• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

小檗胺通过抑制局部炎症和NF-κB核转位促进慢性肢体威胁性缺血下肢肌肉损伤的修复。

Berbamine Promotes the Repair of Lower Limb Muscle Damage in Chronic Limb-Threatening Ischemia by Inhibiting Local Inflammation and NF-κB Nuclear Translocation.

作者信息

Zheng Lei, Zhao Biao, Zhang Zhenxi, Liu Yutong, Zhang Yingying, Cai Jing, Qiao Tong

机构信息

Department of Vascular Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Zhongshan Road 321, Nanjing 210008, China.

Department of Neurosurgery, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Zhongshan Road 321, Nanjing 210008, China.

出版信息

Pharmaceuticals (Basel). 2024 Nov 25;17(12):1583. doi: 10.3390/ph17121583.

DOI:10.3390/ph17121583
PMID:39770425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11679954/
Abstract

: Chronic Limb-Threatening Ischemia (CLTI) is a chronic limb ischemic disease caused by vascular lesions, characterized by pain, ulcers, and gangrene, which can be life-threatening in severe cases. The objective of this study is to explore whether Berbamine (BBM) can protect against and repair ischemic muscle tissue in the lower limbs; : Using a mouse hindlimb ischemia (HLI) model, 36 C57BL6 mice were divided into sham, HLI, and HLI+BBM treatment groups. : Our findings indicate that BBM can restore motor function and muscle tissue pathology in mice, potentially by inhibiting the nuclear translocation of nuclear factor kappa-B (NF-κB), thereby alleviating tissue inflammation caused by chronic ischemia, reducing muscle cell apoptosis, inhibiting M1 macrophage polarization, and promoting angiogenesis. : Our research suggests that BBM has the potential to protect against ischemic damage in lower limb muscle tissue, providing a new approach to the treatment of CLTI.

摘要

慢性肢体威胁性缺血(CLTI)是一种由血管病变引起的慢性肢体缺血性疾病,其特征为疼痛、溃疡和坏疽,严重时可危及生命。本研究的目的是探讨小檗胺(BBM)是否能保护和修复下肢缺血性肌肉组织;使用小鼠后肢缺血(HLI)模型,将36只C57BL6小鼠分为假手术组、HLI组和HLI+BBM治疗组。我们的研究结果表明,BBM可以恢复小鼠的运动功能和肌肉组织病理学,可能是通过抑制核因子κB(NF-κB)的核转位,从而减轻慢性缺血引起的组织炎症,减少肌肉细胞凋亡,抑制M1巨噬细胞极化,并促进血管生成。我们的研究表明,BBM有潜力保护下肢肌肉组织免受缺血损伤,为CLTI的治疗提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/d22834ce0f17/pharmaceuticals-17-01583-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/32c3dec2f968/pharmaceuticals-17-01583-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/dc92ffe415e3/pharmaceuticals-17-01583-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/cf9d9d226d6d/pharmaceuticals-17-01583-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/2aa13990f29c/pharmaceuticals-17-01583-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/d22834ce0f17/pharmaceuticals-17-01583-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/32c3dec2f968/pharmaceuticals-17-01583-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/dc92ffe415e3/pharmaceuticals-17-01583-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/cf9d9d226d6d/pharmaceuticals-17-01583-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/2aa13990f29c/pharmaceuticals-17-01583-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb36/11679954/d22834ce0f17/pharmaceuticals-17-01583-g005.jpg

相似文献

1
Berbamine Promotes the Repair of Lower Limb Muscle Damage in Chronic Limb-Threatening Ischemia by Inhibiting Local Inflammation and NF-κB Nuclear Translocation.小檗胺通过抑制局部炎症和NF-κB核转位促进慢性肢体威胁性缺血下肢肌肉损伤的修复。
Pharmaceuticals (Basel). 2024 Nov 25;17(12):1583. doi: 10.3390/ph17121583.
2
Berbamine attenuates hind limb ischemia-reperfusion injury by eliminating lipid ROS and inhibiting p65 nuclear translocation.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。
Front Pharmacol. 2025 Mar 11;16:1509860. doi: 10.3389/fphar.2025.1509860. eCollection 2025.
3
PER1 promotes functional recovery of mice with hindlimb ischemia by inducing anti-inflammatory macrophage polarization.PER1 通过诱导抗炎性巨噬细胞极化促进后肢缺血小鼠的功能恢复。
Biochem Biophys Res Commun. 2023 Feb 12;644:62-69. doi: 10.1016/j.bbrc.2023.01.001. Epub 2023 Jan 2.
4
Skeletal muscle regeneration failure in ischemic-damaged limbs is associated with pro-inflammatory macrophages and premature differentiation of satellite cells.缺血性损伤肢体中的骨骼肌再生失败与促炎巨噬细胞和卫星细胞的过早分化有关。
Genome Med. 2023 Nov 10;15(1):95. doi: 10.1186/s13073-023-01250-y.
5
Macrophage scavenger receptor A1 promotes skeletal muscle regeneration after hindlimb ischemia.巨噬细胞清道夫受体A1促进后肢缺血后的骨骼肌再生。
J Biomed Res. 2024 May 29;39(1):23-35. doi: 10.7555/JBR.38.20240117.
6
Allogenic Vertebral Body Adherent Mesenchymal Stromal Cells Promote Muscle Recovery in Diabetic Mouse Model of Limb Ischemia.同种异体椎体黏附间充质基质细胞促进肢体缺血糖尿病小鼠模型的肌肉恢复。
Ann Vasc Surg. 2025 Jan;110(Pt A):522-533. doi: 10.1016/j.avsg.2024.08.004. Epub 2024 Sep 27.
7
A novel model of chronic limb ischemia to therapeutically evaluate the angiogenic effects of drug candidates.一种新型慢性肢体缺血模型,用于治疗评估候选药物的血管生成作用。
Am J Physiol Heart Circ Physiol. 2021 Mar 1;320(3):H1124-H1135. doi: 10.1152/ajpheart.00470.2020. Epub 2021 Jan 22.
8
Buyang Huanwu Decoction Enhances Revascularization via Akt/GSK3/NRF2 Pathway in Diabetic Hindlimb Ischemia.补阳还五汤通过 Akt/GSK3/NRF2 通路促进糖尿病性下肢缺血血管新生。
Oxid Med Cell Longev. 2021 Dec 3;2021:1470829. doi: 10.1155/2021/1470829. eCollection 2021.
9
Unilateral hindlimb ischaemia-induced systemic inflammation is associated with non-ischaemic skeletal muscle inflammation.单侧后肢缺血引起的全身炎症与非缺血性骨骼肌炎症有关。
Exp Physiol. 2024 Sep;109(9):1604-1613. doi: 10.1113/EP091901. Epub 2024 Jun 18.
10
Nuanxinkang protects against ischemia/reperfusion-induced heart failure through regulating IKKβ/IκBα/NF-κB-mediated macrophage polarization.暖心康通过调节 IKKβ/IκBα/NF-κB 介导的巨噬细胞极化来防治缺血/再灌注诱导的心力衰竭。
Phytomedicine. 2022 Jul;101:154093. doi: 10.1016/j.phymed.2022.154093. Epub 2022 Mar 30.

本文引用的文献

1
Reversion of the Inflammatory Markers in Patients With Chronic Limb-Threatening Ischemia.慢性肢体威胁性缺血患者炎症标志物的逆转。
J Am Heart Assoc. 2024 Apr 16;13(8):e031922. doi: 10.1161/JAHA.123.031922. Epub 2024 Apr 12.
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
Transcriptomic and Proteomic of Gastrocnemius Muscle in Peripheral Artery Disease.
腓肠肌在周围动脉疾病中的转录组学和蛋白质组学研究。
Circ Res. 2023 May 26;132(11):1428-1443. doi: 10.1161/CIRCRESAHA.122.322325. Epub 2023 May 8.
4
Berbamine dihydrochloride suppresses the progression of colorectal cancer via RTKs/Akt axis.盐酸小檗胺通过 RTKs/Akt 轴抑制结直肠癌的进展。
J Ethnopharmacol. 2023 Mar 1;303:116025. doi: 10.1016/j.jep.2022.116025. Epub 2022 Dec 7.
5
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。
Front Pharmacol. 2022 Nov 2;13:1032866. doi: 10.3389/fphar.2022.1032866. eCollection 2022.
6
Surgery or Endovascular Therapy for Chronic Limb-Threatening Ischemia.慢性肢体威胁性缺血的手术或血管内治疗。
N Engl J Med. 2022 Dec 22;387(25):2305-2316. doi: 10.1056/NEJMoa2207899. Epub 2022 Nov 7.
7
Berbamine and thymoquinone exert protective effects against immune-mediated liver injury NF-κB dependent pathway.小檗胺和百里醌通过NF-κB依赖途径对免疫介导的肝损伤发挥保护作用。
Front Vet Sci. 2022 Jul 26;9:960981. doi: 10.3389/fvets.2022.960981. eCollection 2022.
8
Inflammation and Loss of Skeletal Muscle Mass in Chronic Limb Threatening Ischemia.慢性肢体威胁性缺血中的炎症与骨骼肌质量丧失
Ann Vasc Surg. 2023 Jan;88:164-173. doi: 10.1016/j.avsg.2022.07.009. Epub 2022 Aug 2.
9
Update on the pathophysiology and medical treatment of peripheral artery disease.外周动脉疾病的病理生理学和医学治疗进展。
Nat Rev Cardiol. 2022 Jul;19(7):456-474. doi: 10.1038/s41569-021-00663-9. Epub 2022 Jan 7.
10
Berbamine reduces body weight via suppression of small GTPase Rab8a activity and activation of paraventricular hypothalamic neurons in obese mice.小檗胺通过抑制肥胖小鼠中小 GTPase Rab8a 的活性和激活室旁下丘脑神经元来降低体重。
Eur J Pharmacol. 2022 Feb 5;916:174679. doi: 10.1016/j.ejphar.2021.174679. Epub 2022 Jan 1.