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胰岛素对糖尿病诱导的大鼠前列腺β-肾上腺素能和毒蕈碱受体改变的逆转作用。

The reversal effect of insulin on diabetes-induced alterations in beta adrenergic and muscarinic receptors in rat prostate.

作者信息

Fukumoto Y, Yoshida M, Dokita S, Kamai T, Weiss R M, Latifpour J

机构信息

Section of Urology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

J Urol. 1993 Jun;149(6):1602-6. doi: 10.1016/s0022-5347(17)36459-5.

Abstract

Previous studies from our laboratory demonstrated that 8 weeks after the induction of diabetes by the administration of streptozotocin (STZ) there was a downregulation of beta adrenergic and muscarinic cholinergic receptors in rat prostate, and that early insulin treatment (started 3 days after the onset of diabetes) prevented these alterations from occurring. In the present study, the effects of later insulin treatment (started 8 weeks after the onset of diabetes) on the reversibility of diabetes-induced alterations in beta adrenergic and muscarinic receptors in rat prostate were investigated. Three groups of rats were maintained for 16 weeks: 1) diabetics, 2) insulin-treated diabetics (subcutaneously injected with 5 to 8 U per day starting 8 weeks after the onset of diabetes) and 3) age matched controls. Binding studies with [3H]dihydroalprenolol (DHA) and [3H]quinuclidinyl benzilate (QNB) showed a significantly lower density of beta adrenergic and muscarinic cholinergic receptors in the diabetic rat prostate than in prostate from either controls or insulin-treated diabetic animals. Inhibition of [3H]DHA binding by isoproterenol, a beta adrenergic agonist, and binding of [3H]QNB by carbachol, a muscarinic agonist, indicated the presence of low and high affinity agonist binding sites for each receptor. The relative proportion of high affinity to total binding sites as well as the low and high affinity constants were similar in all groups. These data indicate that insulin treatment, begun 8 weeks after the onset of diabetes, can reverse the diabetes-induced downregulation of both beta adrenergic and muscarinic cholinergic receptors in STZ-diabetic rat prostates.

摘要

我们实验室之前的研究表明,通过注射链脲佐菌素(STZ)诱导糖尿病8周后,大鼠前列腺中的β-肾上腺素能和毒蕈碱胆碱能受体下调,并且早期胰岛素治疗(糖尿病发病后3天开始)可防止这些改变的发生。在本研究中,研究了后期胰岛素治疗(糖尿病发病后8周开始)对大鼠前列腺中糖尿病诱导的β-肾上腺素能和毒蕈碱受体改变的可逆性的影响。三组大鼠维持16周:1)糖尿病组,2)胰岛素治疗的糖尿病组(糖尿病发病后8周开始每天皮下注射5至8 U)和3)年龄匹配的对照组。用[3H]二氢阿普洛尔(DHA)和[3H]喹核醇基苯甲酸酯(QNB)进行的结合研究表明,糖尿病大鼠前列腺中β-肾上腺素能和毒蕈碱胆碱能受体的密度明显低于对照组或胰岛素治疗的糖尿病动物的前列腺。β-肾上腺素能激动剂异丙肾上腺素对[3H]DHA结合的抑制以及毒蕈碱激动剂卡巴胆碱对[3H]QNB结合的抑制表明每个受体存在低亲和力和高亲和力激动剂结合位点。所有组中高亲和力与总结合位点的相对比例以及低亲和力和高亲和力常数相似。这些数据表明,糖尿病发病后8周开始的胰岛素治疗可以逆转STZ糖尿病大鼠前列腺中糖尿病诱导的β-肾上腺素能和毒蕈碱胆碱能受体的下调。

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