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多沙唑嗪对自发性高血压大鼠血管胶原合成、动脉血压及血脂的影响。

Effects of doxazosin on vascular collagen synthesis, arterial pressure and serum lipids in the spontaneously hypertensive rat.

作者信息

Chichester C O, Rodgers R L

机构信息

Department of Pharmacology and Toxicology, University of Rhode Island, Kingston 02881.

出版信息

J Cardiovasc Pharmacol. 1987;10 Suppl 9:S21-6.

PMID:2447437
Abstract

Hypertension in various experimental models, including spontaneously hypertensive rats (SHR), is associated with elevated rates of vascular collagen synthesis. The sympathetic nervous system is an important factor in the etiology of hypertension in SHR. The primary purpose of this study was to determine the effects of the alpha 1-adrenergic receptor antagonist doxazosin on aortic collagen synthesis and on systolic arterial pressure in SHR. Doxazosin was administered either short-term (20 or 200 mg/kg/day by gavage over 5 days) or long-term (0.02 or 0.20 g/L in the drinking water over 8 weeks). Rates of collagen synthesis were determined by incubating aortic segments with 14C-proline in vitro and then measuring either the formation of 14C-hydroxyproline by means of high-performance liquid chromatography, or the amount of radioactivity liberated by collagenase digestion. Systolic arterial pressure was monitored with the standard tail-cuff technique. Both doses of doxazosin depressed aortic collagen synthesis at 8 weeks of treatment, but neither dose had any effect at 4 weeks. In the short-term study only the higher acute dose of doxazosin significantly reduced aortic collagen synthesis; the lower dose had no effect. In the short-term study doxazosin reduced systolic arterial pressure, with a maximum effect at 1-2 days. Tolerance to the depressor effect developed over the remaining 3-4 days, especially with the higher dose. In the 8-week study, the lower doxazosin dose had no effect on systolic arterial pressure, and the higher dose exerted a biphasic effect, moderately but significantly reducing systolic arterial pressure at 1 and 8 weeks of treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在包括自发性高血压大鼠(SHR)在内的各种实验模型中,高血压与血管胶原合成速率升高有关。交感神经系统是SHR高血压病因中的一个重要因素。本研究的主要目的是确定α1肾上腺素能受体拮抗剂多沙唑嗪对SHR主动脉胶原合成和收缩压的影响。多沙唑嗪采用短期给药(5天内每天经口灌胃20或200 mg/kg)或长期给药(8周内饮水中含0.02或0.20 g/L)。通过在体外将主动脉段与14C-脯氨酸孵育,然后用高效液相色谱法测量14C-羟脯氨酸的形成,或通过胶原酶消化测量释放的放射性活度来确定胶原合成速率。用标准尾袖法监测收缩压。治疗8周时,两种剂量的多沙唑嗪均能抑制主动脉胶原合成,但在4周时两种剂量均无作用。在短期研究中,只有较高的急性剂量多沙唑嗪能显著降低主动脉胶原合成;较低剂量无作用。在短期研究中,多沙唑嗪可降低收缩压,在1-2天达到最大效应。在其余3-4天内对降压作用产生耐受性,尤其是较高剂量时。在8周研究中,较低剂量的多沙唑嗪对收缩压无作用,较高剂量产生双相效应,在治疗1周和8周时适度但显著降低收缩压。(摘要截短于250字)

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Selective alpha 1-adrenoreceptor blockers in the treatment of hypertension: should we be using them more?
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Clin Auton Res. 1991 Sep;1(3):251-8. doi: 10.1007/BF01824996.