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ω-芋螺毒素GVIA是大鼠小肠系膜动脉交感神经源性反应的强效抑制剂。

Omega-conotoxin GVIA is a potent inhibitor of sympathetic neurogenic responses in rat small mesenteric arteries.

作者信息

Pruneau D, Angus J A

机构信息

Baker Medical Research Institute, Prahran, Victoria, Australia.

出版信息

Br J Pharmacol. 1990 May;100(1):180-4. doi: 10.1111/j.1476-5381.1990.tb12073.x.

Abstract
  1. We have investigated the effects of the N-type calcium channel blocker, omega-conotoxin GVIA, on contractile responses to nerve stimulation, noradrenaline and KCl in rat small mesenteric arteries. In separate experiments, single and summated excitatory junctional potentials (e.j.ps) evoked by nerve stimulation were recorded with an intracellular electrode in the absence and presence of omega-conotoxin. 2. Electrical field stimulation of intramural sympathetic nerves (30 V; 0.25 ms pulse width; 3 s train length; 4-24 Hz) caused frequency-dependent contractions. Cumulative concentration-response curves for the contractions induced by noradrenaline and KCl were constructed in the same preparations. Stimulation at 0.2 Hz and 10 Hz induced respectively single e.j.ps without contractions and summated e.j.ps associated with a contractile response. 3. omega-Conotoxin (0.1 to 3 nM) inhibited markedly and in a concentration-dependent manner both the contractions and e.j.ps to electrical field stimulation. The concentration-response curves to exogenous noradrenaline and KCl remained unaffected. 4. The time-course for the effects of omega-conotoxin (0.3 to 3 nM) indicated a slow onset of action with at least one hour to achieve an equilibrium. 5. The experiments indicate that omega-conotoxin acts prejunctionally to inhibit sympathetic neurotransmission in rat small arteries presumably by inhibition of noradrenaline release. We suggest that omega-conotoxin could be a useful tool to study the control of vascular tone through the autonomic nervous system.
摘要
  1. 我们研究了N型钙通道阻滞剂ω-芋螺毒素GVIA对大鼠小肠系膜动脉神经刺激、去甲肾上腺素和氯化钾收缩反应的影响。在单独的实验中,在有无ω-芋螺毒素的情况下,用细胞内电极记录神经刺激诱发的单个和总和兴奋性突触后电位(e.j.ps)。2. 对壁内交感神经进行电场刺激(30V;0.25ms脉冲宽度;3s串长;4 - 24Hz)引起频率依赖性收缩。在相同的标本中构建去甲肾上腺素和氯化钾诱发收缩的累积浓度-反应曲线。0.2Hz和10Hz的刺激分别诱发无收缩的单个e.j.ps和与收缩反应相关的总和e.j.ps。3. ω-芋螺毒素(0.1至3nM)以浓度依赖性方式显著抑制对电场刺激的收缩和e.j.ps。对外源性去甲肾上腺素和氯化钾的浓度-反应曲线不受影响。4. ω-芋螺毒素(0.3至3nM)作用的时间进程表明起效缓慢,至少需要一小时才能达到平衡。5. 实验表明,ω-芋螺毒素可能通过抑制去甲肾上腺素释放,在突触前发挥作用,抑制大鼠小动脉中的交感神经传递。我们认为,ω-芋螺毒素可能是研究通过自主神经系统控制血管张力的有用工具。

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