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黄精多糖对老年糖尿病小鼠脑组织糖基化终产物受体mRNA表达的影响 被引量:18

Effect of polygona polysaccharose on expression of RGEP mRNA in brain of the aged diabetic rat
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摘要 目的 探讨黄精多糖对老年糖尿病小鼠脑组织糖基化终产物受体mRNA (RAGEmRNA)表达的调节作用。 方法 BALB/C小鼠 30只 ,随机分为对照组、糖尿病模型组和治疗组 ,每组 1 0只 ;糖尿病模型组和治疗组腹腔注射链脲佐菌素建立小鼠糖尿病模型 ,治疗组给予黄精多糖2ml/kg ,每日 1次灌胃给药 ,共 1 2周。各组实验动物脑组织RAGEmRNA表达的测定采用RT PCR法。 结果 糖尿病模型组实验鼠脑组织RAGEmRNA表达增加 ,RAGE/ β actin相对值 (0 1 5 3±0 0 5 4 )明显高于对照组 (0 ,P <0 0 1 )。应用黄精多糖治疗后 ,治疗组鼠脑组织RAGEmRNA表达较模型组降低 ,RAGE/ β actin相对值 (0 0 92± 0 0 33)显著低于模型组 (P <0 0 5 )。  结论 黄精多糖能抑制老年糖尿病鼠脑组织RAGEmRNA表达 ,对高血糖及糖基化终产物 (AGE) Objective To study the regulative effect of polygona polysaccharose on the mRNA expression of RGEP(receptor of glycosy lated end products) in brain of aged diabetic rats Methods Diabetic rat model was made by injecting streptozotocin into its abdominal cavity RT PCR method was used to examine the expression of RAGE mRNA in rat brain Results RAGE mRNA in tissue of brain in aged diabetic rats was increased The value of RAGE/ actin (0 153±0 054) in aged diabetic rats was significantly higher than that in the control group ( P <0 01) After the treatment of polygona polysaccharose the expression of RAGE mRNA in tissue of brain was decreased in the model group The RGEP/ actin value in the treated group(0 092±0 033) was significantly lower than that in the animal model group( P <0 05) Conclusions Polygona polysaccharose may decrease the expression of RGEP mRNA in the tissue of brain in aged diabetic rats and has protective effect on the tissue damage caused by hyperglycemia and advanced glycosy lated end products
出处 《中华老年医学杂志》 CAS CSCD 北大核心 2004年第11期817-819,共3页 Chinese Journal of Geriatrics
基金 海南省自然科学基金重点资助项目 (No 30 2 2 3)
关键词 黄精多糖 老年人 糖尿病 小鼠 脑组织 受体 mRNA表达 RAGE mRNA 糖基化终产物 多糖类 Diabetes,mellitus, experimental Glycosylation end products, advanced Polygonstum sibiricum Polysaccharides
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  • 1AM Schmidt,Shi DuYan, Jean-Luc, et al. Activation of receptor for advanced glycation end products: a mechanism for chronic vascular dysfuction in diabetic vasculopathy and atherosclerosis. Circ Res, 1999, 84:489-497.
  • 2Shi Du Yan, Xi Chen, Jin Fu, et al. RAGE and amyloid-β peptide neurotoxicity in Alzheimer's disease. Nature ,1996,382:685-691.
  • 3Sasaski N,Fukatsu R, Tsuzuki K, et al.Advanced glycation end products in Alzheimer's disease and other neurodegenerative disease. Am J Pathol, 1998,153:1149-1155.
  • 4Li JJ,Dickson D, Hof PR, et al.Receptors for advanced glycosylation endproducts in human brain:role in brain homeostasis. Mol Med, 1998,4:46-60.
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  • 6Renard C, Chappey O, Wautier MP, et al. Recombinant advanced glycation end product receptor pharmacokinetics in normal and diabetic rats. Molecular Pharmacology, 1997,52:54-62.

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