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Pi-class glutathione-S-transferase-positive hepatocytes in aging B6C3F1 mice undergo apoptosis induced by dietary restriction.

Abstract
Liver sections from aging ad libitum-fed and diet-restricted B6C3F1 male mice were evaluated immunohistochemically for pi-class glutathione S-transferase (GST-II). GST-II immunostaining of hepatocytes was diffuse and occurred in periportal regions of hepatic acinus, whereas perivenous areas were weakly stained or were stain-free. Expression of GST-II was significantly diminished in diet-restricted mice in all age groups and was associated with a marked decrease in liver tumor development. As most spontaneous liver tumors were GST-II positive, it can be speculated that they developed from GST-II positive initiated hepatocytes. To determine whether dietary restriction induces apoptosis in GST-II-positive hepatocytes, 24-month-old ad libitum-fed mice were introduced to 40% diet restriction. After 1 week of diet restriction, a decrease in GST-II expression was associated with a threefold increase in the frequency of apoptotic bodies as detected by terminal deoxynucleotidyl transferase-mediated d-UTP nick end labeling of DNA fragments. A two-step immunohistochemical procedure revealed that approximately 70% of apoptotic bodies were GST-II positive. These results suggest that spontaneous, potentially preneoplastic hepatocytes in tumor-prone B6C3F1 mice are eliminated by apoptosis with dietary restriction.
AuthorsL Muskhelishvili, A Turturro, R W Hart, S J James
JournalThe American journal of pathology (Am J Pathol) Vol. 149 Issue 5 Pg. 1585-91 (Nov 1996) ISSN: 0002-9440 [Print] United States
PMID8909248 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Glutathione Transferase
Topics
  • Aging (pathology)
  • Animals
  • Apoptosis
  • Cells, Cultured
  • Female
  • Food Deprivation
  • Glutathione Transferase (analysis, classification)
  • Immunohistochemistry
  • Liver (enzymology, pathology)
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL

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