Chronic gastrointestinal (GI) disorders are becoming increasingly common throughout the world, but many of them still lack effective treatment. Researchers have now turned to natural compounds, such as those present in traditional medicines, to search for potential drug candidates for difficult-to-treat diseases. The latest issue of the Journal of Pharmaceutical Analysis (JPA) features three articles that report promising findings and could pave the way to treatments for complex diseases affecting the liver and intestine.
The first study focuses on 1,8-cineole, a compound found in volatile oil extracts of the Amomum compactum plant, for treating ulcerative colitis (UC). Motivated by its established use for the treatment of pneumonia and preliminary data on its beneficial effects on the gut, a group of researchers investigated the anti-inflammatory mechanisms of this compound in the context of UC. To this end, they employed dextran sulfate sodium to induce colitis in C57BL/6 mice and conducted several assays on cell cultures to determine 1,8-cineole’s targets and its effects. The article was available online in July 2023 and published in Volume 13, Issue 9 of JPA in September 2023. Their findings revealed that this molecule inhibits the binding between heat shock protein 90 (HSP90) and nucleotide-binding and oligomerization domain-, leucine rich repeat-, and pyrin domain-containing 3 (NLRP3), thereby inhibiting the activation of the NLPR3 inflammasome and the M1 polarization of macrophages. This prevents the activation of inflammatory pathways and promotes the recovery of the intestinal wall. “Our findings provide convincing evidence that 1,8-cineole is a promising candidate in the search for a novel therapeutic strategy for UC treatment,” comments corresponding author Dr. Xiaoyin Chen.
In the second study, scientists turned to ginsenoside Rk2, a bioactive component found in steamed ginseng (Panax notoginseng), and investigated its potential as a treatment for alcoholic lived disease (ALD). They used an ethanol feeding regime to induce ALD-like liver injury in mice and then showed that Rk2 could alleviate the observed deleterious effects. Simply put, as an NLPR3 inhibitor, Rk2 could ameliorate liver inflammation. Moreover, Rk2 also restored intestinal barrier function by enhancing NLPR6 signaling in the intestine, demonstrating the multifaceted nature of its therapeutic potential. “Our findings indicate that Rk2 is a promising agent for the prevention and treatment of ALD and other NLPR3-driven diseases,” concludes corresponding author Dr. Jian-Bo Wan.
Finally, in the third study, researchers explored the relationship between gut microbiota and specnuezhenide (SNZ), an active component of the traditional Chinese medicine Fructus Ligustri Lucidi. Their findings revealed that SNZ is metabolized by the enzyme carboxylesterase produced by intestinal bacteria, yielding the metabolites salidroside and tyrosol. In mice, orally administered SNZ could modify the makeup of the gut microbiota and fungal groups, and also had the potential to inhibit colorectal tumor growth. Taken together, these results suggest the importance of the metabolism of gut microbiota. “Intestinal bacterial metabolic enzymes are an important supplement to human liver and kidney metabolism. Thus, in clinical drug use, the characteristics of the gut microbiota in individuals must be taken into account for personalized treatment,” remarks corresponding author Dr. Yan Wang.
These studies will hopefully pave the way to naturally effective treatments for challenging GI disorders.
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Reference
DOI: https://doi.org/10.1016/j.jpha.2023.07.001
Authors: Shengsuo Ma1,2, Bing Yang1,2, Yang Du1,2, Yiwen Lv1,2, Jiarong Liu1,2, Yucong Shi1, Ting Huang1, Huachong Xu1,2, Li Deng1,2, and Xiaoyin Chen1
Affiliations
1School of Traditional Chinese Medicine, Jinan University, Guangzhou, China
2Guangzhou Key Laboratory of Formula-Pattern of Traditional Chinese Medicine, Jinan University, Guangzhou, China
Journal
Journal of Pharmaceutical Analysis
Method of Research
Experimental study
Subject of Research
Animals
Article Title
1,8-cineole ameliorates colon injury by downregulating macrophage M1 polarization via inhibiting the HSP90-NLRP3-SGT1 complex
Article Publication Date
1-Sep-2023
COI Statement
The authors declare that there are no conflicts of interest.