US20130197000A1 - Drug and food/drink for preventing or improving cerebral dysfunction - Google Patents

Drug and food/drink for preventing or improving cerebral dysfunction Download PDF

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US20130197000A1
US20130197000A1 US13/642,639 US201113642639A US2013197000A1 US 20130197000 A1 US20130197000 A1 US 20130197000A1 US 201113642639 A US201113642639 A US 201113642639A US 2013197000 A1 US2013197000 A1 US 2013197000A1
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sepiapterin
brain
tetrahydrobiopterin
cells
cerebral dysfunction
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Hiroyuki Hasegawa
Shin Aizawa
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Nihon University
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A23L1/296—
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52—Adding ingredients
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D475/00—Heterocyclic compounds containing pteridine ring systems
    • C07D475/02—Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4
    • C07D475/04—Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4 with a nitrogen atom directly attached in position 2

Definitions

  • the present invention relates to a drug and food/drink which contain sepiapterin for preventing or improving cerebral dysfunction. More specifically, the present invention relates to a drug and food/drink for preventing, improving and treating diseases in which neurotransmitters in the brain are involved, for example, central mental disorders (such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance) or central motor disorders (such as myotonia, rigidity and tremor).
  • central mental disorders such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance
  • central motor disorders such as myotonia, rigidity and tremor
  • the brain is the highest center of information transmission via nerves such as motor and consciousness, playing an important role in human mental activities such as feeling, emotion and reason as well as optional control of motor.
  • the brain is constructed with an innumerable number of neurons, and information between the neurons is transmitted by neurotransmitters in the brain.
  • a monoamine neurotransmitter is a generic name for any non-amino acid neurotransmitter which contains one amino group.
  • a monoamine neurotransmitter biosynthesized in the body from tyrosine or tryptophan of a naturally occurring L-amino acid as a precursor is referred to as an aromatic monoamine.
  • Representative aromatic monoamines include serotonin, noradrenaline, dopamine and adrenaline.
  • Aromatic monoamines are present in the brain and peripheries as well. It is known that aromatic monoamines present in the brain play an important role in transmitting information in the brain and are also deeply involved in control of mental activities, emotion and motor.
  • Serotonin is an aromatic monoamine which is commonly contained in plants and animals including humans and primarily present in chromaffin cells of mucous membranes of the small intestine and in platelets, etc. Serotonin is also partially present in the central nervous system. This substance functions as a neurotransmitter in the central nervous system. Serotonin nerves extend their nerve fibers diversely from nuclei raphes of the medullary to the brain and spinal cord including the hypothalamus, basal ganglion and corpus striatum, thereby greatly influencing mental activities of humans such as emotion, fatigue, pain and appetite.
  • SSRI Serotonin Selective Reuptake Inhibitor
  • Noradrenaline is an aromatic monoamine which is widely present at sympathetic nerve endings and in the central nervous system and also a precursor of adrenaline. This substance works as an adrenocortical hormone and a neurotransmitter at the peripheries. On the other hand, noradrenaline nerves of the locus ceruleus project throughout the brain and it is thought that these are involved in attention, drive impulse, etc. A correlation has also been found with a change in the noradrenaline system with depression.
  • An SNRI (Serotonin and Norepinephrine Reuptake Inhibitor) is a drug which inhibits reabsorption of serotonin and noradrenaline in a synapse, thereby increasing concentration of the neurotransmitters at perineural cavities to improve symptoms of depression. It is thought that this drug not only increases the concentration of serotonin to improve symptoms of depression but also inhibits reabsorption of noradrenaline to stimulate sympathetic nerves, thereby exhibiting effects of enhancing ambition and feeling. However, as in the case of an SSRI, it has been pointed out that an SNRI also decreases the total amount of serotonin in neurons and may exacerbate symptoms of depression on longer administration.
  • Dopamine is an aromatic monoamine present in the central nervous system and also a precursor of adrenaline and noradrenaline.
  • the brainstem ventral tegmental area and nigral dopamine nerves project on the cerebrum frontal lobe, corpus striatum, etc., and are involved in control of motor, regulation of hormones, feelings of pleasure, motivation, learning, etc.
  • Parkinson's disease the nigrostriatal dopamine nerves are decreased to cause motor symptoms such as muscle rigidity, tremor and akinesia. There is an assumption that links dopamine with some forms of schizophrenia and depression.
  • aromatic monoamines some are present in peripheral cells, etc., are present in neurons of the central nervous system.
  • aromatic monoamines in the brain do not pass through the blood-brain barrier but they are synthesized and metabolized independently. That is, no mutual migration or complementation occurs between the aromatic monoamines present in peripheral cells and the aromatic monoamines present in neurons of the central nervous system.
  • aromatic monoamines such as serotonin, noradrenaline and dopamine
  • Tetrahydrobiopterin is a coenzyme of phenylalanine hydroxylase, tyrosine hydroxylase, tryptophan hydroxylase and nitric oxide synthase. This substance is a coenzyme which is essential for enzymatic reactions such as reactions for synthesis of tyrosine from phenylalanine, synthesis of serotonin from tryptophan, synthesis of dopa from tyrosine and synthesis of nitric oxide and citrulline from arginine.
  • the above-described enzymes are incapable of exhibiting catalytic actions sufficiently, if cells are deficient in tetrahydrobiopterin. This causes hyperphenylalaninemia and reduction in bioavailability of monoamine neurotransmitters such as dopamine, noradrenaline and serotonin.
  • tetrahydrobiopterin Diseases caused by defective production of tetrahydrobiopterin include malignant hyperphenylalaninemia and Segawa disease (dopa-responsive dystonia). Furthermore, such a possibility has been suggested that abnormal metabolism of tetrahydrobiopterin may be responsible for or exacerbate depression, hyperphagia, Parkinson's disease, autism, schizophrenia, etc.
  • tetrahydrobiopterin In cases where tetrahydrobiopterin is transmitted from the peripheries to the brain, a part of tetrahydrobiopterin is slightly captured by brain tissues but rapidly discharged outside of brain tissues at a stage that it does not reach aromatic monoamine neurons. That is, tetrahydrobiopterin is extremely difficult in passing through the blood-brain barrier.
  • sepiapterin 7,8-Dihydro-6-[(S)-2-hydroxy-1-oxopropyl]-pterin
  • Sepiapterin is inevitably produced in the human body by auto-oxidation of tetrahydro-6-lactoyl-tetrahydropterin (an intermediate in the synthesis of tetrahydrobiopterin from GTP). However, this substance amounts in trace and is nearly undetectable in blood or urine.
  • Non-Patent Document 2 has disclosed findings on cell membrane transport of a pterin compound.
  • Patent Document 1 has disclosed a pterin-derivative containing drug for treating depression and Parkinson's disease
  • Patent Document 2 has disclosed a tetrahydrobiopterin-containing composition for treating attention deficit hyperactivity disorders and hyperphenylalaninemia
  • Patent Document 3 has disclosed a drug having tetrahydrobiopterin as an active ingredient for treating spinocerebellar degeneration
  • Patent Document 4 has disclosed a cancer metastasis depressant having a pterin derivative as an active ingredient.
  • Non-Patent Document 3 evaluation has been made for monotherapy with tetrahydrobiopterin or sepiapterin given to patients with biopterin metabolism deficiency phenylketonuria.
  • Non-Patent Document 4 evaluation has been made for biosynthesis of biopterin in the brain of a rat.
  • Non-Patent Document 5 it has been demonstrated that aromatic monoamines in the brain are increased in concentration only on peripheral administration of tetrahydrobiopterin at a dose close to a lethal dose.
  • Non-Patent Document 6 is literature covering formulation of a prodrug to be described below
  • Non-Patent Document 7 is literature covering synthesis of sepiapterin to be described below
  • Non-Patent Document 8 is literature covering the Fukushima-Nixon method to be described below
  • Non-Patent Document 9 is literature covering a method for measuring amounts of serotonin, 5-hydroxytryptophan and 5-hydroxyindole acetic acid.
  • peripheral administration of tetrahydrobiopterin facilitates metabolism of phenylalanine, synthesis of aromatic monoamines and synthesis of nitric oxide at the peripheries but hardly facilitates biosynthesis of monoamine neurotransmitters in the brain. This is assumed to be due to the fact that tetrahydrobiopterin hardly passes through the blood-brain barrier and is less likely to pass through cell membranes of aromatic monoamine neurons, even if a small amount of tetrahydrobiopterin reaches the brain.
  • tetrahydrobiopterin is effective in facilitating metabolism of phenylalanine, synthesis of aromatic monoamines and synthesis of nitric oxide at the peripheries but not effective in facilitating synthesis of aromatic monoamines in the brain. That is, in cerebral dysfunction such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance, tetrahydrobiopterin administration hardly improves their symptoms in reality, and is also not practically viable.
  • an object of the present invention is to provide new means for improving symptoms of cerebral dysfunction, for example, central mental disorders (such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance) and central motor disorders (such as myotonia, rigidity and tremor).
  • central mental disorders such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance
  • central motor disorders such as myotonia, rigidity and tremor
  • the inventor has newly found that sepiapterin passes through the blood-brain barrier on peripheral administration of sepiapterin and is taken up into neurons in the brain and also facilitates production of aromatic monoamines in the brain, thereby increasing their bioavailability.
  • the present invention provides a drug which contains at least one of sepiapterin and its salt for preventing or improving cerebral dysfunction, and the invention further provides a food and or drink which contains at least one of sepiapterin and its salt for preventing or improving cerebral dysfunction.
  • sepiapterin is capable of preventing decrease in the levels of aromatic monoamines in the brain (for example, any one of or a plurality of serotonin, dopamine and noradrenaline) in neurons in the brain on peripheral administration and also increasing the bioavailability. Therefore, sepiapterin may be effective against cerebral dysfunction arising from decreased levels of aromatic monoamines in neurons in the brain, for example, central mental disorders such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance or central motor disorders such as myotonia, rigidity and tremor.
  • central mental disorders such as depression, hyperphagia, autism, impaired consciousness and concentration
  • cognitive disturbance or central motor disorders such as myotonia, rigidity and tremor.
  • a mechanism by which the bioavailability of aromatic monoamines in the brain increases by sepiapterin is assumed to be as follows. After peripheral administration, sepiapterin passes through the blood-brain barrier more easily than tetrahydrobiopterin and reaches neurons in the brain by a certain amount. Unlike tetrahydrobiopterin, sepiapterin permeates through cell membranes of neurons in the brain by facilitated transport and is taken up into cells. In the neurons in the brain, sepiapterin is converted to tetrahydrobiopterin through two-step enzymatic reactions by SPR (Sepiapterin Reductase) and DHFR (Dihydrofolate Reductase) present in the cells. Thereby, tetrahydrobiopterin in neurons in the brain is increased in amount, facilitating biosynthesis of aromatic monoamines in the brain and elevating the intracellular level of aromatic monoamines in the brain, thus resulting in an increase in the bioavailability.
  • SPR Sepiapterin Reduct
  • the present invention may be capable of improving symptoms of various types of cerebral dysfunction.
  • Substances necessary for neurons in the brain such as nutrients, humoral regulators and physiologically active substances are supplied from the blood stream (as “blood” in FIG. 1 , and the same shall apply hereinafter) across the blood-brain barrier (“blood-brain barrier” in FIG. 1 , and the same shall apply hereinafter) to neurons (a site described as “monoaminergic neuron” in FIG. 1 , and the same shall apply hereinafter).
  • the blood-brain barrier is mainly constituted of (1) a blood vessel wall in the brain (“blood vessel wall” in FIG. 1 , and the same shall apply hereinafter), (2) a glia cell in the perineural cavity (“perineural cavity” in FIG. 1 , a region between a blood vessel wall and a neuron, the same shall apply hereinafter), etc.
  • a blood vessel wall in the brain (“blood vessel wall” in FIG. 1 , and the same shall apply hereinafter)
  • a glia cell in the perineural cavity (“perineural cavity” in FIG. 1 , a region between a blood vessel wall and a neuron, the same shall apply hereinafter)
  • a substance whose migration to neurons in the brain is restricted by the blood-brain barrier is discharged (1) by active outward transport at blood vessel walls and glia cells after reaching the vicinity of a neuron by physico-chemical diffusion, or discharged (2) from the vicinity of the neuron by finally returning to the blood stream of the brain without being taken up into the neuron after reaching the vicinity of the neuron.
  • a substance taken up into neurons in the brain reaches the neurons first at the perineural cavity (1) by physico-chemical permeation and diffusion at cell membranes or cellular gaps of glia cells, etc., or (2) by cooperative mediation of a transporter protein group present in the glia cells.
  • a substance which has reached a neuron is taken up into the neuron (1) by physico-chemical permeation and diffusion at the cell membrane of the neuron or (2) by cooperative mediation of a transporter protein group present in the neuron.
  • concentration of each substance in a neuron is determined for each substance, a substance which has been taken up into the neuron and thereafter rapidly metabolized is further taken up continuously depending on an amount that has been metabolized.
  • serotonin is metabolized by the following mechanism as shown in FIG. 1 .
  • tryptophan of L-amino acid (“Tryptophan” in FIG. 1 and the same shall apply hereinafter) is taken up from the blood stream via the blood-brain barrier into the monoaminergic neuron.
  • This tryptophan is converted to 5-hydroxytryptophan (“5HTP” in FIG. 1 and the same shall apply hereinafter) by actions of tryptophan hydroxylase (“TPH” in FIG. 1 and the same shall apply hereinafter) and a coenzyme thereof, that is, tetrahydrobiopterin (“BH4” in FIG.
  • 5-hydroxytryptophan is a substance which is now used as the drug of first choice on peripheral administration to a patient with tetrahydrobiopterin deficiency for the purpose of increasing the amount of serotonin in the brain. It is known that, as with tryptophan, 5-hydroxytryptophan is taken up into an aromatic monoaminergic neuron from the blood stream via the blood-brain barrier on peripheral administration.
  • Biosynthesized serotonin is taken up into neurotransmitter-releasing granules in an aromatic monoaminergic neuron and released outside of the cell.
  • serotonin does not migrate to the blood stream but remains in the brain and (1) is again taken up into the releasing granules in the aromatic monoaminergic neuron mediated by a serotonin transporter (“SERT” in FIG. 1 and the same shall apply hereinafter) and (2) flows out to the blood stream mediated by an organic anion transporter or others after being subjected to metabolic deactivation by 5HIAA by actions of monoamine oxidase (“MAO” in FIG. 1 and the same shall apply hereinafter).
  • SERT serotonin transporter
  • MAO monoamine oxidase
  • Aromatic monoamines in the brain are in principle do novo synthesized and metabolized therein without passing through the blood-brain barrier.
  • aromatic monoamines in the brain are biosynthesized and accumulated in neurons in the brain. Release of aromatic monoamines into perineural cavities, reuptake into the neurons and metabolic deactivation is also carried out in the brain. Metabolic deactivation is carried out primarily in glia cells and partially in neurons.
  • an appropriate level of aromatic monoamines in the brain is determined by a balance of various factors such as the rate of biosynthesis in the brain, accumulation at releasing granules, synaptic release into pericellular cavities by neurons, reuptake and metabolic deactivation.
  • Tetrahydrobiopterin (BH4) is a coenzyme which is essential in action of tryptophan hydroxylase (TPH). Tetrahydrobiopterin (BH4) is capable of passing through a blood vessel wall in the blood-brain barrier at a rate similar to 5-hydroxytryptophan (5HTP) but is taken up very little by glia cells, etc., present in a perineural cavity. Furthermore, since tetrahydrobiopterin (BH4) is present substantially at a constant level in neurons, it is taken up very little into the neurons even when elevation of the concentration of tetrahydrobiopterin (BH4) elevates near the neurons. Therefore, as shown in FIG. 1 , it is thought that the majority of tetrahydrobiopterin (BH4) is not taken up into glia cells or neurons after reaching the vicinity of the neurons and thereafter finally returns to the blood stream in the brain.
  • TPH tryptophan hydroxylase
  • sepiapterin As shown in FIG. 1 , sepiapterin (“SP” in FIG. 1 and the same shall apply hereinafter) is peripherally administered, passes through the blood-brain barrier after reaching the brain by the blood stream and is taken up into a monoaminergic neuron. In the monoaminergic neuron, sepiapterin is converted to tetrahydrobiopterin (BH4) via dihydrobiopterin (“BH2” in FIG. 1 ) and facilitates biosynthesis of serotonin and release thereof as a coenzyme of tryptophan hydroxylase (TPH) which is the rate limiting enzyme.
  • BH4 tetrahydrobiopterin
  • BH2 dihydrobiopterin
  • TPH tryptophan hydroxylase
  • Sepiapterin (SP) passes through the blood vessel wall in the blood-brain barrier at a rate substantially similar to 5-hydroxytryptophan (5HTP) and is also taken up by glia cells, etc., present at a perineural cavity 10 times or more efficiently than tetrahydrobiopterin (BH4). Therefore, sepiapterin (SP) is thought to reach neurons in a greater amount than tetrahydrobiopterin (BH4).
  • 5HTP 5-hydroxytryptophan
  • BH4 tetrahydrobiopterin
  • sepiapterin SP
  • BH4 tetrahydrobiopterin
  • BH2 dihydrobiopterin
  • sepiapterin in the neuron is kept relatively low in concentration.
  • sepiapterin is continuously further taken up by the amount which has been converted to tetrahydrobiopterin (BH4).
  • sepiapterin is thought to be taken up into the neuron in a greater amount than tetrahydrobiopterin (BH4).
  • peripheral supply of sepiapterin (SP) makes it possible to keep tetrahydrobiopterin (BH4) in a neuron in a greater amount than peripheral supply of tetrahydrobiopterin (BH4). Therefore, it is possible to activate tryptophan hydroxylase (TPH) more effectively and facilitate the biosynthesis of serotonin and release thereof.
  • Drugs such as an SSRI and an SNRI are those which increase the level of serotonin at a perineural cavity in the brain by inhibiting reuptake of serotonin by a serotonin transporter (SERT).
  • SERT serotonin transporter
  • a monoamine oxidase inhibitor is a drug which increases the level of serotonin in the brain by suppressing metabolic deactivation caused by monoamine oxidase (MAO).
  • the present invention covers a wide variety of drugs which contain at least one of sepiapterin and its salt for preventing, improving and treating cerebral dysfunction.
  • sepiapterin means 7,8-dihydro-6-[(S)-2-hydroxy-1-oxopropyl]-pterin.
  • An oxo group present in a substituent arranged in the 6-position of pterin may play an important role in allowing sepiapterin to pass through the blood-brain barrier. Therefore, if such a structure is kept that the oxo group is retained in the substituent to effect intracellular conversion to tetrahydrobiopterin, any drug, the structure of which is partially modified, is also included in sepiapterin of the present invention.
  • isosepiapterin (7,8-dihydro-6-[(S)-2-oxo-1-hydroxypropyl]-pterin) is different in position of an oxo group but has an oxo group in the substituent, as with sepiapterin, and also maintains a structure which can be converted to tetrahydrobiopterin by actions of enzymes in the body such as sepiapterin reductase, aldose reductase and dihydrofolate reductase. Therefore, in the present invention, isosepiapterin is included in sepiapterin of the present invention as a compound similar to sepiapterin.
  • the drug of the present invention includes not only sepiapterin in itself and similar products (such as isosepiapterin) but also pharmaceutically acceptable salts and solvates.
  • the salts include alkaline metal salts (such as sodium salt, potassium salt and lithium salt), alkaline earth metal salts (such as calcium salt, magnesium salt and lithium salt), metal salts (such as aluminum salt, iron salt, zinc salt, copper salt and nickel salt), inorganic salts (such as phosphate, sulfate, hydrobromate, ammonium salt), organic acid salts (such as methanesulfonate, p-toluenesulfonate, lactate, acetate, trifluoroacetate, citrate, succinate, fumarate, maleate and salicylate), organic amine salts (such as methylamine salt, dimethylamine salt, trimethylamine salt, ethylenediamine salt, diethylamine salt, triethylamine salt, ethanolamine salt, diethanolamine salt, dibenzyl
  • the drug of the present invention also includes a prodrug composed of a compound having at least one of the protective groups which are pharmacologically acceptable and dissociable under physiological conditions.
  • the prodrug is made available by a publicly known method (for example, refer to Non-Patent Document 6).
  • the prodrug is made available by adding free carboxylic acid, an alkoxy group (for example, ethoxy group), phenalkyloxy group (for example, benzyloxy group), OCH (R a ) OCOR b group (for example, pivaloyloxymethyloxy group), OCH(R a ) OCO 2 R b group (for example, [[(1-methylethoxy) carbonyl]oxy]ethylester group and proxetil group), OCH(R a )OR b group, 2-alkyl group, 2-cycloalkyl group, 2-cycloalkyl alkyl group, oxycarbonyl-2-alkylidene-ethoxy group, 5-alkyl[1,3]dioxyl-2-on-oil-methyloxy group, dialkylamino-alkoxyl group, and acryloxy group (R a is a hydrogen atom or (C 1 -C 4 ) alkyl group, and R b is any one of
  • a protective group such as sulphate (OSO 3 H), phosphate (OPO 3 H 3 ), oxymethylene phosphate (OCH 2 OPO 3 H 3 ), succinate ester (OCOCH 3 CH 3 COOH), ester of dimethylaminoglycine, a natural amino acid, an inorganic salt or others is added to make the prodrug available.
  • the drug of the present invention is not in particular restricted to the dosage form.
  • the drug is available, for example, in solid preparations (such as tablets, capsules, granules, powders, and sustained-release tablets) and liquid preparations (such as syrups and injections).
  • a carrier which is pharmacologically acceptable may be used to formulate a compound of the present invention into a drug.
  • the carrier includes a variety of organic and inorganic carrier substances which are commonly used as pharmaceutical ingredients.
  • a diluting agent, a smoothing agent, a binder, a disintegrating agent, etc. are formulated into the drug of the present invention and its carrier.
  • a solvent, a solubilizing agent, a suspending agent, an isotonic agent, a buffering agent, a soothing agent, etc. are appropriately formulated into the drug of the present invention and its carrier.
  • pharmaceutical additives such as an antiseptic, an antioxidant agent, a coloring agent and a sweetening agent may be added whenever necessary.
  • a preferable diluting agent includes, for example, lactose, sucrose, D-mannitol, starch, crystalline cellulose and light silicic anhydride.
  • a preferable smoothing agent includes, for example, magnesium stearate, calcium stearate, talc and colloidal silica.
  • a preferable binder includes, for example, crystalline cellulose, sucrose, D-mannitol, dextrin, hydroxypropyl cellulose, hydroxypropylmethyl cellulose and polyvinyl pyrrolidone.
  • a preferable disintegrating agent includes, for example, starch, carboxymethyl cellulose, carboxymethyl cellulose calcium, croscarmellose sodium and sodium carboxylmethyl starch.
  • a preferable solvent includes, for example, injection solvent, alcohol, propylene glycol, macrogol, sesame oil and corn oil.
  • a preferable solubilizing agent includes, for example, polyethylene glycol, propylene glycol, D-mannitol, benzyl benzoate, ethanol, trisaminomethane, cholesterol, triethanolamine, sodium carbonate and sodium citrate.
  • a preferable suspending agent includes, for example, surface active agents (such as stearyltriethanolamine, sodium lauryl sulfate, laurylamino propionate, lecithin, benzalkonium chloride, benzethonium chloride and glyceryl monostearate) and hydrophilic high polymers (such as polyvinyl alcohol, polyvinyl pyrrolidone, sodium carboxymethyl cellulose, methylcellulose, hydroxymethyl cellulose, hydroxyethyl cellulose and hydroxypropyl cellulose).
  • surface active agents such as stearyltriethanolamine, sodium lauryl sulfate, laurylamino propionate, lecithin, benzalkonium chloride, benzethonium chloride and glyceryl monostearate
  • hydrophilic high polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, sodium carboxymethyl cellulose, methylcellulose, hydroxymethyl cellulose, hydroxyethyl
  • a preferable isotonic agent includes, for example, sodium chloride, glycerin and D-mannitol.
  • a preferable buffering agent includes, for example, buffering solutions of phosphate, acetate, carbonate, citrate, etc.
  • a preferable soothing agent includes, for example, benzyl alcohol.
  • a preferable antiseptic includes, for example, p-parahydroxybenzoate esters, chlorobutanol, benzyl alcohol, phenethyl alcohol, dehydroacetic acid and sorbic acid.
  • a preferable antioxidant agent includes, for example, sulfite and ascorbic acid.
  • the drug of the present invention may contain auxiliaries, for example, a light absorption pigment helpful in storage and efficacy retention (such as riboflavin, adenine and adenosine), a chelating agent/reducing agent for stabilization (such as vitamin C and citric acid), an amino acid substrate which enhances effects of sepiapterin in the brain (such as tryptophan) and analogous substances (such as tetrahydrobiopterin and dihydrobiopterin).
  • auxiliaries for example, a light absorption pigment helpful in storage and efficacy retention (such as riboflavin, adenine and adenosine), a chelating agent/reducing agent for stabilization (such as vitamin C and citric acid), an amino acid substrate which enhances effects of sepiapterin in the brain (such as tryptophan) and analogous substances (such as tetrahydrobiopterin and dihydrobiopterin).
  • the drug of the present invention can be produced according to common procedures in which sepiapterin is allowed to be contained usually in a range of 0.1 to 99% (w/w) with respect to a total amount of formulation.
  • the indications are not in particular restricted and may include any type of cerebral dysfunction which is decreased in the intracellular level of aromatic monoamines in the brain.
  • Cerebral dysfunction may be prevented, improved and treated by, for example, administration of sepiapterin at an effective dose to patients with cerebral dysfunction.
  • the drug of the present invention is applicable to mammals (for example, humans, horses, cattle, dogs, cats, rats, mice, pigs and monkeys).
  • the drug can be administered orally, for example, as tablets, capsules (including soft capsules and micro-capsules), powders and granules, or parenterally as injections, suppositories and pellets.
  • Parenteral administration includes intravenous, intramuscular, subcutaneous, intraorgan, intranasal, intradermal, eye drop, intracerebral, intrarectal, vaginal and intraperitoneal administrations.
  • the drug of the present invention varies in dosage, depending on an administration route and symptoms.
  • the drug On intravenous administration to a patient, the drug is administered once daily at a dose of 0.1 to 100 mg/kg ⁇ the body weight.
  • the drug is given at this dose once daily or in one to three divided doses.
  • the drug of the present invention may be administered solely or concomitantly with other drugs, depending on the aim, usage or symptoms.
  • an SSRI and an SNRI have certain medicinal benefits.
  • aromatic monoamines may be decreased in amount on long-term administration.
  • sepiapterin may also be possible to improve effects of sepiapterin in combination with, for example, an inhibitor of a retrograde transporter which prevents intracerebral migration of sepiapterin or an inhibitor of an extravert transporter which shortens the retention time of tetrahydrobiopterin in the brain by administration of sepiapterin.
  • probenecid which is a renal excretion-type inhibitor is capable of prolonging in vivo retention of tetrahydrobiopterin at the peripheries. Therefore, it may be possible to increase the effect or prolong the retention time by using the drug of the present invention together with the renal excretion-type inhibitor.
  • the renal excretion-type inhibitor includes, for example, probenecid, immunomodulators (such as cyclosporine A, FK506 and thymosin ⁇ -1), cytokines (such as TNF and TGF- ⁇ ), interferons (IFN- ⁇ , IFN- ⁇ , IFN- ⁇ ), interleukins (such as interleukins 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 13), macrophage/granular cell colony stimulating factors (such as GM-CSF, G-CSF and M-CSF), erythropoietin, cytokine antagonists (such as reticulose, ADA, AMD-3100, anti-TNF antibody, anti-interleukin antibody, soluble interleukin receptor and proteinkinase C inhibitor), nucleotide transporting inhibitors (such as dipyridamole, pentoxifylline, N-acetylcysteine (NAC), procysteine, ⁇ -trichosanthin, phosphonoformic acid
  • the present invention includes any food/drink for preventing, improving and treating cerebral dysfunction which contains at least one of sepiapterin and its salt as an active ingredient.
  • Sepiapterin and its salt are allowed to contain in, for example, health-promoting food (such as specified health-promoting food and food with nutrient function claims), that is, so-called health-conscious food/drink and other various types of food/drink. Furthermore, sepiapterin and its salt can be formulated into various types of seasoning, etc.
  • the food/drink is not in particular restricted to its form and may be available in liquid, half-solid and solid products. Specifically, it may be available, for example, as confectionery such as cookies, senbei (rice cracker), jelly, yokan (sweat jelly of beans), yogurt and manjyu (bean-jamfilled bun), refreshing drinks, energy drinks and soups. It may also be available as a tea by infusion. Furthermore, the above-described drug may be added by mixture, coating or spraying, for example, in the process of manufacturing the food/drink of the present invention or to final products, thereby providing a health-conscious food/drink. Still furthermore, it may be allowed to be contained in a product that is temporarily kept in the mouth, for example, toothpaste, breath fresheners, chewing gum and mouthwash.
  • Sepiapterin of the present invention can be produced in accordance with a publicly known method. And, the method thereof is not restricted in particular.
  • Sepiapterin is also produced by utilizing the above synthesis system on the basis of organic synthesis. That is, a mixture of tetrahydrobiopterin with the 6th-class diastereomer (6R/6S) is synthesized, thereafter, the mixture is oxidized to produce a crude sepiapterin sample, and the sample is purified to produce sepiapterin (as for an example of the sepiapterin synthesizing method, refer to Non-Patent Document 7, for example). It is noted that, unlike tetrahydrobiopterin, since sepiapterin bears achiral in the 6th-class, it is possible to omit the step of chiral separation in a method for producing sepiapterin.
  • Example 1 where PC12 cells and RBL2H3 cells were used as aromatic monoamine synthesizing cells and sepiapterin was added to a culture medium, evaluation was made for a total amount of biopterin in the cells (a total amount of tetrahydrobiopterin, and its oxidant, dihydrobiopterin and biopterin, the same shall apply hereinafter).
  • the PC12 cells are cultured cells having properties of a neuron and it is known that they synthesize dopamine, noradrenaline and adrenaline, with tetrahydrobiopterin used as a coenzyme.
  • the RBL2H3 cells are cultured cells having properties of a mast cell and it is known that they synthesize serotonin, with tetrahydrobiopterin used as a coenzyme.
  • both cells are capable of synthesizing tetrahydrobiopterin and also retain a certain amount of tetrahydrobiopterin in the cells but do not retain a saturated amount thereof. Furthermore, unlike cells which are not capable of synthesizing aromatic monoamines by themselves but take up aromatic monoamines extracellularly and capable of secreting aromatic monoamines in response to stimulation (for example, platelets are not capable of synthesizing serotonin by themselves but take up serotonin extracellularly and are capable of secreting serotonin in response to stimulation), both cells are capable of synthesizing aromatic monoamines by themselves. In the present example, the inventor, etc., judged that these cells were suitable as models of aromatic monoamine synthetic cells and used them accordingly.
  • the PC12 cells and the RBL2H3 cells were obtained from the JCRB Cell Bank (National Institute of Biomedical Innovation, Japan).
  • the PC12 cells were sub-cultured in a DMEM medium (Dulbecco's Modified Eagle Medium; Dulbecco's medium, and the same shall apply hereinafter) containing 7% bovine fetal serum and 7% horse serum.
  • DMEM medium Dulbecco's Modified Eagle Medium
  • bovine fetal serum 7% horse serum.
  • the cells were plated on a 96-well polylysine-coated plate at 2 ⁇ 10 5 per well, the culture medium was replaced by a serum-free DMEM medium one hour before start of the experiment on the following day to carry out the following uptake experiment.
  • the RBL2H3 cells were cultured in a DMEM medium containing 10% bovine fetal serum and plated on a 96-well coating-free plate at 1 ⁇ 10 5 per well. Similarly, one hour before start of the experiment on the following day, the culture medium was replaced by a serum-free DMEM medium to carry out the following uptake experiment.
  • Sepiapterin or tetrahydrobiopterin was added to the respective media of the PC12 cell and the RBL2H3 cell so as to give a final concentration of 100 ⁇ M.
  • a total amount of biopterin in the cells was measured by using a system of high performance liquid chromatography/fluorescence detection (HPLC/FD) according to the Fukusima-Nixon method (refer to Non-Patent Document 8).
  • HPLC/FD high performance liquid chromatography/fluorescence detection
  • a principle of the Fukushima-Nixon method is as follows. Upon oxidation with iodine under strong acid or alkaline conditions, tetrahydrobiopterin is quantitatively oxidized into oxidized-form biopterin under acid conditions and oxidized into oxidized-form pterin in which a side chain in the 6th-class position is removed under alkaline conditions. Dihydrobiopterin is oxidized into oxidized-form biopterin irrespective of pH conditions. The oxidized-form biopterin and the oxidized-form pterin have strong natural fluorescent characteristics (excitation: 350 nm, fluorescence: 450 nm).
  • the same sample is divided into two portions, and one of them and the other are oxidized with iodine respectively under acid conditions and alkaline conditions.
  • An amount of the oxidized-form biopterin is compared with that of the oxidized-form pterin on fluorescence detection after quantitative determination, thus making it possible to determine the respective amounts of tetrahydrobiopterin and dihydrobiopterin in an original sample.
  • the thus prepared sample was used in the system of high performance liquid chromatography/fluorescence detection. And, the oxidized-form biopterin and the oxidized-form pterin were quantitatively determined according to an external standard comparison method. Then, calculated was an amount of tetrahydrobiopterin and a total amount of biopterin in the cells.
  • “Fine-SIL-C18-5T made by JASCO Corporation
  • a 7% aqueous methanol solution was used as an eluent.
  • An FP model made by JASCO Corporation was used to carry out fluorescence detection.
  • the respective cells used in the present example contain by nature oxidized-form biopterin and oxidized-form pterin only in a trace amount. The experiment was done on the assumption that they were not present.
  • Sepiapterin is not metabolized in the cells by uptake in a period of time during which the experiment was performed except for dihydrobiopterin, irrespective of whether it is exogenous or endogenous.
  • Dihydrobiopterin in the cells is reduced by dihydrofolate reductase to tetrahydrobiopterin but some of dihydrobiopterin remains in the cells. It is found that reactions other than reduction of dihydrobiopterin to tetrahydrobiopterin and decomposition of tetrahydrobiopterin hardly take place in a period of time during which the experiment was performed.
  • Non-Patent Document 1 On the basis of the above findings, a sum of the amount of dihydrobiopterin and the amount of tetrahydrobiopterin was given a total amount of biopterin in the cells.
  • FIG. 2A and FIG. 2B show the results.
  • FIG. 2A is a graph which shows the change in the total amount of biopterin in the PC12 cells with the lapse of time
  • FIG. 2B is a graph which shows a change in the total amount of biopterin in the RBL2H3 cells with the lapse of time.
  • a longitudinal axis indicates the number of moles of a total amount of biopterin per cell population 1 ⁇ 10 6 (total BP, unit: nmol/10 6 cells), while a horizontal axis indicates time after addition of sepiapterin or tetrahydrobiopterin (Time, unit: min).
  • tetrahydrobiopterin was hardly taken up into aromatic monoamine synthetic cells on addition of tetrahydrobiopterin, and there was observed substantially no change in the total amount of biopterin in the cells.
  • sepiapterin was taken up into the aromatic monoamine synthetic cells on addition of sepiapterin and converted to tetrahydrobiopterin in the cells, therein the total amount of biopterin was increased in the cells.
  • the results of the present example have suggested that, on peripheral administration of sepiapterin to animals including humans, unlike tetrahydrobiopterin, sepiapterin passes through the cell membrane of an aromatic monoamine neuron after passing through the blood-brain barrier. And, sepiapterin is taken up into the cells and converted to tetrahydrobiopterin in the cells, thereby facilitating biosynthesis of aromatic monoamines.
  • Example 2 a cell system of a brain blood vessel wall model was used to compare passage of sepiapterin with that of tetrahydrobiopterin across a blood vessel wall.
  • BBB kit As the brain blood vessel wall model, there was used a “BBB kit, RBT24H (made by PharmaCo-Cell Company Ltd. in Japan).”
  • This kit was a model system in which rat vascular endothelical cells were cultured on a porous synthetic resin film having small pores of 3 ⁇ m in inner diameter to form tight intercellular junctions, thereby forming the blood vessel wall.
  • pericytes were cultured in advance on the back side of the porous synthetic resin film and astroglia cells were also cultured at the same time in the well below the film, thereby forming the intercellular tight junctions of vascular endothelical cells.
  • a cultured area was 0.3 cm 2 per well.
  • the cell sheet, an upper side of the cell sheet and a lower side of the cell sheet respectively correspond to the blood vessel wall, an intravascular cavity (lumen) and a perineural cavity in the brain (albumen).
  • each of tetrahydrobiopterin (BH4), sepiapterin (SP) and 5-hydroxytryptophan (5HTP) was dissolved in the upper side of the cell sheet corresponding to the intravascular lumen by using a physiological balanced salt and added at a concentration of 100 ⁇ M. After 30 minutes, each of them was measured for an amount which migrated downward to the cell sheet.
  • BH4 tetrahydrobiopterin
  • SP sepiapterin
  • 5HTP 5-hydroxytryptophan
  • An amount of sepiapterin (SP) was calculated according to an external standard comparison method by treating samples by a system of high performance liquid chromatography/fluorescence detection.
  • SP sepiapterin
  • Example 1 “Fine-SIL-C18-5T (made by JASCO Corporation)” was used as a column, and a 14% aqueous methanol solution was used as an eluent.
  • Fluorescence detection was carried out by setting the exciting wavelength and the fluorescence wavelength to be 412 nm and 527 nm respectively to make measurement using an FP model made by JASCO Corporation.
  • An amount of 5-hydroxytryptophan (5HTP) was calculated according to an internal standard comparison method using N-methyl serotonin by treating samples in the system of high performance liquid chromatography/fluorescence detection (refer to Non-Patent Document 9).
  • high performance liquid chromatography as with Example 1, “Fine-SIL-C18-5T (made by JASCO Corporation)” was used as a column.
  • Formic acid was added to a 40 mM aqueous sodium acetate solution, thereby adjusting pH to 3.5, and the aqueous sodium acetate solution, acetonitrile and methanol were mixed in a volume ratio of 100:10:5 to prepare a solution, and the solution was used as an eluent.
  • Fluorescence detection was carried out by setting the exciting wavelength and the fluorescence wavelength to be 302 nm and 350 nm respectively to make measurement using an FP model made by JASCO Corporation.
  • 5-hydroxytryptophan is a substance which is now used as a drug of the first choice on peripheral administration to patients with tetrahydrobiopterin deficiency for the purpose of increasing the amount of serotonin in the brain.
  • FIG. 3 shows the results.
  • FIG. 3 is a graph which shows an amount of downward migration of each of tetrahydrobiopterin (BH4), sepiapterin (SP) and 5-hydroxytryptophan (5HTP) added over the upper side of the cell sheet of the brain blood vessel wall model.
  • a horizontal axis indicates the respective results on addition of tetrahydrobiopterin (BH4), sepiapterin (SP) and 5-hydroxytryptophan (5HTP)
  • a longitudinal axis indicates the amount of downward migration to the lower face of the cell sheet (unit: pmol/well/30 min).
  • Each value was subjected to the Student t-test (p ⁇ 0.05).
  • tetrahydrobiopterin (BH4) and sepiapterin (SP) were similar to 5-hydroxytryptophan (5HTP) in the amount of migration to the lower side of the cell sheet. That is, the results have suggested that tetrahydrobiopterin (BH4) and sepiapterin (SP) are capable of passing through blood vessel walls which constitute the blood-brain barrier at a rate substantially similar to 5-hydroxytryptophan (5HTP).
  • Example 3 comparison was made between sepiapterin and tetrahydrobiopterin in terms of uptake into astroglia cells.
  • the astroglia cells are major glia cells and present tightly around vessels of the brain. This cell selectively takes up a substance which has passed through the blood vessel walls of the brain and supplies the substance to neurons.
  • CTX TNA2 cells that is, cultured cells derived from the astroglia cells, were used to evaluate the uptake of sepiapterin and that of tetrahydrobiopterin into the astroglia cells. It is noted that the CTX TNA2 cells used were obtained from the ATCC in the U.S.A. (American Type Culture Collection).
  • the CTX TNA2 cells were inoculated at 1 ⁇ 10 5 per well.
  • sepiapterin was added at 50 ⁇ M or tetrahydrobiopterin was added at 100 ⁇ M, each of which was cultured for 0, 5, 10, 20, 40 and 60 minutes.
  • FIG. 4A and FIG. 4B show the results.
  • FIG. 4A is a graph which shows the amounts of sepiapterin (SP), dihydrobiopterin (BH2) and tetrahydrobiopterin (BH4) accumulated in the cells on addition of sepiapterin (SP).
  • FIG. 4B is a graph which shows the amounts of dihydrobiopterin (BH2) and tetrahydrobiopterin (BH4) on addition of tetrahydrobiopterin (BH4).
  • a horizontal axis indicates cultivation time after addition of sepiapterin or tetrahydrobiopterin.
  • a longitudinal axis indicates the amounts of sepiapterin (SP), dihydrobiopterin (BH2) and tetrahydrobiopterin (BH4) which were quantitatively determined (unit: pmol/10 6 cells).
  • the blood-brain barrier is primarily formed with blood vessel walls and glia cells.
  • Astrocytes a major type of glia cell, selectively take up a substance which has passed through blood vessel walls of the brain and supply the substance to neurons. Therefore, it is thought that the substance which has passed through the blood vessel walls and has been taken up by astroglia cells will reach neurons.
  • Example 2 The results of Example 2 and the present example revealed that sepiapterin was substantially similar to tetrahydrobiopterin in amount which has passed through the blood vessel walls further sepiapterin was at least 10 times greater in amount taken up in glia cells than tetrahydrobiopterin.
  • sepiapterin passes through the blood-brain barrier at least 10 times more easily than tetrahydrobiopterin. That is, when the results of Example 1 are also taken into account, sepiapterin passes through the blood-brain barrier more easily than tetrahydrobiopterin on peripheral administration and is also easily taken up by aromatic monoamine neurons.
  • Example 4 rats were used to measure amounts of tetrahydrobiopterin, serotonin and 5-hydroxyindoleacetic acid in the brain on administration of sepiapterin.
  • 5-hydroxyindoleacetic acid which is a metabolic product of serotonin, is thought to be metabolized and converted from serotonin mainly in glia cells or serotonin-producing cells.
  • 5-hydroxyindoleacetic acid was also measured as an index of the bioavailability of an aromatic monoamine (serotonin) in the brain.
  • Rats used were SD rats (7-8 week old, males) purchased from Japan SLC, Inc. The rats were kept in a dark place for 12 hours and in a light place for 12 hours and fed ad libitum with a diet (“MM-3” made by Funabashi Farm Co., Ltd.) and sterilized tap water as drinking water.
  • MM-3 made by Funabashi Farm Co., Ltd.
  • An amount of tetrahydrobiopterin in the brain was measured and calculated according to a method similar to Example 1 by adding 5 times the volume of 100 mM hydrochloric acid to a left brain sample, homogenizing brain tissues and utilized the supernatant solution.
  • Amounts of serotonin and 5-hydroxyindoleacetic acid in the brain were calculated by adding 3.5 times the volume of 1.43% ascorbic acid-containing 100 mM hydrochloric acid which contains N-methyl serotonin as an internal standard to a right brain sample, homogenizing brain tissues, adding potassium perchlorate (final concentration of 5.5%) thereto, ice-cooling the resultant for removing protein and treating a supernatant thereof in a system of high performance liquid chromatography/fluorescence detection (HPLC/FD), (refer to Non-Patent Document 9).
  • HPLC/FD high performance liquid chromatography/fluorescence detection
  • Example 2 As with Example 2, formic acid was added to a 40 mM aqueous sodium acetate solution, thereby adjusting pH to 3.5. Then, the aqueous sodium acetate solution, acetonitrile and methanol were mixed in a volume ratio of 100:10:5 to prepare a solution, and the solution was used as an eluent. As with Example 1, etc., fluorescence detection was carried out by setting the exciting wavelength and the fluorescence wavelength to be 302 nm and 350 nm respectively and making measurement using an FP model made by JASCO Corporation.
  • FIG. 5A The results are shown in FIG. 5A , FIG. 5B , and FIG. 5C .
  • FIG. 5A is a graph which shows change in the amount of tetrahydrobiopterin in the brain with the lapse of time after administration of sepiapterin.
  • a longitudinal axis indicates an amount of tetrahydrobiopterin (BH4, unit: nmol/g brain), and a horizontal axis indicates time after administration of tetrahydrobiopterin or sepiapterin (time, unit: hour).
  • black circles indicate results on addition of sepiapterin (SP), and white circles indicate results on addition of tetrahydrobiopterin (BH4).
  • SP sepiapterin
  • BH4 tetrahydrobiopterin
  • a group treated with tetrahydrobiopterin did not show an increase in the amount of tetrahydrobiopterin in the brain, while a group treated with sepiapterin showed a significant increase in the amount of tetrahydrobiopterin in the brain.
  • peripheral administration of sepiapterin increases the amount of tetrahydrobiopterin in the brain.
  • peripheral administration of tetrahydrobiopterin at the same dose does not increase the amount of tetrahydrobiopterin in the brain.
  • FIG. 5B is a graph which shows change in the amount of serotonin in the brain with the lapse of time after administration of sepiapterin.
  • FIG. 5C is a graph which also shows change in the amount of 5-hydroxyindoleacetic acid (5HIAA) in the brain with the lapse of time.
  • a horizontal axis indicates time from administration of tetrahydrobiopterin or sepiapterin (time, unit: hour) and a longitudinal axis indicates an amount of serotonin (5HT, unit: nmol/g brain) or that of 5-hydroxyindoleacetic acid (5HIAA, unit: nmol/g brain).
  • Example 1 As described above, the results of Example 1 and the present experiment have strongly suggested a series of action mechanisms in which, on peripheral administration of sepiapterin, sepiapterin passes through the blood-brain barrier by a certain amount, reaches the brain, also passes through cell membranes of aromatic monoamine neurons, then, is taken up into aromatic monoamine neurons in the brain, converted to tetrahydrobiopterin in the neurons, and the tetrahydrobiopterin effectively contributes to the synthesis of serotonin, thereby increasing the amount of serotonin in the brain.
  • peripheral administration of tetrahydrobiopterin at the same dose will not enhance the series of action mechanisms in the brain.
  • mice were used to measure the amount of serotonin (5HT) in the brain after administration of sepiapterin.
  • mice used were those of “hph-1” which were provided by Dr. K. Hyland (Institute of Metabolic Disease, Baylor University Medical Center, Dallas, Tex. 75226, USA).
  • the mice are characterized as being defective in biosynthesis functions of tetrahydrobiopterin, with the level of tetrahydrobiopterin in the brain being from 40 to 50% as compared with ordinary mice.
  • the mice were bred in a dark place for 12 hours and also in a light place for 12 hours and fed ad libitum with a diet (“MM-3” made by Funabashi Farm Co., Ltd.) and sterilized tap water as drinking water.
  • MM-3 made by Funabashi Farm Co., Ltd.
  • Measurement of the amount of serotonin was made by obtaining brain samples according to a method similar to Example 4, treating the samples in a system of high-performance liquid chromatography/fluorescence detection (HPLC/FD) after dissolution of the samples and protein removal from them, and setting the excited wavelength and the fluorescence wavelength to be 302 nm and 350 nm respectively. In a control group, measurement was made similarly by orally administering 0.01M hydrochloric acid.
  • HPLC/FD high-performance liquid chromatography/fluorescence detection
  • FIG. 6 shows the results.
  • FIG. 6 is a graph which shows the amount of serotonin in the brain after administration of sepiapterin.
  • a longitudinal axis indicates the amount of serotonin (5HT, unit: nmol/g brain)
  • v-cont shows the results of a control group
  • BH4 shows the results on administration of tetrahydrobiopterin
  • SP shows the result on administration of sepiapterin, respectively.
  • an asterisk shows a significant difference found by t-test (p ⁇ 0.05).
  • a group treated with sepiapterin showed a significant increase in serotonin in the brain as compared with a group treated with tetrahydrobiopterin. That is, the results show that, as with Example 4, a significant increase in the level of an aromatic monoamine in the brain (serotonin) was observed on administration of sepiapterin in the experiment with mice as well.
  • Example 4 and the present example showed that peripheral administration of sepiapterin increased the amount of serotonin in the brain but peripheral administration of tetrahydrobiopterin at the same dose did not increase the amount.
  • Example 4 It is known that intracerebral biosynthesis, release, reuptake and metabolism of dopamine whose starting material is tyrosine of aromatic amino acid are also based on a synthesis amount of dopamine at dopaminergic neurons and dopamine biosynthesis is restricted by the amount of intracellular tetrahydrobiopterin. Therefore, the results of Example 4 and the present example have suggested that dopamine as well as noradrenaline and adrenaline synthesized from dopamine are also increased in intracerebral levels thereof on peripheral administration of sepiapterin. That is, the above results have suggested that peripheral administration of sepiapterin may also be effective in improving central mental disorders and central motor disorders which are involved in decreased levels of dopamine, noradrenaline and adrenaline in the brain.
  • Example 6 the mice were subjected to a forced swim test after administration of sepiapterin.
  • the forced swim test of the mice is a test method for evaluating antidepressant effects, and length of “immobile” time is a criterion of depression. Evaluation is made in such a manner that the shorter the “immobile” time is, the greater the antidepressant effects are.
  • mice used were NZB mice purchased from Japan SLC, Inc (7-week old males). The mice were maintained in a dark place for 12 hours and in a light place for 12 hours and fed ad libitum with a diet (“MM-3” made by Funabashi Farm Co., Ltd.) and sterilized tap water as drinking water, except when they were constrained in an experiment.
  • MM-3 made by Funabashi Farm Co., Ltd.
  • mice are characterized in that they are more likely to develop an auto-immune disease with advancement of age. However, in the present experiment, the mice did not exhibit symptoms of the disease when being used in the experiment (7-week old). The mice which had been subjected to 15-minute preliminary swimming without administration of a drug, etc., on the previous day were used in the experiment.
  • the test was conducted under dim light by using a 15 cm-across and 15 cm-deep water tank kept at a temperature of 22° C. “Immobile” time was measured by calculating an added value of “immobile” time during five-minute-swimming.
  • Desipramine that is, a tricyclic antidepressant, was used because it was judged to be used appropriately as a positive control for demonstrating anti-depressant effects.
  • FIG. 7 shows the above results.
  • FIG. 7 is a graph which shows “immobile” time after administration of sepiapterin in the mice forced swim test.
  • a longitudinal axis indicates “immobile” time (unit: min. during 5 min.)
  • control indicates the result of the control group
  • BH4 indicates the result on administration of tetrahydrobiopterin
  • SP indicates the result on administration of sepiapterin
  • Dsp indicates the result on administration of desipramine to the positive control group.
  • a group treated with sepiapterin was significantly short in “immobile” time as compared with a group treated with tetrahydrobiopterin and the control group. Thus, anti-depressant effects were obtained. Furthermore, the group treated with sepiapterin was also effective in shortening “immobile” time to an extent similar to the positive control group.
  • Examples 1 to 6 have suggested that tetrahydrobiopterin hardly reaches the brain or is not taken up into neurons on peripheral administration, thus resulting in no increase in the level of aromatic monoamines in the brain, and improvement in cerebral dysfunction can be hardly expected.
  • sepiapterin partially reaches the brain and is easily taken up into neurons on peripheral administration, thus resulting in an increased level of aromatic monoamines in the brain, suggesting effectiveness in improving cerebral dysfunction.
  • the present invention is effective in preventing, improving and treating central mental disorders such as depression, hyperphagia, autism, impaired consciousness and concentration, and cognitive disturbance.
  • biosynthesis of dopamine, noradrenaline and adrenaline depends on the level of tetrahydrobiopterin in the neurons, as with serotonin.
  • the present invention is effective in preventing, improving and treating central motor disorders such as myotonia, rigidity and tremor.
  • FIG. 1 is an illustration which depicts a metabolic system of aromatic monoamine in neurons in a brain.
  • FIG. 2A is a graph which shows change in the total amount of biopterin taken up into PC12 cells with the lapse of time in Example 1.
  • FIG. 2B is a graph which shows change in the total amount of biopterin taken up into RBL2H3 cells with the lapse of time in Example 1.
  • FIG. 3 is a graph which shows an amount of downward migration of each of tetrahydrobiopterin (BH4), sepiapterin (SP) and 5-hydroxytryptophan (5HTP) added over the upper side of the cell sheet of the brain blood vessel wall model (RBT24H) in Example 2.
  • BH4 tetrahydrobiopterin
  • SP sepiapterin
  • 5HTP 5-hydroxytryptophan
  • FIG. 4A is a graph which shows amounts of sepiapterin (SP), dihydrobiopterin (BH2) and tetrahydrobiopterin (BH4) accumulated in CTX, TNA2 cells on addition of sepiapterin (SP) in Example 3.
  • SP sepiapterin
  • BH2 dihydrobiopterin
  • BH4 tetrahydrobiopterin
  • FIG. 4B is a graph which shows amounts of dihydrobiopterin (BH2) and tetrahydrobiopterin (BH4) accumulated in the CTX INA 2 cells on addition of tetrahydrobiopterin (BH4) in Example 3.
  • BH2 dihydrobiopterin
  • BH4 tetrahydrobiopterin
  • FIG. 5A is a graph which shows change in the amount of tetrahydrobiopterin in the brain with the lapse of time after administration of sepiapterin in an experiment with rats in Example 4.
  • FIG. 5B is a graph which shows change in the amount of serotonin in the brain with the lapse of time after administration of sepiapterin in the experiment with rats in Example 4.
  • FIG. 5C is a graph which shows change in the amount of 5-hydroxyindoleacetic acid in the brain after administration of sepiapterin in the experiment with rats in Example 4.
  • FIG. 6 is a graph which shows the amount of serotonin in the brain after administration of sepiapterin in an experiment with mice (hph-1) in Example 5.
  • FIG. 7 is a graph which shows “immobile” time after administration of sepiapterin in a forced swim test with mice (NZB) in Example 6.
US13/642,639 2010-04-22 2011-04-22 Drug and food/drink for preventing or improving cerebral dysfunction Abandoned US20130197000A1 (en)

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US11173158B2 (en) 2021-11-16
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