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1.
Neuroscience Bulletin ; (6): 1039-1050, 2021.
Article in Chinese | WPRIM | ID: wpr-951974

ABSTRACT

GABA is the main inhibitory neurotransmitter in the CNS acting at two distinct types of receptor: ligand-gated ionotropic GABA

2.
Chinese journal of integrative medicine ; (12): 932-940, 2016.
Article in English | WPRIM | ID: wpr-229530

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of Bushen Yisui Capsule (, BSYSC) on the oligodendrocyte lineage genes (Olig) 1 and Olig2 in C57BL/6 mice with experimental autoimmune encephalomyelitis (EAE) in order to explore the remyelination effect of BSYSC.</p><p><b>METHODS</b>The mice were randomly divided into normal control (NC), EAE model (EAE-M), prednisone acetate (PA, 6 mg/kg), BSYSC high-dose (3.02 g/kg) and BSYSC low-dose (1.51 g/kg) groups. The mice were induced by immunization with myelin oligodendrocyte glycoprotein (MOG) 35-55. The neurological function scores were assessed once daily. The pathological changes in mice brains were observed with hematoxylin-eosin (HE) staining and transmission electron microscope (TEM). The protein expressions of myelin basic protein (MBP), Olig1 and Olig2 in brains were measured by immunohistochemistry. The mRNA expressions of Olig1 and Olig 2 was also determined by quantitative real-time polymerase chain reaction.</p><p><b>RESULTS</b>Compared with the EAE-M mice, (1) the neurological function scores were significantly decreased in BSYSC-treated mice on days 22 to 40 (P<0.01); (2) the inflammatory cells and demyelination in brains were reduced in BSYSC-treated EAE mice; (3) the protein expression of MBP was markedly increased in BSYSC-treated groups on day 18 and 40 respectively (P<0.05 or P<0.01); (4) the protein expression of Olig1 was increased in BSYSC (3.02 g/kg)-treated EAE mice on day 40 (P<0.01). Protein and mRNA expression of Olig2 was increased in BSYSC-treated EAE mice on day 18 and 40 (P<0.01).</p><p><b>CONCLUSION</b>The effects of BSYSC on reducing demyelination and promoting remyelination might be associated with the increase of Olig1 and Olig2.</p>


Subject(s)
Animals , Female , Basic Helix-Loop-Helix Transcription Factors , Genetics , Metabolism , Brain , Pathology , Bromodeoxyuridine , Metabolism , Capsules , Drugs, Chinese Herbal , Pharmacology , Therapeutic Uses , Encephalomyelitis, Autoimmune, Experimental , Drug Therapy , Genetics , Pathology , Fluorescent Antibody Technique , Mice, Inbred C57BL , Myelin-Oligodendrocyte Glycoprotein , Metabolism , Nerve Tissue Proteins , Genetics , Metabolism , Oligodendrocyte Transcription Factor 2 , RNA, Messenger , Genetics , Metabolism
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