Pruneau D, Angus J A
Baker Medical Research Institute, Prahran, Victoria, Australia.
Eur J Pharmacol. 1990 Aug 2;184(1):127-33. doi: 10.1016/0014-2999(90)90673-t.
The effects of omega-conotoxin GVIA (omega-CTX), a blocker of N-type voltage-operated calcium channels (VOCCs), were investigated in the pithed rat, omega-CTX (1.6 and 3.2 micrograms/kg i.v.) did not alter resting diastolic pressure or heart rate nor the pressor and chronotropic responses to noradrenaline injections (0.1-10 micrograms/kg). In contrast, the pressor responses to electrical stimulation of the whole spinal cord (0.2-6.4 Hz) were dose dependently reduced by omega-CTX whereas the concomitant tachycardia was less affected. When selective stimulation of the cardiac sympathetic outflow was applied, the resulting chronotropic response was more sensitive to omega-CTX. This result is discussed in the light of the possible interference of adrenal catecholamine release during whole spinal cord stimulation which is not sensitive to omega-CTX. These results provide in vivo evidence that omega-CTX is able to reduce sympathetic neurotransmission to the vasculature and the heart, presumably by blocking N-type VOCCs on pre- and post-ganglionic nerve terminals.
研究了N型电压门控钙通道(VOCCs)阻滞剂ω-芋螺毒素GVIA(ω-CTX)对脊髓毁损大鼠的作用。静脉注射ω-CTX(1.6和3.2微克/千克)不会改变静息舒张压或心率,也不会改变对去甲肾上腺素注射(0.1 - 10微克/千克)的升压和变时反应。相反,ω-CTX剂量依赖性地降低了对整个脊髓电刺激(0.2 - 6.4赫兹)的升压反应,而伴随的心动过速受影响较小。当选择性刺激心脏交感神经传出纤维时,所产生的变时反应对ω-CTX更敏感。鉴于在整个脊髓刺激期间肾上腺儿茶酚胺释放可能受到干扰且对ω-CTX不敏感,对该结果进行了讨论。这些结果提供了体内证据,表明ω-CTX能够减少对血管系统和心脏的交感神经传递,推测是通过阻断神经节前和节后神经末梢上的N型VOCCs来实现的。