EP1296668A2 - Compositions a base d'aminoacides permettant d'ameliorer les performances musculaires - Google Patents
Compositions a base d'aminoacides permettant d'ameliorer les performances musculairesInfo
- Publication number
- EP1296668A2 EP1296668A2 EP01940936A EP01940936A EP1296668A2 EP 1296668 A2 EP1296668 A2 EP 1296668A2 EP 01940936 A EP01940936 A EP 01940936A EP 01940936 A EP01940936 A EP 01940936A EP 1296668 A2 EP1296668 A2 EP 1296668A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- amino acids
- compositions
- previous
- active ingredients
- threonine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4172—Imidazole-alkanecarboxylic acids, e.g. histidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Definitions
- the present invention refers to compositions based on amino acids, in particular for oral or parenteral use, suitable for improving muscle performance, particularly but not exclusively in patients suffering of heart insufficiencies.
- CHF chronic heart failure
- National statistics indicate that, in the USA, chronic heart failure (CHF) incidence and prevalence have increased over the last twenty years, despite the increased resources devoted to its prevention (Sytkowski P.A. et al.; New England Journal of Medicine, 1990; 322: 1635-1641), and the significant progresses in availability of treatment of this particular disease (Pitt B. et al.; New England Journal of Medicine, 1999; 341 : 709-717).
- Chronic heart failure is no longer strictly deemed as the consequence of hypertension or valvular heart disease, but rather of coronary heart disease, and therefore of arteriosclerosis (Gheorghiade M. and Bonow R.O.; Circulation, 1998; 97: 282-289).
- intolerance to physical exercise is one of the major clinical feature, which is consistent with the proceeding of the same pathology; in addition, a noticeable skeletal muscle atrophy, often in the absence of signs of severe malnutrition, is a quite constant accompanying feature of chronic heart failure of any grade (Mancini D.M. et al.; Circulation, 1992, 85: 1364- 1373).
- Mechanisms of muscle wasting have been recently reviewed in literature (Mitch W.E. and Goldberg A.L.; New England Journal of Medicine, 1996; 355: 1897- 1905).
- the present invention has the aim of indicating compositions which are capable of determining a noticeable improvement in muscle performances, particularly but not exclusively in patients suffering of heart insufficiencies.
- a further aim of the invention is that of indicating an absolutely innovative therapeutic approach to the problem of heart insufficiency.
- compositions being in particular provided for oral or parenteral use, are characterized by comprising, as main active ingredients, the branched chain amino acids leucine, isoleucine and valine, up to 75% of all the amino acids or active ingredients being present, by expressing the value in molecular weights.
- the compositions according to the invention also comprise, as further active ingredients, threonine and lysine, where in particular threonine plus lysine are present up to 50% of all the amino acids or active ingredients being present, by expressing the value in molecular weights.
- compositions can provide, as further active ingredients, other essential amino acids, in particular methionine and/or phenylalanine ⁇ and/or histidine and/or triphtophan, and non essential amino acids, in particular tyrosine and/or cyst(e)ine (i.e. cystine and cysteine).
- other essential amino acids in particular methionine and/or phenylalanine ⁇ and/or histidine and/or triphtophan
- non essential amino acids in particular tyrosine and/or cyst(e)ine (i.e. cystine and cysteine).
- the sum of the amounts being expressed in molecular weights of threonine and lysine is greater than the sum of the single amounts of the other essential amino acids being provided, but in any case lower than the sum of the single amounts of the branched chain amino acids being provided.
- the amounts being expressed in molecular weight of threonine and of lysine can be each greater than the single amounts of the other essential amino acids being provided, but in any case lower than the single quantities of the branched chain amino acids being provided.
- compositions according to the, invention can also comprise one or more further amino acids, with respect to those as previously indicated, the sum of which, expressed in molecular weight, is preferably lower than 20% with respect to the active ingredients, and less than 10% for each single further amino acid.
- a mixture of amino acids particularly suitable for nutritional use in humans should satisfy different requirements: - the content of essential amino acids in the mixture should be in an adequate ratio to fulfill real human nutritional needs (and this can be optimized by the co-operative adjunction of adequate and small ratios of some non essential amino acids); the pH of the solution of the mixture should be substantially neutral, in order to prevent urinary calcium losses; the mixture should be safe, in respect to calcium balance (i.e.: with no urinary losses) and homocyst(e)ine production (i.e., preferably related to the amount of all amino acids, a strictly correct ratio of sulphur containing amino acids, with a ratio cyst(e)ine / methionine of at least 2: 1 on a sto
- composition according to the invention comprising essential amino acids (leucine, isoleucine, valine, threonine, lysine, methionine, phenylalanine, histidine, triphtophan) and some non essential amino acids (tyrosine and cyst(e)ine), in different but fixed and co-operative molar ratios among them, is the following one: branched chain amino acids leucine (40-60% in molecular weight), isoleucine (20-40% in molecular weight) and valine (20-40% in molecular weight), preferentially in a stoichiometric ratio 2:1 :1 among them, covering from 30 to
- threonine plus lysine preferably in a w/w molar ratio with the above said branched chain amino acids between 20 and 50%, but with a threonine to lysine ratio in which threonine is from 10 to 50% more represented than lysine; the above said branched chain amino acids plus threonine and lysine, whose sum of the molecular weight is in a stoichiometric ratio of 50 to 70% of a mixture also comprising histidine and other amino acids, were histidine is present in molar ratio up to 50% of the following amino acids: - cyst(e)ine (i.e., cystine and cysteine) and methionine, up to 50% of histidine (the ratio between cyst(e)ine and methionine should be preferably of 50 to 200% greater for cyst(e)ine on a w/w molar ratio), phenylalanine and tyrosine, in m
- any other amino acid can be summed to the above formulation, without altering the expected effects, if their sum would be in a percentage lower than 20% with respect to the other active ingredients (less that
- a significant characteristic of the above said formulation is that of having a pH in water solution comprised between 6.5 and 8.5, and therefore suitable for a safe oral or parenteral use, in humans or animals, according to needs. This feature prevents the excessive calcium urinary losses induced by protein sources of amino acids.
- the effects on energy balance of the an amino acids mixture according to the invention as above indicated were the subject of a comparative study with creatine, on a weight ratio (w/w), or with no treatment, on a large group of volunteers submitted to a rigid protocol of alimentation and training.
- Table 1 which follows shows the result of such a study , were the effect of the amino acids mixture according to the invention (24 g/d "1 ), creatine (25 g/d "1 ) and placebo have been compared to each other, after one month of and homogeneous treatment and training, in groups of athletes were:
- Group 1 is the group treated with the mixture according to the invention.
- Tables 2 shows in particular the modifications induced by chronic administration of the amino acids mixture according to the invention in normal athletes (healthy).
- FC Cardiac frequency
- Watt peak power production
- Cysteine 3 ⁇ 1 4 ⁇ 3 Cardiac cachexia (the severe muscle wasting observed even in absence of malnutrition in chronic heart insufficiency patients), is a quite constant and noxious condition, clinically associated to chronic heart failure and potentially life threatening (Anker S.D. et al.; Lancet, 1997; 349:1050-1053).
- Table 4 plasma profiles are reported of amino acids as they can be detected in healthy athletes (weight lifters), that underwent to leg strenuous exercise (i.e., leading to exhaustion) for 45 minutes, after an overnight fasting.
- fuel availability is the main control of the origin of energy from one or another substrate.
- citric acid cycle the main energy producer of any body cell
- citric acid cycle the main energy producer of any body cell
- acetyl groups and intermediates of the said cycle mostly at committed steps as ⁇ -ketoglutarate and succinate
- oxaloacetate-citrate The part of them not utilized for energy production is exported to cytoplasm as malonylCoA-malate or glutamic acid-glutamine, via mitochondria co-transporter systems.
- this peculiar metabolic flow will inhibit pyruvate dehydrogenase, by activation of pyruvate dehydrogenase kinase in presence of acetylcoA and NADH, avoiding pyruvate from lipid syntheses.
- compositions according to the invention are particularly efficacious for improving the muscle performances, particularly but not exclusively in patients suffering of chronic heart failure patients. From the above, it is also clear that the compositions according to the invention are particularly efficacious also for treating chronic heart failure. Within these frames, the compositions according to the invention are particularly efficacious:
- compositions according to the invention are suitable for being added to and/or improving clinical effects of any other therapeutic schedule.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITTO000675 | 2000-07-04 | ||
IT2000TO000675A IT1320783B1 (it) | 2000-07-04 | 2000-07-04 | Composizioni a base di aminoacidi, atte al miglioramento delleprestazioni muscolari. |
PCT/IB2001/001182 WO2002002092A2 (fr) | 2000-07-04 | 2001-06-28 | Compositions a base d'aminoacides permettant d'ameliorer les performances musculaires |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1296668A2 true EP1296668A2 (fr) | 2003-04-02 |
Family
ID=11457894
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01940936A Withdrawn EP1296668A2 (fr) | 2000-07-04 | 2001-06-28 | Compositions a base d'aminoacides permettant d'ameliorer les performances musculaires |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1296668A2 (fr) |
AU (1) | AU2001274422A1 (fr) |
IT (1) | IT1320783B1 (fr) |
WO (1) | WO2002002092A2 (fr) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ITTO20010580A1 (it) * | 2001-06-15 | 2002-12-15 | Professional Dietetics Srl | Composizioni a base di aminoacidi per il miglioramento della funzioneventricolare miocardica in pazienti affetti da diabete. |
GB2394698A (en) | 2002-11-01 | 2004-05-05 | Gibbs Tech Ltd | Amphibious vehicle wheel transmission arrangement |
IT1397023B1 (it) * | 2009-11-27 | 2012-12-20 | Professional Dietetics Srl | Composizioni comprendenti amminoacidi, per il trattamento della broncopneumopatia cronica ostruttiva |
IT1397446B1 (it) * | 2010-01-12 | 2013-01-10 | Professional Dietetics Srl | Compositions comprising amino acids for prevention and/or treatment of renal disorders. |
DK3006027T3 (en) * | 2014-10-08 | 2017-12-18 | Professional Dietetics Spa | Compositions comprising amino acids for use in the treatment of systemic inflammation associated with stroke in dysphagia patients |
JOP20190146A1 (ar) | 2016-12-19 | 2019-06-18 | Axcella Health Inc | تركيبات حمض أميني وطرق لمعالجة أمراض الكبد |
PE20200747A1 (es) | 2017-08-14 | 2020-07-24 | Axcella Health Inc | Composiciones de aminoacidos para el tratamiento de enfermedad hepatica |
AR115585A1 (es) | 2018-06-20 | 2021-02-03 | Axcella Health Inc | Composiciones y métodos para el tratamiento de la infiltración de grasa en músculo |
IT202000021664A1 (it) * | 2020-09-14 | 2022-03-14 | Iaf Network S P A | Formulazione amminoacidica bilanciata |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5276018A (en) * | 1992-07-17 | 1994-01-04 | Brigham And Women's Hospital | Composition comprising amino acids and methods for decreasing muscle breakdown |
IT1289754B1 (it) * | 1996-12-16 | 1998-10-16 | Professional Dietetics Srl | Composizioni a base di aminoacidi |
-
2000
- 2000-07-04 IT IT2000TO000675A patent/IT1320783B1/it active
-
2001
- 2001-06-28 AU AU2001274422A patent/AU2001274422A1/en not_active Abandoned
- 2001-06-28 WO PCT/IB2001/001182 patent/WO2002002092A2/fr not_active Application Discontinuation
- 2001-06-28 EP EP01940936A patent/EP1296668A2/fr not_active Withdrawn
Non-Patent Citations (2)
Title |
---|
None * |
See also references of WO0202092A3 * |
Also Published As
Publication number | Publication date |
---|---|
ITTO20000675A0 (it) | 2000-07-04 |
IT1320783B1 (it) | 2003-12-10 |
AU2001274422A1 (en) | 2002-01-14 |
WO2002002092A2 (fr) | 2002-01-10 |
ITTO20000675A1 (it) | 2002-01-04 |
WO2002002092A3 (fr) | 2002-06-20 |
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Legal Events
Date | Code | Title | Description |
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AX | Request for extension of the european patent |
Extension state: AL LT LV MK RO SI |
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17Q | First examination report despatched |
Effective date: 20030904 |
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17Q | First examination report despatched |
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STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
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18D | Application deemed to be withdrawn |
Effective date: 20070605 |