Reda Abo- Elsoud, Amany Elfakhrany, Anwaar Shaban, A. Gaafar
{"title":"非诺贝特对老年大鼠生化及血管反应性变化的影响","authors":"Reda Abo- Elsoud, Amany Elfakhrany, Anwaar Shaban, A. Gaafar","doi":"10.21608/besps.2022.120408.1118","DOIUrl":null,"url":null,"abstract":"Background: Risk of vascular hemodynamic impairment increases with age. So, finding a new therapeutic approach to counter the age-related vascular complications has been a challenge. Hence, we evaluated the therapeutic effects of fenofibrate (FEN) in ageing. We also studied the FEN anti-ageing effects, and the possible molecular mechanisms that may clarify these effects. Methods: Thirty male rats were equally divided into three groups: 1Control group: Received (1% CMC) via gastric lavage, 2aged non treated group: Received (1% CMC) via gastric lavage, and 3Aged (FEN) treated group: received FEN (30 mg/kg) dissolved in (1% CMC) via gastric lavage for 7 weeks. At the end of study, serum lipid profile, inflammatory and oxidative stress markers were performed. Lastly, rats were subjected for measurement of invasive mean arterial blood pressure (MABP) and vascular reactivity to NE and Ach. Results: Aging resulted in dyslipidemia and elevation of inflammatory biomarkers, with altered oxidative stress markers. Increased MABP and decreased vascular reactivity to NE and Ach were also notice. FEN restored significantly aged related biochemical and vascular pathophysiological changes. Conclusion: FEN could be a good candidate for cardiovascular deficits due to ageing via amelioration of dyslipidemia, inflammation, attenuation of oxidative stress, reduction of MABP and improvement of vascular reactivity.","PeriodicalId":9347,"journal":{"name":"Bulletin of Egyptian Society for Physiological Sciences","volume":"11 1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of fenofibrate on biochemical and vascular reactivity changes in aged rats\",\"authors\":\"Reda Abo- Elsoud, Amany Elfakhrany, Anwaar Shaban, A. Gaafar\",\"doi\":\"10.21608/besps.2022.120408.1118\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Risk of vascular hemodynamic impairment increases with age. So, finding a new therapeutic approach to counter the age-related vascular complications has been a challenge. Hence, we evaluated the therapeutic effects of fenofibrate (FEN) in ageing. We also studied the FEN anti-ageing effects, and the possible molecular mechanisms that may clarify these effects. Methods: Thirty male rats were equally divided into three groups: 1Control group: Received (1% CMC) via gastric lavage, 2aged non treated group: Received (1% CMC) via gastric lavage, and 3Aged (FEN) treated group: received FEN (30 mg/kg) dissolved in (1% CMC) via gastric lavage for 7 weeks. At the end of study, serum lipid profile, inflammatory and oxidative stress markers were performed. Lastly, rats were subjected for measurement of invasive mean arterial blood pressure (MABP) and vascular reactivity to NE and Ach. Results: Aging resulted in dyslipidemia and elevation of inflammatory biomarkers, with altered oxidative stress markers. Increased MABP and decreased vascular reactivity to NE and Ach were also notice. FEN restored significantly aged related biochemical and vascular pathophysiological changes. Conclusion: FEN could be a good candidate for cardiovascular deficits due to ageing via amelioration of dyslipidemia, inflammation, attenuation of oxidative stress, reduction of MABP and improvement of vascular reactivity.\",\"PeriodicalId\":9347,\"journal\":{\"name\":\"Bulletin of Egyptian Society for Physiological Sciences\",\"volume\":\"11 1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of Egyptian Society for Physiological Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/besps.2022.120408.1118\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Egyptian Society for Physiological Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/besps.2022.120408.1118","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Effect of fenofibrate on biochemical and vascular reactivity changes in aged rats
Background: Risk of vascular hemodynamic impairment increases with age. So, finding a new therapeutic approach to counter the age-related vascular complications has been a challenge. Hence, we evaluated the therapeutic effects of fenofibrate (FEN) in ageing. We also studied the FEN anti-ageing effects, and the possible molecular mechanisms that may clarify these effects. Methods: Thirty male rats were equally divided into three groups: 1Control group: Received (1% CMC) via gastric lavage, 2aged non treated group: Received (1% CMC) via gastric lavage, and 3Aged (FEN) treated group: received FEN (30 mg/kg) dissolved in (1% CMC) via gastric lavage for 7 weeks. At the end of study, serum lipid profile, inflammatory and oxidative stress markers were performed. Lastly, rats were subjected for measurement of invasive mean arterial blood pressure (MABP) and vascular reactivity to NE and Ach. Results: Aging resulted in dyslipidemia and elevation of inflammatory biomarkers, with altered oxidative stress markers. Increased MABP and decreased vascular reactivity to NE and Ach were also notice. FEN restored significantly aged related biochemical and vascular pathophysiological changes. Conclusion: FEN could be a good candidate for cardiovascular deficits due to ageing via amelioration of dyslipidemia, inflammation, attenuation of oxidative stress, reduction of MABP and improvement of vascular reactivity.