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脂肪变性不足以导致大鼠部分肝切除术后再生反应受损。

Steatosis is not sufficient to cause an impaired regenerative response after partial hepatectomy in rats.

作者信息

Picard Christian, Lambotte Luc, Starkel Peter, Sempoux Christine, Saliez Alain, Van den Berge Véronique, Horsmans Yves

机构信息

Gastroenterology Laboratory, Department of Gastroenterology, University of Louvain Medical School, Saint Luc University Hospital, Avenue Hippocrate 10, 1200 Brussels, Belgium.

出版信息

J Hepatol. 2002 May;36(5):645-52. doi: 10.1016/s0168-8278(02)00038-7.

Abstract

BACKGROUND/AIMS: Fatty liver is known to be associated with increased mortality and morbidity after liver resection. The ability of fatty liver to regenerate after two-thirds partial hepatectomy was studied in three different models of steatosis in rats: obese Zucker rats, orotic acid-fed Wistar rats and Wistar rats fed a methionine-low, choline-deficient diet.

METHODS

Liver regeneration was assessed 24 h after partial hepatectomy by bromodeoxyuridine incorporation (immunohistochemistry), proliferating cell nuclear antigen, cyclin E and cyclin-dependent kinase 2 protein expression (Western blot analysis) and cyclin-dependent kinase 2 activity (kinase assays using histone H1 as a substrate).

RESULTS

No significant difference of proliferative response was found between orotic acid or methionine-low, choline-deficient diet-fed and control Wistar rats 24 h after partial hepatectomy. In contrast, hepatocyte proliferation in obese Zucker rats after partial hepatectomy was significantly reduced when compared with their lean controls.

CONCLUSIONS

Steatosis per se does not impair liver regeneration. The reduced liver regeneration observed in obese Zucker rats may not be due to fatty infiltration itself but to other factors such as leptin receptor dysfunction.

摘要

背景/目的:已知脂肪肝与肝切除术后死亡率和发病率的增加相关。在大鼠的三种不同脂肪变性模型中研究了脂肪肝在三分之二部分肝切除术后的再生能力:肥胖 Zucker 大鼠、喂饲乳清酸的 Wistar 大鼠和喂饲低蛋氨酸、胆碱缺乏饮食的 Wistar 大鼠。

方法

在部分肝切除术后 24 小时,通过溴脱氧尿苷掺入(免疫组织化学)、增殖细胞核抗原、细胞周期蛋白 E 和细胞周期蛋白依赖性激酶 2 蛋白表达(蛋白质印迹分析)以及细胞周期蛋白依赖性激酶 2 活性(使用组蛋白 H1 作为底物的激酶测定)评估肝再生。

结果

部分肝切除术后 24 小时,喂饲乳清酸或低蛋氨酸、胆碱缺乏饮食的大鼠与对照 Wistar 大鼠之间未发现增殖反应有显著差异。相比之下,肥胖 Zucker 大鼠部分肝切除术后的肝细胞增殖与瘦对照相比显著降低。

结论

脂肪变性本身并不损害肝再生。肥胖 Zucker 大鼠中观察到的肝再生减少可能不是由于脂肪浸润本身,而是由于其他因素,如瘦素受体功能障碍。

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