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2022 年第 8 期 第 17 卷

平腑调代方对肥胖2型糖尿病小鼠脂代谢和炎症及氧化应激水平的影响

Effects of Pingfutiaodai decoction on lipid metabolism, inflammation and oxidative stress in obese type 2 diabetic mice

作者:陈弘东1王耀献1刘伟敬1郭敬1张超1孙浩1娄文娇1贺仲晨2

英文作者:Chen Hongdong1 Wang Yaoxian1 Liu Weijing1 Guo Jing1 Zhang Chao1 Sun Hao1 Lou Wenjiao1 He Zhongchen2

单位:1北京中医药大学东直门医院肾病内分泌科,北京100700;2北京市和平里医院内分泌科,北京100013

英文单位:1Department of Nephrology and Endocrinology Dongzhimen Hospital of Beijing University of Chinese Medicine Beijing 100700 China; 2Department of Endocrinology Beijing Hepingli Hospital Beijing 100013 China

关键词:

英文关键词:Obese;Type2diabetesmellitus;Pingfutiaodaidecoction;Lipidmetabolism;Inflammatoryfactors;Oxidativestress

  • 摘要:
  • 目的 观察平腑调代方对肥胖2型糖尿病小鼠脂代谢、炎症及氧化应激水平的影响。方法 36只无特定病原体级健康雄性6周龄C57BL/6J小鼠依据随机数字表法分为对照组、模型组和中药组,模型组选用高脂饲料联合链脲佐菌素诱导建立肥胖2型糖尿病小鼠模型,并给予纯水灌胃干预,中药组诱导建立肥胖2型糖尿病小鼠模型并给予平腑调代方灌胃干预。对照组不诱导肥胖2型糖尿病模型并给予纯水灌胃干预。干预12周后,检测各组总胆固醇、三酰甘油、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)C反应蛋白(CRP)、白细胞介素6IL-6)、肿瘤坏死因子α(TNF-α)、超氧化物歧化酶(SOD)、丙二醛、总抗氧化能力(T-AOC)水平。结果 造模结束后,剔除不达标小鼠,最终对照组10只小鼠,模型组与中药组各9只小鼠进行药物干预。干预12周后,模型组总胆固醇、三酰甘油、LDL-C水平高于对照组,HDL-C水平低于对照组,中药组总胆固醇、三酰甘油、LDL-C水平均低于模型组,HDL-C水平高于模型组(P0.05)。模型组CRPIL-6TNF-α水平明显高于对照组,中药组CRPIL-6TNF-α水平低于模型组[(48±5)μg/L比(55±6)μg/L、(66.1±5.8ng/L比(71.9±2.5ng/L、(97±9ng/L比(126±11ng/L](均P0.05)。模型组SODT-AOC水平低于对照组,丙二醛水平高于对照组,中药组SODT-AOC水平高于模型组,丙二醛水平低于模型组(均P0.05)。结论 平腑调代方能够改善肥胖2型糖尿病小鼠脂代谢紊乱,减轻炎症反应并提高抗氧化能力,对肥胖2型糖尿病的治疗有参考意义。

  • Objective To observe the effects of Pingfutiaodai decoction on lipid metabolism, inflammation and oxidative stress in obese type 2 diabetic mice. Methods Totally 36 healthy male C57BL/6J mice without specific pathogens at the age of 6 weeks were divided into control group, model group and traditional Chinese medicine group according to random number table method. The model group was induced to establish obese type 2 diabetic mice model by high-fat diet combined with streptozotocin and was given pure water gavage intervention. The traditional Chinese medicine group was induced to establish obese type 2 diabetic mice model and was given Pingfutiaodai decoction gavage intervention. The control group was not induced to obese type 2 diabetic model and was given pure water gavage intervention. After 12 weeks of intervention, levels of total cholesterol, triacylglycerol, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), C-reactive protein (CRP), interleukin-6 (IL-6), tumor necrosis factor-α(TNF-α), superoxide dismutase (SOD), malondialdehyde and total-antioxidant capacity (T-AOC) were measured in each group. Results After modeling and removing non-compliance mice, 10 mice in the control group, 9 mice in the model group and 9 mice in the traditional Chinese medicine group were given drug intervention. Twelve weeks after intervention, the levels of total cholesterol, triglyceride and LDL-C in the model group were higher than those in the control group, and the level of HDL-C was lower than that in the control group; the levels of total cholesterol, triglyceride and LDL-C in the traditional Chinese medicine group were lower than those in the model group, and the level of HDL-C was higher than that in the model group(all P0.05). The levels of CRP, IL-6 and TNF-α in the model group were higher than those in the control group, and the levels in the traditional Chinese medicine group were lower than those in the model group[(48±5)μg/L vs 55±6)μg/L,66.1±5.8ng/L vs 71.9±2.5ng/L,97±9ng/L vs 126±11ng/L(all P0.05). The levels of SOD and T-AOC in the model group were lower than those in the control group, and the level of malondialdehyde was higher than that in the control group; the levels of SOD and T-AOC in the traditional Chinese medicine group were higher than those in the model group, and the level of malondialdehyde was lower than that in the model group(all P0.05). Conclusion Pingfutiaodai decoction can improve the disorder of lipid metabolism, reduce inflammatory response and increase antioxidant capacity in obese type 2 diabetic mice, which has reference significance for the treatment of obese type 2 diabetes mellitus.

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