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超极化激活环核苷酸门控通道在糖尿病膀胱病中的作用。

The function of hyperpolarization-activated cyclic nucleotide-gated channel in diabetic cystopathy.

机构信息

Department of Urology, Southwest Hospital, Third Military Medical University, PLA, Chongqing, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Oct;22(20):6575-6582. doi: 10.26355/eurrev_201810_16131.

Abstract

OBJECTIVE

We aimed at investigating changes in the expression and physiological function of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels in interstitial cells of Cajal (ICC) in diabetic state.

MATERIALS AND METHODS

Twenty adult female Sprague-Dawley (SD) rats were randomly assigned to control and Zucker diabetic fatty (ZDF) group. The protein and mRNA expression of HCN isoforms and C-kit in the rat bladders were detected using Western blotting and reverse transcription-polymerase chain reaction (RT-PCR). The bladder contraction was evaluated using a bladder smooth muscle strip test. Whole cell patch-clamp techniques were used to detect the activity of HCN channels. Immunofluorescent staining was used to the positive expression of HCN and C-kit in ICC.

RESULTS

cAMP, as HCN channel-specific stimulant, could increase the frequency and amplitude of spontaneous contractions in both group, while cAMP inducing contraction of ZDF rats, was still significantly lower compared with the control group. Acute bladder ICCs were isolated by collagenase digestion. Classic Ih current pattern was recorded on ICCs while Ih current amplitude of ICCs from ZDF diabetic rats was significantly lower than the control group. The expression and mRNA of HCN1-4 isoforms in ZDF diabetic rats were both significantly lower compared with the control group. Meanwhile, the number of c-kit positive cells in ZDF diabetic rats showed no significant differences compared with controls. The morphological structure of ICC in the bladder of ZDF rats was relatively loose and the number of their cell process was apparently decreased.

CONCLUSIONS

The structure of ICCs in ZDF rats was relatively loose, their connection to each other was also diminished. The expression of HCN was down-regulated and its response to cAMP was also decreased. HCN channels in bladder ICCs might regulate detrusor contraction. Changes in HCN expression and activity in bladder ICCs might be one of the most important mechanisms of diabetic cystopathy.

摘要

目的

研究高极化激活环核苷酸门控(HCN)通道在糖尿病状态下 Cajal 间质细胞(ICC)中的表达和生理功能变化。

材料和方法

将 20 只成年雌性 Sprague-Dawley(SD)大鼠随机分为对照组和 Zucker 糖尿病肥胖(ZDF)组。使用 Western blot 和逆转录-聚合酶链反应(RT-PCR)检测大鼠膀胱中 HCN 同工型和 C-kit 的蛋白和 mRNA 表达。使用膀胱平滑肌条测试评估膀胱收缩。使用全细胞膜片钳技术检测 HCN 通道的活性。免疫荧光染色检测 ICC 中 HCN 和 C-kit 的阳性表达。

结果

cAMP 作为 HCN 通道特异性激动剂,可增加两组自发性收缩的频率和幅度,而 ZDF 大鼠的 cAMP 诱导收缩仍明显低于对照组。通过胶原酶消化分离急性膀胱 ICC。在 ICC 上记录经典 Ih 电流模式,而 ZDF 糖尿病大鼠 ICC 的 Ih 电流幅度明显低于对照组。ZDF 糖尿病大鼠 HCN1-4 同工型的表达和 mRNA 均明显低于对照组。同时,ZDF 糖尿病大鼠 c-kit 阳性细胞数量与对照组相比无显著差异。ZDF 大鼠膀胱 ICC 的形态结构相对疏松,细胞突起数量明显减少。

结论

ZDF 大鼠 ICC 的结构相对疏松,彼此之间的连接也减少。HCN 的表达下调,对 cAMP 的反应也减弱。膀胱 ICC 中的 HCN 通道可能调节逼尿肌收缩。膀胱 ICC 中 HCN 表达和活性的变化可能是糖尿病膀胱病变的重要机制之一。

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