Additive renoprotective effects of B2-kinin receptor blocker and PPAR-γ agonist in uninephrectomized db/db mice

被引:20
作者
Tang, Sydney C. W. [1 ]
Chan, Loretta Y. Y. [1 ]
Leung, Joseph C. K. [1 ]
Cheng, Amy Shan [1 ]
Lan, Hui Yao [2 ,3 ]
Lai, Kar Neng [1 ]
机构
[1] Univ Hong Kong, Dept Med, Queen Mary Hosp, Div Nephrol, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
关键词
B2-kinin receptor blockade; diabetic nephropathy; inflammation; PPAR-gamma agonist; renal pathology; signaling; uninephrectomy; CONVERTING ENZYME-INHIBITION; KALLIKREIN-KININ SYSTEM; DIABETIC-NEPHROPATHY; BRADYKININ RECEPTOR; TISSUE KALLIKREIN; MESANGIAL CELLS; ROSIGLITAZONE; ACTIVATION; PROTECTS; KIDNEY;
D O I
10.1038/labinvest.2011.81
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We recently showed that the bradykinin B2 receptor (B2R) blocker icatibant (Icat) and the peroxisome proliferator-activated receptor-g agonist rosiglitazone (Ros) exerted anti-inflammatory effects in renal tubular cells exposed to a diabetic milieu. This study aims to explore whether these effects can be translated to an experimental model of type 2 diabetic nephropathy (DN). db/db mice and their nondiabetic db/m littermates underwent sham operation or uninephrectomy (Unx) at 10 weeks and received vehicle (Veh), metformin (Met), Icat, Ros, or Icat plus Ros for 8 weeks before killing. Among the db/db group with Unx, mice that received Icat or Ros had significantly lower serum creatinine and albuminuria, which was further reduced when Icat and Ros were given in combination. These beneficial effects were not observed in the Met group that achieved similar glycemic control as Ros-treated animals. Likewise, the severity of reactive glomerular and proximal tubular hypertrophy, glomerulosclerosis, interstitial injury, cortical F4/80 and alpha-smooth muscle actin immunostaining, and CCL-2, ICAM-1 and TGF-beta overexpression were all attenuated by Icat and Ros, and these effects were enhanced when both agents were combined. Immunohistochemical staining confirmed the proximal tubular expression of CCL-2 (inflammation) and TGF-beta (fibrosis). Treatment with Icat was associated with decreased B2R, but increased, B1R expression, which was exaggerated in Unx animals. At the signaling level, Icat and Ros reduced extracellular signal-regulated kinase 1/2 and STAT1 activation, respectively. Our results suggest a deleterious role of the kallikrein-kinin system in murine-accelerated DN, which can be ameliorated by the B2R blocker Icat and enhanced by the addition of Ros. This calls for further evaluation of this novel therapeutic approach in more animal models of diabetic nephropathy. Laboratory Investigation (2011) 91, 1351-1362; doi: 10.1038/labinvest.2011.81; published online 2 May 2011
引用
收藏
页码:1351 / 1362
页数:12
相关论文
共 27 条
[1]   Inhibition of IGF-I-induced Erk 1 and 2 activation and mitogenesis in mesangial cells by bradykinin [J].
Alric, C ;
Pecher, C ;
Cellier, E ;
Schanstra, JP ;
Poirier, B ;
Chevalier, J ;
Bascands, JL ;
Girolami, JP .
KIDNEY INTERNATIONAL, 2002, 62 (02) :412-421
[2]   Kallikrein protects against microalbuminuria in experimental type I diabetes [J].
Bodin, Sophie ;
Chollet, Catherine ;
Goncalves-Mendes, Nicolas ;
Gardes, Joelle ;
Pean, Franck ;
Heudes, Didier ;
Bruneval, Patrick ;
Marre, Michel ;
Alhenc-Gelas, Francois ;
Bouby, Nadine .
KIDNEY INTERNATIONAL, 2009, 76 (04) :395-403
[3]   Pharmacological blockade of B2-kinin receptor reduces renal protective effect of angiotensin-converting enzyme inhibition in db/db mice model [J].
Buleon, Marie ;
Allard, Julien ;
Jaafar, Acil ;
Praddaude, Francoise ;
Dickson, Zara ;
Ranera, Marie-Therese ;
Pecher, Christiane ;
Girolami, Jean-Pierre ;
Tack, Ivan .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2008, 294 (05) :F1249-F1256
[4]   Increased tissue kallikrein levels in type 2 diabetes [J].
Campbell, D. J. ;
Kladis, A. ;
Zhang, Y. ;
Jenkins, A. J. ;
Prior, D. L. ;
Yii, M. ;
Kenny, J. F. ;
Black, M. J. ;
Kelly, D. J. .
DIABETOLOGIA, 2010, 53 (04) :779-785
[5]   Icatibant [J].
Deeks, Emma D. .
DRUGS, 2010, 70 (01) :73-81
[6]   Vasoactive potential of the B1 bradykinin receptor in normotension and hypertension [J].
Duka, I ;
Kintsurashvili, E ;
Gavras, I ;
Johns, C ;
Bresnahan, M ;
Gavras, H .
CIRCULATION RESEARCH, 2001, 88 (03) :275-281
[7]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[8]  
GOLDSTEIN RH, 1984, J BIOL CHEM, V259, P9263
[9]   Role of tissue kallikrein in the cardioprotective effects of ischemic and pharmacological preconditioning in myocardial ischemia [J].
Griol-Charhbili, V ;
Messadi-Laribi, E ;
Bascands, JL ;
Heudes, D ;
Meneton, P ;
Giudicelli, JF ;
Alhenc-Gelas, F ;
Richer, C .
FASEB JOURNAL, 2005, 19 (06) :1172-+
[10]   Increased vascular permeability in C1 men inhibitor-deficient mice mediated by the bradykinin type 2 receptor [J].
Han, ED ;
MacFarlane, RC ;
Mulligan, AN ;
Scafidi, J ;
Davis, AE .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (08) :1057-1063