首页> 外文期刊>The Journal of Urology >Aldose reductase inhibitor ONO-2235 restores the alterations of bladder nerve growth factor and neurotrophin receptor p75 genetic expression in streptozotocin induced diabetic rats.
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Aldose reductase inhibitor ONO-2235 restores the alterations of bladder nerve growth factor and neurotrophin receptor p75 genetic expression in streptozotocin induced diabetic rats.

机译:醛糖还原酶抑制剂ONO-2235恢复链脲佐菌素诱导的糖尿病大鼠膀胱神经生长因子和神经营养蛋白受体p75基因表达的改变。

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PURPOSE: We assessed the treatment effect of the aldose reductase inhibitor ONO-2235 (China Chemical and Pharmaceutical, Taipei, Taiwan) on diabetes associated alterations in bladder nerve growth factor and the nerve growth factor neurotrophin receptor p75 mRNA expressions using the streptozotocin (Sigma) induced diabetic rat model. MATERIALS AND METHODS: Male Wistar rats were divided into 3 groups, including group 1--vehicle treated normal rats, group 2--vehicle treated 9-week streptozotocin diabetic rats and group 3--ONO-2235 treated 9-week streptozotocin diabetic rats. In vivo cystometry was performed using anesthesia. Bladder nerve growth factor levels were measured by enzyme linked immunosorbent assay. Expression of the mRNA encoding nerve growth factor and neurotrophin receptor p75 in the rat bladder was studied using reverse transcriptase-polymerase chain reaction. RESULTS: Cystometry showed increased bladder capacity and decreased emptying function in diabetic rats. ONO-2235 treatment improved voiding volume, voiding fraction and residual volume. The nerve growth factor concentration in streptozotocin induced diabetic rat bladders was significantly lower than the control level in 8 experiments each (mean +/- SEM 45.78 +/- 4.36 and 96.44 +/- 8.73 pg/microg protein, respectively, p <0.01). The mRNA expression of bladder nerve growth factor and neurotrophin receptor p75 in diabetic rats was significantly decreased compared to that in controls in 8 experiments each (p <0.01 and <0.001, respectively). Treatment with ONO-2235 did not significantly change the blood sugar level in diabetic rats. However, administration of the drug significantly increased the bladder nerve growth factor concentration as well as nerve growth factor mRNA and neurotrophin receptor p75 mRNA expression to normal levels in 8 experiments each (p <0.01, <0.01 and <0.001, respectively). CONCLUSIONS: ONO-2235 improved bladder emptying function and restored the decreased genetic expression of bladder nerve growth factor and neurotrophin receptor p75 in 9-week streptozotocin induced diabetic rats, indicating involvement of the sorbitol pathway in the genetic down-regulations of nerve growth factor and p75(NTR) during diabetic cystopathy.
机译:目的:我们使用链脲佐菌素(Sigma)评估了醛糖还原酶抑制剂ONO-2235(中国化学和制药,台湾台北)对糖尿病相关的膀胱神经生长因子和神经生长因子神经营养因子受体p75 mRNA表达的影响。诱导的糖尿病大鼠模型。材料与方法:雄性Wistar大鼠分为3组,分别为:第1组动物治疗的正常大鼠,第2组动物治疗的9周链脲佐菌素糖尿病大鼠和第3组-ONO-2235治疗的9周链脲佐菌素糖尿病大鼠。 。使用麻醉进行体内膀胱测压。通过酶联免疫吸附试验测定膀胱神经生长因子水平。使用逆转录酶-聚合酶链反应研究了编码神经生长因子和神经营养蛋白受体p75的mRNA在大鼠膀胱中的表达。结果:膀胱测量显示糖尿病大鼠膀胱容量增加,排空功能降低。 ONO-2235处理改善了排空体积,排空分数和残留体积。链脲佐菌素诱导的糖尿病大鼠膀胱中神经生长因子的浓度均显着低于对照组,分别为8个实验(平均+/- SEM 45.78 +/- 4.36和96.44 +/- 8.73 pg / microg蛋白,p <0.01) 。在8个实验中,与对照组相比,糖尿病大鼠中膀胱神经生长因子和神经营养蛋白受体p75的mRNA表达显着降低(分别为p <0.01和<0.001)。用ONO-2235治疗并没有显着改变糖尿病大鼠的血糖水平。但是,在每项8个实验中,给药均显着增加了膀胱神经生长因子浓度以及神经生长因子mRNA和神经营养因子受体p75 mRNA的表达,使其达到正常水平(分别为p <0.01,<0.01和<0.001)。结论:ONO-2235改善了9周链脲佐菌素诱导的糖尿病大鼠膀胱排空功能,并恢复了降低的膀胱神经生长因子和神经营养因子受体p75的基因表达,表明山梨糖醇途径参与了神经生长因子和神经元的基因下调。糖尿病性膀胱病变期间的p75(NTR)。

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