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Inhibition of brain protein kinase C subtypes by lead

K Murakami, G Feng and SG Chen

Department of Biochemical Pharmacology, School of Pharmacy, State University of New York, Buffalo.

Protein kinase C (PKC) is an important enzyme in mediating cellular signal transduction and neuronal plasticity. Extremely low concentrations (picomolar range) of Pb++ have been reported to activate partially purified PKC from rat brain (Markovac and Goldstein, 1988). However, the lead activation of PKC at such low concentrations is still a matter of discussion (Simons, 1989). To clarify this point, we have examined the lead effect on highly purified PKC subtypes. Pb++ was found to be a potent inhibitor for all three PKC subtypes (types I, II and III) with IC50 of 2 to 10 microM. Characterization of this lead inhibition of PKC suggests that 1) the inhibition is not due to the competition with Ca++, 2) the site of action of lead is on the catalytic domain of PKC, 3) the inhibition is not dependent on the mode of activation (phosphatidylserine/diacylglycerol vs. cis-unsaturated fatty acid) and 4) the inhibition is totally reversible.

Volume 264, Issue 2, pp. 757-761, 02/01/1993
Copyright © 1993 by American Society for Pharmacology and Experimental Therapeutics







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Copyright © 1993 by the American Society for Pharmacology and Experimental Therapeutics.