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降低去甲肾上腺素摄取的药物对家兔升压和血管反应性的影响。

Effect on pressor and vascular responsiveness in rabbits of drugs that decrease norepinephrine uptake.

作者信息

Koivunen D G, Johnson J A

机构信息

H. S. Truman Memorial Veterans Administration Medical Center, Columbia 65201.

出版信息

Proc Soc Exp Biol Med. 1994 Sep;206(4):375-83. doi: 10.3181/00379727-206-43774.

Abstract

The purpose of this study was to determine if decreases in norepinephrine (NE) uptake would result in pressor and vascular hyperresponsiveness to vasoconstrictor substances. These experiments examined the effects of cocaine and imipramine, drugs known to decrease NE uptake, on the changes in arterial pressure and total peripheral resistance (TPR) in response to NE and arginine vasopressin (AVP) in conscious rabbits. The infusion of graded doses of NE resulted in significantly greater increases in mean arterial pressure at all dose levels following the administration of cocaine (0.6 mg/kg iv) or imipramine (0.5 mg/kg) than following the administration of the vehicle alone. The infusion of NE also resulted in greater increases in TPR as well as blood pressure following cocaine or imipramine administration than occurred prior to the administration of these drugs. The infusion of AVP caused significantly larger increases in arterial pressure and in TPR following cocaine or imipramine administration than was seen after the administration of AVP to control rabbits not treated with these drugs. These studies demonstrated that cocaine and imipramine, substances known to decrease NE uptake by the sympathetic nerve terminals, will induce pressor and vascular hyperresponsiveness to NE and AVP in rabbits. These results are in keeping with the concept that pressor and vascular hyperresponsiveness in renal prehypertensive rabbits may be the result of decreases in NE uptake by sympathetic fibers supplying vascular smooth muscle cells.

摘要

本研究的目的是确定去甲肾上腺素(NE)摄取的减少是否会导致对血管收缩物质的升压反应和血管高反应性。这些实验研究了可卡因和丙咪嗪(已知可减少NE摄取的药物)对清醒兔体内动脉压和总外周阻力(TPR)变化的影响,这些变化是对NE和精氨酸加压素(AVP)的反应。静脉注射可卡因(0.6mg/kg)或丙咪嗪(0.5mg/kg)后,在所有剂量水平下,输注分级剂量的NE导致平均动脉压的升高显著大于单独注射溶剂后的升高。与这些药物给药前相比,注射可卡因或丙咪嗪后,输注NE还导致TPR以及血压有更大的升高。与未用这些药物治疗的对照兔相比,注射可卡因或丙咪嗪后,输注AVP导致动脉压和TPR的升高显著更大。这些研究表明,可卡因和丙咪嗪(已知可减少交感神经末梢对NE的摄取的物质)会在兔体内诱导对NE和AVP的升压反应和血管高反应性。这些结果与以下概念一致,即肾性高血压前期兔的升压反应和血管高反应性可能是供应血管平滑肌细胞的交感纤维对NE摄取减少的结果。

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