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高浓度山莨菪碱对离体犬血管α-肾上腺素能反应的抑制作用。

Anisodamine at higher concentrations in inhibiting alpha-adrenergic responses in isolated canine blood vessels.

作者信息

Guo H Y, Lorenz R R, Vanhoutte P M

机构信息

Department of Pathophysiology, Faculty of Basic Medicine, Peking Union Medical College, Beijing.

出版信息

Chin Med J (Engl). 1993 Jun;106(6):452-7.

PMID:7900973
Abstract

The present study was designed to examine the effect of higher concentration of anisodamine on alpha-adrenergic responses in isolated canine blood vessels. Up to 10(-3) mol/L, anisodamine did not significantly affect the responses of saphenous vein to alpha 2-adrenergic agonist UK-14, 304. In contrast, anisodamine (10(-5), 10(-4), 10(-3) mol/L) caused the concentration-response curves of femoral artery to norepinephrine (pA2 = 4.81 +/- 0.11) to phenylephrine (pA2 = 4.86 +/- 0.20) shift markedly. However, the antagonism on the alpha 1-adrenergic responses of canine femoral artery to norepinephrine and phenylephrine by higher concentrations of anisodamine produces dose ratios which yield a linear Schild regression with a slope less than unity, indicating an inequilibrium between agonist, antagonist, and receptors. The probable mechanisms involved are discussed.

摘要

本研究旨在考察高浓度山莨菪碱对离体犬血管α-肾上腺素能反应的影响。高达10⁻³mol/L时,山莨菪碱对隐静脉对α₂-肾上腺素能激动剂UK-14,304的反应无显著影响。相反,山莨菪碱(10⁻⁵、10⁻⁴、10⁻³mol/L)使股动脉对去甲肾上腺素(pA₂ = 4.81 ± 0.11)和去氧肾上腺素(pA₂ = 4.86 ± 0.20)的浓度-反应曲线明显右移。然而,高浓度山莨菪碱对犬股动脉对去甲肾上腺素和去氧肾上腺素的α₁-肾上腺素能反应的拮抗作用产生的剂量比,其Schild回归呈线性,斜率小于1,表明激动剂、拮抗剂和受体之间存在不平衡。文中讨论了可能涉及的机制。

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