禁食时间对Sprague-Dawley大鼠非酒精性脂肪性肝炎伴晚期纤维化模型中葡萄糖和脂质代谢的影响。

Pub Date : 2023-01-01 DOI:10.3177/jnsv.69.357
Katsuhisa Omagari, Ayumi Maruta, Natsuki Yayama, Yuki Yoshida, Kyoko Okamoto, Bungo Shirouchi, Shouhei Takeuchi, Kazuhito Suruga, Kazunori Koba, Mayuko Ichimura-Shimizu, Koichi Tsuneyama
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引用次数: 0

摘要

非酒精性脂肪性肝炎(NASH)可发展为肝纤维化,并与心血管和肝脏相关的死亡率有关。为了了解NASH的发病机制,可靠的疾病动物模型是有用的。在动物研究中,动物通常在采集生物样本前禁食过夜,但对禁食的影响知之甚少。在这里,我们研究了与正常SD大鼠相比,在饮食诱导的中度和晚期NASH的Sprague-Dawley(SD)大鼠模型中,过夜禁食约9-17小时对葡萄糖和脂质代谢的影响。我们的研究结果表明,在中度NASH模型大鼠中,禁食时间不影响葡萄糖和脂质代谢、组织病理学表现或与脂质代谢、胆固醇代谢、炎症、纤维化和氧化应激相关的基因的肝脏mRNA表达水平。相反,在正常大鼠中,观察到附睾脂肪垫重量和肝脏脂肪分化相关蛋白和血红素加氧酶-1的mRNA表达水平的显著禁食时间依赖性降低。此外,在晚期NASH模型大鼠中,观察到血清胰岛素水平和α-平滑肌肌动蛋白的mRNA表达水平分别显著降低和增加。我们目前的结果表明,夜间禁食时间的影响在健康状况、中度NASH和晚期NASH状态之间有所不同。需要对人类进行进一步的研究,以确定合适的夜间禁食时间,从而准确评估NASH患者的葡萄糖和脂质代谢。
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The Effects of Overnight Fasting Duration on Glucose and Lipid Metabolism in a Sprague-Dawley Rat Model of Nonalcoholic Steatohepatitis with Advanced Fibrosis.

Nonalcoholic steatohepatitis (NASH) can progress to hepatic fibrosis, and is associated with cardiovascular and liver-related mortality. To understand the pathogenesis of NASH, reliable animal models of the disease are useful. In animal studies, the animals are usually fasted overnight before biospecimens are taken, but little is known about the effects of fasting. Here, we investigated the impact of overnight fasting for approximately 9 to 17 h on glucose and lipid metabolism in a Sprague-Dawley (SD) rat model of diet-induced moderate and advanced NASH in comparison to normal SD rats. Our results revealed that in the moderate NASH model rats, the fasting duration did not affect glucose and lipid metabolism, the histopathological findings, or the hepatic mRNA expression levels of genes related to lipid metabolism, cholesterol metabolism, inflammation, fibrosis, and oxidative stress. In contrast, in the normal rats, significant fasting time-dependent reductions were observed in the epididymal fat pad weight and the hepatic mRNA expression levels of adipose differentiation-related protein and heme oxygenase-1. Moreover, in the advanced NASH model rats, a significant fasting time-dependent reduction and increase were observed in the serum insulin level and mRNA expression level of alpha-smooth muscle actin, respectively. Our present results suggest that the influence of the overnight fasting duration differs among the healthy condition, moderate NASH, and advanced NASH statuses. Further studies are needed in humans to determine the appropriate overnight fasting duration for the accurate evaluation of glucose and lipid metabolism in NASH patients.

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