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  • 标题:The Enhancing Effects of S-Allylcysteine on Liver Regeneration Are Associated with Increased Expression of mRNAs Encoding IGF-1 and Its Receptor in Two-Thirds Partially Hepatectomized Rats
  • 本地全文:下载
  • 作者:Kazuki Kurihara ; Hajime Moteki ; Hideshi Natsume
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2020
  • 卷号:43
  • 期号:11
  • 页码:1776-1784
  • DOI:10.1248/bpb.b20-00495
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:Two-thirds partial hepatectomy (PHx) was performed in rats, and the differences in effects between S -allylcysteine (SAC) and other sulfur-containing compounds on regeneration of the remaining liver and restoration of the injury were examined. Three days after two-thirds PHx, rats treated with 300 mg/kg/d, per os ( p.o. ) SAC showed a 1.2-fold increase in liver weight per 100 g body weight compared with saline-treated controls. In contrast, S -methylcysteine (SMC) (300 mg/kg/d, p.o. ) or cysteine (Cys) (300 mg/kg/d, p.o. ) did not have a regeneration-promoting effect. In the comparison with control rats, the regenerating liver of SAC-treated rats showed a significantly higher 5-bromo-2′-deoxyuridine labeling index on day 1. In contrast, serum alanine aminotransferase activity, which increases following PHx, was significantly inhibited by SAC and SMC (but not Cys) on day 1 after two-thirds PHx. In addition, SAC induced increases in insulin-like growth factor (IGF)-1 and its receptor mRNA expressions at 1 h after two-thirds PHx, and it increased phosphorylation of extracellular signal-regulated kinase (ERK)2 and Akt at 3 h after two-thirds PHx without affecting serum growth hormone levels. These results demonstrate that SAC is a mitogenic effector of normal remnant liver and promotes recuperation of liver function after two-thirds PHx. Moreover, SAC-induced proliferative effects are mediated via increased mRNA expressions of IGF-1 and its receptor and subsequent phosphorylation of ERK2 and Akt.
  • 关键词:partial hepatectomy (PHx);liver regeneration;S-allylcysteine (SAC);insulin-like growth factor (IGF)-1;serum alanine aminotransferase (ALT)
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