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Zhongguo Zhong Yao Za Zhi ; 36(23): 3315-8, 2011 Dec.
Article in Chinese | MEDLINE | ID: mdl-22393743

ABSTRACT

OBJECTIVE: To study the effect of GABA transporter (GAT-1) on the analgesic action of oxysophoridine (OSR) in the central nervous system of mice. METHOD: Hot plate test was used to observe and analyze the effect of gamma aminobutyric acid and the inhibitor of GAT-1 (NO-711) on the analgesic action of oxysophoridine. Real time RT-PCR was used to investigate the influence of OSR on the expression of GAT-1 mRNA induced by formalin in spinal cord and brain of mice. RESULT: Both GABA (2.0 mg x kg(-1), icv) and NO-711(0.125 mg x kg(-1), icv) enhanced the analgesic action of OSR (32.0 mg x kg(-1), iv) in the hot plate test, and the latencies was markedly increased (P < 0.05, P < 0.01). OSR (500.0 mg x kg(-1), iv) significantly inhibited the expression of GAT-1 mRNA induced by formalin (P < 0.05). CONCLUSION: GAT-1 was involved in the analgesia effect of OSR and the down-regulation of GAT-1 mRNA enhanced the analgesic effect.


Subject(s)
Alkaloids/pharmacology , Analgesics/pharmacology , Down-Regulation/drug effects , GABA Plasma Membrane Transport Proteins/genetics , Animals , Brain/drug effects , Brain/metabolism , Female , GABA Plasma Membrane Transport Proteins/metabolism , Gene Expression Regulation/drug effects , Male , Mice , RNA, Messenger/analysis , Spinal Cord/drug effects , Spinal Cord/metabolism
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