TRPV4 受体对血管紧张素II 诱导的小鼠肾损害的影响
作者:
作者单位:

(1. 河南中医药大学第一附属医院,中心实验室,郑州 450000; 2. 河南中医药大学中西医结合临床学科,郑州 450008)

中图分类号:

R-33

基金项目:

河南省科技攻关计划项目(162102410048);国家自然科学基金面上项目(81170243)


Effect of TRPV4 on angiotensin II-induced renal injury in mice
Author:
  • (1. The Central Lab of The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, Henan 450000, China; 2. Clinical Department of Integrated Traditional Chinese and Western Medicine, Henan University of Traditional Chinese Medicine, Zhengzhou, Henan 450008)
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Affiliation:

(1. The Central Lab of The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, Henan 450000, China; 2. Clinical Department of Integrated Traditional Chinese and Western Medicine, Henan University of Traditional Chinese Medicine, Zhengzhou, Henan 450008)

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    摘要:

    目的 通过利用瞬时受体电位香草酸亚型4(transient receptor potential vanilloid type 4,TRPV4)基因敲除(TRPV4 - / - )小鼠,探讨TRPV4 受体在血管紧张素II(angiotensin II,Ang II)所诱导的肾损害中的作用?方法 实验小鼠分为假手术组和Ang II 处理组?在野生型和TRPV4 - / - 小鼠中通过皮下灌注Ang II 建立Ang II 依赖型高血压模型,而假手术组小鼠皮下只灌注生理盐水?处理4 周后,分别检测小鼠的尾动脉收缩压?24 h 尿白蛋白排泄量及8-异构前列腺素?血清肌酐的改变,并且同时对肾组织病理学的变化进行分析?结果 与相应的假手术组比较,Ang II 处理组小鼠血压升高?尿白蛋白及8-异构前列腺素排泄量增加,并同时伴有血清肌酐升高(P < 0.05); 肾小球纤维样硬化及肾小管间质损伤程度均出现明显加重,并伴有肾胶原蛋白水平的增高(P < 0.05)?除血压外,TRPV4 基因敲除能显著抑制上述所有病理变化,从而缓解Ang II 所诱导的肾损害(P < 0.05)?结论 在AngII 所诱导高血压的过程中,TRPV4 基因敲除能够明显减弱由上述过程所诱发的肾损害?因此,上述研究结果提示TRPV4 受体在促进Ang II 所诱导的肾损害中发挥重要的病理生理学作用?

    Abstract:

    Objective This study was designed to determine the effect of transient receptor potential vanilloid type 4 (TRPV4) on angiotensin II (Ang II)-induced renal injury in TRPV4-null mutant (TRPV4 - / - ) mice. Methods The mice were divided into sham group and Ang II-treated group. Ang II was infused systemically into wild type (WT) and TRPV4 - / - mice via a miniosmotic pump for 4 weeks, and the sham mice were given with normal saline. Systolic blood pressure, urinary excretion of albumin and 8-isoprostane, serum creatinine, and the pathological changes in the kidney tissues were assayed after the 4-week treatment. Results Compared with corresponding sham mice, Ang II infusion led to enhanced systolic blood pressure, increased urinary excretion of albumin and 8-isoprostane, increased serum creatinine (P< 0.05), and enhanced glomerulosclerosis degree and renal tubulointerstitial injury index (P < 0.05) in the WT and TRPV4 - / - mice. The result were associated with enhanced collagen levels in the kidney (P < 0.05). All of them were attenuated by the deletion of TRPV4 in the absence of alteration in blood pressure (P < 0.05). Conclusions Deletion of TRPV4 could alleviate renal injury during Ang II-induced hypertension, suggesting that TRPV4 may contribute to the pathophysiology of angiotensin II-induced renal injury.

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. TRPV4 受体对血管紧张素II 诱导的小鼠肾损害的影响[J].中国比较医学杂志,2018,28(2):1~6.

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  • 收稿日期:2017-04-17
  • 在线发布日期: 2018-03-14
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