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Modulation of calcium by the carcinogenic process in the liver induced by a choline-deficient diet.

Abstract
A diet devoid of choline and low in methionine (CD), without any added carcinogen, has been shown to induce 100% preneoplastic nodules and more than 50% cancer in the rat liver. Attempts to understand the mechanism by which a CD diet induces liver cell cancer revealed that like chemical carcinogens, a CD diet also appears to cause alterations in DNA, perhaps mediated by free radicals. Indeed, a CD diet induces nuclear lipid peroxidation prior to the changes in DNA. The CD diet induced DNA alterations coupled with continuing liver cell proliferation may account for the induction of initiated hepatocytes by the CD diet. To gain insight into the nature of free radicals generated by the CD diet, experiments were designed to determine whether agents that modulate free radical effects influence the CD diet induced changes in the liver. We investigated the effect of Ca2+ in the modulation of CD diet induced alterations in the liver. The results show that extra Ca2+ when added to the CD diet prevented some of the early changes due to choline deficiency, such as nuclear lipid peroxidation and DNA damage, but had little or no effect on the triglyceride accumulation in the liver. Also, the same CD diet with extra Ca2+, when used as a promoter after initiation by diethylnitrosamine, decreased the number and size of early putative preneoplastic foci and nodules.
AuthorsA K Ghoshal, E Laconi, F Willemsen, A Ghoshal, T H Rushmore, E Farber
JournalCanadian journal of physiology and pharmacology (Can J Physiol Pharmacol) Vol. 65 Issue 3 Pg. 478-82 (Mar 1987) ISSN: 0008-4212 [Print] Canada
PMID2884028 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • DNA
  • gamma-Glutamyltransferase
  • Calcium
Topics
  • Animals
  • Calcium (pharmacology, therapeutic use)
  • Choline Deficiency (complications)
  • DNA (metabolism)
  • Liver (drug effects, metabolism, pathology)
  • Liver Neoplasms (etiology, pathology, prevention & control)
  • Male
  • Rats
  • Rats, Inbred F344
  • gamma-Glutamyltransferase (metabolism)

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