Protective effect of Ferula gummosa hydroalcoholic extract against nitric oxide deficiency-induced oxidative stress and inflammation in rats renal tissues

被引:14
作者
Moosavi, Seyed Jafar [1 ]
Habibian, Masoumeh [1 ]
Peeri, Maghsoud [2 ]
Azarbayjani, Mohammad Ali [2 ]
Nabavi, Seyed Mohammad [3 ]
Nabavi, Seyed Fazel
Sureda, Antoni [4 ]
机构
[1] Islamic Azad Univ, Qaemshahar Branch, Dept Phys Educ & Sports Sci, Qaemshahar, Iran
[2] Islamic Azad Univ, Cent Tehran Branch, Dept Exercise Physiol, Tehran, Iran
[3] Baqiyatallah Univ Med Sci, Appl Biotechnol Res Ctr, Tehran, Iran
[4] Univ Balearic Isl, Inst Salud Carlos III, CIBERobn, Res Grp Community Nutr & Oxidat Stress,Dept Funda, Palma de Mallorca, Balearic Island, Spain
关键词
Antioxidant; nitric oxide; pro-inflammatory cytokines; stress protein; BLOOD-PRESSURE; HYPERTENSION; KIDNEY; CYTOKINES; INFILTRATION; ANGIOTENSIN; PROPOLIS; CELLS;
D O I
10.3109/10641963.2014.913609
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nitric oxide (NO) synthase inhibition increases hypertension and causes renal injury. Ferula gummosa is used in Iranian traditional medicine for treatment of several diseases and has been reported to exert a potent anti-inflammatory and antioxidant action. The aim of this investigation was to evaluate the renoprotective effects of hydroalcoholic extract of Ferula gummosa (HEG) on N omega-nitro-L-arginine methyl ester (L-NAME)-induced oxidative stress and inflammation and explore the mechanisms that link NO deficiency with altered renal heat shock protein (HSP70). Rats were injected intraperitoneally with L-NAME (10 mg/kg) to induce renal injury. Simultaneously, HEG (90 mg/kg) was administered by gastric gavage to L-NAME-treated rats for 6 days/week during an 8-week period. Renal thiobarbituric acid reactive substances (TBARS), superoxide dismutase (SOD), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-alpha), HSP70, plasma NO and total antioxidant capacity (TAC) were evaluated. The administration of L-NAME significantly increased renal TBARS, TNF-alpha, IL-6, HSP70 levels and decreased renal SOD activity, that these changes were accompanied by the reduced plasma NO and TAC levels. HEG administration decreased TBARS, HSP70, TNF-alpha and IL-6 levels and increased SOD activity in the kidney tissues of L-NAME treated rats (p<0.05). Also, plasma TAC level and NO bioavailability have been elevated after administration of HEG (p<0.05). These findings support that NO deficiency induces renal stress oxidative and inflammation, which markedly increased renal HSP70 and HEG could protect kidney against these damaging effects via its anti-oxidative, anti-inflammatory action and modulate renal HSP70.
引用
收藏
页码:136 / 141
页数:6
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