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小檗胺通过清除脂质活性氧和抑制p65核转位减轻后肢缺血再灌注损伤。

Berbamine attenuates hind limb ischemia-reperfusion injury by eliminating lipid ROS and inhibiting p65 nuclear translocation.

作者信息

Zheng Lei, Zhao Biao, Ji Run, Zhang Zhenxi, Liu Yutong, Zhao Xiaoqi, Cai Jing, Qiao Tong

机构信息

Department of Vascular Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Department of Vascular Surgery and Intervention, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China.

出版信息

Front Pharmacol. 2025 Mar 11;16:1509860. doi: 10.3389/fphar.2025.1509860. eCollection 2025.

DOI:10.3389/fphar.2025.1509860
PMID:40135236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11933021/
Abstract

This research aims to explore whether Berbamine (BBM) can mitigate tissue damage in mice resulting from hind limb muscle ischemia-reperfusion by scavenging lipid ROS and inhibiting p65 nuclear translocation. The hind limb ischemia-reperfusion (IR) injury model in mice was employed. Forty-eight mice (n = 12 per group) were randomly allocated into four groups: Sham group, IR group, IR + BBM (20 mg/kg) group, and IR + BBM (50 mg/kg) group. We observed that BBM pretreatment shielded against muscle damage and diminished levels of cell apoptosis compared to the control group. The mechanism likely involves reducing the movement of p65 into the nucleus and lessening the build-up of lipid ROS in muscle tissue. This action helps to decrease the release of substances that cause inflammation, ultimately reducing the inflammation in tissues that occurs as a result of hind limb IR. Our findings suggest that BBM has a protective impact on hindlimb ischemia-reperfusion injury, potentially due to its capacity to eliminate tissue lipid ROS and prevent p65 nuclear translocation.

摘要

本研究旨在探讨小檗胺(BBM)是否能通过清除脂质活性氧(ROS)和抑制p65核转位来减轻小鼠后肢肌肉缺血再灌注所致的组织损伤。采用小鼠后肢缺血再灌注(IR)损伤模型。48只小鼠(每组n = 12只)随机分为四组:假手术组、IR组、IR + BBM(20 mg/kg)组和IR + BBM(50 mg/kg)组。我们观察到,与对照组相比,BBM预处理可减轻肌肉损伤并降低细胞凋亡水平。其机制可能涉及减少p65进入细胞核的移动以及减少肌肉组织中脂质ROS的积累。这一作用有助于减少引起炎症的物质的释放,最终减轻后肢IR所致的组织炎症。我们的研究结果表明,BBM对后肢缺血再灌注损伤具有保护作用,这可能归因于其清除组织脂质ROS和防止p65核转位的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/fcc02a0ad31c/fphar-16-1509860-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/05e7aa50a6de/fphar-16-1509860-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/5f81966a5e29/fphar-16-1509860-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/f0554436e9a4/fphar-16-1509860-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/5f790bdf11af/fphar-16-1509860-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/97a4f9527a3c/fphar-16-1509860-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/fcc02a0ad31c/fphar-16-1509860-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/05e7aa50a6de/fphar-16-1509860-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/5f81966a5e29/fphar-16-1509860-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/f0554436e9a4/fphar-16-1509860-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/5f790bdf11af/fphar-16-1509860-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/97a4f9527a3c/fphar-16-1509860-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f08/11933021/fcc02a0ad31c/fphar-16-1509860-g006.jpg

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本文引用的文献

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2
Berbamine Inhibits the Biological Activities of Prostate Cancer Cells by Modulating the ROS/NF-κB Axis.小檗胺通过调节 ROS/NF-κB 轴抑制前列腺癌细胞的生物学活性。
Anticancer Agents Med Chem. 2023;23(14):1626-1633. doi: 10.2174/1871520623666230503094540.
3
Mechanisms of ferroptosis regulating oxidative stress and energy metabolism in myocardial ischemia-reperfusion injury and a novel perspective of natural plant active ingredients for its treatment.
铁死亡调控心肌缺血再灌注损伤氧化应激和能量代谢的机制及天然植物活性成分治疗的新视角。
Biomed Pharmacother. 2023 Sep;165:114706. doi: 10.1016/j.biopha.2023.114706. Epub 2023 Jul 1.
4
Ferroptotic mechanisms and therapeutic targeting of iron metabolism and lipid peroxidation in the kidney.肾脏中铁代谢和脂质过氧化的铁死亡机制及治疗靶点
Nat Rev Nephrol. 2023 May;19(5):315-336. doi: 10.1038/s41581-023-00689-x. Epub 2023 Mar 15.
5
Identification of a group of bisbenzylisoquinoline (BBIQ) compounds as ferroptosis inhibitors.鉴定出一组双苄基异喹啉(BBIQ)类化合物为铁死亡抑制剂。
Cell Death Dis. 2022 Nov 26;13(11):1000. doi: 10.1038/s41419-022-05447-8.
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Berbamine inhibits RANKL- and M-CSF-mediated osteoclastogenesis and alleviates ovariectomy-induced bone loss.小檗胺抑制RANKL和M-CSF介导的破骨细胞生成,并减轻去卵巢诱导的骨质流失。
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