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锰疗法对小鼠模型血脂异常和斑块逆转的作用

Manganese therapy for dyslipidemia and plaque reversal in murine models.

作者信息

Wang Yawei, Feng Xin, Zhou Wenjing, Huang Runze, Hu Yating, Hui Hui, Tian Jie, Wang Xiao, Chen Xiao-Wei

机构信息

State Key Laboratory of Membrane Biology, Peking University, Beijing 100871, China.

PKU-THU Joint Center for Life Sciences, Peking University, Beijing 100871, China.

出版信息

Life Metab. 2023 Oct 26;2(6):load040. doi: 10.1093/lifemeta/load040. eCollection 2023 Dec.

Abstract

Precise control of circulating lipid levels is vital in both health and disease. We recently uncovered that bulk lipids, transported by lipoproteins, enter the circulation initially via the coat protein complex II (COPII) in a condensation-dependent manner. Divalent manganese, acting as a signaling messenger, selectively controls COPII condensation to regulate lipid homeostasis . Here, we present evidence for a manganese-based therapy in murine models of hypolipidemia and hyperlipidemia, aided by advanced multimodal imaging of atherosclerosis. Dietary titration of manganese supply enables tailored control of circulating lipid levels in whole animals, with no apparent toxicity. Strikingly, elevating the manganese signal through diets could not only effectively treat pathological hyperlipidemia but also further achieve significant reversal of atherosclerotic plaques. Hence, the study provides critical proof-of-principle for a novel therapy for deadly cardiovascular diseases with a potentially broad impact.

摘要

精确控制循环脂质水平在健康和疾病状态下都至关重要。我们最近发现,由脂蛋白转运的大量脂质最初以依赖凝聚的方式通过II型被膜小泡蛋白复合体(COPII)进入循环。二价锰作为一种信号信使,选择性地控制COPII凝聚以调节脂质稳态。在此,我们借助先进的动脉粥样硬化多模态成像技术,展示了在高脂血症和低脂血症小鼠模型中基于锰的治疗证据。通过饮食对锰供应进行滴定,能够对全动物的循环脂质水平进行定制控制,且无明显毒性。引人注目的是,通过饮食提高锰信号不仅能有效治疗病理性高脂血症,还能进一步显著逆转动脉粥样硬化斑块。因此,该研究为一种对致命心血管疾病具有潜在广泛影响的新型疗法提供了关键的原理证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8b/11749556/27617f54542b/load040_fig2.jpg

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