Antidepressant-like effect of atorvastatin in the forced swimming test in mice: The role of PPAR-gamma receptor and nitric oxide pathway

被引:32
|
作者
Shahsavarian, Arash [1 ,2 ]
Javadi, Shiva [3 ]
Jahanabadi, Samane [3 ,4 ]
Khoshnoodi, Mina [3 ]
Shamsaee, Javad [3 ]
Shafaroodi, Hamed [1 ,2 ]
Mehr, Shahram Ejtemaei [3 ,5 ]
Dehpour, Ahmadreza [3 ,5 ]
机构
[1] Islamic Azad Univ, Dept Pharmacol & Toxicol, Pharmaceut Sci Branch, Tehran, Iran
[2] Islamic Azad Univ, Pharmaceut Sci Res Ctr, Tehran, Iran
[3] Univ Tehran Med Sci, Sch Med, Dept Pharmacol, Tehran, Iran
[4] Shahid Sadoughi Univ Med Sci, Fac Pharm, Yazd, Iran
[5] Univ Tehran Med Sci, Expt Med Res Ctr, Tehran, Iran
关键词
Depression; Atorvastatin; Pioglitazonc; Nitric oxide; FST; Mice; HIPPOCAMPAL CELL-DEATH; SYNTHASE INHIBITORS; SERUM-CHOLESTEROL; MAJOR DEPRESSION; PIOGLITAZONE; STATINS; PATHOPHYSIOLOGY; INFLAMMATION; REDUCTION; DISORDER;
D O I
10.1016/j.ejphar.2014.10.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Atorvastatin is a synthetic and lipophilic statin which has been reported to have a positive role in reducing depression. The potential antidepressant-like effects of atorvastatin and the possible involvement of peroxisome proliferator-activated receptor gamma (PEAR_gamma) and nitric oxide system were determined using forced swimming test (FST) in mice was studied. Atorvastatin (0.01, 0.1 and 1 mg/kg, p.o.) was administered 1 h before FST. To assess the involvement of PEAR_gamma in the possible antidepressant effect of atorvastatin, pioglitazone, a PEAR_gamma agonist (5 mg/kg), and GW-9662, a specific PEAR_gamma antagonist (2 mg/kg), was co-administered with atorvastatin (0.01 mg/kg, p.o.) and then FST was performed. The possible role of nitric oxide pathway was determined by using co-administration of a nonspecific NOS inhibitor, N-nitro-L-arginine methyl ester (L-NAME, 10 mg/kg, i.p.), and a NO precursor, L-arginine (750 mg/kg, i.p.) with sub-effective doses of atorvastatin and pioglitazone. Immobility time was significantly decreased after atorvastatin administration (0.1 and 1 mg/kg, p.o.). Administration of pioglitazone or L-NAME in combination with the sub-effective dose of atorvastatin (0.01 mg/kg, p.o.) reduced the immobility time in the FST compared to drugs alone, showing the participation of these pathways; while co-administration of non-effective doses of atorvastatin and pioglitazone with GW9662 or L-arginine reversed antidepressant-like effect of atorvastatin in FST. Data From concurrent use of GW9662 and atorvastatin also demonstrated that the antidepressant effect of atorvastatin was significantly reversed by GW9662. The antidepressant-like effect of atorvastatin on mice in the EST is mediated at least in part through PPAR_gamma receptors and NO pathway. (C) 2014 Elsevier By. All rights reserved.
引用
收藏
页码:52 / 58
页数:7
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