期刊
EUROPEAN JOURNAL OF PHARMACOLOGY
卷 666, 期 1-3, 页码 165-172出版社
ELSEVIER
DOI: 10.1016/j.ejphar.2011.05.035
关键词
Rosuvastatin; Pulmonary hypertension; Monocrotaline; Akt/eNOS; ADMA/DDAH2
资金
- Education Ministry of P. R. China [NCET-06-0916]
- Ningxia Natural Science Foundation of P. R. China [NZ08106]
This study was designed to investigate whether rosuvastatin could attenuate monocrotaline-induced pulmonary hypertension via regulation of Akt/eNOS signaling pathway and asymmetric dimethylarginine (ADMA) metabolism in rats. After a single-dose injection of monocrotaline (60 mg/kg), oral administration of rosuvastatin (5 mg/kg) was started from day 1 to day 28 (preventive administration) or from day 15 to day 28 (therapeutic administration), or with vehicle as corresponding controls. 28 days after monocrotaline, significant pulmonary hypertension characterized by pulmonary arterial medial wall thickening, right ventricular hypertrophy and right heart failure was observed. Rosuvastatin (5 mg/kg, for 14 days and 28 days) treatment significantly attenuated monocrotaline-induced pulmonary vascular remodeling, right ventricular hypertrophy and dysfunction, and normalized the down-regulated pulmonary Akt/p-Akt and eNOS/p-eNOS expressions, while increased DDAH2 expression accompanied by decreased serum level of ADMA. However expression of PRMT1 and GSK3 beta/p-GSK3 beta did not differ among all groups (all P>0.05). We concluded that rosuvastatin inhibits monocrotaline-induced pulmonary hypertension through normalization of Akt, eNOS and DDAH2 expressions, and decreasing the level of ADMA. (C) 2011 Elsevier B.V. All rights reserved.
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