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豚鼠回肠的α和β肾上腺素能受体介导反应以及神经元摄取抑制的作用

Alpha- and beta-adrenoceptor-mediated responses of the guinea-pig ileum and the effects of neuronal uptake inhibition.

作者信息

Broadley K J, Grassby P F

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Dec;331(4):316-23. doi: 10.1007/BF00500813.

Abstract

The effects of noradrenaline and isoprenaline were examined on preparations of guinea-pig ileum, in which contractions were induced by three different methods; by transmural electrical stimulation, by exogenous carbachol and by potassium depolarization. Alpha- or beta-adrenoceptor-mediated responses were examined by construction of cumulative concentration-response curves in the presence of propranolol (10(-6) M) and phentolamine (5 X 10(-6) M) respectively. Stimulation of alpha-adrenoceptors by noradrenaline virtually abolished the twitches from transmural stimulation, but only partially inhibited the carbachol- and potassium-induced contractions. The effects on the last two preparations were attributed to a post-synaptic inhibition at alpha-adrenoceptors on the longitudinal smooth muscle. In the transmurally-stimulated preparation there was an additional pre-synaptic alpha-adrenoceptor-mediated inhibition of cholinergic transmission. The maximum beta-adrenoceptor-mediated inhibition of all three preparations to noradrenaline and isoprenaline was of the same magnitude and attributed only to a post-synaptic action on longitudinal smooth muscle. The predominant post-synaptic beta-adrenoceptor-mediated (carbachol-contracted ileum) and pre-synaptic alpha-adrenoceptor-mediated (transmurally-stimulated ileum) relaxations were significantly (P less than 0.05) potentiated by the neuronal uptake inhibitor desmethylimipramine. These receptors may therefore be considered to be closely associated with the sympathetic innervation. The effect on the post-synaptic alpha-adrenoceptor-mediated relaxation was equivocal. Additional minor excitatory responses were identified as a direct alpha-adrenoceptor-mediated contractile response to noradrenaline and as a beta-adrenoceptor-mediated potentiation of transmural stimulation by isoprenaline, possibly due to facilitation of cholinergic transmitter release.

摘要

研究了去甲肾上腺素和异丙肾上腺素对豚鼠回肠标本的作用,其中通过三种不同方法诱导收缩:经壁电刺激、外源性卡巴胆碱和钾去极化。分别在普萘洛尔(10⁻⁶ M)和酚妥拉明(5×10⁻⁶ M)存在的情况下构建累积浓度-反应曲线,以检测α-或β-肾上腺素能受体介导的反应。去甲肾上腺素对α-肾上腺素能受体的刺激实际上消除了经壁刺激引起的抽搐,但仅部分抑制了卡巴胆碱和钾诱导的收缩。对后两种标本的作用归因于纵向平滑肌上α-肾上腺素能受体的突触后抑制。在经壁刺激的标本中,存在额外的突触前α-肾上腺素能受体介导的胆碱能传递抑制。所有三种标本对去甲肾上腺素和异丙肾上腺素的最大β-肾上腺素能受体介导的抑制作用强度相同,且仅归因于对纵向平滑肌的突触后作用。神经元摄取抑制剂去甲替林显著(P<0.05)增强了主要的突触后β-肾上腺素能受体介导的(卡巴胆碱收缩的回肠)和突触前α-肾上腺素能受体介导的(经壁刺激的回肠)松弛。因此,这些受体可能被认为与交感神经支配密切相关。对突触后α-肾上腺素能受体介导的松弛的影响不明确。额外的轻微兴奋反应被确定为对去甲肾上腺素的直接α-肾上腺素能受体介导的收缩反应以及异丙肾上腺素对经壁刺激的β-肾上腺素能受体介导的增强作用,这可能是由于胆碱能递质释放的促进。

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