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慢性去甲肾上腺素输注对家兔肾上腺素能受体数量的调节作用。

Regulation of adrenergic receptor number following chronic noradrenaline infusion in the rabbit.

作者信息

Deighton N M, Brown A D, Hamilton C A, Reid J L

机构信息

University Department of Materia Medica, Stobhill General Hospital, Glasgow, United Kingdom.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 Nov;338(5):517-22. doi: 10.1007/BF00179323.

Abstract

In order to study noradrenaline-induced regulation of alpha- and beta-adrenoceptors, groups of male New Zealand White rabbits (n = 8) were treated with intravenous noradrenaline (0.09 mumol/kg x h) or ascorbate (0.1%) for 10 days via osmotic minipumps implanted in the femoral vein, and the number of cardiac, lung and lymphocyte beta-adrenoceptors as well as renal and platelet alpha 2-adrenoceptors were determined. 1. The mean arterial blood pressure, heart rate and catecholamine levels were measured before commencing, and after 24 h and 10 days infusion. Circulating noradrenaline concentrations were elevated approximately 6-fold at 24 h and were sustained at these levels after 10 days administration of noradrenaline. There were no significant alterations in the blood pressure while a significant decrease in the heart rate was observed at 24 h. 2. Alpha 2-adrenoceptor density was assessed using [3H]-yohimbine. A significant decrease in the number of alpha 2-adrenoceptors in the kidney was observed following the 10 days infusion with noradrenaline. This down-regulation was in marked contrast to the lack of alteration in platelet alpha 2-adrenoceptor number and the platelet alpha 2-adrenoceptor mediated aggregatory response. 3. The density of beta-adrenoceptors in lymphocytes, heart and lung were quantified using (-)[125I]iodocyanopindolol (ICYP). The noradrenaline infusions caused significant reductions in beta-adrenoceptor number in the heart and lung (containing predominantly beta 1-adrenoceptors) but not in lymphocytes (possessing mainly beta 2-adrenoceptors). The KD-values (pM) for ICYP binding to heart and lung were also significantly decreased in the present studies.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了研究去甲肾上腺素诱导的α和β肾上腺素能受体的调节,将雄性新西兰白兔分成几组(n = 8),通过植入股静脉的渗透微型泵,用静脉注射去甲肾上腺素(0.09 μmol/kg·h)或抗坏血酸(0.1%)处理10天,然后测定心脏、肺和淋巴细胞β肾上腺素能受体以及肾脏和血小板α2肾上腺素能受体的数量。1. 在开始输注前、输注24小时和10天后测量平均动脉血压、心率和儿茶酚胺水平。去甲肾上腺素输注24小时后,循环中的去甲肾上腺素浓度升高约6倍,给药10天后维持在这些水平。血压没有显著变化,而在24小时时观察到心率显著下降。2. 使用[3H]育亨宾评估α2肾上腺素能受体密度。去甲肾上腺素输注10天后,观察到肾脏中α2肾上腺素能受体数量显著减少。这种下调与血小板α2肾上腺素能受体数量和血小板α2肾上腺素能受体介导的聚集反应缺乏变化形成明显对比。3. 使用(-)[125I]碘氰吲哚洛尔(ICYP)对淋巴细胞、心脏和肺中的β肾上腺素能受体密度进行定量。去甲肾上腺素输注导致心脏和肺(主要含有β1肾上腺素能受体)中的β肾上腺素能受体数量显著减少,但淋巴细胞(主要含有β2肾上腺素能受体)中的数量没有减少。在本研究中,ICYP与心脏和肺结合的KD值(pM)也显著降低。(摘要截断于250字)

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