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Sirtuin 1 减轻创伤性脑损伤后神经炎症诱导的细胞凋亡。

Sirtuin 1 alleviates neuroinflammation-induced apoptosis after traumatic brain injury.

机构信息

Department of Emergency, The Second Affiliated Hospital, Fujian Medical University, Quanzhou, China.

Department of Neurosurgery, Anxi County Hospital of Traditional Chinese Medicine, Quanzhou, China.

出版信息

J Cell Mol Med. 2021 May;25(9):4478-4486. doi: 10.1111/jcmm.16534. Epub 2021 Apr 8.

Abstract

Sirtuin 1 (SIRT1) plays a very important role in a wide range of biological responses, such as metabolism, inflammation and cell apoptosis. Changes in the levels of SIRT1 have been detected in the brain after traumatic brain injury (TBI). Further, SIRT1 has shown a neuroprotective effect in some models of neuronal death; however, its role and working mechanisms are not well understood in the model of TBI. This study aimed to address this issue. SIRT1-specific inhibitor (sirtinol) and activator (A3) were introduced to explore the role of SIRT1 in cell apoptosis. Results of the study suggest that SIRT1 plays an important role in neuronal apoptosis after TBI by inhibiting NF-κB, IL-6 and TNF-α deacetylation and the apoptotic pathway sequentially, possibly by alleviating neuroinflammation.

摘要

Sirtuin 1(SIRT1)在广泛的生物学反应中起着非常重要的作用,例如代谢、炎症和细胞凋亡。创伤性脑损伤(TBI)后,大脑中 SIRT1 的水平发生了变化。此外,SIRT1 在某些神经元死亡模型中表现出神经保护作用;然而,其在 TBI 模型中的作用和工作机制尚不清楚。本研究旨在解决这一问题。引入 SIRT1 特异性抑制剂(sirtinol)和激活剂(A3)来探索 SIRT1 在细胞凋亡中的作用。研究结果表明,SIRT1 通过抑制 NF-κB、IL-6 和 TNF-α 的去乙酰化和凋亡途径来依次发挥作用,从而在 TBI 后神经元凋亡中发挥重要作用,可能通过减轻神经炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68c2/8093975/24e3f18980f0/JCMM-25-4478-g004.jpg

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