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Effects of aluminium on the hepatic inositol polyphosphate phosphatase.

Abstract
There is speculation that some of the toxic effects of Al3+ may originate from it perturbing inositol phosphate/Ca2+ signalling. For example, in permeabilized L1210 mouse lymphoma cells, 10-50 microM Al3+ activated Ins(1,3,4,5)P4-dependent Ca2+ mobilization and Ins(1,3,4,5)P4 3-phosphatase activity [Loomis-Husselbee, Cullen, Irvine and Dawson (1991) Biochem. J. 277, 883-885]. Ins(1,3,4,5)P4 3-phosphatase activity is performed by a multiple inositol polyphosphate phosphatase (MIPP) that also attacks Ins(1,3,4,5,6)P5 and InsP6 [Craxton, Ali and Shears (1995) Biochem. J. 305, 491-498]: 5-50 microM Al3+ increased MIPP activity towards both Ins(1,3,4,5)P4 (by 30%) and Ins(1,3,4,5,6)P5 (by up to 500%), without affecting metabolism of InsP6. Higher concentrations of Al3+ inhibited metabolism of all three substrates, and in the case of InsP6, Al3+ altered the pattern of accumulating products. When 1-50 microM Al3+ was present, InsP6 became a less effective inhibitor of Ins(1,3,4,5)P4 3-phosphatase activity; this effect did not depend on the presence of cellular membranes, contrary to a previous proposal. The latter phenomenon largely explains how, in a cell-free system where Ins(1,3,4,5)P4 3-phosphatase is inhibited by endogenous InsP6, the addition of Al3+ can apparently increase the enzyme activity. However, there was no effect of either 10 or 25 microM Al3+ (in either the presence or absence of apotransferrin) on inositol phosphate profiles in either Jurkat E6-1 lymphoma cells or AR4-2J pancreatoma cells.
AuthorsN Ali, A Craxton, M Sumner, S B Shears
JournalThe Biochemical journal (Biochem J) Vol. 305 ( Pt 2) Pg. 557-61 (Jan 15 1995) ISSN: 0264-6021 [Print] England
PMID7832774 (Publication Type: Journal Article)
Chemical References
  • Inositol Phosphates
  • Phytic Acid
  • Aluminum
  • Phosphoric Monoester Hydrolases
  • multiple inositol-polyphosphate phosphatase
  • phosphatidylinositol-3-phosphatase
Topics
  • Aluminum (pharmacology)
  • Dose-Response Relationship, Drug
  • Humans
  • Inositol Phosphates (metabolism)
  • Microsomes, Liver (enzymology)
  • Phosphoric Monoester Hydrolases (drug effects)
  • Phytic Acid (metabolism)
  • Tumor Cells, Cultured

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