Influence of triiodothyronine on the contractile effect of D-nor-pseudoephedrine.

Carlos Castillo-Henkel, Jorge López-Canales, María del Carmen Castillo-Hernández, Juan Asbun-Bojalil, Raul Morín-Zaragoza, Daniel Rodríguez-Choreño
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Abstract

Here we contrast the vascular smooth muscle contractility produced by D-nor-pseudoephedrine, alone or combined with triiodothyronine, on the aorta and coronary vasculature of the rat. At high concentrations (greater than those found in normal therapeutic dosing) D-nor-pseudoephedrine contracted the aorta. In contrast, it produced vasodilation on pre-contracted aorta independently of the vasoconstrictor employed or the presence of vascular endothelium. D-nor-pseudoephedrine increased coronary perfusion pressure, but the effect was smaller than the vasoconstriction produced by phenylephrine (a full alpha 1 adrenergic agonist), and was blocked by the pre-treatment with triiodothyronine. These results suggest cardiovascular risks in the use of D-nor-pseudoephedrine for weight loss.

三碘甲状腺原氨酸对d -非伪麻黄碱收缩作用的影响。
在这里,我们对比了d -非伪麻黄碱单独或与三碘甲状腺原氨酸联合对大鼠主动脉和冠状血管的血管平滑肌收缩力。在高浓度(大于正常治疗剂量)下,d -非伪麻黄碱收缩主动脉。相反,它对预收缩的主动脉产生血管扩张,而不依赖于血管收缩剂的使用或血管内皮的存在。d -去伪麻黄碱增加冠状动脉灌注压,但作用小于苯肾上腺素(一种全α - 1肾上腺素能激动剂)产生的血管收缩作用,并被三碘甲状腺原氨酸预处理阻断。这些结果表明,使用d -非伪麻黄碱减肥有心血管风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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