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Shenling Guchang prescription ameliorates intestinal barrier inflammation in gestational diabetes rats <i>via</i> TLR4/NF-κB pathway

TLR4型 妊娠期糖尿病 医学 炎症 后代 免疫印迹 二甲双胍 NF-κB 内科学 H&E染色 内分泌学 药理学 糖尿病 妊娠期 免疫组织化学 生物 怀孕 基因 生物化学 遗传学
作者
Manling Li,Lisha Li,Xingman Liu,Tao Yang,Jingyun Gao,Anqin Wu,Zhaozhao Hua,Lingling Wang
出处
期刊:Drug discoveries and therapeutics [International Research and Cooperation Association for Bio & Socio-Sciences Advancement]
卷期号:18 (6): 343-352
标识
DOI:10.5582/ddt.2024.01066
摘要

Gestational diabetes mellitus (GDM) is linked to a greater risk of various maternal and fetal complications, including the possibility of long-term metabolic issues in offspring. Our initial research suggests that the Traditional Chinese Medicine formula, Shenling Guchang prescription (SLGP), may have an impact on the gut microbiota. However, the specific mechanisms through which it affects intestinal barrier inflammation in GDM are still not fully understood. This study explored SLGP's mechanisms in GDM. Firstly, network pharmacology predicted key bioactive constituents targeting toll-like receptor 4 (TLR4)/nuclear factor-kappa B (NF-κB), guiding experimental design. Subsequently, the pregnant female rats were induced with GDM through intraperitoneal streptozotocin injection and then divided into control, model, metformin, and SLGP treatment groups. Blood samples were collected for ELISA analysis to measure levels of inflammatory markers, intestinal tissues were examined histologically using hematoxylin-eosin (HE) staining, and western blot analysis was conducted to evaluate TLR4 and NF-κB expression. Relative to control rats, model group animals exhibited significant increases in the levels of inflammatory markers (IL-1β, IL-6, TNF-α, TGF-β, CRP), as well as enhanced TLR4 and p-NF-κB p65 expression, along with intestinal histopathological changes. Treatment with SLGP notably reduced inflammatory markers and protein expression in the colonic tissue of GDM rats, leading to a decrease in histopathological damage. Overall, SLGP was found to modulate the TLR4/NF-κB pathway, resulting in enhancements in insulin resistance and a reduction in inflammatory responses in GDM rats, thereby providing protection for the intestines. This study demonstrates the potential therapeutic effectiveness of SLGP in addressing intestinal inflammation linked to GDM.

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