时间标签:数据日期 2026-10-31 · 生成时间 2026-11-01 05:30(Asia/Shanghai)| 检索窗口 PubMed edat 2026/10/28–2026/10/31 | 情报发生日期 2026-10-31
研究问题
However, oral delivery exposes phytochemicals to harsh gastrointestinal conditions and first-pass hepatic metabolism, which not only reduces the fraction reaching systemic circulation but also generates variable and unpredictable metabolite profiles [].;However, most existing systems rely on injection or wound dressing formats, underscoring the need for a minimally invasive, targeted delivery approach suitable for long-term management of chronic conditions like obesity.;As a result, there is a significant gap in the development of multi-target synergistic therapeutic approaches [].
方法
BCA Protein Assay Kit (P0011), dNTPs (D7373), Hoechst 33,342 (C1027), and sulfobutylether-β-cyclodextrin (SBE-β-CD, Y027108) were purchased from Beyotime Biotechnology.;Phi29 DNA polymerase (0.5 U/µL, D7053L, Beyotime) was then added, and isothermal amplification was performed at 30 °C for 24 h, followed by enzyme inactivation at 70 °C for 20 min.;Superoxide dismutase (SOD)-like activity was quantified using a Total SOD Activity Assay Kit (S0101S, Beyotime). 3T3-L1 and RAW264.7 cells were obtained from the Chinese Academy of Sciences Cell Bank.;Intracellular NAD⁺ and NADH levels were measured using an NAD⁺/NADH Assay Kit (S0175, Beyotime).
核心结论
In the presence of Mn²⁺, the abundant pyrophosphate (PPi⁴⁻) and phosphate (PO₄²⁻) groups generated during RCA reacted with Mn²⁺ to form manganese pyrophosphate/phosphate, which co-biomineralized with nucleic acids into flower-like MNF (Fig. a).;Compared with Mn-free NF, M2NF exhibited increased particle size and a decreased zeta potential, due to the enhanced RCA efficiency resulting from Mn²⁺ acting as a cofactor for Phi29 DNA polymerase (Figure S1).;When the Mn²⁺ concentration was increased to 4 mM, M4NF adopted a petal-like morphology with higher specific surface area. ‖ 结论:Collectively, this work presents a promising strategy for long-term obesity management that aims to promote favorable metabolic changes through a multi-pronged approach, simultaneously addressing impaired beiging, oxidative stress, and chronic inflammation, all within a single, patient-friendly platform.
局限
Given that MNF scavenges ROS and alleviates oxidative stress, we propose that reduced oxidative damage suppresses PARP1 expression, thereby limiting NAD⁺ consumption.;While our study demonstrates the therapeutic efficacy of the MNF-allicin microneedle system, several limitations should be acknowledged.;Future studies will directly measure glucose tolerance, insulin sensitivity and energy expenditure to fully characterize the systemic metabolic improvements conferred by this microneedle system.
对本项目的价值
★☆☆☆☆ 代谢轴既干预敏感性最高,也是老药新用供给最充足的来源。
全文来源
PMC JATS 全文(正文 48,698 字符,已过标题/DOI 逐字归属校验)
原文题录
- 英文标题:Synergistic promotion of white-to-beige adipocyte transition by manganese-nucleic acid framework and allicin for alleviating obesity.
- 期刊与标识:J Nanobiotechnology · PMID 42958258 · DOI 10.1186/s12951-026-04857-6
C 级证据分级:C 级(预印本 / 观点评论,非原始研究)
本文属观点/评论类文献,不是原始研究。其论点依赖于作者对既有证据的梳理与判断,不构成新的实验证据。本站标注 C 级即为此意——阅读时请把它当作「领域内的思考框架」,而非「研究发现」。
关于本文的文献来源:本站依据 IMA 知识库「五刊监控·深度文献卡片」撰写,依据已获取的期刊全文(方法、样本量与结论已回到原文核对);未能获取全文的同批条目另行标注「摘要级」,全程未做任何数值推算补全。