Early Treatment With Enalapril and Later Renal Injury in Programmed Obese Adult Rats
- Authors
- Yim, Hyung Eun; Yoo, Kee Hwan; Bae, In Sun; Hong, Young Sook
- Issue Date
- 2월-2017
- Publisher
- WILEY-BLACKWELL
- Citation
- JOURNAL OF CELLULAR PHYSIOLOGY, v.232, no.2, pp.447 - 455
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF CELLULAR PHYSIOLOGY
- Volume
- 232
- Number
- 2
- Start Page
- 447
- End Page
- 455
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/84813
- DOI
- 10.1002/jcp.25444
- ISSN
- 0021-9541
- 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 21days of life. These pups were treated with enalapril (Obese enalapril, OE; Lean enalapril, LE) or vehicle (Obese control, OC; Lean control, LC) for 15-28days. 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. (c) 2016 Wiley Periodicals, Inc.
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