Mackenzie I, Burnstock G
Eur J Pharmacol. 1984 Oct 1;105(1-2):85-94. doi: 10.1016/0014-2999(84)90651-4.
A comparison was made between the effects of several neuropeptides and ATP as possible mediators of the non-adrenergic, non-cholinergic excitatory response in detrusor strips from the guinea-pig urinary bladder. Both substance P and vasoactive intestinal polypeptide produced contractions of the guinea-pig bladder, but the form of the atropine-resistant neurogenic excitation was mimicked more precisely by ATP. Neither methionine enkephalin nor leucine enkephalin had a prominent direct action on the smooth muscle (up to 100 microM) and did not significantly modify the cholinergic or non-cholinergic components of the response elicited by field stimulation. A proteolytic enzyme, chymotrypsin (10 U/ml), antagonised the excitatory effect of substance P, but not that of the non-adrenergic, non-cholinergic excitatory response or ATP. The slow excitation elicited by a high concentration of vasoactive intestinal polypeptide (10 microM), in contrast to responses elicited by ATP or field stimulation, was attenuated by preincubation with the structurally related polypeptide PHI, which was itself inactive (up to 10 microM). The present observations argue against a role for the peptides studied as neuromuscular transmitters in the detrusor but do not preclude such a role for ATP.
对几种神经肽和ATP的作用进行了比较,它们可能是豚鼠膀胱逼尿肌条中非肾上腺素能、非胆碱能兴奋反应的介质。P物质和血管活性肠肽均可引起豚鼠膀胱收缩,但ATP更精确地模拟了阿托品抵抗性神经源性兴奋的形式。甲硫氨酸脑啡肽和亮氨酸脑啡肽对平滑肌均无显著直接作用(高达100μM),且对场刺激引起的反应中的胆碱能或非胆碱能成分无显著影响。一种蛋白水解酶,胰凝乳蛋白酶(10 U/ml),可拮抗P物质的兴奋作用,但不拮抗非肾上腺素能、非胆碱能兴奋反应或ATP的兴奋作用。与ATP或场刺激引起的反应相反,高浓度血管活性肠肽(10μM)引起的缓慢兴奋可被与结构相关的无活性肽PHI(高达10μM)预孵育所减弱。目前的观察结果不支持所研究的肽作为逼尿肌神经肌肉递质的作用,但不排除ATP有此作用。