Beta-hydroxy-beta-methylbutyrate (HMB) ameliorates DSS-induced colitis by inhibiting ERK/NF-κB activation in macrophages

IF 8.3 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2025-04-01 Epub Date: 2025-02-13 DOI:10.1016/j.phymed.2025.156492
Jiao Liu , Danye Niu , Yu Tang , Ruoheng Zheng , Yinyin Qin , Xiuqin Cheng , Shubo Pan , Jinfei Yuan , Xiaohua Shi , Jiao Yang
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Abstract

Background

β-Hydroxy β-Methylbutyrate (HMB), derived from leucine, is known for its role in anti-oxidation and anti-inflammation. But, the application of HMB in IBD treatment is not fully understood, highlighting the requirement for further research.

Purpose

We aimed to examine the effects of HMB treatment on DSS-induced chronic colitis in mice and explore its underlying mechanisms.

Methods

To simulate colonic inflammation, a murine colitis model was generated by using DSS induction. Critical indicators such as body weight, colon length, disease activity index (DAI), and gross pathology were thoroughly monitored. Immunohistochemistry assay was conducted to assess the expression of Occludin and F4/80. Flow cytometry was employed to evaluate the expression levels of CD80 and CD86. qPCR was performed to measure cytokine expression (IL-6, IL-1β, TNF-α, IL-22, CXCL2, iNOS). RNA sequencing was carried out using bone-marrow derived dendritic macrophage cells (BMDMs).

Results

Our study indicates that HMB treatment substantially mitigated colonic damage in murine models of DSS-induced colitis, highlighting its anti-inflammatory potential. Notably, HMB significantly enhanced the expression of Occludin in these mice. Furthermore, HMB downregulated proinflammatory markers such as IL-6, IL-1β, and TNF-α as well as CXCL2 in the colon tissue. In vitro experiments also revealed that HMB reduced production of proinflammatory cytokines induced by DSS and suppressed the expression levels of CD80 and CD86 in macrophage cells. On a mechanistic level, we demonstrated the anti-inflammatory effects of HMB by reducing the phosphorylation of p-ERK and p-p65, thereby limiting cytokine production in both in vivo and in vitro settings.

Conclusion

These findings indicate that HMB possesses anti-inflammation against intestinal inflammation and may hold promise as a potential therapeutic candidate for IBD treatment. There's growing interest in combining traditional anti-inflammatory agents with supplements like HMB to improve outcomes in complex IBD cases. HMB's role in established muscle preservation and reduction of systemic inflammation as described in this study could make it a valuable adjunct in IBD therapy.

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β -羟基- β -甲基丁酸酯(HMB)通过抑制巨噬细胞ERK/NF-κB活化来改善dss诱导的结肠炎
β-羟基β-甲基丁酸酯(HMB)是由亮氨酸衍生而来,具有抗氧化和抗炎症的作用。但HMB在IBD治疗中的应用尚不完全清楚,需要进一步研究。目的观察HMB对dss诱导的小鼠慢性结肠炎的影响,并探讨其作用机制。方法采用DSS诱导建立小鼠结肠炎模型,模拟结肠炎症反应。全面监测体重、结肠长度、疾病活动指数(DAI)和大体病理等关键指标。免疫组化检测Occludin和F4/80的表达。流式细胞术检测CD80和CD86的表达水平。采用qPCR检测细胞因子(IL-6、IL-1β、TNF-α、IL-22、CXCL2、iNOS)的表达。利用骨髓来源的树突状巨噬细胞(bmdm)进行RNA测序。结果我们的研究表明,HMB治疗显著减轻了dss诱导的小鼠结肠炎模型的结肠损伤,突出了其抗炎潜力。值得注意的是,HMB显著增强了Occludin在这些小鼠中的表达。此外,HMB下调结肠组织中的促炎标志物如IL-6、IL-1β和TNF-α以及CXCL2。体外实验还发现,HMB可减少DSS诱导的促炎细胞因子的产生,抑制巨噬细胞CD80和CD86的表达水平。在机制水平上,我们通过降低p-ERK和p-p65的磷酸化,从而在体内和体外环境中限制细胞因子的产生,证明了HMB的抗炎作用。结论HMB具有抗肠道炎症的作用,有望成为IBD治疗的潜在候选药物。人们对将传统抗炎药与HMB等补充剂结合使用以改善复杂IBD病例的预后越来越感兴趣。正如本研究所描述的,HMB在已建立的肌肉保存和减少全身性炎症中的作用可能使其成为IBD治疗中有价值的辅助手段。
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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