王灿红,彭德乾,刘洋洋,余章昕,郭鹏,魏建和.沉香醇提物对大鼠气滞血瘀心肌缺血的保护作用[J].药物评价研究,2019,42(7):1279-1285
沉香醇提物对大鼠气滞血瘀心肌缺血的保护作用
Protective effect of agarwood alcohol extracts on myocardial ischemia injury in rats with qi stagnation and blood stasis
投稿时间:2018-10-25  
DOI:10.7501/j.issn.1674-6376.2019.07.004
中文关键词:  沉香醇提物;气滞血瘀;异丙肾上腺素;心肌缺血;血液黏度;抗氧化作用
英文关键词:agarwood alcohol extracts;qi stagnation and blood stasis;isoproterenol;myocardial ischemia;blood viscosity;antioxidant effect
基金项目:海南省自然科学基金(817290);海南省重大科技计划项目(ZDKJ2016004);海南省自然科学基金(217291)
作者单位E-mail
王灿红 中国医学科学院 北京协和医学院 药用植物研究所海南分所 海南省南药资源保护与开发重点实验室和国家中医药管理局沉香可持续利用重点研究室, 海南 海口 570311  
彭德乾 海南医学院药学院, 海南 海口 571199  
刘洋洋 中国医学科学院 北京协和医学院 药用植物研究所海南分所 海南省南药资源保护与开发重点实验室和国家中医药管理局沉香可持续利用重点研究室, 海南 海口 570311  
余章昕 中国医学科学院 北京协和医学院 药用植物研究所海南分所 海南省南药资源保护与开发重点实验室和国家中医药管理局沉香可持续利用重点研究室, 海南 海口 570311  
郭鹏 中国医学科学院 北京协和医学院 药用植物研究所 中草药物质基础与资源利用教育部重点实验室和濒危药材繁育国家工程实验室, 北京 100193 pguo@implad.ac.cn 
魏建和 中国医学科学院 北京协和医学院 药用植物研究所海南分所 海南省南药资源保护与开发重点实验室和国家中医药管理局沉香可持续利用重点研究室, 海南 海口 570311
中国医学科学院 北京协和医学院 药用植物研究所 中草药物质基础与资源利用教育部重点实验室和濒危药材繁育国家工程实验室, 北京 100193 
wjianh@263.net 
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中文摘要:
      目的 研究沉香醇提物对大鼠气滞血瘀心肌缺血损伤的保护作用及机制。方法 大鼠随机分成6组:对照组、模型组、野生沉香醇提物(2.84 g/kg)组和通体沉香醇提物低、中、高剂量(0.71、1.42、2.84 g/kg)组,每天1次,连续ig给药7 d,对照组和模型组ig等体积蒸馏水。除对照组外,采用sc异丙肾上腺素(ISO)联合冰水浸泡诱导大鼠气滞血瘀心肌缺血模型,检测生化指标全血黏度(WBV)、血浆比黏度(PSV),血清中肌酸激酶(CK)、乳酸脱氢酶(LDH)、丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)活性;观察心电图及心肌病理损伤情况;检测血浆中脂质过氧化物(LPO)、过氧化氢(H2O2)、总抗氧化能力(T-AOC)和过氧化氢酶(CAT)的水平;酶联免疫法(ELISA)检测血清中细胞因子5-羟色胺(5-HT)、内皮素(ET)、血栓烷素B2(TXB2)及前列腺素E2(PGE2)的分泌水平。结果 与模型组比较,通体沉香醇提物各剂量组均能显著降低WBV和PSV,改善心电图的异常,显著降低心电图ST段的抬高(P<0.05、0.01);中、高剂量组显著降低血清中心肌酶CK、LDH、ALT和AST活性(P<0.05、0.01、0.001);各剂量组明显减轻心肌组织的病理损伤程度;高、中剂量组均显著降低LPO和H2O2水平,升高T-AOC和SOD水平(P<0.05、0.01、0.001);高剂量组显著降低5-HT水平,各剂量组均显著降低ET、TXB2和PEG2水平(P<0.05、0.01、0.001)。同等剂量下通体沉香醇提物与野生沉香醇提物作用相当。结论 通体沉香醇提物对大鼠气滞血瘀心肌缺血有保护作用,其作用机制与抗氧化、改善血管微循环、调节内皮细胞生长及调节细胞因子的分泌有关。
英文摘要:
      Objective To investigate the cardioprotective effect and its mechanism of agarwood alcohol extract on qi stagnation blood stasis myocardial ischemia injury in rats. Methods Rats were randomly divided into six groups:control group, model group, wild agarwood ethanol extract (2.84 g/kg) group and low, medium and high dose (0.71, 1.42, 2.84 g/kg) groups of agarwood alcohol extract produced by whole-tree agarwood-inducing technique (WTAAE). Rats were ig administrated corresponding drug once a day for 7 d. Rats in control and model group were ig administrated with distilled water of equal volume. Myocardial ischemia injury rat model was established by injecting with isoproterenol (ISO) and stimulated with ice water. The whole blood and plasma specific viscosity (WBV and PSV) were measured by viscometer. The activities of creatine kinase (CK), lactic dehydrogenase (LDH), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were measured in serum. Electrocardiograph (ECG) and myocardial pathological injury were observed. The plasma levels of lipid peroxide (LPO), hydrogen peroxide (H2O2), total antioxidant capacity (T-AOC) and catalase (CAT) were measured. The secreted levels of 5-hydroxyptamine (5-HT), endothelin (ET), thromboxane B2 (TXB2) and prostaglandin E2 (PGE2) were measured by enzyme-linked immunosorbent assay (ELISA). Results Compared with model group, WTAAE could significantly reduce WBV and PSV, improve ECG abnormalities, and significantly reduce ST segment elevation (P<0.05, 0.01); The activities of serum myosin CK, LDH, ALT and AST were significantly decreased in the middle and high dose groups (P<0.05, 0.01 and 0.001); The pathological damage degree of myocardium was significantly reduced in each dose group; LPO and H2O2 levels were significantly decreased in the middle and high dose group, and T-AOC and SOD levels were increased (P<0.05, 0.01 and 0.001); 5-HT levels were significantly decreased in the high dose group, and ET, TXB2 and PEG2 levels were significantly decreased in each dose group (P<0.05, 0.01 and 0.001). At the same dosage, WTAAE had the same effect as that of wild agarwood. Conclusion WTAAE shows a significantly protective effect on myocardial ischemia in rats, and its mechanism is related to the antioxidant activity, regulation of vascular microcirculation, endothelial growth and cytokines secretion.
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