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从亚麻籽中分离出的开环异落叶松脂素二葡萄糖苷(SDG),可作为治疗高血压的血管紧张素转换酶抑制剂替代品。

Secoisolariciresinol Diglucoside (SDG) Isolated from Flaxseed, an Alternative to ACE Inhibitors in the Treatment of Hypertension.

作者信息

Prasad Kailash

机构信息

Department of Physiology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

出版信息

Int J Angiol. 2013 Dec;22(4):235-8. doi: 10.1055/s-0033-1351687.

Abstract

Secoisolariciresionol diglucoside (SDG) is a plant lignan isolated from flaxseed and is phytoestrogen. SDG is a potent and long-acting hypotensive agent. Plant phytoestrogens have inhibitory effects on angiotensin-converting enzyme (ACE). The hypotensive effects of SDG, a phytoestrogen, may be mediated through inhibition of ACE. The objective of this study was to investigate if SDG-induced hypotension is mediated through inhibition of ACE. The Sprague Dawley male rats were anesthetized and trachea was cannulated. The right jugular vein was cannulated to administer the drug and the carotid artery was cannulated to record arterial pressures using PIOEZ-1 miniature model transducer (Becton, Dickinson and Company, Franklin Lakes, NJ) and Beckman dynograph (Beckman Instruments, Inc., Schiller Park, IL). The effects of angiotensin I (0.2 µg/kg, intravenously [IV]) in the absence and presence of SDG (10 mg/kg, IV), and SDG alone on systolic, diastolic, and mean arterial pressures were measured before and after 15, 30, and 60 minutes of drug administration. SDG decreased the systolic, diastolic, and mean arterial pressure by 37, 47, and 43%, respectively, at 15 minutes and 18.8, 21.2, and 20.3%, respectively, at 60 minutes. Angiotensin I increased the arterial pressure. SDG decreased angiotensin I-induced rise in the systolic, diastolic, and mean arterial pressures by 60, 58, and 51%, respectively, at 15 minutes and 48, 46, and 30%, respectively, at 60 minutes. The data suggest that SDG reduced the angiotensin I-induced rise in the arterial pressures and hence SDG is a potent ACE inhibitor.

摘要

开环异落叶松树脂酚二葡萄糖苷(SDG)是一种从亚麻籽中分离出来的植物木脂素,属于植物雌激素。SDG是一种强效长效的降压剂。植物雌激素对血管紧张素转换酶(ACE)有抑制作用。作为植物雌激素的SDG的降压作用可能是通过抑制ACE介导的。本研究的目的是调查SDG诱导的低血压是否通过抑制ACE介导。将雄性Sprague Dawley大鼠麻醉并进行气管插管。通过右颈静脉插管给药,通过颈动脉插管,使用PIOEZ - 1微型传感器(Becton, Dickinson and Company, Franklin Lakes, NJ)和贝克曼记纹鼓(Beckman Instruments, Inc., Schiller Park, IL)记录动脉血压。在给药前以及给药15、30和60分钟后,测量在不存在和存在SDG(10 mg/kg,静脉注射)的情况下血管紧张素I(0.2 µg/kg,静脉注射)以及单独使用SDG对收缩压、舒张压和平均动脉压的影响。SDG在15分钟时分别使收缩压、舒张压和平均动脉压降低了37%、47%和43%,在60分钟时分别降低了18.8%、21.2%和20.3%。血管紧张素I使动脉血压升高。SDG在15分钟时分别使血管紧张素I诱导的收缩压、舒张压和平均动脉压升高降低了60%、58%和51%,在60分钟时分别降低了48%、46%和30%。数据表明,SDG降低了血管紧张素I诱导的动脉血压升高,因此SDG是一种强效的ACE抑制剂。

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