阿尔哈吉-蜂蜜对肝脏代谢和肠道微生物群的调节减轻了热应激引起的肝损伤。

Jing Xu, Yundie Liu, Xuanhong Cao, Xinrui Guo, Jie Wang, Yang Liu, Hongda Zhou, Baohua Ma, Sha Peng
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引用次数: 0

摘要

阿尔哈吉蜂蜜(Alhagi-honey,AH)是一种历史悠久的传统民族药物,对腹泻和头痛有很好的疗效。我们的目的是探讨阿尔哈吉蜂蜜对热应激(HS)引起的肝损伤的预防作用及其内在机制。通过恒温箱建立热应激模型,在39 ℃下处理小鼠10小时,持续7天。组织学观察采用血红素-伊红(H&E)染色和过期酸-希夫(PAS)染色,透射电子显微镜(TEM)检查肝细胞的超微结构。16S rRNA测序和非靶向代谢组测序分别分析了肠道微生物群(GM)组成和肝脏代谢物。AH 预处理减轻了热应激对小鼠肝脏的损伤。主要表现为 AH 可缓解血清天门冬氨酸转氨酶(AST)和天门冬氨酸转氨酶(ALT)。研究发现,AH 可改善肝细胞损伤的症状。此外,AH 还改变了 f_Rikenellaceae、g_Incertae_Sedis 和 s_Staphylococcus_Orisratti、g_Lachnoclostridium、g_GCA-900066575 和 s_Alistipes_inops 的相对丰度,这些细菌属与 6 种代谢物(2-(3,4-二羟基苯基)乙酰胺、3-羟基-3-甲基戊二酸、PC(17:0/17:1)、Y-L-谷氨酸、L-异亮氨酸、5-甲基尿苷和 8,8-二甲基-2-苯基-4H,8H-吡喃 [2,3-h]色烯-4-酮)。皮尔逊分析还显示,这些微生物与肝损伤的两个风险指标(谷草转氨酶和谷丙转氨酶)之间存在很强的相关性。AH 可通过调节肝脏代谢和维持正常的 GM 来减轻 HS 引起的肝损伤。研究表明,AH 具有作为预防药物的潜力,可预防 HS 引起的肝损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of liver metabolism and gut microbiota by Alhagi-honey alleviated heat stress-induced liver damage.

Alhagi-honey (AH) is a well-established traditional ethnic medicine with advantageous effects against diarrhea and headaches. We aimed to explore the preventive effect of AH on liver damage induced by heat stress (HS) and its underlying mechanism. HS models were established by thermostat, and mice were treated at 39 ℃ for 10 h, lasting for 7 days. Hematoxylin-eosin (H&E) staining and Periodic Acid-Schiff (PAS) staining were used for histological observation, and transmission electron microscopy (TEM) was used for ultrastructure examination of hepatocytes. Gut microbiota (GM) composition and liver metabolites were respectively analyzed by 16S rRNA sequencing and non-targeted metabolome sequencing. AH pretreatment alleviated liver damage caused by heat stress in mice. The main manifestation was that AH alleviated serum aspartate transferase (AST) and aspartate transaminase (ALT). It was found that AH improved symptoms of hepatocyte damage. In addition, the relative abundance of f_Rikenellaceae, g_Incertae_Sedis and s_Staphylococcus_Orisratti, g_Lachnoclostridium, g_GCA-900066575, and s_Alistipes_inops were modified by AH and these bacterial genera showed association with 6 metabolites (2- (3,4-dihydroxyphenyl) acetamide, 3-hydroxy-3-methylpentanedioic acid, PC (17:0/17:1), Y-L-Glutamy-L-glutamic acid, L-Isoleucine, 5-Methyluridine, 8,8-dimethyl-2-phenyl-4H,8H-pyrano [2, 3-h] chromen-4-one). The Pearson analysis also showed a strong correlation between these microbes and 2 risk indicators (AST and ALT) of liver damage. AH alleviated HS-induced liver damage by regulating liver metabolism and maintaining normal GM. It demonstrated that AH held potential as a prophylactic drug for the prevention of HS-induced liver damage.

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