抽象来源: plos One。 2023; 18(9):E0282275。 EPUB 2023 9月21日。PMID: 37733659“> 37733659 Bo,Shuang-Yuan Hu,Ju-Yi Xiang,Zheng-ru Yang,Xiao-Mei Zhang,An-Jing Chen,Jin-Hao Zeng,Xiao MA,Jing Guo xue-exue-er Zhang Zhang Zhang Zhang Zhang Zhang Zhang Zhang Zhang Zhang Zhang Zhang Zhang actract 目的: 方法: 每项研究中偏见的风险是使用Camarades 10项质量清单的,其标准的数量从4/10到7/10,平均为5.44。从成立到2022年7月,我们搜索了八个数据库。我们使用了Cochrane Complocrations 10-项目清单和Revman 5.3软件来评估偏见的风险并分析数据。进行了三维剂量/时间效应分析,以检查pf和dn。进行系统的审查,以评估PF在改善DN动物模型中的有效性。 Meta-analysis data and intergroup comparisons indicated that PF slowed the index of mesangial expansion and tubulointerstitial injury, 24-h urinary protein excretion rate, expression of anti-inflammatory mediators (mRNA of MCP-1, TNF-α, iNOS, and IL-1β), and expression of immune downstream factors (P-IRAK1, TIRF, P-IRF3, MYD88和NF-κBP-P65)。 Furthermore, modeling methods, animal species, treatment duration, thickness of tissue sections during the experiment, and experimental procedures were subjected to subgroup analyses. CONCLUSION: The present study demonstrated that the reno-protective effects of PF were associated with its inhibition on macrophage infiltration, reduction炎症介质和免疫调节作用。总之,PF可以有效地降低DN的进展,并保持诺言作为ProtectivE治疗DN的药物。由于PF的生物利用度较低,因此迫切需要对动物肾脏组织学的进一步研究。因此,我们建议对诊所和动物中PF的剂量和治疗时间框架进行积极探索。此外,建议积极探索改善PF生物利用度以扩展PF在诊所中的生物利用度的方法。