摘要
目的:探讨次乌头碱(HA)与甘草苷、甘草次酸配伍对心肌细胞的减毒作用。方法:以新生SD乳鼠心肌细胞为研究对象,观察甘草苷、甘草次酸对HA引起心肌细胞的形态变化和超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-PX)活性的影响。结果:与120μmol/L HA组比较,120μmol/L甘草次酸、480μmol/L甘草苷与120μmol/L HA配伍可使SOD、GSH-PX的活性由(56.38±0.41)U/mL和(81.89±3.67)U/mgprot分别增加到(65.39±0.25)U/mL、(101.69±7.17)U/mgprot和(62.69±0.54)U/mL、(100.85±7.32)U/mgprot(P<0.05),120μmol/L的甘草次酸和120μmol/L HA配伍作用更显著(P<0.01)。结论:480μmol/L甘草苷、120μmol/L甘草次酸与120μmol/L HA配伍可以降低HA对心肌细胞的毒性作用,增强其活力,这与甘草苷、甘草次酸减少了HA对心肌细胞的氧化损伤有关。
Objective: To explore the compatibility of hypaconitine(HA) and liquiritin, glycyrrhetinic acid on the detoxicated effect to myocardial ceils. Methods: Using the primary cultured myocardial cells as reseach subjects, to observe the changes of myocardial cells and vigour of superoxide dismutase (SOD), glutathione peroxidase(GSH-PX) through liquiritin and glycyrrhetinic acid for HA. Results: By comparison with HA 120μmol/L, compatibility of HA 120μmol/L and liquirilin 480μmol/L with compatibility of HA 120μmol/L and glycyrrhetinic acid 120μmol/L increased vigour of SOD, GSH-PX, from (56.38±0.41)U/mL and (81.89±3.67)U/mgprot to (65.39±0.25)U/mL, (101.69±7.17)U/mgprot and (62.69±0.54)U/mL, (100.85±7.32)U/mgprot (P〈0.05), compatibility of HA 120μmol/L and glycyrrhetinic acid 120μmol/L worked best (P〈0.01). Conclusion: Compatibility of liquiritin 4800mol/L, glycyrrhetinic 1200rnol/L and HA1201amol/L can reduce the toxicity of HA to myocardial cells and increase vigor. There is a relationship between reducing oxidation and damaging of myocardial cells.
出处
《中华中医药杂志》
CAS
CSCD
北大核心
2013年第9期2601-2604,I0001,共5页
China Journal of Traditional Chinese Medicine and Pharmacy
基金
国家自然科学基金项目(No.81073139)
高等学校博士学科点专项科研基金(No.20113322110002
No.20093322110001)
浙江省中医药科技计划项目(No.2010ZA017)
浙江省中医药重点学科(No.2012-XK-A06)~~