Antonaccio M J, Robson R D
Br J Pharmacol. 1974 Sep;52(1):41-50. doi: 10.1111/j.1476-5381.1974.tb09685.x.
1 The ability of intravenous L-DOPA to block sympathetic and parsympathetic nerves has been studied in cats and dogs pretreated with a monoamine oxidase inhibitor.2 L-DOPA inhibited positive chronotropic and pressor responses to dimethylphenylpiperazinium (DMPP) and McN-A-343 in dogs, and contractions of the nictitating membrane produced by these ganglion stimulants in cats.3 Responses of the cat nictitating membrane to preganglionic stimulation were inhibited by L-DOPA to a greater extent than those to postganglionic stimulation of the cervical sympathetic chain.4 In dogs, L-DOPA had no vagolytic action, but depressed vasoconstrictor responses elicited in the perfused hind-limb by electrical stimulation of the lumbar sympathetic chain.5 The degree of lumbar sympathetic chain inhibition correlated with the pressor response following L-DOPA, and both effects were prevented by prior decarboxylase inhibition.6 These results suggest that the decarboxylation products of L-DOPA do not impair parasympathetic nerve activity but depress sympathetic nerve function predominantly by inhibiting both muscarinic and nicotinic sites of sympathetic ganglia.
已在预先用单胺氧化酶抑制剂处理过的猫和狗身上研究了静脉注射左旋多巴阻断交感神经和副交感神经的能力。
左旋多巴抑制了狗对二甲基苯基哌嗪(DMPP)和 McN - A - 343 的正性变时性和升压反应,以及猫中这些神经节兴奋剂引起的瞬膜收缩。
左旋多巴对猫瞬膜对节前刺激的反应的抑制程度大于对颈交感链节后刺激的反应。
在狗身上,左旋多巴没有迷走神经解阻遏作用,但抑制了通过电刺激腰交感链在灌注后肢中引发的血管收缩反应。
腰交感链抑制程度与左旋多巴后的升压反应相关,并且两种效应都可通过预先抑制脱羧酶来预防。
这些结果表明,左旋多巴的脱羧产物不会损害副交感神经活动,但主要通过抑制交感神经节的毒蕈碱和烟碱部位来抑制交感神经功能。