AN Jie, CHEN Chang-hua, GUAN Bing-cai, TANG Ming, YU Cheng-gao, LI Zhi-wang. 5-HT2 receptor mediated the potentiation of GABA-activated current in the membrane of the dorsal root ganglion neurons of ratJ. Acta Pharmaceutica Sinica, 2005, 40(1): 1-1.
Citation: AN Jie, CHEN Chang-hua, GUAN Bing-cai, TANG Ming, YU Cheng-gao, LI Zhi-wang. 5-HT2 receptor mediated the potentiation of GABA-activated current in the membrane of the dorsal root ganglion neurons of ratJ. Acta Pharmaceutica Sinica, 2005, 40(1): 1-1.

5-HT2 receptor mediated the potentiation of GABA-activated current in the membrane of the dorsal root ganglion neurons of rat

  • AimTo explore the modulation of 5-HT on GABA-activated current (IGABA) in the membrane of rat dorsal root ganglion (DRG) neurons and its mechanism. MethodsRat DRG neurons were isolated mechanically and enzymatically, on which whole-cell patch clamp recording and repatch technique for intracellular dialysis were performed. ResultsIn the majority of neurons examined (92.0%, 69/75) GABA induced a concentration-dependent inward current. In neurons sensitive to GABA preapplication of 5-HT produced potentiation effect (82.6%, 57/69) on IGABA. Preapplication of 5-HT at concentrations of 1×10-6, 1×10-5, 1×10-4 and 1×10-3 mol·L-1 potentiated IGABA by (35±8)% (n=8), (47±11)% (n=10), (65±17)% (n=9) and (75±18)% (n=11), respectively. This effect was mimicked by α-methyl-5-HT (1×10-6 mol·L-1), a specific 5-HT2 receptor agonist, and reversed by cyproheptadine, a selective 5-HT2 receptor antagonist. The potentiation of IGABA by 5-HT was irrespective to whether the I5-HT presents or not in a subset of neurons. The concentration-response curves for GABA before and after pretreatment with 5-HT manifested the same threshold value and similar EC50 (2.0×10-5 and 1.9×10-5 mol·L-1, respectively), while the maximal value of IGABA for the latter was 33.6% higher than that for the former. Intracellular dialysis with GDP-β-S or H-7 abolished the potentiation of IGABA by 5-HT, while H-9 did not. Conclusion5-HT can potentiate GABA-activated current via PKC-dependent phosphorylation of GABAA receptor following the activation of 5-HT2 receptor.
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