Literature DB >> 7030354

Clinical evaluation of GABA in the treatment of cerebrovascular disorders. Multi-center double-blind study in comparison with pyrithioxine and placebo.

E Otomo, G Araki, A Mori, M Kurihara.   

Abstract

The therapeutic efficacy of GABA was compared with pyrithioxine and placebo in 432 patients with cerebrovascular disorders by a multi-center (50 hospitals) double-blind clinical trial. 12 tablets (3 g) of GABA and 3 tablets (600 mg) of pyrithioxine were given daily for 8 weeks. Subjective complaints, neurological and psychiatric findings, activity of daily living were checked at the 4th and 8th weeks after medication. The global improvement rates in GABA-treated groups were 59% and 70% each after 4 and 8 weeks of medication, and were significantly superior to the other two groups. Especially on cerebral arteriosclerosis GABA was more effective than the other two drugs, with statistical significance. As for improvement rates of symptoms there were significant differences between GABA and the other two drugs in subjective complaints and in psychiatric findings. The incidence of side effects was 5%, 20% and 8% in GABA, pyrithioxine and placebo, respectively. The incidence of abnormal laboratory data was 2% (3 cases), 8% (11 cases) and 4% (6 cases), respectively. Those in GABA group were transient and restored to normal values after the trial. It is concluded from these results that GABA is safe and effective in the treatment of cerebrovascular disorders.

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Year:  1981        PMID: 7030354

Source DB:  PubMed          Journal:  Arzneimittelforschung        ISSN: 0004-4172


  11 in total

1.  Oral GABA treatment downregulates inflammatory responses in a mouse model of rheumatoid arthritis.

Authors:  Jide Tian; Jing Yong; Hoa Dang; Daniel L Kaufman
Journal:  Autoimmunity       Date:  2011-05-23       Impact factor: 2.815

Review 2.  gamma-Aminobutyric acid and cardiovascular function.

Authors:  F V DeFeudis
Journal:  Experientia       Date:  1983-08-15

3.  Combining antigen-based therapy with GABA treatment synergistically prolongs survival of transplanted ß-cells in diabetic NOD mice.

Authors:  Jide Tian; Hoa Dang; Daniel L Kaufman
Journal:  PLoS One       Date:  2011-09-22       Impact factor: 3.240

4.  γ-Aminobutyric acid regulates both the survival and replication of human β-cells.

Authors:  Jide Tian; Hoa Dang; Zheying Chen; Alice Guan; Yingli Jin; Mark A Atkinson; Daniel L Kaufman
Journal:  Diabetes       Date:  2013-08-30       Impact factor: 9.461

5.  Combined therapy with GABA and proinsulin/alum acts synergistically to restore long-term normoglycemia by modulating T-cell autoimmunity and promoting β-cell replication in newly diabetic NOD mice.

Authors:  Jide Tian; Hoa Dang; An Viet Nguyen; Zheying Chen; Daniel L Kaufman
Journal:  Diabetes       Date:  2014-09       Impact factor: 9.461

6.  Homotaurine Treatment Enhances CD4+ and CD8+ Regulatory T Cell Responses and Synergizes with Low-Dose Anti-CD3 to Enhance Diabetes Remission in Type 1 Diabetic Mice.

Authors:  Jide Tian; Hoa Dang; Karen Anne O'Laco; Min Song; Bryan-Clement Tiu; Spencer Gilles; Christina Zakarian; Daniel L Kaufman
Journal:  Immunohorizons       Date:  2019-10-21

7.  GABA induces a hormonal counter-regulatory response in subjects with long-standing type 1 diabetes.

Authors:  Daniel Espes; Hanna Liljebäck; Henrik Hill; Andris Elksnis; José Caballero-Corbalan; Per-Ola Carlsson
Journal:  BMJ Open Diabetes Res Care       Date:  2021-10

8.  GABAA-Receptor Agonists Limit Pneumonitis and Death in Murine Coronavirus-Infected Mice.

Authors:  Jide Tian; Blake Middleton; Daniel L Kaufman
Journal:  Viruses       Date:  2021-05-23       Impact factor: 5.048

9.  GABA administration prevents severe illness and death following coronavirus infection in mice.

Authors:  Jide Tian; Blake Middleton; Daniel L Kaufman
Journal:  bioRxiv       Date:  2020-10-04

10.  GABA Administration Ameliorates Sjogren's Syndrome in Two Different Mouse Models.

Authors:  Min Song; Jide Tian; Blake Middleton; Cuong Q Nguyen; Daniel L Kaufman
Journal:  Biomedicines       Date:  2022-01-07
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