番茄粉对健康大鼠衰老过程中NF-κB、mTOR和Nrf2通路的调节作用

IF 1.6 Q4 GERIATRICS & GERONTOLOGY
Journal of Aging Research Pub Date : 2019-01-02 eCollection Date: 2019-01-01 DOI:10.1155/2019/1643243
Kazim Sahin, Cemal Orhan, Mehmet Tuzcu, Hakki Tastan, Birdal Bilir, Nurhan Sahin, Deniz Aslar Oner, Omer Kucuk
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引用次数: 11

摘要

目的:本研究旨在探讨番茄粉(TP)对健康大鼠衰老过程中糖脂代谢、氧化应激及NF-κB、mTOR、Nrf2通路的影响。方法与结果:将雄性Wistar大鼠随机分为4组:(i)对照组1 (n=15只,3周龄):饲喂标准日粮7周;(ii) TP组1 (n=15, 3周龄):在标准饲粮中添加TP,饲喂7周;(iii)对照组2 (n=15, 8周龄):饲喂标准日粮69周;(iv) TP组2(8周龄):在标准饲粮中添加TP,饲喂69周。与对照组相比,添加TP显著降低了77周龄大鼠的高血糖、高甘油三酯血症和高胆固醇血症,改善了肝功能和肾功能(P < 0.05)。此外,与对照组相比,TP显著降低了10周龄和77周龄大鼠血清和肝脏MDA水平(P < 0.003和P < 0.001),提高了肝脏SOD (P < 0.001)、CAT (P < 0.008)和GPx (P < 0.01)活性(P < 0.05)。与10周龄大鼠相比,77周龄大鼠肝脏中NF-κBp65、mTOR、4E-BP1和P70S6K的磷酸化水平与年龄相关(P < 0.001)。与对照动物相比,补充TP降低了77周龄大鼠肝脏中NF-κBp65的表达和mTOR、4E-BP1和P70S6K的激活。此外,添加TP显著提高了10周龄和77周龄大鼠肝脏中Nrf2的表达(P < 0.05)。结论:TP通过抑制NF-κBp65、mTOR通路和Nrf2激活来改善年龄相关性炎症和氧化应激,这可能解释了观察到的糖脂代谢改善和肝肾功能改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tomato Powder Modulates NF-<i>κ</i>B, mTOR, and Nrf2 Pathways during Aging in Healthy Rats.

Tomato Powder Modulates NF-<i>κ</i>B, mTOR, and Nrf2 Pathways during Aging in Healthy Rats.

Tomato Powder Modulates NF-κB, mTOR, and Nrf2 Pathways during Aging in Healthy Rats.

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.

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来源期刊
Journal of Aging Research
Journal of Aging Research Medicine-Geriatrics and Gerontology
CiteScore
5.40
自引率
0.00%
发文量
11
审稿时长
30 weeks
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