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利多卡因对大鼠回肠肠道平滑肌的作用。

Effect of lignocaine on intestinal smooth muscle of rat ileum.

作者信息

Wali F A

出版信息

Acta Physiol Hung. 1986;68(1):61-71.

PMID:3751621
Abstract

The effect of lignocaine on tone and contractility of intestinal smooth muscle, and on contractures produced by ACh or TEA, was studied in isolated ileum of the rat. Lignocaine (0.1-100 microM) produced concentration-dependent contractures in the rat ileum. In low concentrations, lignocaine increased the amplitude of spontaneous contractions and contractions produced by transmural stimulation. High concentrations of lignocaine abolished all contractile responses and produced a marked contracture in rat ileum. Lignocaine (10 microM) also reduced the contractures produced by ACh (0.01-10 microM). In contrast, the contractures produced by TEA (0.1-10 mM) were markedly increased by lignocaine. Furthermore, the contracture produced by lignocaine was reduced by lowering the external calcium from 2.5 mM to 1.5 mM. It was concluded that lignocaine in moderate and high concentrations produces a contracture in rat intestinal smooth muscle. Whereas lignocaine reduces the ACh-induced contracture, it increases that produced by TEA in the same preparation. The results further suggest that lignocaine modifies cholinergic responses and affects excitation-contraction coupling in rat intestinal smooth muscle.

摘要

在大鼠离体回肠中研究了利多卡因对肠道平滑肌张力和收缩性以及对乙酰胆碱(ACh)或四乙铵(TEA)所致挛缩的影响。利多卡因(0.1 - 100微摩尔)在大鼠回肠中产生浓度依赖性挛缩。在低浓度时,利多卡因增加自发收缩的幅度以及经壁刺激所产生收缩的幅度。高浓度的利多卡因消除所有收缩反应并在大鼠回肠中产生明显的挛缩。利多卡因(10微摩尔)也减少了由ACh(0.01 - 10微摩尔)所产生的挛缩。相反,利多卡因使TEA(0.1 - 10毫摩尔)所产生的挛缩明显增加。此外,通过将细胞外钙从2.5毫摩尔降至1.5毫摩尔,可减少利多卡因所产生的挛缩。得出的结论是,中等浓度和高浓度的利多卡因在大鼠肠道平滑肌中产生挛缩。虽然利多卡因减少ACh诱导的挛缩,但在同一标本中它增加TEA所产生的挛缩。结果进一步表明,利多卡因改变胆碱能反应并影响大鼠肠道平滑肌中的兴奋 - 收缩偶联。

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