Nirmala C, Puvanakrishnan R
Department of Biotechnology, Central Leather Research Institute, Madras, India.
Mol Cell Biochem. 1996 Jun 21;159(2):85-93. doi: 10.1007/BF00420910.
The effect of curcumin on the biochemical changes induced by isoproterenol (ISO) administration in rats was examined. ISO (300 mg Kg-1 administered subcutaneously twice at an interval of 24 h) caused a decrease in body weight and an increase in heart weight, water content as well as in the levels of serum marker enzymes viz creatine kinase (CK), lactate dehydrogenase (LDH) and LDH1 isozyme. It also produced electrocardiographic changes such as increased heart rate, reduced R amplitude and ST elevation. Curcumin at a concentration of 200 mg.Kg-1, when administered orally, showed a decrease in serum enzyme levels and the electrocardiographic changes got restored towards normalcy. Myocardial infarction was accompanied by the disintegration of membrane polyunsaturated fatty acids expressed by increase of thiobarbituric acid reactive substance (TBARS), a measure of lipid peroxides and by the impairment of natural scavenging, characterized by the decrease in the levels of superoxide dismutase, catalase, glutathione peroxidase, ceruloplasmin, alpha tocopherol, reduced glutathione (GSH) and ascorbic acid. The oral pretreatment with curcumin two days before and during ISO administration decreased the effect of lipid peroxidation. It was shown to have a membrane stabilizing action by inhibiting the release of beta-glucuronidase from nuclei, mitochondria, lysosome and microsome. Curcumin pre- and co-treatment decreased the severity of pathological changes and thus, could have a protective effect against the damage caused by myocardial infarction (MI).
研究了姜黄素对异丙肾上腺素(ISO)诱导的大鼠生化变化的影响。ISO(以300 mg·kg⁻¹皮下注射,间隔24 h注射两次)导致体重下降、心脏重量增加、含水量增加以及血清标志物酶即肌酸激酶(CK)、乳酸脱氢酶(LDH)和LDH1同工酶水平升高。它还引起心电图变化,如心率加快、R波振幅降低和ST段抬高。口服浓度为200 mg·kg⁻¹的姜黄素后,血清酶水平降低,心电图变化恢复正常。心肌梗死伴随着膜多不饱和脂肪酸的分解,表现为硫代巴比妥酸反应物质(TBARS,一种脂质过氧化物的指标)增加,以及天然清除功能受损,表现为超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、铜蓝蛋白、α-生育酚、还原型谷胱甘肽(GSH)和抗坏血酸水平降低。在ISO给药前两天及给药期间口服姜黄素预处理可降低脂质过氧化作用。它通过抑制β-葡萄糖醛酸酶从细胞核、线粒体、溶酶体和微粒体的释放而具有膜稳定作用。姜黄素预处理和联合处理可减轻病理变化的严重程度,因此可能对心肌梗死(MI)造成的损伤具有保护作用。