MISC

2012年2月

Conophylline Suppresses Pancreatic Stellate Cells and Improves Islet Fibrosis in Goto-Kakizaki Rats

ENDOCRINOLOGY
  • Rie Saito
  • ,
  • Satoko Yamada
  • ,
  • Yoritsuna Yamamoto
  • ,
  • Tsutomu Kodera
  • ,
  • Akemi Hara
  • ,
  • Yuji Tanaka
  • ,
  • Fumihiko Kimura
  • ,
  • Izumi Takei
  • ,
  • Kazuo Umezawa
  • ,
  • Itaru Kojima

153
2
開始ページ
621
終了ページ
630
記述言語
英語
掲載種別
DOI
10.1210/en.2011-1767
出版者・発行元
ENDOCRINE SOC

Activin A is a differentiation factor for beta-cells and is effective to promote beta-cell neogenesis. Activin A is also an autocrine activator of pancreatic stellate cells, which play a critical role in fibrogenesis of the pancreas. Conophylline (CnP) is a natural compound, which reproduces the effect of activin on beta-cell differentiation and promotes beta-cell neogenesis when administered in vivo. However, its effect on stellate cells is not known. We therefore investigated the effect of CnP on stellate cells both in vitro and in vivo. Unlike activin A, CnP inhibited activation of cultured stellate cells and reduced the production of collagen. We then analyzed the involvement of stellate cells in islet fibrosis in Goto-Kakizaki (GK) rats, a model of type 2 diabetes mellitus. In pancreatic sections obtained from 6-wk-old GK rats, CD68-positive macrophages and glial fibrillary acidic protein-and alpha-smooth muscle actin-positive stellate cells infiltrated into islets. Later, the number of macrophages was increased, and the alpha-smooth muscle actin staining of stellate cells became stronger, indicating the involvement of stellate cells in islet fibrosis in GK rats. When CnP was administered orally for 4 wk, starting from 6 wk of age, invasion of stellate cells and macrophages was markedly reduced and islet fibrosis was significantly improved. The insulin content was twice as high in CnP-treated rats. These results indicate that CnP exerts antifibrotic actions both in vitro and in vivo and improves islet fibrosis in Goto-Kakizaki rats. (Endocrinology 153: 621-630, 2012)

リンク情報
DOI
https://doi.org/10.1210/en.2011-1767
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000299928200012&DestApp=WOS_CPL
ID情報
  • DOI : 10.1210/en.2011-1767
  • ISSN : 0013-7227
  • Web of Science ID : WOS:000299928200012

エクスポート
BibTeX RIS