临床荟萃 ›› 2021, Vol. 36 ›› Issue (11): 1005-1008.doi: 10.3969/j.issn.1004-583X.2021.11.009

• 论著 • 上一篇    下一篇

血管紧张素Ⅱ1型受体拮抗剂对早期糖尿病肾病患者尿液中足细胞相关蛋白nephrin、自噬基因Beclin-1 mRNA排泄的影响

刘伦志(), 邓璐, 张明霞   

  1. 湖北民族大学附属民大医院 肾内科 湖北省肾脏病临床研究中心 风湿病发生与干预湖北省重点实验室, 湖北 恩施 445000
  • 收稿日期:2021-04-14 出版日期:2021-11-20 发布日期:2021-12-01
  • 通讯作者: 刘伦志 E-mail:liulunzhi@163.com
  • 基金资助:
    恩施州科技局科技计划项目——糖尿病肾病尿液足细胞nephrin、podocin mRNA排泄及氯沙坦对其的影响(D20170017);湖北省卫生健康委员会联合基金项目——金蝉花对糖尿病肾病足细胞保护及机制的研究(WJ2019H140)

Effects of angiotensin Ⅱ type 1 receptor blockers on urinary nephrin and Beclin-1 mRNA excretion in urine of patients with early diabetic nephropathy

Liu Lunzhi(), Deng Lu, Zhang Mingxia   

  1. Department of Nephrology, Minda Hospital of Hubei Minzu Uuiversity, Hubei Provincial Clinic Research Center of Kindney Diseases, Hubei Provincial Key Laboratory of Occurrence and Intervention of Rheumatic Diseases, Enshi 445000, China
  • Received:2021-04-14 Online:2021-11-20 Published:2021-12-01
  • Contact: Liu Lunzhi E-mail:liulunzhi@163.com

摘要:

目的 观察早期糖尿病肾病(diabetic nephropathy, DN)患者尿液中足细胞、足细胞相关蛋白nephrin、自噬基因Beclin-1 mRNA 排泄及氯沙坦对上述指标的影响。方法 入选2018年1月-2021年1月我院确诊的符合标准的早期DN患者48 例,给予氯沙坦50 mg或100 mg口服6个月,观察治疗前后患者尿液中微量白蛋白、足细胞、足细胞相关蛋白nephrin mRNA、自噬基因Beclin-1 mRNA排泄。结果 早期DN患者尿液中微量白蛋白排泄、足细胞及足细胞相关蛋白nephrin、自噬基因Beclin-1 mRNA排泄均较健康人明显增加(P<0.01)。给予氯沙坦治疗6个月后,与治疗前比较,患者尿液中微量白蛋白、足细胞排泄减少(P<0.05),nephrin mRNA排泄呈下降趋势(P<0.05),自噬基因Beclin-1 mRNA排泄较治疗前有一定增加,但差异无统计学意义(P=0.067)。结论 早期DN患者可通过尿液检查证实存在足细胞损伤。血管紧张素Ⅱ1型受体拮抗剂可以减少DN患者尿微量白蛋白排泄,保护足细胞,并可能增强足细胞自噬作用。

关键词: 糖尿病肾病, 血管紧张素Ⅱ1型受体拮抗剂, 足细胞

Abstract:

Objective To observe the urinary excretion of podocytes, podocyte-related protein nephrin and autophay gene Beclin-1 mRNA of patients with early diabetic nephropathy(DN) and the effects of Losartan on the above indicators.Methods Forty-eight cases of early DN patients in our hospital from January 2018 to January 2021 were selected and given Losartan 50 mg or 100 mg orally for 6 months. The urine of early DN patients was sampled to determine the excretion of microalbumin, podocytes, podocyte-related protein nephrin mRNA, and autophagy gene Beclin-1 mRNA before and after treatment.Results The urinary excretion of microalbumin, podocyte, podocyte-related protein nephrin, autophagy gene Beclin-1 mRNA of early DN patients were significantly increased compared with healthy people (P<0.01). After six months of treatment with Losartan, urinary excretion of microalbumin and podocytes in patients with early DN decreased (P<0.05).The urinary excretion of nephrin mRNA showed a downward trend (P<0.05). The autophagy gene Beclin-1 mRNA excretion increased to a certain extent after treatment, but the difference was not statistically significant (P=0.067).Conclusion Podocyte damage can be confirmed by urine examination in patients with early DN.Angiotensin Ⅱ type 1 receptor blockers can reduce the excretion of microalbumin to protect podocytes and enhance podocyte autophagy in early ND patients.

Key words: diabetic nephropathy, angiotensin Ⅱ type 1 receptor blockers, podocyte

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