Duckles S P, Kennedy C D
J Pharmacol Exp Ther. 1982 Sep;222(3):562-5.
There is a cholinergic system in large cerebral arteries, but acetylcholine does not mediate the vasodilator response to nerve stimulation. Therefore, the possibility that acetylcholine modulates norepinephrine release must be considered. The effects of cholinergic agonists and antagonists on stimulation-evoked endogenous norepinephrine release from cat and rabbit cerebral arteries were tested at a stimulation frequency of 8 Hz. Acetylcholine (5 X 10(-7) M) decreased norepinephrine release from the cat middle cerebral artery by 40% and by 30% from the rabbit basilar artery. In both species, the effect of acetylcholine was not blocked by hexamethonium but was blocked by atropine. Under the conditions of these experiments, cholinergic and adrenergic nerves are activated simultaneously, so the possibility that cholinergic nerves modulate adrenergic transmission was tested by blocking presynaptic acetylcholine receptors with atropine. However, in both cat and rabbit cerebral arteries, atropine alone had no effect on norepinephrine overflow. These findings suggest that the cholinergic system present in cerebral blood vessels does not modulate norepinephrine release, even though presynaptic cholinergic receptors are present.
在大脑的大动脉中存在胆碱能系统,但乙酰胆碱并不介导对神经刺激的血管舒张反应。因此,必须考虑乙酰胆碱调节去甲肾上腺素释放的可能性。在8Hz的刺激频率下,测试了胆碱能激动剂和拮抗剂对猫和兔脑动脉刺激诱发的内源性去甲肾上腺素释放的影响。乙酰胆碱(5×10⁻⁷M)使猫大脑中动脉的去甲肾上腺素释放减少40%,使兔基底动脉的去甲肾上腺素释放减少30%。在这两个物种中,乙酰胆碱的作用未被六甲铵阻断,但被阿托品阻断。在这些实验条件下,胆碱能神经和肾上腺素能神经同时被激活,因此通过用阿托品阻断突触前乙酰胆碱受体来测试胆碱能神经调节肾上腺素能传递的可能性。然而,在猫和兔的脑动脉中,单独使用阿托品对去甲肾上腺素溢出没有影响。这些发现表明,尽管存在突触前胆碱能受体,但脑血管中的胆碱能系统并不调节去甲肾上腺素的释放。