US3908007A - Treatment of mental depression - Google Patents

Treatment of mental depression Download PDF

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US3908007A
US3908007A US503732A US50373274A US3908007A US 3908007 A US3908007 A US 3908007A US 503732 A US503732 A US 503732A US 50373274 A US50373274 A US 50373274A US 3908007 A US3908007 A US 3908007A
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mesterolone
administered
acid
depression
mental
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Turan M Itil
Werner Martin Herrmann
Reinhard Horowski
Wolfgang Kehr
Dieter Palenschat
Gerd Paschelke
Helmut Wachtel
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PROF DR TURAN M ITIL NEW YORK MEDICAL COLLEGE DIVISION OF BIOLOGICAL PHYCHIATRY
PROF DR WERNER MARTIN HERRMANN
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Schering AG
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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
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
    • A61K31/568—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone

Definitions

  • Testosterone was reported to delay a drop in functional capacity in certain psychological testing processes upon infusion into healthy persons (W. Vogel et .al., Electroenceph. Clin. Neurophysiol. I971, 400).
  • Androgens having an improved oral effectiveness can moreover lead to serious liver damage.
  • psychopharmacological agents with antidepressant effectiveness contain, as the active components, the so-called tricyclic antidepressants, such as amitryptiline, imipramine, and desipramine, and monoamine oxidase inhibitors, such as nialamide and parglyline, as'well as stimulants of the amphetamine type.
  • tricyclic antidepressants such as amitryptiline, imipramine, and desipramine
  • monoamine oxidase inhibitors such as nialamide and parglyline
  • Particularly undesired side effects of the tricyclic antidepressants are neurological and vegetative symptoms, such as, for example, visual disturbances, heart rhythm disturbances, dry mouth, consciousness changes, as well as, in some instances, dangerous alterations of the blood picture.
  • Undesirable side effects of the monoamine oxidase inhibitors are, in particular, liver damage and dangerous hypertonic crises upon the ingestion of tyramine-containing foods.
  • mesterolone or a 17- ester thereof is administered to a patient in a mentally depressed state in an amount effective to evoke at least one of a psyehostimulating and an antidepressant effect.
  • DETAILED DISCUSSION Mesterolone and its l7-esters exhibit neuropsychotropic effects, especially antidepressant, moodelevating and efficiency-raising properties. At lower dosages, e.g.,about 0.1-10 mg. per dose, they evoke a psyehostimulating effect and at higher dosages, e.g., about 25-300 mg. per dose, an antidepressant effect.
  • the preferred l7-esters of mesterolone are esters of hydrocarbon carboxylic acids of 1-8 carbon atoms, preferably 28 carbon atoms, e.g., a monobasic alkanoic acid, e.g.,-'formic, acetic, propionic, butyric', isobutyric, a-ethylbutyric, valeric, isovaleric, a-ethylvaleric, trimethylacetic, 2-methylbutyric, S-ethylbutyric, hexanoic, diethylacetic, triethylacetic, enanthic, octanoic, a
  • cyclic acid preferably a cycloaliphatic acid, e.g., cyclopropylideneacetic, cyclobutylcarboxylic, cyclopentylcarboxylic, cyclopentylacetic, B-cyclopentylpropionic, cyclohexylcarboxylic, cyclohexylacetic, a carbocyclic aryl or an alkaryl acid, e.g., benzoic, 2-, 3- or 4- methylbenzoic acid.
  • a cycloaliphatic acid e.g., cyclopropylideneacetic, cyclobutylcarboxylic, cyclopentylcarboxylic, cyclopentylacetic, B-cyclopentylpropionic, cyclohexylcarboxylic, cyclohexylacetic, a carbocyclic aryl or an alkaryl acid, e.g., benzoic, 2-, 3- or 4-
  • a preferred class of acyl groups are those of straight or branched chain monobasic alkanoic acids, preferably 2-8 carbon atoms, e.g., acetyl, propionyl, butyryl, isobutyryl, of which acetyl is most preferred.
  • acyl radical of the l7-ester group is not critical, as long as it is not physiologically toxic and it can be formed on mesterolone l7-hydroxy' group
  • contemplated equivalents of the preferred esters described above, insofar as they can be formed are those formed with other aliphatic and aromatic unsubstituted and substituted and monobasic, dibasic and polybasic carboxylic acid, saturated or unsaturated aliphatic, araliphatic and aromatic carboxylic acids containing up to 18 and preferably up to 8 carbon atoms, e.g., undecylic, palmitic, B-cyclohexylpropionic acid, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- and 3,5- dimethylbenzoic, ethylbenzoic, 2,4,6-trimethylbenzoic, cinnamic, naphthoic, S-methyI-a-naphthoic, B-
  • Such contemplated equivalents can also be esters with an acid containing one, two or more simple substituents in the molecule, e.g., hydroxy, halo, alkoxy, acyloxy, sulfonyloxy, amido, sulfato, nitro, mercapto and cyano, in the molecule, e.g., glycolic, lactic,'citric, tartaric, d-maleic, d-glyceric, mannoic, gluconic and salicylic acid; of an amino acid, e. g., glycine, aminopropionic, diglycollamic, triglycollamic, methy'lglycine,
  • mesterolone and the esters thereof the desired effect occurs shortly, e.g., about 2-3 hours, after administration. This is surprising, since it is generally known from endocrine-active steroids that the effect manifests itself only after a longer treatment period. In case of mesterolone, in its conventional applications, it is known per se that the effect occurs only after weeks of treatment. Whereas, the desired psychotropic and CNS-stimulating effects of mesterolone occurs within hours after administration.
  • this invention relates to a method for the treatment of mental depressions and disturbances in mood, behavior and functional capacity employing mesterolone or a l7-ester thereof.
  • mesterolone or a l7-ester thereof employing mesterolone or a l7-ester thereof.
  • mesterolone or a l7-ester thereof employing mesterolone or a l7-ester thereof.
  • mesterolone or a l7-ester thereof employing mesterolone or a l7-ester thereof.
  • mesterolone or a l7-ester thereof employing mesterolone or a l7-ester thereof.
  • the medicinal agents of this invention are also suitable for the treatment of weaknesses of concentration and memory, also in persons without androgen deficiency, as well as of psychophysiological illnesses, such as a drop in general functional capacity, fatigue. loss of interest, and in case of sleep disturbances, such as loss of sleep during the night with tiredness during the day, disturbances in sexuality, such as loss of libido and potency in younger patients without steroid hormone deficiency.
  • compositions of this invention are thus useful for the treatment of mental depressions generally and the amelioration of and relief from the symptoms thereof
  • mental depression as used herein meaning any mental state which is abnormally depressed for that individual (as opposed to congenital-defect or traumaor physical disease-related reduced mental capacity), including both depressed mood and mental outlook and depressed level of mental activity or function.
  • antidepressant effect is used in the conventional sense. It is associated with a reversal of or a reduction in the severity of a depressed mood or state of mind. Subclassification of the patients with depressions to be treated are manic depressive psychoses depressive type, neurotic depression, reactive depression as well as involutional depression, climacteric depression and depression of the old aged.
  • psychostimulating effect is associated in an increase in the overall level of mental activity. It is related to patients with lack of energy, drive and desire as well as lack of concentration and memory.
  • the drugs based on mesterolone or a l7-ester thereof according to this invention can be administered systemically, including parenterally, e.g., subcutaneously and intramuscularly, and orally.
  • the daily dosage is 0.1 1000 mg.
  • a psychostimulating effect is predominant among the components of the above-mentioned spectrum of effectiveness, whereas, in the upper daily dosage range of 25 1000 mg., a specifically antidepressant activity can be determined in addition to the psychostimulating effect.
  • the dosage can be administered at once or in several doses of a pharmaceutical composition containing 0.1 200 mg., preferably 1-50 mg., per unit dosage.
  • the formulation of the medicinal agents of this invention comprising mesterolone or a l7-ester thereof can be conducted in a conventional manner by processing mesterolone or a l7-ester thereof with the vehicles, diluents, flavor-ameliorating agents, etc., customary in galenic pharmacy, and converting these formulations into the desired form of application, such as, for example, tablets, dragees, capsules, solutions, etc.
  • Suitable for injections are, in particular, oily solutions, such as, for example, solutions in sesame oil, castor oil and cottonseed oil.
  • diluents or solubilizers such as, for example, benzyl benzoate or benzyl alcohol to increase the solubility.
  • mesterolone and the l7-esters thereof can also be utilized in microencapsulated form.
  • especially suitable are tablets, capsules, dragees, pills, suspensions and solutions.
  • the desired effects of mesterolone and its l7-esters according to this invention occur not only by injection but equally well in case of oral administration, which is preferred.
  • the amount of effective agent in the thusformulated medicinal agents is 0.1 200 mg., preferably 1 50 mg., per day in a single or in divided doses.
  • the above-mentioned dosage range is related to oral administration. Among the parenteral administrations the intramuscular administration is preferred. If a prolonged release is desired, the mesterolone is intramuscular administered as l7-Ester, e.g., as mesterolone cipionate, in a dosage range between 10 and 500 mg per 2 weeks, preferably in a dosage of 10 to 200 respectively 50 to 500 mg per two weeks, according to the desired effect.
  • the intra muscular form is normally given in one dosage.
  • EXAMPLE I 10.0 mg. of 17B-hydroxy-la-methyl-Sa-androstan- 3-one (mesterolone) having a specific external surface of 20,000 cm l g. and an average particle diameter of 7 p. is homogeneously mixed with:
  • EXAMPLE 5 Respectively 0.5 mg. of mesterolone (micronized, particle size 2-8 p) is mixed homogeneously with 150 mg. of lactose (USP XVII) and filled into hard-gelatin capsules (5 X 15 mm.).
  • EXAMPLE '6 Five male depressive patients in theage range of 20-25 (two patients with .psychoneurotic depressive reaction, two patients with reactive depression, and
  • a method for the treatment of mental depression in an affected person which comprises administering systemically to the affected person an amount of mesterolone or a l7-ester thereof with a hydrocarboncarboxylic acid of 1-8 carbon atoms effective to evoke at least one of a psychostimulating and an antidepressant effect.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
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  • Steroid Compounds (AREA)

Abstract

Mesterolone and its 17-esters possess neuropsychotropic activity and are administered to persons in a mentally depressed state to treat the depression.

Description

United States Patent [191 m1 et al.
[ Sept. 23, 1975 TREATMENT OF MENTAL DEPRESSION [73] Assignee: Schering Aktiengesellschaft, Berlin 7 and Bergkamen, Germany [22] Filed: Sept. 6, 1974 [21] Appl. No.: 503,732
[30] Foreign Application Priority Data Sept, 6, 1973 Germany 2345376 52 US. cl, 424/242 [51] 1m. (:13 A61K 27/00 [58] Field of Search 424/242 [56] Y References Cited UNITED STATES PATENTS 3,361,773 ll/i968 Wieckert 260/239.55 R
Primary Examiner-Stanley J. Friedman Attorney, Agent, or Firm-Millen, Raptes & White 57 ABSTRACT Mesterolonand its l7-ester's possess neuropsychotropic activity and are administered to persons in a mentally depressed state to treat the depression.
11 Claims, No Drawings TREATMENT OF MENTAL DEPRESSION BACKGROUND OF THE INVENTION duce a marked depression of the central nervous system.
It is known that it is possible, in case of a lack of steroidal sexual body hormones, e.g., androgen deficiency, to eliminate also the psychic disturbances connected with the deficiency by the administration of endocrin-active steroids.
Testosterone was reported to delay a drop in functional capacity in certain psychological testing processes upon infusion into healthy persons (W. Vogel et .al., Electroenceph. Clin. Neurophysiol. I971, 400).
However, these effects have no significance for the utilization according to this invention, either, since testosterone shows such effect only when administered as an alcoholic infusion. Additionally, testosterone leads,
due to its gonadotropin-inhibiting activity, to atrophy of the testes and a reduction in the body androgens. Androgens having an improved oral effectiveness, such as methyltestosterone, can moreover lead to serious liver damage. i
It is known that psychopharmacological agents with antidepressant effectiveness contain, as the active components, the so-called tricyclic antidepressants, such as amitryptiline, imipramine, and desipramine, and monoamine oxidase inhibitors, such as nialamide and parglyline, as'well as stimulants of the amphetamine type. These active agents have in common that they possess a high toxicity. Furthermore, they have the disadvantage that the antidepressant effect occurs only after weeks of administration. These disadvantages represent a high risk, especially in case of suicide-prone persons. Furthermore, these effective agents show anumber of side effects. Particularly undesired side effects of the tricyclic antidepressants are neurological and vegetative symptoms, such as, for example, visual disturbances, heart rhythm disturbances, dry mouth, consciousness changes, as well as, in some instances, dangerous alterations of the blood picture. Undesirable side effects of the monoamine oxidase inhibitors are, in particular, liver damage and dangerous hypertonic crises upon the ingestion of tyramine-containing foods. In
case of amphetamines, the strong central-stimulating 'and dependency-forming effect of these substances has led to the result that for all practical purposes, they are no longer used as antidepressants.
It has now been found that mesterolone and its esters .exhibit a psyehostimulating effect at lower doses and a pronounced antidepressant effect at higher doses. This result has been obtained for the first time with a substance having a steroid structure.
SUMMARY OF THE INVENTION According to this invention, mesterolone or a 17- ester thereof is administered to a patient in a mentally depressed state in an amount effective to evoke at least one of a psyehostimulating and an antidepressant effect.
DETAILED DISCUSSION Mesterolone and its l7-esters exhibit neuropsychotropic effects, especially antidepressant, moodelevating and efficiency-raising properties. At lower dosages, e.g.,about 0.1-10 mg. per dose, they evoke a psyehostimulating effect and at higher dosages, e.g., about 25-300 mg. per dose, an antidepressant effect.
The preferred l7-esters of mesterolone are esters of hydrocarbon carboxylic acids of 1-8 carbon atoms, preferably 28 carbon atoms, e.g., a monobasic alkanoic acid, e.g.,-'formic, acetic, propionic, butyric', isobutyric, a-ethylbutyric, valeric, isovaleric, a-ethylvaleric, trimethylacetic, 2-methylbutyric, S-ethylbutyric, hexanoic, diethylacetic, triethylacetic, enanthic, octanoic, a
cyclic acid, preferably a cycloaliphatic acid, e.g., cyclopropylideneacetic, cyclobutylcarboxylic, cyclopentylcarboxylic, cyclopentylacetic, B-cyclopentylpropionic, cyclohexylcarboxylic, cyclohexylacetic, a carbocyclic aryl or an alkaryl acid, e.g., benzoic, 2-, 3- or 4- methylbenzoic acid.
A preferred class of acyl groups are those of straight or branched chain monobasic alkanoic acids, preferably 2-8 carbon atoms, e.g., acetyl, propionyl, butyryl, isobutyryl, of which acetyl is most preferred.
Since the exact chemical nature of the acyl radical of the l7-ester group is not critical, as long as it is not physiologically toxic and it can be formed on mesterolone l7-hydroxy' group, contemplated equivalents of the preferred esters described above, insofar as they can be formed, are those formed with other aliphatic and aromatic unsubstituted and substituted and monobasic, dibasic and polybasic carboxylic acid, saturated or unsaturated aliphatic, araliphatic and aromatic carboxylic acids containing up to 18 and preferably up to 8 carbon atoms, e.g., undecylic, palmitic, B-cyclohexylpropionic acid, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- and 3,5- dimethylbenzoic, ethylbenzoic, 2,4,6-trimethylbenzoic, cinnamic, naphthoic, S-methyI-a-naphthoic, B-phenylpropionic, diph'enylacetic, biphenylacetic or a-naphthylacetic acid or a dibasic alkanoic acid, e.g., oxalic, maleic, furnaric, succinic, malonic, glutaric, a-methylglutaric, B-rnethylglutaric, [3,B-dimethylglutaric, adipic, pimelic and suberic acid, a dibasic aryl acid, especially those capable of forming a cyclic anhydride, e.g., phthalic acid, or a carbamic acid, e.g., carbamic acid, phenylcarbamic, n-butylcarbamic, dimethylcarbamic, diethylcarbamic and allophanic acid; or of a heterocyclic acid, e.g., B-furylcarboxylic pyrrolecarboxylic, B -pyrrolidylpropionic, N-methylpyrrolidyl- Z-carboxylic, a-picolinic, nicotinic, indole-2- carboxylic, 6-hydroxylindolyl-3-acetic and N- methylmorpholyl-Z-carboxylic I and pyrrolyl-2- carboxylic acid, or a sulfonic acid of l-18, preferably ll2, carbon atoms, including alkanesulfonic, e.g., methaneand ethanesulfonic, and aryl sulfonic, e.g., benzeneand p-toluenesulfonic acid.
Such contemplated equivalents can also be esters with an acid containing one, two or more simple substituents in the molecule, e.g., hydroxy, halo, alkoxy, acyloxy, sulfonyloxy, amido, sulfato, nitro, mercapto and cyano, in the molecule, e.g., glycolic, lactic,'citric, tartaric, d-maleic, d-glyceric, mannoic, gluconic and salicylic acid; of an amino acid, e. g., glycine, aminopropionic, diglycollamic, triglycollamic, methy'lglycine,
dimethylglycinc, diethylglycine, para-aminosalicylic, paraaminobenzoic, ethylmercaptoacetic, benzylmercaptoacetic, chloroacetic, fluoroacetic, trichloroacetic, trifluoroacetic, thioglycolic. m-nitrobenzoic, 2,3,4- trimethoxybenzoic, phenoxyacetic and a-naphthoxyacetic acid. 7
- Mesterolone and l7-esters thereof were tested on humans in several, respectively independent, placebocontrolled double blank experiments by quantitative pharmaco-electroencephalography (CEEG) and by the method of evoked potentials (EP). The effects and side effects were also recorded by means of various rating scales, for example for neurological and psychosomatic symptom spectra, by self-rating scales for sedation, fear and depression, as well as by interviews with physicians. In clinical tests, the effect determined in the CEEG and EP was confirmed in low as well as high doses. During the clinical investigations, detailed case reports on the therapeutic success were conducted and placed into an objective form in rating scales, e.g., Hamilton Depression Scale.
In the practical application of mesterolone and the esters thereof, the desired effect occurs shortly, e.g., about 2-3 hours, after administration. This is surprising, since it is generally known from endocrine-active steroids that the effect manifests itself only after a longer treatment period. In case of mesterolone, in its conventional applications, it is known per se that the effect occurs only after weeks of treatment. Whereas, the desired psychotropic and CNS-stimulating effects of mesterolone occurs within hours after administration.
The advantage of use of medicinal agents based on mesterolone or a l7-ester thereof resides particularly in that even a huge individual oral dose, on the order of 2 g., no neurological, vegetative, or other side effects are ordinarily evoked. Therefore, a large overdose is not inevitably lethal.
Furthermore, it is also advantageous that even in case of a long-term use of mesterolone and its esters, no dependency is created, as is possible in case of the conventional antidepressants.
In its method of use aspect, this invention relates to a method for the treatment of mental depressions and disturbances in mood, behavior and functional capacity employing mesterolone or a l7-ester thereof. Among these are, in particular, endogenic, neurotic and reactive depressions, depressions of the aging, climacteric and involution depressions, as well as the conditions related to the climacteric depressions with changes and disturbances in the affective region, waning functional power and concentration, and increased irritability, with and without a lack of body hormones.
Moreover, the medicinal agents of this invention are also suitable for the treatment of weaknesses of concentration and memory, also in persons without androgen deficiency, as well as of psychophysiological illnesses, such as a drop in general functional capacity, fatigue. loss of interest, and in case of sleep disturbances, such as loss of sleep during the night with tiredness during the day, disturbances in sexuality, such as loss of libido and potency in younger patients without steroid hormone deficiency.
The compositions of this invention are thus useful for the treatment of mental depressions generally and the amelioration of and relief from the symptoms thereof, the term mental depression as used herein meaning any mental state which is abnormally depressed for that individual (as opposed to congenital-defect or traumaor physical disease-related reduced mental capacity), including both depressed mood and mental outlook and depressed level of mental activity or function.
The term antidepressant effect is used in the conventional sense. It is associated with a reversal of or a reduction in the severity of a depressed mood or state of mind. Subclassification of the patients with depressions to be treated are manic depressive psychoses depressive type, neurotic depression, reactive depression as well as involutional depression, climacteric depression and depression of the old aged. The term psychostimulating effect, as the term implies, is associated in an increase in the overall level of mental activity. It is related to patients with lack of energy, drive and desire as well as lack of concentration and memory.
In the medical practice, the drugs based on mesterolone or a l7-ester thereof according to this invention can be administered systemically, including parenterally, e.g., subcutaneously and intramuscularly, and orally. The daily dosage is 0.1 1000 mg. In the lower daily dosage range of 0.1 20 mg., a psychostimulating effect is predominant among the components of the above-mentioned spectrum of effectiveness, whereas, in the upper daily dosage range of 25 1000 mg., a specifically antidepressant activity can be determined in addition to the psychostimulating effect. The dosage can be administered at once or in several doses of a pharmaceutical composition containing 0.1 200 mg., preferably 1-50 mg., per unit dosage.
The formulation of the medicinal agents of this invention comprising mesterolone or a l7-ester thereof can be conducted in a conventional manner by processing mesterolone or a l7-ester thereof with the vehicles, diluents, flavor-ameliorating agents, etc., customary in galenic pharmacy, and converting these formulations into the desired form of application, such as, for example, tablets, dragees, capsules, solutions, etc. Suitable for injections are, in particular, oily solutions, such as, for example, solutions in sesame oil, castor oil and cottonseed oil. If desired, it is possible to add diluents or solubilizers, such as, for example, benzyl benzoate or benzyl alcohol to increase the solubility. To obtain a protracted effect, mesterolone and the l7-esters thereof can also be utilized in microencapsulated form. For oral application, especially suitable are tablets, capsules, dragees, pills, suspensions and solutions.
The desired effects of mesterolone and its l7-esters according to this invention occur not only by injection but equally well in case of oral administration, which is preferred. The amount of effective agent in the thusformulated medicinal agents is 0.1 200 mg., preferably 1 50 mg., per day in a single or in divided doses. The above-mentioned dosage range is related to oral administration. Among the parenteral administrations the intramuscular administration is preferred. If a prolonged release is desired, the mesterolone is intramuscular administered as l7-Ester, e.g., as mesterolone cipionate, in a dosage range between 10 and 500 mg per 2 weeks, preferably in a dosage of 10 to 200 respectively 50 to 500 mg per two weeks, according to the desired effect.
For oral administration divided dosages are pre-.
For special purposes and in depressed patients it may be givenin addition to this in the evening. The intra muscular form is normally given in one dosage.
Without further claboration, it. is believed that one skilled in the art can, using the preceding description, 5 utilize the present invention to its fullest extent. The following preferred specific embodiments are, therefore, to be construed as merely illustrative and not limitative of the remainder of the disclosure in any way whatsoever.
EXAMPLE I 10.0 mg. of 17B-hydroxy-la-methyl-Sa-androstan- 3-one (mesterolone) having a specific external surface of 20,000 cm l g. and an average particle diameter of 7 p. is homogeneously mixed with:
36.0 mg. lactose (DAB [German Pharmacopoeial]6;
USP XVII),
66.565 mg. corn starch (USP XVII),
1.4 mg. gelatin (DAB 6; USP XVII),
0.024 mg. methyl parahydroxybenzoate (DAB 6,
USP XVII),
0.01 1 mg. propyl parahydroxybenzoate (DAB 6,
USP XVII),
4.8 mg. talc (DAB 6, USP XVII), and
1.2 mg. magnesium stearate (USP XVII),
and compressed into tablets without previous granulation, these tablets having a dividing notch and a weight of 120 mg., with a diameter of about 7 mm. and a thick ness of 2.7-2.9 mm.
EXAMPLE 2 EXAMPLE 3 In order to prepare an injection solution,
20.0 mg. of mesterolone is dissolved in:
618.6 mg. benzyl benzoate (USP XVII) and 353.4 mg. castor oil (DAB 7, USP XVII); the solution is filtered aseptically and filled into l-ml. ampoules under sterile conditions.
EXAMPLE 4 Analogously to Example 3,
25.0 mg. of l7B-cyclopenty1propionyloxy-1amethyl-5a-androstan-3-one (mesterolone cipionate) is dissolved in:
152.3 mg. benzyl benzoate and 86.4 mg. castor oil,
and filled into l-ml. ampoules.
EXAMPLE 5 Respectively 0.5 mg. of mesterolone (micronized, particle size 2-8 p) is mixed homogeneously with 150 mg. of lactose (USP XVII) and filled into hard-gelatin capsules (5 X 15 mm.).
. EXAMPLE '6 Five male depressive patients in theage range of 20-25 (two patients with .psychoneurotic depressive reaction, two patients with reactive depression, and
one patient with bipolar depressive illness) were included in this study. Except for one, it was a first-time illness for all other patients. None, but one, was treated before with any psychotropic drugs. The one occasionally received different anxiolytics and antidepressive drugs.
With daily dosages of 25200 mg (mean daily dosages ranged from l02l31 mg. and the total dosages from 2,4403,150 mg.) two of the patients showed complete remission in symptomatology, two showed nearly complete remission, and one showed slight degree of remission (the length of treatment ranged from 2 /2 3 weeks).
EXAMPLE 7 Five male subjects in the age range of 20-23 with a diagnosis of depression (one patient with psychoneurotic depression, four patients with reactive depression) were included in this study. All patients with the exception of one had never been treated with any psychotropic drug. All patients had, in addition to typical depressive symptoms, psychomotor retardation, apathy, lack of energy and drive.
With daily dosages of 2-6 mg (mean daily dosage ranged from 3.7 4.2 mg and total dosages from 91-101 mg), three of the patients showed complete remission in depressive symptomatology and two of the patients almost complete remission. The length of the treatment was 24 days.
The preceding examples can be repeated with similar success by substituting the generically and specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.
What is claimed is:
l. A method for the treatment of mental depression in an affected person which comprises administering systemically to the affected person an amount of mesterolone or a l7-ester thereof with a hydrocarboncarboxylic acid of 1-8 carbon atoms effective to evoke at least one of a psychostimulating and an antidepressant effect.
2. A method according to claim 1 wherein mesterolone is administered.
3. A method according to claim 2 wherein the mesterolone is administered orally.
4. A method according to claim 1 wherein mesterolone cipionate is administered.
5. A method according to claim 4 wherein the mesterolone cipionate is administered parenterally.
6. A method according to claim 1 wherein the mental alteration is a depressed mood.
7. A method according to claim 6 wherein the amount administered is 251,000 mg. daily, for oral administration.
amount administered is 0.1 20 mg daily, for oral administration.
ll. A method according to claim 1 wherein the amount administered is 10 200 mg per two weeks. for
parenteral administration.

Claims (11)

1. A METHOD FOR THE TREATMENT OF METAL DEPRESSION IN AN AFFECTED PERSON WHICH COMPRISES ADMINISTERING SYSTEMICALLY TO THE AFFECTED PERSON AN AMOUNT OF MESTEROLONE OR A 17-ESTER THEREOF WITH A HYDROCARBONCARBOXYLIC ACID OF 1-8 CARBON ATOMS EFFECTIVE TO EVOKE AT LEAST ONE OF A PSYCHOSTIMULATING AND AN ANTIDEPRESSANT EFFECT.
2. A method according to claim 1 wherein mesterolone is administered.
3. A method according to claim 2 wherein the mesterolone is administered orally.
4. A method according to claim 1 wherein mesterolone cipionate is administered.
5. A method according to claim 4 wherein the mesterolone cipionate is administered parenterally.
6. A method according to claim 1 wherein the mental alteration is a depressed mood.
7. A method according to claim 6 wherein the amount administered is 25-1,000 mg. daily, for oral administration.
8. A method according to claim 6 wherein the amount administered is 50-500 mg per two weeks, for parenteral administration.
9. A method according to claim 1 wherein the mental alteration is reduced mental activity.
10. A method according to claim 1 wherein the amount administered is 0.1 - 20 mg. daily, for oral administration.
11. A method according to claim 1 wherein the amount administered is 10 - 200 mg per two weeks, for parenteral administration.
US503732A 1973-09-06 1974-09-06 Treatment of mental depression Expired - Lifetime US3908007A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4415591A (en) * 1981-06-04 1983-11-15 Georgia Tech Research Institute Use of aminoalkyl phenyl sulfide derivatives for the treatment of hypertension
WO1994028904A1 (en) * 1993-06-15 1994-12-22 Pherin Corporation Androstane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical compositions and methods
US5591732A (en) * 1992-06-03 1997-01-07 Mattern; Claudia Medicament for influencing the degree of activation of the central nervous system
US5883087A (en) * 1991-01-07 1999-03-16 Pherin Corporation Androstane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical compositions and methods
CN1057531C (en) * 1993-06-15 2000-10-18 弗林公司 Androstane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical
WO2009049030A1 (en) * 2007-10-09 2009-04-16 Triton Biopharma, Llc Method to use compositions having antidepressant anxiolytic and other neurological activity and compositions of matter
BE1027858B1 (en) * 2019-12-13 2021-07-14 Georges Debled Pharmaceutical composition for contraception in women

Citations (1)

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Publication number Priority date Publication date Assignee Title
US3361773A (en) * 1960-04-06 1968-01-02 Schering Ag 1alpha-methyl steroids

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1152100B (en) * 1960-12-23 1963-08-01 Schering Ag Process for the preparation of 1ª ‡ -Methyl-3-ketosteroids

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3361773A (en) * 1960-04-06 1968-01-02 Schering Ag 1alpha-methyl steroids

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4415591A (en) * 1981-06-04 1983-11-15 Georgia Tech Research Institute Use of aminoalkyl phenyl sulfide derivatives for the treatment of hypertension
US5883087A (en) * 1991-01-07 1999-03-16 Pherin Corporation Androstane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical compositions and methods
US5965552A (en) * 1991-01-07 1999-10-12 Pherin Pharmaceuticals, Inc. Androstane steroids as neurochemical initators of change in human hypothalamic compositions and methods
US5591732A (en) * 1992-06-03 1997-01-07 Mattern; Claudia Medicament for influencing the degree of activation of the central nervous system
WO1994028904A1 (en) * 1993-06-15 1994-12-22 Pherin Corporation Androstane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical compositions and methods
AU691474B2 (en) * 1993-06-15 1998-05-21 Pherin Pharmaceuticals, Inc. Androstane steroids as neurochemical initiators of change inhuman hypothalamic function and related pharmaceutical compositions and methods
CN1057531C (en) * 1993-06-15 2000-10-18 弗林公司 Androstane steroids as neurochemical initiators of change in human hypothalamic function and related pharmaceutical
WO2009049030A1 (en) * 2007-10-09 2009-04-16 Triton Biopharma, Llc Method to use compositions having antidepressant anxiolytic and other neurological activity and compositions of matter
BE1027858B1 (en) * 2019-12-13 2021-07-14 Georges Debled Pharmaceutical composition for contraception in women

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GB1483650A (en) 1977-08-24
DE2345376A1 (en) 1975-03-20

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