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糖尿病和利尿诱导的大鼠膀胱穹窿部毒蕈碱受体改变的可逆性

Reversibility of diabetes- and diuresis-induced alterations in rat bladder dome muscarinic receptors.

作者信息

Fukomoto Y, Yoshida M, 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

Diabetes. 1994 Jun;43(6):819-26. doi: 10.2337/diab.43.6.819.

Abstract

Previous studies from our laboratory demonstrated that 8 weeks of streptozocin (STZ)-induced diabetes and sucrose-fed diuresis resulted in increases in the density of muscarinic receptors in rat bladder dome and that early insulin treatment (started 3 days after the onset of diabetes) prevented the diabetes-induced upregulation (J Pharmacol Exp Ther 248:81-88, 1989; Diabetes 40: 1150-1156, 1991; J Urol 147:760-763, 1992). To determine whether diabetes- and diuresis-induced alterations in muscarinic receptors in rat bladder dome are reversible, we administered insulin (beginning 8 weeks after the onset of diabetes) or removed sucrose from drinking water of diuretic rats (beginning 8 weeks after the onset of diuresis). Five groups of rats were maintained for 16 weeks: 1) STZ-induced diabetic rats (65 mg/kg intravenously); 2) insulin-treated diabetic rats (5-8 U/day insulin subcutaneously beginning 8 weeks after the onset of diabetes); 3) sucrose-fed diuretic rats (5% sucrose in drinking water throughout 16 weeks); 4) sucrose-removed rats (sucrose withdrawn from drinking water after 8 weeks of the sucrose-induced diuretic state); and 5) age-matched control rats. Radioligand receptor binding experiments with [3H]quinuclidinyl benzilate showed an increase in the density of muscarinic receptors in bladder dome of diabetic and sucrose-fed rats compared with age-matched control rats. Removing the 5% sucrose from the drinking water of diuretic rats reversed the increased water intake and urine output, decreased the bladder hypertrophy that accompanied the diuretic state, and corrected the upregulation of the muscarinic receptors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们实验室之前的研究表明,链脲佐菌素(STZ)诱导的糖尿病持续8周以及蔗糖喂养导致多尿,会使大鼠膀胱穹窿部毒蕈碱受体的密度增加,而早期胰岛素治疗(糖尿病发病后3天开始)可防止糖尿病诱导的上调(《药理学与实验治疗学杂志》248:81 - 88, 1989;《糖尿病》40: 1150 - 1156, 1991;《泌尿学杂志》147:760 - 763, 1992)。为了确定糖尿病和多尿诱导的大鼠膀胱穹窿部毒蕈碱受体改变是否可逆,我们给予胰岛素(糖尿病发病后8周开始)或从多尿大鼠的饮用水中去除蔗糖(多尿开始后8周开始)。五组大鼠维持16周:1)STZ诱导的糖尿病大鼠(静脉注射65 mg/kg);2)胰岛素治疗的糖尿病大鼠(糖尿病发病后8周开始皮下注射5 - 8 U/天胰岛素);3)蔗糖喂养的多尿大鼠(16周内饮用水中含5%蔗糖);4)去除蔗糖的大鼠(蔗糖诱导的多尿状态8周后从饮用水中撤去蔗糖);5)年龄匹配的对照大鼠。用[3H]喹核醇基苯甲酸酯进行的放射性配体受体结合实验表明,与年龄匹配的对照大鼠相比,糖尿病大鼠和蔗糖喂养大鼠膀胱穹窿部毒蕈碱受体的密度增加。从多尿大鼠的饮用水中去除5%的蔗糖可逆转饮水量和尿量的增加,减少伴随多尿状态的膀胱肥大,并纠正毒蕈碱受体的上调。(摘要截短至250字)

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