HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Effects of GABAergic Agents on Multiple Sclerosis. A Narrative Review of In-vivo Models.

AbstractBACKGROUND:
Multiple sclerosis (MS) is a lifelong deteriorating disease characterized by multiple heterogeneous symptoms. Being an autoimmune disease of the central nervous system, mainly affecting the myelin sheath of the nerves ordinarily results in neurological symptoms. GABA has numerous effects on the immune cells, altering cytokine production, cell migration and proliferation. Immune cells express GABA receptors making GABA an inflammation modulator. Therefore, GABAergic- associated agents could provide a compatible add-on therapy for MS patients alleviating their symptoms and providing better quality years.
OBJECTIVE:
This review aims to highlight and provide evidence of the potential benefits of a secondary treatment option in MS patients, aiming to better manage this disease.
METHODS:
We conducted a literature search through PubMed, Scopus and Google Scholar for GABA agonists, antagonists and modulators used in the in vivo model of experimental autoimmune encephalomyelitis (EAE), taking into consideration certain inclusion and exclusion criteria.
RESULTS:
In vivo studies for GABA-a and GABA-b agonists and modulators showed regulation of the autoimmune response in EAE mice. Increased preservation of myelinated sensitive fibers and diminished axonal damage in the CNS was also demonstrated. Further, decreased mononuclear inflammatory infiltration, pro-inflammatory cytokines reduction and reduced levels of Reactive oxygen species (ROS) were also reported. Biological results included decreased peak disease severity, duration, clinical scores and EAE incidence in the treatment groups.
CONCLUSION:
GABA agonists and modulators efficiently challenged different aspects of disease pathophysiology in vivo models of EAE. The studies showed a significant relevance of neuroprotection via modulation of the autoimmune response in EAE rats, indicating that they should be considered proper therapeutic candidates for clinical use, while also further clinical studies could empower their administration in clinical practice.
AuthorsЕleni Stamoula, Alexandra Ainatzoglou, Ioannis Dardalas, Theofanis Vavilis, Vasileios-Periklis Stamatellos, Spyridon Siafis, Thomas Psathas, Ioanna Boskou, Georgios Papazisis
JournalCNS & neurological disorders drug targets (CNS Neurol Disord Drug Targets) Vol. 22 Issue 10 Pg. 1439-1452 ( 2023) ISSN: 1996-3181 [Electronic] United Arab Emirates
PMID36200199 (Publication Type: Review, Journal Article)
CopyrightCopyright© Bentham Science Publishers; For any queries, please email at [email protected].
Chemical References
  • GABA Agonists
  • gamma-Aminobutyric Acid
Topics
  • Mice
  • Rats
  • Animals
  • Multiple Sclerosis (drug therapy)
  • Encephalomyelitis, Autoimmune, Experimental (drug therapy)
  • Central Nervous System
  • GABA Agonists (therapeutic use)
  • gamma-Aminobutyric Acid
  • Mice, Inbred C57BL

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: