Wang X M, Wang X J, Han J S
Sheng Li Xue Bao. 1989 Apr;41(2):179-83.
Behavioral observations have repeatedly shown that the analgesic effect of morphine can be antagonized by intracerebroventricular injection of angiotensin I (A I), although mechanisms underlying the action were obscure. Since a prevention of Ca2+ uptake into the nerve terminals was considered as one of the mechanisms for morphine analgesia, we examined the effect of A I and morphine on the 45Ca uptake by rat brain synaptosomal preparations. Morphine of 10(-8)-10(-6) mol/L produced a dose-related suppression on synaptosomal 45Ca uptake, which was completely reversed by the opioid antagonist naloxone of 10(-6) mol/L. A I of 10(-8)-10(-6) mol/L, on the contrary, enhanced 45Ca uptake. This effect was totally abolished by saralasin, a A I antagonist, at 10(-6) mol/L. When synaptosomal preparations were incubated in a mixture of morphine (10(-6) mol/L) and A I (10(-8)-10(-6) mol/L), the effect of morphine was almost completely reversed. The results suggest that the distinct effect of A I may account for, at least in part, the antagonistic effect of A I on morphine analgesia.
行为学观察反复表明,脑室内注射血管紧张素I(AI)可拮抗吗啡的镇痛作用,但其作用机制尚不清楚。由于阻止Ca2+进入神经末梢被认为是吗啡镇痛的机制之一,我们研究了AI和吗啡对大鼠脑突触体45Ca摄取的影响。10(-8)-10(-6)mol/L的吗啡对突触体45Ca摄取产生剂量相关的抑制作用,10(-6)mol/L的阿片拮抗剂纳洛酮可完全逆转这种抑制作用。相反,10(-8)-10(-6)mol/L的AI可增强45Ca摄取。10(-6)mol/L的AI拮抗剂沙拉新可完全消除这种作用。当突触体制剂在吗啡(10(-6)mol/L)和AI(10(-8)-10(-6)mol/L)的混合物中孵育时,吗啡的作用几乎完全被逆转。结果表明,AI的独特作用可能至少部分解释了AI对吗啡镇痛的拮抗作用。