Sangeetha T, Darlin Quine S
School of Chemical and Biotechnology, SASTRA-University, Thirumalaisamudram, Tanjore 613 402, Tamil Nadu, India.
J Biochem Mol Toxicol. 2007;21(3):118-24. doi: 10.1002/jbt.20166.
In this study, S-allyl cysteine sulfoxide (SACS) was used to evaluate its preventive effect in isoproterenol (ISO)-induced myocardial ischemia in male Wistar rats. Rats were pretreated with SACS (40 and 80 mg kg(-1)) orally for 5 weeks. After the treatment period, ISO (150 mg kg(-1)) was administered subcutaneously to rats at an interval of 24 h for 2 days. The activities of beta-D-N-acetyl-glucosaminidase, beta-galactosidase, beta-glucosidase, and acid phosphatase increased in serum and heart in ISO-induced rats. In addition, these rats showed a significant (p < 0.05) increase in the activities of beta-glucuronidase and cathepsin-D in serum and heart and a significant (p < 0.05) decrease in their activities in lysosomal fraction of the heart. The activity of Na(+)K(+)-ATPase declined, while those of Ca(2+)- and Mg(2+)-ATPases significantly (p < 0.05) elevated in the heart of ISO-induced rats. Pretreatment with SACS (40 and 80 mg kg(-1)) showed a significant (p < 0.05) effect in all the biochemical parameters studied. The effect at a dose of 80 mg kg(-1) body weight was more effective than that at 40 mg kg(-1) body weight and brought back all the biochemical parameters to near normal levels. Hereby, our study shows the membrane-stabilizing as well as antioxidant effects of SACS in ISO-induced rats.
在本研究中,使用S-烯丙基半胱氨酸亚砜(SACS)评估其对雄性Wistar大鼠异丙肾上腺素(ISO)诱导的心肌缺血的预防作用。大鼠口服SACS(40和80 mg kg⁻¹)进行预处理,持续5周。在治疗期后,以24小时间隔皮下给予大鼠ISO(150 mg kg⁻¹),共2天。在ISO诱导的大鼠中,血清和心脏中的β-D-N-乙酰氨基葡萄糖苷酶、β-半乳糖苷酶、β-葡萄糖苷酶和酸性磷酸酶的活性增加。此外,这些大鼠血清和心脏中的β-葡萄糖醛酸酶和组织蛋白酶D的活性显著(p < 0.05)增加,而心脏溶酶体部分中它们的活性显著(p < 0.05)降低。在ISO诱导的大鼠心脏中,Na⁺K⁺-ATP酶的活性下降,而Ca²⁺-和Mg²⁺-ATP酶的活性显著(p < 0.05)升高。用SACS(40和80 mg kg⁻¹)预处理对所有研究的生化参数均显示出显著(p < 0.05)效果。80 mg kg⁻¹体重剂量的效果比40 mg kg⁻¹体重剂量更有效,并使所有生化参数恢复到接近正常水平。因此,我们的研究显示了SACS在ISO诱导的大鼠中的膜稳定以及抗氧化作用。