Kazim Sahin, Cemal Orhan, Mehmet Tuzcu, Hakki Tastan, Birdal Bilir, Nurhan Sahin, Deniz Aslar Oner, Omer Kucuk
{"title":"Tomato Powder Modulates NF-<i>κ</i>B, mTOR, and Nrf2 Pathways during Aging in Healthy Rats.","authors":"Kazim Sahin, Cemal Orhan, Mehmet Tuzcu, Hakki Tastan, Birdal Bilir, Nurhan Sahin, Deniz Aslar Oner, Omer Kucuk","doi":"10.1155/2019/1643243","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>In the present study, we aimed to investigate the effects of tomato powder (TP) on glucose and lipid metabolism, as well as oxidative stress and the NF-<i>κ</i>B, mTOR, and Nrf2 pathways during the aging process in healthy rats.</p><p><strong>Methods and results: </strong>Male Wistar rats were randomly assigned to four groups as follows: (i) Control group 1 (<i>n</i>=15, 3-week old): rats were fed standard diet for 7 weeks; (ii) TP group 1 (<i>n</i>=15, 3-week old): rats were fed standard diet supplemented with TP for 7 weeks; (iii) Control group 2 (<i>n</i>=15, 8-week old): rats were fed standard diet for 69 weeks; and (iv) TP group 2 (8-week old): rats were fed standard diet supplemented with TP for 69 weeks. TP supplementation significantly reduced the hyperglycemia, hypertriglyceridemia, and hypercholesterolemia and improved liver function and kidney function in 77-week old rats compared with the control animals (<i>P</i> < 0.05). In addition, TP significantly decreased the serum and liver MDA levels (<i>P</i> < 0.003 and <i>P</i> < 0.001, respectively) while increasing the activities of liver SOD (<i>P</i> < 0.001), CAT (<i>P</i> < 0.008), and GPx (<i>P</i> < 0.01) compared with the control groups in both 10-week-old and 77-week-old rats (<i>P</i> < 0.05). Age-related increases in phosphorylation of NF-<i>κ</i>Bp65, mTOR, 4E-BP1, and P70S6K were observed in livers of 77-week-old rats compared to those of 10-week-old rats (<i>P</i> < 0.001). TP supplementation decreased the expression of NF-<i>κ</i>Bp65 and activation of mTOR, 4E-BP1, and P70S6K in livers of 77-week-old rats compared to the control animals. Moreover, TP supplementation significantly elevated Nrf2 expression in livers of both 10-week-old and 77-week-old rats (<i>P</i> < 0.05).</p><p><strong>Conclusion: </strong>TP ameliorates age-associated inflammation and oxidative stress through the inhibition of NF-<i>κ</i>Bp65, mTOR pathways, and Nrf2 activation may explain the observed improvement in glucose and lipid metabolism as well as the improved liver and kidney functions.</p>","PeriodicalId":14933,"journal":{"name":"Journal of Aging Research","volume":"2019 ","pages":"1643243"},"PeriodicalIF":1.6000,"publicationDate":"2019-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2019/1643243","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Aging Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2019/1643243","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 11
Abstract
Purpose: In the present study, we aimed to investigate the effects of tomato powder (TP) on glucose and lipid metabolism, as well as oxidative stress and the NF-κB, mTOR, and Nrf2 pathways during the aging process in healthy rats.
Methods and results: Male Wistar rats were randomly assigned to four groups as follows: (i) Control group 1 (n=15, 3-week old): rats were fed standard diet for 7 weeks; (ii) TP group 1 (n=15, 3-week old): rats were fed standard diet supplemented with TP for 7 weeks; (iii) Control group 2 (n=15, 8-week old): rats were fed standard diet for 69 weeks; and (iv) TP group 2 (8-week old): rats were fed standard diet supplemented with TP for 69 weeks. TP supplementation significantly reduced the hyperglycemia, hypertriglyceridemia, and hypercholesterolemia and improved liver function and kidney function in 77-week old rats compared with the control animals (P < 0.05). In addition, TP significantly decreased the serum and liver MDA levels (P < 0.003 and P < 0.001, respectively) while increasing the activities of liver SOD (P < 0.001), CAT (P < 0.008), and GPx (P < 0.01) compared with the control groups in both 10-week-old and 77-week-old rats (P < 0.05). Age-related increases in phosphorylation of NF-κBp65, mTOR, 4E-BP1, and P70S6K were observed in livers of 77-week-old rats compared to those of 10-week-old rats (P < 0.001). TP supplementation decreased the expression of NF-κBp65 and activation of mTOR, 4E-BP1, and P70S6K in livers of 77-week-old rats compared to the control animals. Moreover, TP supplementation significantly elevated Nrf2 expression in livers of both 10-week-old and 77-week-old rats (P < 0.05).
Conclusion: TP ameliorates age-associated inflammation and oxidative stress through the inhibition of NF-κBp65, mTOR pathways, and Nrf2 activation may explain the observed improvement in glucose and lipid metabolism as well as the improved liver and kidney functions.