PMID- 22943648 OWN - NLM STAT- MEDLINE DCOM- 20130930 LR - 20151119 IS - 0253-3758 (Print) IS - 0253-3758 (Linking) VI - 40 IP - 6 DP - 2012 Jun TI - [Role of valsartan on myocardial Calpain I, calcineurin and Ca/calmodulin-dependent protein kinase IIdelta expression of renovascular hypertensive rats]. PG - 511-5 AB - OBJECTIVE: To determine the protein expression of Calpain I, mRNA and protein expressions and activity of calcineurin, and the alternative splicing of Ca/calmodulin-dependent protein kinase II (CaMKII) delta in the hypertrophic heart, and to investigate the effect of angiotensin II type 1 receptor blocker valsartan (Val) on cardiac hypertrophy and the level of Calpain I, calcineurin and CaMKIIdelta in renovascular hypertensive rats model. METHODS: Rats were randomly divided into sham-operated control (n=8), hypertension (n=8) and hypertension plus Val (n=8, 30 mgxkg(-1)x(-1)). The renovascular hypertension was induced by two kidney-one clip methods in rats. The ratio of left ventricular weight to body weight was measured, the mRNA expression of calcineurin and alternative splicing of CaMKIIdelta were determined by RT-PCR, the protein expression of Calpain I and calcineurin were measured by Western blot and the activity of calcineurin activity was assayed by a specialized kit. RESULTS: Eight weeks after procedure, hypertension rats developed significantly cardiac hypertrophy, and the protein expression of Calpain I, mRNA and protein expression and the activity of calcineurin were significantly increased compared sham-operated control rats (all P<0.01), the mRNA expression of CaMKIIdeltaA and B increased, CaMKIIdeltaC mRNA decreased (P<0.01). Treatment with valsartan effectively attenuated cardiac hypertrophy and reversed hypertension induced changes on myocardial Calpain I, calcineurin and CaMKIIdelta. CONCLUSION: Valsartan attenuates cardiac hypertrophy in renovascular hypertensive rats, possibly through inhibiting Calpain I, calcineurin and CaMKIIdelta signaling pathways. FAU - Lu, Jin-ya AU - Lu JY AD - Department of Cardiology, Affiliated Hospital of Nantong University, Nantong 226001, China. FAU - Zhu, Jian-hua AU - Zhu JH FAU - Qin, Xiao-tong AU - Qin XT FAU - Yu, Xiao-hong AU - Yu XH FAU - Sheng, Hong-zhuan AU - Sheng HZ LA - chi PT - English Abstract PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. PL - China TA - Zhonghua Xin Xue Guan Bing Za Zhi JT - Zhonghua xin xue guan bing za zhi JID - 7910682 RN - 0 (RNA, Messenger) RN - 0 (Tetrazoles) RN - 80M03YXJ7I (Valsartan) RN - EC 2.7.11.17 (Calcium-Calmodulin-Dependent Protein Kinase Type 2) RN - EC 3.1.3.16 (Calcineurin) RN - EC 3.4.22.- (Calpain) RN - HG18B9YRS7 (Valine) SB - IM MH - Animals MH - Calcineurin/metabolism MH - Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism MH - Calpain/metabolism MH - Hypertension, Renovascular/drug therapy/*metabolism/pathology MH - Male MH - Myocardium/*metabolism/pathology MH - RNA, Messenger/genetics MH - Rats MH - Rats, Sprague-Dawley MH - *Signal Transduction MH - Tetrazoles/*pharmacology/therapeutic use MH - Valine/*analogs & derivatives/pharmacology/therapeutic use MH - Valsartan EDAT- 2012/09/05 06:00 MHDA- 2013/10/01 06:00 CRDT- 2012/09/05 06:00 PHST- 2012/09/05 06:00 [entrez] PHST- 2012/09/05 06:00 [pubmed] PHST- 2013/10/01 06:00 [medline] PST - ppublish SO - Zhonghua Xin Xue Guan Bing Za Zhi. 2012 Jun;40(6):511-5.