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一种合成肽 AWRK6 可缓解脂多糖诱导的肝损伤。

A Synthetic Peptide AWRK6 Alleviates Lipopolysaccharide-Induced Liver Injury.

机构信息

School of Life Science, Liaoning University, Shenyang 110036, China.

Research Center for Computer Simulating and Information Processing of Bio-macromolecules of Liaoning Province, Liaoning University, Shenyang 110036, China.

出版信息

Int J Mol Sci. 2018 Sep 7;19(9):2661. doi: 10.3390/ijms19092661.

Abstract

During lipopolysaccharide (LPS)-induced sepsis, the liver plays central roles in toxins phagocytosis and clearance to protect the whole body. The liver cells were constantly irritated by LPS which leads to liver injury. While most anti-LPS agents showed little clinical activity against LPS-induced liver injury. Here, the protective effects of the synthetic peptide AWRK6 against LPS-induced liver injury have been investigated in vivo and in vitro. In mice liver homogenate, LPS administration elevated ALT (alanine aminotransferase), iNOS (inducible nitric oxide synthase) and repressed SOD (superoxide dismutase) activities and these changes were remarkably reversed by AWRK6. Histologically, AWRK6 effectively alleviated the histological changes and repressed LPS-induced neutrophils infiltration. By TUNEL assay on liver sections, AWRK6 was proven to inhibit apoptosis induced by LPS in mice livers, which was also verified by the protein levels of cleaved-caspase 9, Bax and Bcl-2. In addition, by in vitro study using HepG2 cells, AWRK6 was found to recover the LPS-reduced cell viability and reduce LPS-induced apoptosis. For mechanisms, AWRK6 was demonstrated to alleviate the LPS-induced phosphorylation of ERK, JNK and p38 MAPK, indicating the involvement of MAPKs in the protection of AWRK6 against liver injury. In summary, we have found the synthetic peptide AWRK6 as a promising novel agent for LPS-induced liver injury, by inhibiting cell apoptosis through MAPK signaling pathways, which might bring new strategies for the treatment of acute and chronic liver injuries.

摘要

在脂多糖 (LPS) 诱导的败血症中,肝脏在吞噬和清除毒素以保护全身方面发挥着核心作用。LPS 不断刺激肝脏细胞,导致肝损伤。而大多数抗 LPS 药物对 LPS 诱导的肝损伤几乎没有临床活性。在这里,研究了合成肽 AWRK6 在体内和体外对 LPS 诱导的肝损伤的保护作用。在小鼠肝匀浆中,LPS 给药升高 ALT(丙氨酸氨基转移酶)、iNOS(诱导型一氧化氮合酶)并抑制 SOD(超氧化物歧化酶)活性,这些变化被 AWRK6 显著逆转。组织学上,AWRK6 有效缓解了组织学变化并抑制了 LPS 诱导的中性粒细胞浸润。通过对肝切片进行 TUNEL 检测,证明 AWRK6 抑制了 LPS 在小鼠肝脏中诱导的细胞凋亡,这也通过裂解型 caspase 9、Bax 和 Bcl-2 的蛋白水平得到验证。此外,通过体外研究使用 HepG2 细胞,发现 AWRK6 恢复了 LPS 降低的细胞活力并减少了 LPS 诱导的细胞凋亡。对于机制,证明 AWRK6 减轻了 LPS 诱导的 ERK、JNK 和 p38 MAPK 的磷酸化,表明 MAPKs 参与了 AWRK6 对肝损伤的保护作用。总之,我们发现合成肽 AWRK6 是一种有前途的新型 LPS 诱导肝损伤药物,通过 MAPK 信号通路抑制细胞凋亡,为急性和慢性肝损伤的治疗带来了新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee89/6165536/e39e33cc5129/ijms-19-02661-g001a.jpg

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4
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6
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7
Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016.
Intensive Care Med. 2017 Mar;43(3):304-377. doi: 10.1007/s00134-017-4683-6. Epub 2017 Jan 18.
8
Antimicrobial Peptides: An Introduction.
Methods Mol Biol. 2017;1548:3-22. doi: 10.1007/978-1-4939-6737-7_1.
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Int J Antimicrob Agents. 2017 Feb;49(2):233-238. doi: 10.1016/j.ijantimicag.2016.07.023. Epub 2016 Sep 16.

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