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枸杞多糖通过维持线粒体分裂和融合平衡来降低高血糖加重的缺血性脑损伤。

Lycium Barbarum Polysaccharides Decrease Hyperglycemia-Aggravated Ischemic Brain Injury through Maintaining Mitochondrial Fission and Fusion Balance.

机构信息

School of Basic Medical Science, Ningxia Key Laboratory of Cerebrocranial Diseases-Incubation Base of National Key Laboratory, Ningxia Medical University, Yinchuan 750004, China.

出版信息

Int J Biol Sci. 2017 Jul 7;13(7):901-910. doi: 10.7150/ijbs.18404. eCollection 2017.

DOI:10.7150/ijbs.18404
PMID:28808422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5555107/
Abstract

Although it has been reported that polysaccharides found in possess neuroprotective effects, little is known of their ability to ameliorate hyperglycemia-aggravated ischemia/reperfusion brain injury. In this study, normoglycemic (NG) and hyperglycemic (HG) rats were compared after 30 minutes of middle cerebral artery occlusion (MCAO), followed by 24 or 27 hours of reperfusion, with HG rats pretreated with polysaccharides (LBP) or insulin. In each group, the neurological deficit, infarct volume, pathohistology, and expression of proteins, Opa1 and Drp1, were assessed to determine the efficacy of LBP in alleviating hyperglycemia-aggravated ischemia/reperfusion brain injury. Our results show that, compared to the NG group, the HG group had increases in neurological deficits, infarct volume, and evidence of neuronal pyknosis at 24- and/or 72-h of reperfusion (<0.05) and that pre-treatment with LBP decreased these effects (<0.05). In addition, immunohistochemistry revealed an increase of Drp1 and a decrease of Opa1 positive neurons in the HG group after 24 and 72 hours of reperfusion when compared to the NG group. LBP treatment prevented the HG-induced alterations in Drp-1 and Opa1 expression. Western blots further confirmed these findings showing that HG caused an increase in phospho-Drp1 and a decrease in Opa1 which were subsequently reversed by LBP addition. These results suggest that hyperglycemia-aggravated ischemic brain damage is associated with an alteration of mitochondrial dynamics and that pre-treatment with LBP ameliorates the hyperglycemia-enhanced ischemic brain damage through maintaining mitochondrial dynamic balance.

摘要

尽管已有报道称[X]中存在的多糖具有神经保护作用,但对于其改善高血糖加重的缺血/再灌注脑损伤的能力知之甚少。在这项研究中,对正常血糖(NG)和高血糖(HG)大鼠进行了比较,这些大鼠在大脑中动脉闭塞(MCAO) 30 分钟后,再灌注 24 或 27 小时,HG 大鼠用[X]多糖(LBP)或胰岛素预处理。在每组中,评估神经功能缺损、梗死体积、病理组织学以及 Opa1 和 Drp1 蛋白的表达,以确定 LBP 在缓解高血糖加重的缺血/再灌注脑损伤中的功效。我们的结果表明,与 NG 组相比,HG 组在再灌注 24-和/或 72 小时时神经功能缺损、梗死体积和神经元皱缩的证据增加(<0.05),而 LBP 预处理可降低这些影响(<0.05)。此外,免疫组织化学显示,与 NG 组相比,HG 组在再灌注 24 和 72 小时时 Drp1 增加,Opa1 阳性神经元减少。LBP 治疗可预防 HG 诱导的 Drp1 和 Opa1 表达改变。Western blot 进一步证实了这些发现,表明 HG 导致磷酸化 Drp1 增加,Opa1 减少,随后加入 LBP 逆转。这些结果表明,高血糖加重的缺血性脑损伤与线粒体动力学的改变有关,LBP 预处理通过维持线粒体动力学平衡改善高血糖增强的缺血性脑损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1b580e3cb8ad/ijbsv13p0901g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1b0d839fe989/ijbsv13p0901g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1d389b09092c/ijbsv13p0901g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/06813a73c60b/ijbsv13p0901g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/4ad197c2b08e/ijbsv13p0901g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/e77831753ce4/ijbsv13p0901g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/8a857b95dcb9/ijbsv13p0901g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1b580e3cb8ad/ijbsv13p0901g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1b0d839fe989/ijbsv13p0901g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1d389b09092c/ijbsv13p0901g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/06813a73c60b/ijbsv13p0901g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/4ad197c2b08e/ijbsv13p0901g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/e77831753ce4/ijbsv13p0901g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/8a857b95dcb9/ijbsv13p0901g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b1/5555107/1b580e3cb8ad/ijbsv13p0901g007.jpg

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