大鼠晶状体中谷胱甘肽水平调节的日时差异。

Frontiers in ophthalmology Pub Date : 2024-08-15 eCollection Date: 2024-01-01 DOI:10.3389/fopht.2024.1407582
Bo Li, Haruna Suzuki-Kerr, Renita M Martis, Christopher J J Lim, Zhou-Ai Wang, Tai X Nguyen, Paul J Donaldson, Raewyn C Poulsen, Julie C Lim
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引用次数: 0

摘要

导言:非眼部组织中的证据表明,抗氧化剂谷胱甘肽(GSH)可能会受到昼夜节律的调节,这让人联想到晶状体中的GSH水平也可能受到昼夜节律的控制,以预测氧化应激时期:雄性大鼠 Wistar 晶状体(6 周)在早上 6 点、10 点、下午 2 点、晚上 6 点、10 点和凌晨 2 点的 24 小时内每 4 小时采集一次,并进行定量-PCR、Western 印迹和免疫组化,以检测核心时钟基因和蛋白质(BMAL1、CLOCK、CRY1-2、PER 1-3)的表达及其在 24 小时内的亚细胞定位。还对镜片进行了 Western 印迹,以检测 24 小时内 NRF2 的表达情况,NRF2 是一种转录因子,参与调节涉及 GSH 稳态的基因和 GSH 相关酶(GCLC、GS 和 GR)。最后,使用 HLPC 在 24 小时内每 4 小时测量一次水液和晶状体中的 GSH 水平:结果:大鼠晶状体含有昼夜节律钟的核心分子成分,核心时钟蛋白、NRF2 和 GSH 相关酶的表达在 24 小时内波动。BMAL1的表达在白天最高,上午10点时BMAL1定位于细胞核。NRF2 的表达在 24 小时内保持稳定,但每 4 小时会进出细胞核一次。GSH相关酶的表达量往往在夜晚开始时达到峰值,这与晶状体中GSH水平较高和水液中GSH水平较低有关:结论:晶状体含有昼夜节律钟的关键成分,参与维持GSH平衡的GSH和GSH相关酶的表达存在日时差异。大鼠晶状体中的 GSH 水平在夜间开始时最高,这代表了大鼠的活跃期,此时可能需要高水平的 GSH 来抵消细胞代谢引起的氧化应激。未来将时钟与调节晶状体中 GSH 水平直接联系起来的工作将对确定时钟是否可用于帮助恢复晶状体中 GSH 水平非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time of day differences in the regulation of glutathione levels in the rat lens.

Introduction: Evidence in non-ocular tissues indicate that the antioxidant glutathione (GSH) may be regulated in a circadian manner leading to the idea that GSH levels in the lens may also be controlled in a circadian manner to anticipate periods of oxidative stress.

Methods: Male rat Wistar lenses (6 weeks) were collected every 4 hours over a 24-hour period at 6am, 10am, 2pm, 6pm, 10pm and 2am and quantitative-PCR, western blotting and immunohistochemistry performed to examine the expression of core clock genes and proteins (BMAL1, CLOCK, CRY1-2, PER 1-3) and their subcellular localisation over a 24-hour period. Western blotting of lenses was also performed to examine the expression of NRF2, a transcription factor involved in regulating genes involved in GSH homeostasis and GSH related enzymes (GCLC, GS and GR) over the 24-hour period. Finally, HLPC was used to measure GSH levels in the aqueous humour and lenses every 4 hours over a 24-hour period.

Results: The rat lens contains the core molecular components of a circadian clock with the expression of core clock proteins, NRF2 and GSH related enzymes fluctuating over a 24-hour period. BMAL1 expression was highest during the day, with BMAL1 localised to the nuclei at 10am. NRF2 expression remained constant over the 24-hour period, although appeared to move in and out of the nuclei every 4 hours. GSH related enzyme expression tended to peak at the start of night which correlated with high levels of GSH in the lens and lower levels of GSH in the aqueous humour.

Conclusion: The lens contains the key components of a circadian clock, and time-of-day differences exist in the expression of GSH and GSH related enzymes involved in maintaining GSH homeostasis. GSH levels in the rat lens were highest at the start of night which represents the active phase of the rat when high GSH levels may be required to counteract oxidative stress induced by cellular metabolism. Future work to directly link the clock to regulation of GSH levels in the lens will be important in determining whether the clock can be used to help restore GSH levels in the lens.

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