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多沙唑嗪和普萘洛尔给药对高胆固醇喂养大鼠脂蛋白脂肪酶的影响。

Effects of doxazosin and propranolol administration on lipoprotein lipases in cholesterol-fed rats.

作者信息

Jansen H, Baggen R G

机构信息

Department of Internal Medicine III, Erasmus University Rotterdam, The Netherlands.

出版信息

J Cardiovasc Pharmacol. 1987;10 Suppl 9:S16-20.

PMID:2447435
Abstract

The effects of alpha 1-adrenergic receptor inhibition with doxazosin, and beta-blockade with propranolol on tissue lipoprotein lipases and plasma lipids were studied in rats. In rats fed a normal lab chow, doxazosin increased heart lipoprotein lipase activity (+14%), while propranolol had the opposite effect (-20%). These effects were not statistically significant when compared with nontreated controls, although the difference between the doxazosin and propranolol groups was significant (p less than 0.05). There were no significant effects on adipose tissue lipoprotein lipase activity or hepatic lipase activity. In rats fed a cholesterol-enriched diet there were similar but smaller effects on heart lipoprotein lipase activity (+5% and -12%, respectively). In these rats alpha 1-inhibition also tended to increase adipose tissue lipoprotein lipase (+14%) and hepatic lipase (+13%), while beta-blockade had the opposite effect (-20% and -9%, respectively). The lipase activities were significantly different between the treatment groups in liver and heart but not in adipose tissue. Doxazosin and propranolol did not affect plasma triglyceride or total cholesterol, but high-density lipoprotein cholesterol was increased during alpha 1-blockade (+24%).

摘要

在大鼠中研究了用多沙唑嗪抑制α1 - 肾上腺素能受体以及用普萘洛尔进行β - 受体阻滞对组织脂蛋白脂肪酶和血浆脂质的影响。在喂食正常实验室饲料的大鼠中,多沙唑嗪增加了心脏脂蛋白脂肪酶活性(+14%),而普萘洛尔则产生相反的效果(-20%)。与未治疗的对照组相比,这些影响在统计学上不显著,尽管多沙唑嗪组和普萘洛尔组之间的差异显著(p小于0.05)。对脂肪组织脂蛋白脂肪酶活性或肝脂肪酶活性没有显著影响。在喂食富含胆固醇饮食的大鼠中,对心脏脂蛋白脂肪酶活性有类似但较小的影响(分别为+5%和-12%)。在这些大鼠中,α1 - 抑制也倾向于增加脂肪组织脂蛋白脂肪酶(+14%)和肝脂肪酶(+13%),而β - 受体阻滞则产生相反的效果(分别为-20%和-9%)。治疗组之间肝和心脏的脂肪酶活性有显著差异,但脂肪组织中没有。多沙唑嗪和普萘洛尔不影响血浆甘油三酯或总胆固醇,但在α1 - 受体阻滞期间高密度脂蛋白胆固醇增加(+24%)。

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