Literature DB >> 18682491

Effect of eplerenone, enalapril and their combination treatment on diabetic nephropathy in type II diabetic rats.

Young Sun Kang1, Gang Jee Ko, Mi Hwa Lee, Hye Kyoung Song, Sang Youb Han, Kum Hyun Han, Hyoung Kyu Kim, Jee Young Han, Dae Ryong Cha.   

Abstract

BACKGROUND: Recent data suggest that aldosterone antagonists have beneficial effects on diabetic nephropathy. In this study, we investigated the dose-dependent effect of eplerenone and a combined treatment with eplerenone and enalapril compared with each drug alone on renal function in type II diabetic rats. To further explore the molecular mechanism of action of combination therapy, we also performed in vitro study.
METHODS: The animals were divided into six groups as follows: normal control Long-Evans Tokushima Otsuka (LETO) rats, Otsuka Long-Evans Tokushima Fatty (OLETF) rats, OLETF rats treated with low dose of eplerenone (50 mg/kg/day), OLETF rats treated with high dose of eplerenone (200 mg/kg/day), OLETF rats treated with enalapril (10 mg/kg/day) and OLETF rats treated with a combination of both drugs (eplerenone 200 mg/kg/day and enalapril 10 mg/kg/day) for 6 months.
RESULTS: Treatment of OLETF rats had no significant effect on body weight, kidney weight and blood glucose levels. However, urinary albumin excretion, glomerular filtration rate and glomerulosclerosis were significantly improved in the enalapril group and improvement was observed in a dose-dependent manner in the eplerenone groups; the most dramatic decreases were observed in the combination group. In accordance with these findings, renal expressions of TGF-beta1, type IV collagen and PAI-1 were also markedly decreased in the treatment groups, with the combined treatment providing the most significant level of improvement. In cultured mesangial cells, combined treatment resulted in an additive decrease in TGF-beta1, PAI-1 and collagen gene expressions and protein production induced by high glucose and aldosterone stimulation.
CONCLUSIONS: Aldosterone receptor antagonism provided additional benefits beyond blockade of the renin-angiotensin system in type II diabetic nephropathy.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18682491     DOI: 10.1093/ndt/gfn448

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  19 in total

Review 1.  Therapeutic modalities in diabetic nephropathy: standard and emerging approaches.

Authors:  Emaad M Abdel-Rahman; Lawand Saadulla; W Brian Reeves; Alaa S Awad
Journal:  J Gen Intern Med       Date:  2011-10-18       Impact factor: 5.128

Review 2.  Dual Renin-Angiotensin-Aldosterone System Inhibition for the Treatment of Diabetic Kidney Disease: Adverse Effects and Unfulfilled Promise.

Authors:  Boutros El-Haddad; Scott Reule; Paul E Drawz
Journal:  Curr Diab Rep       Date:  2015-10       Impact factor: 4.810

Review 3.  Aldosterone and diabetic kidney disease.

Authors:  Young Sun Kang; Dae Ryong Cha
Journal:  Curr Diab Rep       Date:  2009-12       Impact factor: 4.810

Review 4.  Aldosterone blockade in chronic kidney disease: can it improve outcome?

Authors:  Robert D Toto
Journal:  Curr Opin Nephrol Hypertens       Date:  2010-09       Impact factor: 2.894

5.  Effects of single and dual RAAS blockade therapy on progressive kidney disease transition to CKD in rats.

Authors:  Devesh Aggarwal; Gaaminepreet Singh
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2019-11-26       Impact factor: 3.000

Review 6.  PPARalpha: an emerging therapeutic target in diabetic microvascular damage.

Authors:  Anne Hiukka; Marianna Maranghi; Niina Matikainen; Marja-Riitta Taskinen
Journal:  Nat Rev Endocrinol       Date:  2010-06-22       Impact factor: 43.330

Review 7.  Clinical therapeutic strategies for early stage of diabetic kidney disease.

Authors:  Munehiro Kitada; Keizo Kanasaki; Daisuke Koya
Journal:  World J Diabetes       Date:  2014-06-15

8.  Mineralocorticoid receptor blockade enhances the antiproteinuric effect of an angiotensin II blocker through inhibiting podocyte injury in type 2 diabetic rats.

Authors:  Akira Nishiyama; Hiroyuki Kobori; Yoshio Konishi; Takashi Morikawa; Isseki Maeda; Michiaki Okumura; Masatsugu Kishida; Masahiro Hamada; Yukiko Nagai; Toshitaka Nakagawa; Naro Ohashi; Daisuke Nakano; Hirofumi Hitomi; Masahito Imanishi
Journal:  J Pharmacol Exp Ther       Date:  2009-11-25       Impact factor: 4.030

9.  An additive effect of eplerenone to ACE inhibitor on slowing the progression of diabetic nephropathy in the db/db mice.

Authors:  Guangyu Zhou; Ulrika Johansson; Xiao-Rong Peng; Krister Bamberg; Yufeng Huang
Journal:  Am J Transl Res       Date:  2016-03-15       Impact factor: 4.060

10.  Preventive and chronic mineralocorticoid receptor antagonism is highly beneficial in obese SHHF rats.

Authors:  G Youcef; A Olivier; N Nicot; A Muller; C Deng; C Labat; R Fay; R-M Rodriguez-Guéant; C Leroy; F Jaisser; F Zannad; P Lacolley; L Vallar; A Pizard
Journal:  Br J Pharmacol       Date:  2016-04-26       Impact factor: 8.739

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.