WO2014178803A1 - A composition for use in the treatment of alcohol addiction - Google Patents
A composition for use in the treatment of alcohol addiction Download PDFInfo
- Publication number
- WO2014178803A1 WO2014178803A1 PCT/TR2013/000325 TR2013000325W WO2014178803A1 WO 2014178803 A1 WO2014178803 A1 WO 2014178803A1 TR 2013000325 W TR2013000325 W TR 2013000325W WO 2014178803 A1 WO2014178803 A1 WO 2014178803A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ginsenoside
- composition
- treatment
- alcohol addiction
- addiction
- Prior art date
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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
Definitions
- the invention relates to a composition formed for the use of methylsalidroside and ginsenoside rg3 in the treatment of the alcohol addiction.
- an object of the invention is to enable the body to repair the imbalance of dopamine and serotonin release in the body within a short time. Another object of the invention is to suppress the catecholamine secretion from the adrenal glands and reduce the production of the substance P having an important effect on addiction. Another object of the invention is to provide effectiveness in the permanent treatment of the alcohol addiction, owing to the ability to stimulate the AMPA receptor, the increase in the sensitivity of serotonin receptor, the suppression of the catecholamine secretion and the simultaneous reduction of the expression of the substance P.
- the invention is a composition for use in the treatment of the alcohol addiction, said composition being obtained by the components selected from the group comprising 20-(s)-ginsenoside rg3, 20-(s)-B- ginsenoside rg3 that are used individually or in combinations.
- the invention is a composition formed for the use of methylsalidroside and ginsenoside rg3 in the treatment of the alcohol addiction.
- 20-(s)-ginsenoside rg3 and 20-(s)-B-ginsenoside rg3, which are active derivatives of ginsenoside rg3, a glucopyranoside derivative naturally contained by ginseng, enable the body to repair the imbalances in the secretion of dopamine and serotonin owing to the ability to stimulate the AMPA receptors, suppress the catecholamine secretion from the adrenal glands and reduce the production of the substance P having an important effect on addiction.
- a permanent treatment is provided for the alcohol addiction, owing to the ability to stimulate the AMPA receptor, the increase in the sensitivity of serotonin receptor, the suppression of the catecholamine secretion and the simultaneous reduction of the expression of the substance P.
- composition according to the invention contains 20-(s)-ginsenoside rg3, 20-(s)- B-ginsenoside rg3.
- Said formulation is obtained by a mixture of the aforesaid components according to the following ratios by weight:
- composition is obtained from the aforesaid components selected from the aforesaid group and used according to the mentioned weight ratio ranges individually or in combinations.
- Said invention also encompasses the use of said composition to enable the use of methylsalidroside and ginsenoside rg3 in the treatment of alcohol addiction and the manufacture thereof for this purpose.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Addiction (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Psychiatry (AREA)
- Neurosurgery (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Abstract
The invention relates to a composition formed for use in the treatment of the alcohol addiction.
Description
Description
A COMPOSITION FOR USE IN THE TREATMENT OF ALCOHOL ADDICTION Technical Field
The invention relates to a composition formed for the use of methylsalidroside and ginsenoside rg3 in the treatment of the alcohol addiction.
State of the Art
Today, tricyclic antidepressants, racetam derivatives, psychological group therapies and meetings are employed as the possible methods for the treatment of alcohol addiction.
The use of antidepressants and other psychotropic drugs usually aggravates the condition in the short term, and irreversibly aggravates the already existing depression caused by the alcohol addiction. Although partially successful results are obtained from the racetam derivatives, the alcohol addiction may relapse when their use is stopped. Group therapies suffer the instability of participation caused by the discomfort that the individuals feel about their situation.
As a result, the presence of the need for a composition formed for the use of methylsalidroside and ginsenoside rg3 in the treatment of the alcohol addiction and the inadequacy of the existing solutions have made it necessary to perform an improvement in the relevant art.
Object of the Invention
In order to eliminate the disadvantages of the state of the art, an object of the invention is to enable the body to repair the imbalance of dopamine and serotonin release in the body within a short time.
Another object of the invention is to suppress the catecholamine secretion from the adrenal glands and reduce the production of the substance P having an important effect on addiction. Another object of the invention is to provide effectiveness in the permanent treatment of the alcohol addiction, owing to the ability to stimulate the AMPA receptor, the increase in the sensitivity of serotonin receptor, the suppression of the catecholamine secretion and the simultaneous reduction of the expression of the substance P. In order to achieve the aforesaid advantages, the invention is a composition for use in the treatment of the alcohol addiction, said composition being obtained by the components selected from the group comprising 20-(s)-ginsenoside rg3, 20-(s)-B- ginsenoside rg3 that are used individually or in combinations. The structural and characteristic features and all the advantages of the invention will become more clearly understood from the detailed description provided below and therefore, the evaluation must be made taking this detailed description into consideration. Detailed Description of the Invention
The invention is a composition formed for the use of methylsalidroside and ginsenoside rg3 in the treatment of the alcohol addiction. 20-(s)-ginsenoside rg3 and 20-(s)-B-ginsenoside rg3, which are active derivatives of ginsenoside rg3, a glucopyranoside derivative naturally contained by ginseng, enable the body to repair the imbalances in the secretion of dopamine and serotonin owing to the ability to stimulate the AMPA receptors, suppress the catecholamine secretion from the adrenal glands and reduce the production of the substance P having an important effect on addiction.
A permanent treatment is provided for the alcohol addiction, owing to the ability to stimulate the AMPA receptor, the increase in the sensitivity of serotonin receptor, the
suppression of the catecholamine secretion and the simultaneous reduction of the expression of the substance P.
The composition according to the invention contains 20-(s)-ginsenoside rg3, 20-(s)- B-ginsenoside rg3.
Said formulation is obtained by a mixture of the aforesaid components according to the following ratios by weight:
1-99% 20-(s)-ginsenoside rg3,
99-1% 20-(s)-B-ginsenoside rg3.
The composition is obtained from the aforesaid components selected from the aforesaid group and used according to the mentioned weight ratio ranges individually or in combinations.
Said invention also encompasses the use of said composition to enable the use of methylsalidroside and ginsenoside rg3 in the treatment of alcohol addiction and the manufacture thereof for this purpose.
Claims
1. A composition for use in the treatment of the alcohol addiction, said composition being obtained by the components selected from the group comprising 20-(s)-ginsenoside rg3, 20-(s)-B-ginsenoside rg3 that are used individually or in combinations.
2. A composition according to Claim 1 characterized in that it comprises 1-99% by weight 20-(s)-ginsenoside rg3.
3. A composition according to Claim 1 characterized in that it comprises 99-1% by weight 20-(s)-B-ginsenoside rg3.
4. Use of the components according to Claims 1 to 3 obtained individually or in combinations from the group consisting of 20-(s)-ginsenoside rg3, 20-(s)-B- ginsenoside rg3 for the manufacture of a composition for the treatment of alcohol addiction.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TR201305046 | 2013-04-29 | ||
TR2013/05046 | 2013-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2014178803A1 true WO2014178803A1 (en) | 2014-11-06 |
Family
ID=49759517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/TR2013/000325 WO2014178803A1 (en) | 2013-04-29 | 2013-10-14 | A composition for use in the treatment of alcohol addiction |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2014178803A1 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE20119321U1 (en) * | 2001-11-19 | 2002-05-29 | mediWirk GmbH, 17489 Greifswald | Pharmaceutical preparation |
CN1911437A (en) * | 2006-06-28 | 2007-02-14 | 杨贻方 | Sobering-up beverage |
WO2009094177A1 (en) * | 2008-01-24 | 2009-07-30 | Raptor Therapeutics Inc. | Protopanaxadiol-type ginsenoside compositions and uses thereof |
-
2013
- 2013-10-14 WO PCT/TR2013/000325 patent/WO2014178803A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE20119321U1 (en) * | 2001-11-19 | 2002-05-29 | mediWirk GmbH, 17489 Greifswald | Pharmaceutical preparation |
CN1911437A (en) * | 2006-06-28 | 2007-02-14 | 杨贻方 | Sobering-up beverage |
WO2009094177A1 (en) * | 2008-01-24 | 2009-07-30 | Raptor Therapeutics Inc. | Protopanaxadiol-type ginsenoside compositions and uses thereof |
Non-Patent Citations (1)
Title |
---|
DATABASE WPI Week 200744, Derwent World Patents Index; AN 2007-446853, XP002719524 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB2545368A (en) | Diversion-resistant opioid formulations | |
WO2013006729A3 (en) | Cannabinoid receptor binding agents, compositions and methods | |
WO2016090287A3 (en) | Transdermal cannabinoid formulations | |
UY35334A (en) | COMPOUNDS AND COMPOSITIONS AS SELECTIVE DEGRADANTS OF THE ESTROGEN RECEIVER | |
WO2012037410A3 (en) | Estrogen receptor modulators and uses thereof | |
MX2019006221A (en) | Preparation of solid cyclodextrin complexes for ophthalmic active pharmaceutical ingredient delivery. | |
SG10201907588XA (en) | Androgen Receptor Modulators And Uses Thereof | |
WO2018042362A9 (en) | Muscarinic m1 receptor positive allosteric modulators | |
JP2017536398A5 (en) | ||
GB201201314D0 (en) | Composition | |
WO2017100700A3 (en) | Peptides for renal therapy | |
AR074240A1 (en) | COMPOUND 3- (4-CHLORO-2-FLUOROBENCIL) -2-METHYL-N- (5- METHYL-1H- PIRAZOL-3-IL) -8- (MORFOLINOMETIL) IMIDAZO (1,2-B) PIRIDAZIN -6- AMINA OR A PHARMACEUTICALLY ACCEPTABLE SALT OF THE SAME, ITS USE TO PREPARE A USEFUL MEDICINAL PRODUCT FOR THE TREATMENT OF CHRONIC MYELOPROLIFERANT DISORDERS AND ASOCI CONDITIONS | |
PH12017501424B1 (en) | Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity | |
TN2011000282A1 (en) | Alkaloid aminoester derivatives and medicinal composition thereof | |
MX2015015589A (en) | Compositions and methods for delivery of hydrophobic active agents. | |
BR112017015487A2 (en) | COMPOUND; COMPOSITION; METHOD OF TREATMENT AND / OR PREVENTION OF MIGRAINE, ALS, ALZHEIMER'S DISEASE, PARKINSON'S DISEASE, EXTRAPYRIMIDAL DISORDERS, DEPRESSION, NAUSEA, AEMESIS, SYNDROME OF THE WASTE LEGS, INSOMENESS, HYGERNESS, AGING , ANXIETY, DRUG DEPENDENCIES, DYSTONIA, PARASSONIA OR HYPERLACTINEMIA IN AN INDIVIDUAL; AGONIZATION METHODS OF D2, 5-HT1D, 5-HT1A AND 5-HT2C RECEPTORS, IN AN INDIVIDUAL; ANTAGONIZATION METHOD OF THE D3 RECEPTOR IN AN INDIVIDUAL; METHODS OF SELECTIVE AGONIZATION OF RECEPTORS 5 -HT1D, AND 5-HT2C, METHOD OF PROVIDING FUNCTIONAL ANTAGONIST ACTIVITY IN RECEPTOR 5 -HT2B OR IN RECEIVER 5-HT7, OR IN BOTH, IN AN INDIVIDUAL; METHOD OF PROVIDING FUNCTIONAL ANTAGONIST ACTIVITY IN ADRENERGIC RECEPTORS IN AN INDIVIDUAL | |
EA201590030A1 (en) | DRY POWDER INHALERS, CONTAINING CARRIER, EXCELLENT FROM LACTOSE, AND THIRD COMPONENT | |
AR097078A1 (en) | COMBINATIONS THAT INCLUDE MABA AND CORTICOSTEROID COMPOUNDS, USE, KIT AND COMPOUND | |
WO2015116856A3 (en) | Farnesoid x receptor antagonists | |
JP2015514739A5 (en) | ||
EP4414037A3 (en) | Morphinan derivatives for the treatment of opioid delta receptor agonist-related diseases | |
WO2014178803A1 (en) | A composition for use in the treatment of alcohol addiction | |
EP4356964A3 (en) | Use of igf-2 receptor agonist ligands for treatment of angelman syndrome and autism | |
MX2017015047A (en) | Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity. | |
WO2014014698A3 (en) | Bitopic muscarinic agonists and antagonists and methods of synthesis and use thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13803303 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
32PN | Ep: public notification in the ep bulletin as address of the adressee cannot be established |
Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FORM 1205N DATED 05/02/2016) |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 13803303 Country of ref document: EP Kind code of ref document: A1 |