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依那普利早期治疗与程序性肥胖成年大鼠后期肾损伤

Early Treatment With Enalapril and Later Renal Injury in Programmed Obese Adult Rats.

作者信息

Yim Hyung Eun, Yoo Kee Hwan, Bae In Sun, Hong Young Sook

机构信息

Department of Pediatrics, College of Medicine, Korea University, Seoul, Korea.

出版信息

J Cell Physiol. 2017 Feb;232(2):447-455. doi: 10.1002/jcp.25444. Epub 2016 Jun 6.

Abstract

Obesity-related kidney disease should be prevented or retarded. We aimed to investigate whether early treatment with enalapril ameliorates later renal injury induced by early postnatal overnutrition. Three or ten male pups per mother were assigned to either the Obese or Lean group during the first 21 days of life. These pups were treated with enalapril (Obese enalapril, OE; Lean enalapril, LE) or vehicle (Obese control, OC; Lean control, LC) for 15-28 days. Body weight, blood pressure (BP), and renal alterations were determined at 3 months. Enalapril decreased body weight only in the Lean group at 3 months (P < 0.05). Systemic BP levels were higher in the LE, OC, and OE groups than in the LC group at 3 months (P < 0.05). Fewer glomeruli per section area were found in the LE, OC, and OE groups than in the LC group and in the OE group than in the OC group (P < 0.05). The LE and OE groups had higher index scores of glomerulosclerosis and tubulointerstitial fibrosis than the controls (P < 0.05). LE pups showed increased intrarenal angiotensin II receptor type (AT)2 and matrix metalloproteinase (MMP)-9 and decreased renin and tissue inhibitor of MMP (TIMP)-1 expression than the LC rats (P < 0.05). OE pups showed increased intrarenal AT2 and decreased AT1 and TIMP-1 expression than the OC rats (P < 0.05). In conclusion, early treatment with enalapril can induce detrimental renal effects in later life and may not be renoprotective in programmed obese adult rats. J. Cell. Physiol. 232: 447-455, 2017. © 2016 Wiley Periodicals, Inc.

摘要

肥胖相关肾病应予以预防或延缓。我们旨在研究依那普利早期治疗是否能改善出生后早期营养过剩所致的后期肾损伤。在出生后的前21天,每只母鼠所产的3只或10只雄性幼崽被分为肥胖组或瘦组。这些幼崽接受依那普利(肥胖组依那普利,OE;瘦组依那普利,LE)或赋形剂(肥胖组对照,OC;瘦组对照,LC)治疗15 - 28天。在3个月时测定体重、血压(BP)和肾脏改变情况。依那普利仅在3个月时使瘦组体重下降(P < 0.05)。3个月时,LE、OC和OE组的全身血压水平高于LC组(P < 0.05)。LE、OC和OE组每单位面积切片中的肾小球数量少于LC组,且OE组少于OC组(P < 0.05)。LE和OE组的肾小球硬化和肾小管间质纤维化指数评分高于对照组(P < 0.05)。与LC大鼠相比,LE幼崽肾内血管紧张素II受体2型(AT)2和基质金属蛋白酶(MMP)-9表达增加,肾素和MMP组织抑制剂(TIMP)-1表达降低(P < 0.05)。与OC大鼠相比,OE幼崽肾内AT2表达增加,AT1和TIMP-1表达降低(P < 0.05)。总之,依那普利早期治疗可在后期生活中诱发有害的肾脏效应,且对程序化肥胖成年大鼠可能无肾脏保护作用。《细胞生理学杂志》2017年第232卷:447 - 455页。© 2016威利期刊公司

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