睡莲对l - name诱导的高血压雄性大鼠组织氧化损伤和勃起功能障碍的保护作用

K. Mireille, D. Désiré, Bilanda Danielle Claude, M. N. Y. Sandrine, Mballa Marguerite Francine, Ngoungoure Madeleine Chantal, O. Carolle, D. Théophile, Kamtchouing Pierre
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引用次数: 5

摘要

探讨莲花水提物对l - name介导的雄性Wistar大鼠性功能障碍和组织氧化应激的影响。方法:50只成年雄性Wistar大鼠随机分为5组;对照,L-NAME (10mg /kg), L-NAME +氯沙坦(10mg /kg), L-NAME + N.莲花,剂量分别为75mg /kg和200mg /kg。L-NAME在8周内给予,但其他治疗从第4周开始,在额外的4周内持续给予L-NAME (10 mg/kg)。结果:L-NAME给药导致性行为明显下降,特别是阴茎插入失败或在测试期间射精困难。与对照组相比,L-NAME进一步导致主动脉和阴茎组织中还原型谷胱甘肽(GSH)和亚硝酸盐(NO)等抗氧化产物显著减少。与仅服用L-NAME的阴性对照组相比,联合治疗4周的荷花组勃起指数和射精率明显高于氯沙坦组。与L-NAME组相比,L-NAME组抗氧化酶活性显著升高,GSH和NO水平显著升高,MDA水平显著降低,阳性药物氯沙坦未引起阳性反应。这些结果表明,荷花可能通过上调抗氧化系统和促进血管舒张因子,对l - name诱导的慢性no缺乏大鼠的组织氧化损伤具有显著的保护作用。莲花的这些缓解作用表明,在主动脉重塑明显减少的组织学检查后,莲花具有促性、抗氧化和血管扩张的特性。结论:莲子可能被认为是限制高血压相关勃起功能障碍和毒性的潜在有效策略。
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Protective effects of Nymphaea lotus Linn (Nymphaeaceae) on L-NAME-induced tissular oxidative damages and erectile dysfunction in hypertensive male rat
To investigate Nymphaea lotus aqueous extract on L-NAME-mediated sexual dysfunction and tissular oxidative stress in male Wistar rats. Methods: Fifty adult male Wistar rats were randomly classified into 5 groups; Control, L-NAME (10 mg/kg), L-NAME + losartan (10 mg/kg), L-NAME + N. lotus at the dose of 75 mg/kg and 200 mg/kg. L-NAME was administered during 8 weeks, but others treatments started from the 4th week and were administered continuously with L-NAME (10 mg/kg) during 4 additional weeks. Results: L-NAME administration caused marked hit of sexual behaviour, specifically failure of penile insertion or difficulty to ejaculate during the test interval. Further L-NAME causes a significant decrease in antioxidant products as reduced gluthatione (GSH) and nitrites (NO) in aorta and penile tissues, as compared to control group. N. lotus co-treatment for 4 weeks increased markedly the erectile index and the ejaculation rates contrarily to losartan in comparison to negative control receiving only L-NAME. N. lotus, but not the positive drug losartan, induced a significant increase in the anti-oxidant enzymes activities and GSH and NO levels, as well as a significant decrease in MDA levels compared to L-NAME group. These results suggests N. lotus may provide significant protection against L-NAME-induced tissular oxidative damages by up-regulation of antioxidant systems and promotion of the vasodilator factors in chronic NO-deficient rats. These alleviating effects of Nymphaea lotus denote a pro-sexual, antioxidant and vasodilatatory properties that was more appreciated after histological examination where remodeling of aorta were visibly reduced. Conclusion: N. lotus may be considered as a potentially useful strategy to limit erectile dysfunction and toxicity associated with hypertension.
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