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Influence of Triiodothyronine on the Contractile Effect of D-Nor-Pseudoephedrine

机译:三碘噻吩对D-NOR-Pseudoephedrine的收缩效果的影响

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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 ciiadrenergic 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.
机译:在这里,我们将D-NOR-PSEUDOEPHEDRINE,单独或与三碘罗酮组合在大鼠的主动脉和冠状动脉脉管系统上形成对比血管平滑肌收缩性。在高浓度(大于正常治疗剂量中发现的高浓度)D-NOR-PSEUDOPHEDRINE收缩了主动脉。相比之下,它在采用的血管收缩剂或血管内皮的存在之外,它在预挛缩主动脉上产生血管舒张。 D-NOR-PSEUDOPHEDRINE增加冠状动脉灌注压力,但效果小于苯肾上腺素产生的血管收缩(全CIADRENICICICART),并通过用三碘罗酮预处理封闭。这些结果表明,在使用D-NOR-PSEUDOPHEDRINE进行体重减轻的心血管风险。

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