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Insulin-Releasing Properties of a Series of Cinnamic Acid Derivatives in Vitro and in Vivo

机译:一系列肉桂酸衍生物的体内和体外胰岛素释放特性

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Cinnamic acid derivatives are naturally occurring substances found in fruits,vegetables,and flowers and are consumed as dietary phenolic compounds.In the present study,cinnamic acid and its derivatives were evaluated for insulin secreting activity in perfused rat pancreas and pancreatic beta-cells(INS-1)as well as an increase in[Ca~(2+)]i in vitro.The presence of m-hydroxy or p-methoxy residues on cinnamic acid was a significantly important substituent as an effective insulin releasing agent.The introduction of p-hydroxy and m-methoxy-substituted groups in cinnamic acid structure(ferulic acid)displayed the most potent insulin secreting agent among those of cinnamic acid derivatives.In particular,the stimulatory insulin secreting activities of test compounds were associated with a rise of[Ca~(2+)];in INS-1.In perfused rat pancreas,m-hydroxycinnamic acid,p-methoxycinnamic acid,and ferulic acid(100 mu M)significantly stimulated insulin secretion during 10 min of administration.The onset time of insulin secretion of those compounds was less than 1 min and reached its peak at 4 min that was about 2.8-,3.3-,and 3.4-fold of the baseline level,respectively.Intravenous administration of p-methoxycinnamic acid and ferulic acid(5 mg/kg)significantly decreased plasma glucose and increased insulin concentration in normal rats and maintained its level for 15 min until the end of experiment.Meanwhile,m-hydroxycinnamic acid induced a significant lowering of plasma glucose after 6 min,but the effects were transient with plasma glucose concentration,rapidly returning to basal levels.Our findings suggested that p-methoxycinnamic acid and ferulic acid may be beneficial for the treatment of diabetes mellitus because they regulated blood glucose level by stimulating insulin secretion from pancreatic beta-cells.
机译:肉桂酸衍生物是在水果,蔬菜和花卉中发现的天然物质,并作为膳食酚类化合物消费。在本研究中,对肉桂酸及其衍生物在灌注的大鼠胰腺和胰腺β细胞(INS)中的胰岛素分泌活性进行了评估。 -1)以及体外[Ca〜(2 +)] i的增加。肉桂酸上的m-羟基或对甲氧基残基的存在是作为有效的胰岛素释放剂的重要重要取代基。肉桂酸结构中的对羟基和间甲氧基取代基(阿魏酸)在肉桂酸衍生物中表现出最强的胰岛素分泌剂。特别是,受试化合物的刺激性胰岛素分泌活性与[ Ca〜(2+)];在INS-1中。在大鼠灌注胰腺中,间羟基肉桂酸,对甲氧基肉桂酸和阿魏酸(100μM)在给药10分钟内显着刺激胰岛素分泌。这些化合物的胰岛素分泌低于1分钟,并在4分钟达到峰值,分别约为基线水平的2.8、3.3和3.4倍。对甲氧基肉桂酸和阿魏酸的静脉给药5 mg / kg)的正常大鼠血浆葡萄糖显着降低,胰岛素浓度升高,并维持其水平15分钟,直到实验结束。同时,间羟基肉桂酸在6分钟后诱导血浆葡萄糖显着降低,但其作用是我们的发现表明对甲氧基肉桂酸和阿魏酸可能对糖尿病的治疗有益,因为它们通过刺激胰腺β细胞分泌胰岛素来调节血糖水平。

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