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乌头类生物碱对体外循环缺血心肌Cu-ZnSOD基因表达的影响 被引量:6

Effect of aconitine akaloid Akaloid (Sini decoction) on Cu-ZnSOD expression in the ischemic myocardium of extracorporeal circulation
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摘要 目的探讨乌头类生物碱(四逆汤煎剂)对体外循环心肌CuZnSOD基因表达的影响。方法28例成年瓣膜置换患者随机分成对照组14例和乌头类生物碱口服(四逆汤煎剂)组14例。术前1周乌头类生物碱组依照中医辩证给予乌头类生物碱每天1剂口服,术后分别取右心耳组织测心肌组织铜锌超氧歧化酶CuZnSODmRNA含量。提取各组心肌组织总RNA通过逆转录聚合酶链反应(RTPCR),以βactin为内参照对CuZnSOD基因的表达水平进行检测。结果乌头类生物碱(四逆汤煎剂)组(1.310±0.135)CuZnSOD基因表达显著强于对照组(1.060±0.183)。结论乌头类生物碱能上调CuZnSOD基因的表达,发挥对体外循环心肌缺血再灌注损伤的保护作用。 Objective To detect the effect of aconitine akaloid akaloid (Sini decoction) on Cu-ZnSOD expression in the ischemic myocardium of extracorporeal circulation.Methods Twenty-eight cardiac valve replacement patients in adult were divided into control and aconitine akaloid akaloid groups.Preoperation the aconitine akaloid group was treated with aconitine akaloid (SND) for 7 days once every day.Total RNA was extracted from the myocardium in each group.The effect of aconitine akaloid (Sini decoction) on the expression of Cu-ZnSOD gene was detected by RT-PCR.Results The expression of Cu-ZnSOD mRNA in aconitine akaloid (Sini decoction) group (1.310± 0.135) was significantly up-regulated as compared with the control group (1.060± 0.183).Conclusion Aconitine akaloid (Sini decoction) can promote the expression of Cu-ZnSOD gene,which may be related to its protective effect on ischemic myocardium.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2005年第7期782-783,共2页 Chinese Journal of Experimental Surgery
基金 广东省科委资助项目(99M04602G)
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  • 1吴伟康,罗汉川,侯灿.四逆汤清除氧自由基及抑制心肌脂质过氧化反应的体外试验[J].中国中药杂志,1995,20(11):690-691. 被引量:41
  • 2吴伟康,尧宏斌,侯灿,罗汉川.四逆汤保护缺血心肌功能的实验研究[J].中国中医基础医学杂志,1995,1(3):24-26. 被引量:30
  • 3段沁江.谷胱甘肽S-转移酶与肝脏病变研究的新进展[J].国外医学(卫生学分册),1995,22(1):8-11. 被引量:10
  • 4吴伟康,何光耀,罗汉川,谭红梅,谭炳炎,侯灿.四逆汤与缺血心肌的能量代谢[J].中国中医基础医学杂志,1996,2(2):26-29. 被引量:41
  • 5Altavilla D, Deodato B, Campo GM, et al. IRFI 042, a novel dual vitamin E-like antioxidant, inhibits activation of nuclear factor-kappa B and reduces the inflammatory response in myocardial ischemia-reperfusion injury. Cardiovasc Res, 2000,47(3):515-528.
  • 6Ishikawa H, Claudio E, Dambach D, et al. Chronic inflammation and susceptibility to bacterial infections in mice lacking the polypeptide(p) 105 precursor (NF- kappa B1) but expressing p50. J Exp Med,1998,187(7):985-996.
  • 7Bours V, Franzoso G, Azarenko V, et al. The oncoprotein Bcl-3 directly transactivates through kappa B motifs via association with DNA-binding p50 B homodimers. Cell,1993,72(5):729-739.
  • 8Pan J, McEver RP. Regulation of the human P-selectin promoter by Bcl-3 and specific homodimeric members of the NF- kappa B/Rel family. J Biol Chem, 1995,270(39):23077-23083.
  • 9Yeh KY, Yeh M, Glass J, et al. Rapid activation of NF- kappa B and AP-1 and target gene expression in postischemic rat intestine. Gastroenterology, 2000,118(3):525-534.
  • 10Lawrence T, Gilroy DW, Colville-Nash PR, et al. Possible new role for NF-kappa B in the resolution of inflammation. Nat Med, 2001,7(12):1291-1297.

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