K. Mireille, D. Désiré, Bilanda Danielle Claude, M. N. Y. Sandrine, Mballa Marguerite Francine, Ngoungoure Madeleine Chantal, O. Carolle, D. Théophile, Kamtchouing Pierre
{"title":"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","authors":"K. Mireille, D. Désiré, Bilanda Danielle Claude, M. N. Y. Sandrine, Mballa Marguerite Francine, Ngoungoure Madeleine Chantal, O. Carolle, D. Théophile, Kamtchouing Pierre","doi":"10.5455/JEIM.121216.OR.165","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":16091,"journal":{"name":"Journal of Experimental and Integrative Medicine","volume":"40 9 1","pages":"178-184"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Protective effects of Nymphaea lotus Linn (Nymphaeaceae) on L-NAME-induced tissular oxidative damages and erectile dysfunction in hypertensive male rat\",\"authors\":\"K. Mireille, D. Désiré, Bilanda Danielle Claude, M. N. Y. Sandrine, Mballa Marguerite Francine, Ngoungoure Madeleine Chantal, O. Carolle, D. Théophile, Kamtchouing Pierre\",\"doi\":\"10.5455/JEIM.121216.OR.165\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":16091,\"journal\":{\"name\":\"Journal of Experimental and Integrative Medicine\",\"volume\":\"40 9 1\",\"pages\":\"178-184\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Experimental and Integrative Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5455/JEIM.121216.OR.165\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental and Integrative Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5455/JEIM.121216.OR.165","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.