Sharma J N, Sandrew B B, Wang S C
Arch Int Pharmacodyn Ther. 1979 Sep;241(1):92-9.
The central site and mechanism of alpha-methyldopa-induced hypotension were examined with the microiontophoretic technique which permits the topical application of drugs to single neurons of the bulbar vasomotor center in decerebrate cats. Cardiovascular neurons were identified by their response to an increase in arterial blood pressure following a small intravenous pressor dose of norepinephrine. Microiontophoretic application of alpha-methyldopa was found to have an inhibitory effect on the spontaneous firing rate of cardiovascular neurons. Furthermore, alpha-methyldopa was found to completely block the excitatory response of cardiovascular neurons to iontophoretically applied norepinephrine. Non-cardiovascular neurons, recorded from the same brain area, were unaffected by iontophoretic application of alpha-methyldopa at the same or greater doses that produced responses in cardiovascular neurons. While peripheral factors cannot be entirely ruled out, the present findings are contrary to the postulate that alpha-methyldopa lowers arterial blood pressure by stimulating central alpha-adrenoceptors, causing a reduction of sympathetic outflow to the periphery. Rather, the data indicate that alpha-methyldopa or its metabolites act directly on central alpha-adrenoceptors in a manner which results in reduced activity.
采用微离子电泳技术研究了α-甲基多巴诱导低血压的中枢部位和机制,该技术可将药物局部应用于去大脑猫延髓血管运动中枢的单个神经元。通过对小剂量静脉注射去甲肾上腺素后动脉血压升高的反应来识别心血管神经元。发现微离子电泳应用α-甲基多巴对心血管神经元的自发放电频率有抑制作用。此外,还发现α-甲基多巴能完全阻断心血管神经元对离子电泳应用去甲肾上腺素的兴奋反应。从同一脑区记录的非心血管神经元,在产生心血管神经元反应的相同或更大剂量下,不受α-甲基多巴离子电泳应用的影响。虽然不能完全排除外周因素,但目前的研究结果与α-甲基多巴通过刺激中枢α-肾上腺素能受体降低动脉血压,导致外周交感神经输出减少的假设相反。相反,数据表明α-甲基多巴或其代谢产物以导致活性降低的方式直接作用于中枢α-肾上腺素能受体。