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胶原肽修饰的羧甲基纤维素作为抗氧化药物和药物载体,用于治疗视网膜缺血/再灌注损伤。

Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury.

机构信息

Department of Ophthalmology, the First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.

出版信息

J Cell Mol Med. 2018 Oct;22(10):5008-5019. doi: 10.1111/jcmm.13768. Epub 2018 Jul 20.

DOI:10.1111/jcmm.13768
PMID:30030883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6156360/
Abstract

Oxidative stress can cause injury in retinal endothelial cells. Carboxymethyl cellulose modified with collagen peptide (CMCC) is of a distinct antioxidant capacity and potentially a good drug carrier. In this study, the protective effects of CMCC against H O -induced injury of primary retinal endothelial cells were investigated. In vitro, we demonstrated that CMCC significantly promoted viability of H O -treated cells, efficiently restrained cellular reactive oxygen species (ROS) production and cell apoptosis. Then, the CMCC was employed as both drug and anti-inflammatory drug carrier for treatment of retinal ischaemia/reperfusion (I/R) in rats. Animals were treated with CMCC or interleukin-10-loaded CMCC (IL-10@CMCC), respectively. In comparisons, the IL-10@CMCC treatment exhibited superior therapeutic effects, including better restoration of retinal structural thickness and less retinal apoptosis. Also, chemiluminescence demonstrated that transplantation of IL-10@CMCC markedly reduced the retinal oxidative stress level compared with CMCC alone and potently recovered the activities of typical antioxidant enzymes, SOD and CAT. Therefore, it could be concluded that CMCC provides a promising platform to enhance the drug-based therapy for I/R-related retinal injury.

摘要

氧化应激可导致视网膜内皮细胞损伤。经胶原肽修饰的羧甲基纤维素(CMCC)具有明显的抗氧化能力,可能是一种良好的药物载体。本研究探讨了 CMCC 对 H2O2诱导的原代视网膜内皮细胞损伤的保护作用。体外实验表明,CMCC 显著促进了 H2O2处理细胞的活力,有效抑制了细胞活性氧(ROS)的产生和细胞凋亡。随后,将 CMCC 用作药物和抗炎药物载体,用于治疗大鼠视网膜缺血/再灌注(I/R)损伤。动物分别用 CMCC 或白细胞介素 10 负载的 CMCC(IL-10@CMCC)进行处理。结果表明,与 CMCC 单独处理相比,IL-10@CMCC 处理表现出更好的治疗效果,包括更好地恢复视网膜结构厚度和更少的视网膜细胞凋亡。此外,化学发光实验表明,与单独使用 CMCC 相比,移植 IL-10@CMCC 可显著降低视网膜氧化应激水平,并有效恢复典型抗氧化酶 SOD 和 CAT 的活性。因此,CMCC 为增强 I/R 相关视网膜损伤的药物治疗提供了一个有前途的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/0ca219a44008/JCMM-22-5008-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/8ab437df0f00/JCMM-22-5008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/6bfbd0cc9a8d/JCMM-22-5008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/7fe12c6169b1/JCMM-22-5008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/1be97965fa30/JCMM-22-5008-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/dbefacd656cb/JCMM-22-5008-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/87d2f4981948/JCMM-22-5008-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/0ca219a44008/JCMM-22-5008-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/8ab437df0f00/JCMM-22-5008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/6bfbd0cc9a8d/JCMM-22-5008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/7fe12c6169b1/JCMM-22-5008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/1be97965fa30/JCMM-22-5008-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/dbefacd656cb/JCMM-22-5008-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/87d2f4981948/JCMM-22-5008-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c891/6156360/0ca219a44008/JCMM-22-5008-g007.jpg

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