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撤稿文章:卡尔施肽的结构表征及在人血管内皮细胞中的抗炎效力评估

Retracted Article: Structural characterization of Karsch peptides and anti-inflammatory potency evaluation in human vascular endothelial cells.

作者信息

Zheng Man, Yan Xiafeng, Bu Fanli, Zhang Fenglei, Li Zhenhua, Cui Jiali, Liu Jie, Dong Minya

机构信息

Department of Cardiology, Dongying People's Hospital Dongying Shandong 257091 China

People's Hospital of Shule County Kashi Xinjiang 844043 China.

出版信息

RSC Adv. 2019 Jun 20;9(34):19365-19374. doi: 10.1039/c9ra01609k. eCollection 2019 Jun 19.

Abstract

Studies have reported that scorpion toxins have excellent anti-cancer effects; however, the anti-inflammatory activity of scorpion peptides has rarely been studied. Here, a series of Karsch peptides (MMKPs) were isolated and the amino acid sequence was identified. The MMKPs mitigated TNF-α-mediated inflammation in human umbilical vein endothelial cells (HUVECs). The results showed that MMKP-1 (His-Glu-Gly-His) treatment (43.0 μM) significantly attenuated the reactive oxygen species (ROS) generation and mitochondrial membrane potential collapse in HUVECs. Moreover, MMKP-1 down-regulated the intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) expressions and blocked the NF-κB pathway to alleviate the damage caused by TNF-α. Of note, our study provides a good reference for the anti-inflammation research on scorpion oligopeptides.

摘要

研究报告称,蝎毒素具有出色的抗癌作用;然而,蝎肽的抗炎活性鲜有研究。在此,一系列卡尔施肽(MMKPs)被分离出来并鉴定了氨基酸序列。MMKPs减轻了人脐静脉内皮细胞(HUVECs)中肿瘤坏死因子-α(TNF-α)介导的炎症。结果表明,MMKP-1(组氨酸-谷氨酸-甘氨酸-组氨酸)处理(43.0 μM)显著减弱了HUVECs中活性氧(ROS)的产生和线粒体膜电位崩溃。此外,MMKP-1下调了细胞间黏附分子-1(ICAM-1)和血管细胞黏附分子-1(VCAM-1)的表达,并阻断了核因子-κB(NF-κB)途径以减轻TNF-α造成的损伤。值得注意的是,我们的研究为蝎寡肽的抗炎研究提供了良好的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b180/9065169/be0018853675/c9ra01609k-f1.jpg

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