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前列腺素对大鼠离体肠系膜血管床肾上腺素能反应的调节作用。

Modulation of adrenergic responses by prostanoids in the isolated mesenteric vascular bed of the rat.

作者信息

Mantelli L, Amerini S, Filippi S, Ledda F

机构信息

Department of Pharmacology, University of Florence, Italy.

出版信息

Gen Pharmacol. 1993 Jul;24(4):911-9. doi: 10.1016/0306-3623(93)90169-x.

Abstract
  1. The influences of PGE2, PGE1, iloprost and carbocyclic thromboxane A2 (cTxA2) on the response to adrenergic nerve stimulation, exogenous noradrenaline and perfusion with methoxamine, have been compared in the rat mesenteric vascular bed. 2. PGE2, PGE1 and cTxA2 enhanced the vasoconstrictor response elicited by field stimulation, as well as that induced by noradrenaline and methoxamine. 3. Iloprost did not affect the increase in perfusion pressure induced by field stimulation, slightly reduced the vasoconstrictor response to high concentrations of noradrenaline, and significantly attenuated the increase in vascular tone induced by perfusion with methoxamine. 4. These findings suggest that, in the rat mesenteric vascular bed, prejunctional mechanisms are not involved in the interference exerted by different prostanoids on the vascular response to adrenergic activation.
摘要
  1. 在大鼠肠系膜血管床中,比较了前列腺素E2(PGE2)、前列腺素E1(PGE1)、伊洛前列素和环戊烷前列环素A2(cTxA2)对肾上腺素能神经刺激、外源性去甲肾上腺素及甲氧明灌注反应的影响。2. PGE2、PGE1和cTxA2增强了场刺激引发的血管收缩反应,以及去甲肾上腺素和甲氧明诱导的血管收缩反应。3. 伊洛前列素不影响场刺激诱导的灌注压升高,轻微降低高浓度去甲肾上腺素引起的血管收缩反应,并显著减弱甲氧明灌注诱导的血管张力增加。4. 这些发现表明,在大鼠肠系膜血管床中,不同前列腺素对肾上腺素能激活的血管反应产生干扰时,不涉及突触前机制。

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