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短期高脂肪和高碳水化合物饮食通过诱导不同平衡的肝促凝和促炎状态增加肝脏损伤易感性。

Short-term high-fat and high-carbohydrate diets increase susceptibility to liver injury by inducing hepatic procoagulant and proinflammatory conditions with different balances.

机构信息

Department of Anatomy, Aichi Medical University, Nagakute-city, Aichi, Japan.

Department of Anatomy, Aichi Medical University, Nagakute-city, Aichi, Japan.

出版信息

Nutrition. 2022 Sep;101:111710. doi: 10.1016/j.nut.2022.111710. Epub 2022 May 6.

Abstract

OBJECTIVES

High-fat diet (HFD) and high-carbohydrate diet (HCD) are strongly linked to nonalcoholic fatty liver disease, a hepatic manifestation of metabolic syndrome. The mechanism of pathologic progression from nonalcoholic fatty liver disease to nonalcoholic steatohepatitis, which is a more severe form associated with inflammation and fibrosis, remains poorly understood. Thus, the aim of this study was to investigate and compare the inflammatory and coagulative state of the liver in short-term HFD- or HCD-fed mice with acute liver injury induced by concanavalin A (Con A).

METHODS

Histopathologic evaluation, real-time polymerase chain reaction, and immunohistochemical evaluation were performed on the liver of mice fed HFDs and HCDs for 4 d before and after Con A administration.

RESULTS

The liver of the HFD-fed mice had larger fibrinogen/fibrin depositions than those fed the HCD. HCD induced the expression of the proinflammatory cytokine tumor necrosis factor-α in the liver. Moreover, the expression of proinflammatory cytokines and chemokines was further enhanced after Con A stimulation in HCD (e.g., interleukin-1α, interleukin-6 at 1 h), with a strong tendency for inflammatory cell infiltration also found (24 h).

CONCLUSIONS

Short-term HCD and HFD increased susceptibility to liver injury. HCD tended to induce more intense inflammation, whereas HFD tended to induce more intense hypercoagulation, suggesting that HCD and HFD may have different mechanisms of pathologic progression to nonalcoholic steatohepatitis.

摘要

目的

高脂肪饮食(HFD)和高碳水化合物饮食(HCD)与非酒精性脂肪性肝病密切相关,后者是非酒精性代谢综合征的肝脏表现。从非酒精性脂肪性肝病向更严重的伴有炎症和纤维化的非酒精性脂肪性肝炎进展的病理机制仍知之甚少。因此,本研究旨在研究和比较短期 HFD 或 HCD 喂养的小鼠在给予刀豆蛋白 A(Con A)后急性肝损伤时肝脏的炎症和凝血状态。

方法

在给予 Con A 前后,对 HFD 和 HCD 喂养 4 天的小鼠的肝脏进行组织病理学评估、实时聚合酶链反应和免疫组织化学评估。

结果

HFD 喂养的小鼠的肝脏比 HCD 喂养的小鼠有更大的纤维蛋白原/纤维蛋白沉积。HCD 诱导了肝脏中促炎细胞因子肿瘤坏死因子-α的表达。此外,Con A 刺激后,HCD 中促炎细胞因子和趋化因子的表达进一步增强(例如,1 小时时白细胞介素-1α、白细胞介素-6),也发现炎症细胞浸润的强烈趋势(24 小时)。

结论

短期 HCD 和 HFD 增加了肝脏损伤的易感性。HCD 倾向于诱导更强烈的炎症,而 HFD 倾向于诱导更强烈的高凝状态,这表明 HCD 和 HFD 可能具有非酒精性脂肪性肝炎进展的不同机制。

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