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4-氯-2,6-双吡啶双氧钒化合物降低1型糖尿病大鼠血糖的生物学作用
  • ISSN号:2095-6134
  • 期刊名称:《中国科学院大学学报》
  • 时间:0
  • 分类:R587.1[医药卫生—内分泌;医药卫生—临床医学;医药卫生—内科学]
  • 作者机构:[1]中国科学院研究生院生物系,北京100049
  • 相关基金:国家自然科学基金(20571084)资助
中文摘要:

通过1型和2型糖尿病动物模型的研究,发现过渡金属元素钒(V)具有降糖作用.有机钒化合物与无机钒相比,其副作用低、体内吸收率和生物利用度高.主要探讨了4价有机钒化合物4-氯-2,6-双吡啶双氧钒化合物(4-chloro-2,6-dipicolinatodioxovanadium(IV),v4dipic—C1)对链脲佐菌素(STZ,55mg/kg)诱导的1型糖尿病大鼠的生物学作用.大鼠通过自由饮水的方式口服V4dipic-Cl(o.5mg/mL)8天.结果表明,V4dipic—C1组的大鼠血糖和血清碱性磷酸酶(ALP)活性显著低于糖尿病对照组,并且其葡萄糖耐量水平得到明显改善.但有机配体H2dipic—Cl对糖尿病大鼠的血糖和血清ALP活性的影响不显著.结果提示V4dipic-Cl具有降低糖尿病大鼠的血糖,提高葡萄糖耐量和改善肝功能的作用.

英文摘要:

The insulin-mimic effect of vanadium compounds has been widely reported in both type 1 and 2 diabetes animal models. Recently, various organic vanadium compounds have been synthesized to lower the side effect of inorganic vanadium and improve its poor absorption efficiency. In the present study, we evaluated the biological effects of V4dipic-Cl in streptozotocin (STZ)-induced diabetic rats. V4dipic-Cl was orally administrated to diabetic rats for eight days at the dose of 0.5mg/mL through drinking water. The blood glucose level, serum alkaline phosphorase (ALP), aspartate amino transferase (AST) and blood urea nitrogen (BUN) were determined. In addition, an oral glucose tolerance test was carried out. The results showed that blood glucose, serum ALP, AST and BUN were significantly increased in STZ induced-diabetic rats. The level of glucose tolerance in diabetic rats was lower than that in the controls. At the end of the experiment, blood glucose and serum ALP in Vadipic-Cl- treated diabetic rats were significantly decreased. Meanwhile, oral glucose tolerance of diabetic rats was improved as compared to the H2dipic-Cl-treated diabetic rats. In conclusion, it was found that V4dipic-Cl could decrease blood glucose level and restore the hyperglycemia-induced hepatic dysfunction in STZ-induced diabetic rats.

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期刊信息
  • 《中国科学院大学学报》
  • 中国科技核心期刊
  • 主管单位:中国科学院
  • 主办单位:中国科学院大学
  • 主编:石耀霖
  • 地址:北京玉泉路19号(甲)
  • 邮编:100049
  • 邮箱:journal@gucas.ac.cn
  • 电话:010-88256013
  • 国际标准刊号:ISSN:2095-6134
  • 国内统一刊号:ISSN:10-1131/N
  • 邮发代号:82-583
  • 获奖情况:
  • 国内外数据库收录:
  • 中国中国科技核心期刊,中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版)
  • 被引量:416