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前列腺素DP受体激动剂BW245C对麻醉大鼠全身和局部血流动力学的影响。

Effects of BW245C, a prostaglandin dp receptor agonist, on systemic and regional haemodynamics in the anaesthetized rat.

作者信息

Koch Kristin A, Wessale Jerry L, Moreland Robert, Reinhart Glenn A, Cox Bryan F

机构信息

Neurological Diseases Research, Global Pharmaceutical Research and Development, Pharmaceutical Products Division, Abbott Laboratories, Abbott Park, Illinois 60064-6119, USA.

出版信息

Clin Exp Pharmacol Physiol. 2005 Nov;32(11):931-5. doi: 10.1111/j.1440-1681.2005.04287.x.

Abstract
  1. Prostaglandin D (DP) receptor agonists have been shown to induce hypotension in rat models, possibly via peripheral vasodilation. However, it is not known which tissues and organs are most responsive. 2. In the present study, BW245C, a DP receptor-selective agonist, was administered to Inactin (Sigma, St Louis, MO, USA)-anaesthetized rats. Animals received three serial i.v. infusions (17 min each) of either BW245C (escalating doses of 0.3, 3 and 30 microg/kg; n=6) or vehicle (6% ethanol in normal saline; n=6). Mean arterial pressure (MAP) and heart rate were monitored continuously and regional blood flow was determined by the radionuclide-labelled microsphere method at baseline and at the end of each infusion. 3. It was found that BW245C dose-dependently reduced MAP; blood flow increased in forelimb skeletal muscle and skin, resulting in decreases in the regional vascular resistance (RVR) of skeletal muscle to -6+/-13, -53+/-11 and -68+/-6% of baseline following 0.3, 3 and 30 microg/kg BW245C, respectively (P<0.05 vs vehicle treatment for the two higher doses), and skin to -29+/-8, -55+/-8 (P<0.05) and -30+/-16% of baseline, respectively. Relative to vehicle, blood flow and RVR for brain, heart, lung, liver, stomach and kidney were not significantly affected by BW245C. 4. These results demonstrate that the hypotension resulting from DP receptor activation in the rat is mediated primarily through vasodilation of arterioles of skeletal muscle independent of changes in blood flow to vital organs.
摘要
  1. 前列腺素D(DP)受体激动剂已被证明在大鼠模型中可诱导低血压,可能是通过外周血管舒张实现的。然而,尚不清楚哪些组织和器官对此最为敏感。2. 在本研究中,将DP受体选择性激动剂BW245C给予用英纳克(西格玛,美国密苏里州圣路易斯)麻醉的大鼠。动物接受了三次连续的静脉输注(每次17分钟),分别输注BW245C(剂量递增,分别为0.3、3和30微克/千克;n = 6)或赋形剂(生理盐水中含6%乙醇;n = 6)。在基线时以及每次输注结束时,连续监测平均动脉压(MAP)和心率,并通过放射性核素标记微球法测定局部血流。3. 发现BW245C可剂量依赖性地降低MAP;前肢骨骼肌和皮肤的血流增加,导致骨骼肌局部血管阻力(RVR)在分别给予0.3、3和30微克/千克BW245C后降至基线的-6±13%、-53±11%和-68±6%(与两个较高剂量的赋形剂处理相比,P<0.05),皮肤的RVR分别降至基线的-29±8%、-55±8%(P<0.05)和-30±16%。相对于赋形剂,BW245C对脑、心、肺、肝、胃和肾的血流和RVR没有显著影响。4. 这些结果表明,大鼠中DP受体激活导致的低血压主要是通过骨骼肌小动脉的血管舒张介导的,而与重要器官的血流变化无关。

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