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20E对急性肝损伤模型小鼠抗氧化作用研究 被引量:1

Anti-oxidative Ability Study of 20-hydroxyecdysone on Acute Liver Injury of Mice
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摘要 目的:为了探讨20-羟基蜕皮甾酮(20E)对四氯化碳(CCl4)急性肝损伤的保护作用及相关机制。方法:小鼠体重(20±2)g随机分成3组,20E治疗组皮下注射2mg.kg-1的20E注射液,正常组和模型组注射等量的生理盐水。给药7天后,模型组和20E治疗组腹腔注射剂量为10mL.kg-1的0.25%CCl4大豆油溶液,正常组注射等体积大豆油,摘除眼球取血,制备血清,解剖肝脏。测定血清中谷丙转氨酶(ALT)、谷草转氨酶(AST)、碱性磷酸酶(ALP)的含量,采用real-time PCR测定过氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)、谷胱甘肽还原酶(GR)和肿瘤坏死因子(TNF-α)的表达。结果:20E处理之后血清ALT、AST和ALP含量分别比模型组降低了31.3%、35.2%和50.7%(P<0.05);肝脏的组织学病变较模型组显著减轻;SOD和GSH-PxmRNA水平分别比模型组升高84.5%(P<0.01)和105.3%(P<0.01),ACT和TNF-α分别减少了53.7%(P<0.05)和71.2%(P<0.05)。结论:20E对小鼠急性肝损伤有显著的保护作用,其机制可能与增强肝组织抗氧化能力有关。 Objective : To study the 20E protecting-mechanism in acute liver injury induced by carbon tetrachloride ( CC14 ). Methods : The mice, ( 20 ± 2 ) g weight, were randomly divided into three groups. The 20E treatment group was injected of 20E solution at a concentration of 2rag . kg^-1 and with similar volume saline solution in normal group and model group, respectively. On the 7th day, model group and 20E treatment group was injected 10mL . kg^-1 with a concentration of 0.25% CC14, normal group with similar volume soybean oil. The expressions of alanine aminotransferase ( ALT ), aspartate aminotransferase ( AST ) and Alkaline phosphatase ( ALP ) were analyzed by automatic biochemical analyzer in serum. The real-time PCR was used to measure the expressions of superoxide dismutase ( SOD ), catalase ( CAT ), glutathione peroxidase ( GSH-Px ), glutathione reductase ( GR ) and tumor necrosis factor- ct ( TNF- ct ). Results : Compared with that of mode group, the contents of ALT, AST and ALP decreased 31.3%, 35.2% and 50.7% ( P〈0.05 ), respectively. The levels of SOD and GSH-Px in 20E treatment group increased 84.5% ( P〈0.01 ) and 105.5% (P〈0.01)than that in mode group, respectively. But, the ACT and TNF-o~ mRNA levels reduced 53.7% (P〈0.05)and 71.2% (P〈0.05). Conclusion: 20E administration results in protection for acute liver injury of mice may be through enhancing liver anti-oxidative ability
出处 《辽宁中医药大学学报》 CAS 2012年第10期81-83,共3页 Journal of Liaoning University of Traditional Chinese Medicine
基金 河南省重点科技攻关项目(122102310103)
关键词 20-羟基蜕皮甾酮 小鼠 急性肝损伤 抗氧化能力 20-hydroxyecdysone mice acute liver injury anti-oxidative ability
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  • 1王宗舜.蜕皮激素在动物界的发生[J].动物学杂志,1993,28(2):45-47. 被引量:6
  • 2何令媛,洪长福,钟惠仙.超氧化物歧化酶测定方法的改良[J].职业卫生与病伤,1994,9(4):198-201. 被引量:7
  • 3刘广义,毕秀荣,张桂英,杨金龙,乔保书,于廷祥.蜕皮激素对破伤风毒素的体外中和作用[J].内蒙古畜牧科学,1995,16(3):48-48. 被引量:1
  • 4吴旭,林水金,杨映波,冯素珍.蜕皮甾酮对人脐静脉内皮细胞增殖的影响[J].中国药理学通报,1997,13(2):176-179. 被引量:33
  • 5KLEIN R. Phytoecdy,,teroids[ J ]. J Am Herbalists Guild (fall/ winter issue) ,2004,9(5 ) : 18 - 28.
  • 6SCHLATTNER U, VAFOPOULOU X, STEEL CGH, et al. Nongenomic ecdysone effects and the invertebrate nuclear steroid hormone receptor EcR - new role for an ‘ old' receptor[ J]. Mol Cell Endocrinol, 2006, 247 ( 1/2 ) :64 - 72.
  • 7HENRICH VC. The ecdysteroid receptor [ M ]//Comprehensive Molecular Insect Science, vol 3, 2005:243 - 285.
  • 8CARMICHAEL JA, LAWRENCE MC, GRAHAM LD, et al. The X-ray structure cf a hemipteran ecdysone receptor ligand binding domain[J]. J Biol Chem, 2005,280(6):22258 - 22269.
  • 9DEVARAKONDA S, HARP JM, KIM Y, et al. Structure of the heterodimeric ecdysone receptor DNA-bindlng complex[ J ]. EMBO J, 2003, 22(21) : 5827 -5840.
  • 10DINAN L, HORMANN RE. Ecdysteroid agonists and antagonists [ M ]//Comprehensive Molecular Insect Science, vol 3, 2005: 197 - 242.

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  • 1赵红刚,陈贤均.硒中毒对小鼠器官蛋白质含量及SOD活性影响的实验研究[J].环境与职业医学,2006,23(3):262-263. 被引量:7
  • 2Youssef DM, Fawzy FM. Value of renal resistive index as an early marker of diabetic nephropathy in children with type-1 diabetes mellitus [J]. Saudi J Kidney Dis Transpl, 2012, 23 (5) : 985- 992.
  • 3Hu Wenchao, Yu Qian, Zhang Jie, et at. Rosiglitazone ameliorates diabetic nephropathy by reducing the expression of chemerin and ChemR23 in the kidney of Streptozotocin-lnduced diabetic rats [J]. Inflammation, 2012, 35 (4): 1287-1293.
  • 4Brownlee M, Vlassara H, Kooney A, et al. Aminoguanidine pre- vents diabetes-induced arterial wall protein cross-linking [J]. Sci- ence, 1986, 232 (4758): 1629-1632.
  • 5Hirasawa Y, Sakai T, Ito M, et at. Advanced-glycation-end- product-cholesterol-aggregated-protein accelerates the proliferation of mesangial cells mediated by transforming-growth-factor- beta 1 receptors and the ERK-MAPK pathway [J]. Eur J Pharmacol, 2011, 672 (1/3): 159-168.
  • 6Yang Lan, Wang Chengzhang, Ye Jianzhong, et al. Hepatoprotec- tive effects of polyprenols from Ginkgo biloba L. leaves on CC14- induced hepatotoxicity in rats [J]. Fitoterapia, 2011, 82 (6) : 834-840.
  • 7Liou KT, Shen YC, Chen CF, et al. The anti-inflammatory effect of honokiol on neutrophils: mechanisms in the inhibition of reactive Oxygen species production [J]. Eur J Pharmacol, 2003, 475 (1/3) : 19-27.
  • 8Jian Congxiang, Liu Xiaofei, Hu Jun, et al. 20-Hydrox- yeedysone-induced bone morphogenetic protein-2-dependent os- teogenic differentiation through the ERK pathway in human periodontal ligament stem cells [J]. Eur J Pharmacol, 2013, 698 (1/3) : 48-56.
  • 9Hu Jun, Luo Chunxia, Chu Weihua, et al. 20-Hydroxyeedysone protects against oxidative stress-induced neuronal injury by scaveng- ing free radicals and medulatitag NF- K B and JNK pathways [J]. PLoSOne, 2012, 7 (12): e50764.
  • 10Liao YC, Lee YH, Chuang LY, et al. Advanced glyeation end products-mediated hypertrophy is negatively regulated by tetrahydro- biopterin in renal tubular cells [J]. Mol Cell Endoerinol, 2012, 355 (1): 71-77.

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