- 期刊International journal of molecular sciences(Int J Mol Sci)
- 发表时间2026-09-28
- 作者Charoenchon N, Korprasertthaworn P, Thammavoharnkul J, Kiatsurayanon N, Prathomthong P, Chimmanee D, Sitthipunya A
- 卷期页码V27(19)
- DOI10.3390/ijms27198684
- PMID42883929
摘要机译
Zingiber purpureum Roscoe(Phlai)在东南亚以其抗炎、抗氧化和抗菌活性而闻名,但其安全性和对体内肠道健康的影响尚不清楚。
本研究调查了乙醇溶性Phlai提取物(ESPE)在斑马鱼(Danio rerio)中的生物学效应,重点关注苯基丁烷类化合物和葫芦素类化合物中的化学标记标准化、发育毒性、肠道微生物群调查和组织病理学。斑马鱼胚胎暴露于ESPE以评估毒性,而成年雌性接受含有20 mg ESPE/g饮食(2%w/w)的ESPE丰富饮食14天。
治疗后分析包括肠道和多器官组织学,以及用于微生物组分析的16S rRNA测序。高效液相色谱分析证实,ESPE含有9.91%(w/w)的(E)-1-(3,4-二甲氧基苯基)丁二烯(DMPBD)和0.49%(w/w)姜黄素。胚胎的96小时LC50为45.54μg/mL。在成人中,ESPE改善了肠道健康,如更大的粘膜厚度、增加的杯状细胞和增强的肠细胞组织所示。
微生物组分析显示,组间整体肠道微生物α多样性和β多样性没有显著差异。然而,探索性差异丰度分析确定了ESPE治疗组中特定属的相对丰度差异,包括克雷诺杆菌、细胞弧菌、假单胞菌和Starkeya。肌肉组织表现出健康的肌原纤维再生,没有纤维化。
ESPE耐受性良好,肠功能增强,无全身毒性。这些发现支持ESPE作为生物活性提取物在转化药理学应用中进一步研究肠道健康和安全性的潜力。
展开英文摘要原文
Zingiber purpureum Roscoe (Phlai) is renowned in Southeast Asia for its anti-inflammatory, antioxidant, and antibacterial activities, yet its safety and effects on gut health in vivo are not well characterized. This study investigated the biological effects of ethanolic-soluble Phlai extract (ESPE) in zebrafish (Danio rerio), focusing on chemical marker standardization in phenylbutanoids and cucurminoids, developmental toxicity, gut microbiota investigation, and tissue histopathology. Zebrafish embryos were exposed to ESPE to assess toxicity while adult females received an ESPE-enriched diet containing 20 mg ESPE/g diet (2% w/w) for 14 days. Post-treatment analyses included intestinal and multi-organ histology, and 16S rRNA sequencing for microbiome profiling. HPLC analysis confirmed that ESPE contained 9.91% (w/w) of (E)-1-(3,4-dimethoxyphenyl)butadiene (DMPBD) and 0.49% (w/w) curcumin. The 96-h LC50 for embryos was 45.54 µg/mL. In adults, ESPE improved gut health, as shown by greater mucosal thickness, increased goblet cells, and enhanced enterocyte organization. Microbiome analysis showed that overall gut microbial alpha diversity and beta diversity did not differ significantly between groups. However, exploratory differential abundance analysis identified differences in the relative abundance of specific genera in the ESPE-treated group, including Crenobacter, Cellvibrio, Pseudaeromonas, and Starkeya. Muscle tissue demonstrated healthy myofibril regeneration without fibrosis. ESPE was well tolerated, enhanced intestinal function, and without systemic toxicity. These findings support the potential of ESPE as a bioactive extract for further investigation of intestinal health and safety in translational pharmacology applications.
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