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去氧肾上腺素与前列腺素E1和F1α对血管肌肉收缩反应的相互作用。

Interaction between phenylephrine and prostaglandins E1 and F1 alpha on the contractile responses of vascular muscle.

作者信息

Pfaffman M A, Chu-Sun D

出版信息

Prostaglandins. 1979 Mar;17(3):375-84. doi: 10.1016/s0090-6980(79)80005-2.

Abstract

Prostaglandins (PGs) E1 or F1 alpha (1.4--8.4 x 10(-8) M) contracted strips of rabbit aorta and increased the contractions produced by 1--6 x 10(-7) M phenylephrine (PE). The addition of the PGs simultaneously with PE or after a low concentration of PE (2 x 10(-7) M) significantly increased the PE-induced contractions. However, when the PGs were added after a higher concentration of PE (6 x 10(-7) M) an additional increase in the PE-induced contraction was produced with PGF1 alpha but not with PGE1. Isobolic plots of the data obtained from the simultaneous addition of PE and the PGs indicate that both PGs interact with PE in a synergistic or potentiative manner, suggesting that their effects are mediated through different receptor mechanisms. Addition of the PGs after a high dose of PE indicates that there may also be either qualitative or quantitative differences between PGE1 and PGF1 alpha.

摘要

前列腺素(PGs)E1或F1α(1.4 - 8.4×10⁻⁸ M)使兔主动脉条收缩,并增强了由1 - 6×10⁻⁷ M去氧肾上腺素(PE)所产生的收缩作用。PGs与PE同时添加或在低浓度PE(2×10⁻⁷ M)之后添加,均显著增强了PE诱导的收缩作用。然而,当在高浓度PE(6×10⁻⁷ M)之后添加PGs时,PGF1α可使PE诱导的收缩作用进一步增强,但PGE1则无此作用。从PE与PGs同时添加所获得的数据的等效应线图表明,两种PGs均以协同或增效方式与PE相互作用,提示它们的作用是通过不同的受体机制介导的。在高剂量PE之后添加PGs表明,PGE1和PGF1α之间可能还存在质或量的差异。

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