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褪黑素通过 AMPK/DRP1 调控线粒体动力学和自噬减轻肾缺血再灌注损伤。

MELATONIN ATTENUATES RENAL ISCHEMIA-REPERFUSION INJURY BY REGULATING MITOCHONDRIAL DYNAMICS AND AUTOPHAGY THROUGH AMPK/DRP1.

机构信息

Department of Urology, Institute of Urology, Gansu Urological Clinical Center, Lanzhou University Second Hospital, Lanzhou, China.

Department of Anesthesiology, Lanzhou University Second Hospital, Lanzhou, China.

出版信息

Shock. 2024 Jul 1;62(1):74-84. doi: 10.1097/SHK.0000000000002330. Epub 2024 Apr 26.

Abstract

Ischemia-reperfusion injury (IRI) often stems from an imbalance between mitochondrial dynamics and autophagy. Melatonin mitigates IRI by regulating mitochondrial dynamics. However, the precise molecular mechanism underlying the role of melatonin in reducing IRI through modulating mitochondrial dynamics remains elusive. The objective of this study was to investigate whether pretreatment with melatonin before IRI confers protective effects by modulating mitochondrial dynamics and mitophagy. Melatonin pretreatment was administered to HK-2 cells and live rats before subjecting them to hypoxia-reoxygenation or IRI, respectively. Cells and rat kidney models were evaluated for markers of oxidative stress, autophagy, mitochondrial dynamics, and the expression of adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) and phospho-AMPKα (P-AMPK). After renal IRI, increased mitochondrial fission and autophagy were observed, accompanied by exacerbated cellular oxidative stress injury and aggravated mitochondrial dysfunction. Nevertheless, melatonin pretreatment inhibited mitochondrial fission, promoted mitochondrial fusion, and attenuated autophagy levels. This intervention was correlated with a notable reduction in oxidative stress injury and remarkable restoration of mitochondrial functionality. Ischemia-reperfusion injury led to a decline in P-AMPK levels, whereas melatonin pretreatment increased the level of P-AMPK levels. Silencing AMPK with small interfering RNA exacerbated mitochondrial damage, and in this context, melatonin pretreatment did not alleviate mitochondrial fission or autophagy levels but resulted in sustained oxidative stress damage. Collectively, these findings indicate that melatonin pretreatment shields the kidneys from IRI by mitigating excessive mitochondrial fission, moderating autophagy levels, and preserving appropriate mitochondrial fission, all in an AMPK-dependent manner.

摘要

缺血再灌注损伤(IRI)通常源于线粒体动力学和自噬之间的失衡。褪黑素通过调节线粒体动力学来减轻 IRI。然而,褪黑素通过调节线粒体动力学来减轻 IRI 的精确分子机制仍不清楚。本研究旨在探讨 IRI 前给予褪黑素预处理是否通过调节线粒体动力学和线粒体自噬发挥保护作用。在分别进行缺氧复氧或 IRI 之前,将褪黑素预处理给予 HK-2 细胞和活大鼠。评估细胞和大鼠肾脏模型的氧化应激、自噬、线粒体动力学标志物以及腺苷 5'-单磷酸(AMP)激活的蛋白激酶(AMPK)和磷酸化-AMPKα(P-AMPK)的表达。在肾 IRI 后,观察到线粒体裂变和自噬增加,同时伴有细胞氧化应激损伤加剧和线粒体功能恶化。然而,褪黑素预处理抑制了线粒体裂变,促进了线粒体融合,并降低了自噬水平。这种干预与氧化应激损伤显著减少和线粒体功能显著恢复有关。缺血再灌注损伤导致 P-AMPK 水平下降,而褪黑素预处理增加了 P-AMPK 水平。用小干扰 RNA 沉默 AMPK 加剧了线粒体损伤,在这种情况下,褪黑素预处理不能减轻线粒体裂变或自噬水平,但会导致持续的氧化应激损伤。总之,这些发现表明,褪黑素预处理通过减轻过度的线粒体裂变、调节自噬水平和维持适当的线粒体裂变来保护肾脏免受 IRI 的影响,所有这些都依赖于 AMPK。

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