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姜黄素对雄性 Wistar 大鼠 SCN 中时钟基因和 Sirt1 表达的年龄诱导的日常节律变化的治疗作用。

Therapeutic effects of curcumin on age-induced alterations in daily rhythms of clock genes and Sirt1 expression in the SCN of male Wistar rats.

机构信息

Neurobiology and Molecular Chronobiology Laboratory, Department of Animal Biology, School of Life Sciences, University of Hyderabad, Hyderabad, 500046, India.

出版信息

Biogerontology. 2019 Aug;20(4):405-419. doi: 10.1007/s10522-018-09794-y. Epub 2019 Jan 3.

Abstract

The aging brain is linked to accumulation of oxidative stress and increase in damage to biomolecules which in turn may cause or promote circadian dysfunction by disruption of biological clock, the suprachiasmatic nucleus (SCN). Age associated alterations in clock gene expression in the SCN has been reported earlier. In the present study we have examined therapeutic effects of the antioxidant curcumin on age induced alterations in daily rhythms and levels of core clock genes in SCN of young [3 months (m)], middle (12 months) and old (24 months) male Wistar rats. Curcumin was administered orally at ZT-11, 1 hour (h) before the onset of darkness. The effect of curcumin administration on daily rhythms and levels of expression of clock genes such as rBmal1, rPer1, rPer2, rCry1, rCry2 and rRev-erbα as well as on the clock modulator rSirt1 were studied. There was restoration of phase of rPer1, rPer2, rCry1, rCry2 and daily pulse of rPer2 in middle aged animals. However, in old aged rats the phase and daily pulse of rPer1 were restored with curcumin treatment. rSirt1 did not show age related alterations in its transcript levels though the rhythms were abolished in old aged rat SCN. Pearson correlation analysis showed that curcumin administration to 12 and 24 months animals had resulted in restorations of several correlations among clock genes which were found to be altered/abolished in age matched control groups. In addition, strong interlocking interactions between rSirt1 and clock genes were observed in young age which were disrupted with aging and curcumin administration resulted in partial restoration.

摘要

衰老的大脑与氧化应激的积累和生物分子损伤的增加有关,这反过来可能通过破坏生物钟、视交叉上核(SCN),导致或促进昼夜节律功能障碍。先前有报道称,SCN 中时钟基因表达的年龄相关改变。在本研究中,我们研究了抗氧化剂姜黄素对年轻[3 个月(m)]、中年(12 个月)和老年(24 个月)雄性 Wistar 大鼠 SCN 中年龄引起的每日节律和核心时钟基因水平变化的治疗作用。姜黄素在 ZT-11 时经口给药,即在黑暗开始前 1 小时(h)给药。研究了姜黄素给药对时钟基因如 rBmal1、rPer1、rPer2、rCry1、rCry2 和 rRev-erbα 的表达的昼夜节律和水平的影响,以及对时钟调节剂 rSirt1 的影响。中年动物的 rPer1、rPer2、rCry1、rCry2 的相位和每日脉冲得到恢复。然而,在老年大鼠中,rPer1 的相位和每日脉冲在姜黄素治疗后得到恢复。rSirt1 的转录水平与年龄无关,但在老年大鼠 SCN 中其节律被消除。Pearson 相关分析表明,向 12 个月和 24 个月龄动物给予姜黄素导致几个时钟基因之间的相关性得到恢复,而这些相关性在年龄匹配的对照组中被改变/消除。此外,在年轻年龄中观察到 rSirt1 和时钟基因之间的强连锁相互作用,随着衰老而中断,姜黄素给药导致部分恢复。

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