综述解读

综述:天然多糖调控线粒体稳态的结构决定因素与转化瓶颈

来源:Frontiers in pharmacology · PMID 42953059 · DOI 10.3389/fphar.2026.1948381 · 来源:IMA 知识库《文献层·文献监控卡片》2026-11-01 期 · 全文级(file_id dlMXdlgtPZzo,实际下载核验) · 全文已获取并通过归属校验

时间标签:数据日期 2026-11-01 · 生成时间 2026-11-01 05:30(Asia/Shanghai)| 检索窗口 PubMed edat 2026/10/31–2026/11/01 | 情报发生日期 2026-11-01

研究问题

Unlike previous reviews mainly focusing on the general antioxidant or anti-inflammatory activities, this review emphasizes the links among NP structural features, mitochondrial homeostasis, and disease-context-specific therapeutic…;We also discuss current challenges and future directions for developing NPs as mitochondria-regulating therapeutic candidates. 2

方法

(原文未给出可直接抽取的对应表述)

核心结论

In NAFLD-related models, LBP activated the PGC-1α/NRF1/TFAM pathway to promote mitochondrial biogenesis, accompanied by increased ATP production, reduced oxidative stress, and decreased hepatic lipid accumulation ( ).;These effects were accompanied by ROS accumulation, altered oxygen consumption, reduced UCP2 protein expression, and decreased lactate production ( ).;Likewise, Ganoderma lucidum polysaccharides (GLP) decreased p-Drp1 and Fis1 expression while increasing Mfn1, Mfn2, and OPA1 levels, thereby attenuating pathological mitochondrial fragmentation in mice ( ).;In cardiomyocyte injury associated with metabolic stress, aging, or other stressors, NPs appear to attenuate mitochondria-dependent apoptosis and calcium-related mitochondrial dysfunction.

局限

Fifth, clinical translation requires stronger human evidence. polysaccharide-K and lentinan have been used regionally as adjunctive cancer therapies, while fucoidan has undergone preliminary clinical evaluation ( ; ; ).;Despite advances in targeted therapy and immunotherapy, treatment failure remains common because of tumor heterogeneity, recurrence, and drug resistance ( ).

对本项目的价值

临床前机制证据,需评估物种外推与剂量可行性:线粒体是衰老干预的共同下游效应器,可用于跨器官效应的统一读数。 | 价值分 1.7/5(★★☆☆☆)

全文来源

PubMed PMC JATS 全文(正文 49,547 字符,已过 DOI 逐字 + 题名指纹双重归属校验)

原文题录

  • 英文标题:Natural polysaccharides as modulators of mitochondrial homeostasis: structural determinants, pharmacological mechanisms, and translational challenges.
  • 期刊与标识:Frontiers in pharmacology · PMID 42953059 · DOI 10.3389/fphar.2026.1948381

C 级证据分级:C 级(预印本 / 观点评论,非原始研究)

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