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Endocrinology Vol. 138, No. 5 2033-2042
Copyright © 1997 by The Endocrine Society


Articles

Insulin and Insulin-Like Growth Factor-I Inhibit the L-Type Calcium Channel Current in Rat Pinealocytes1

Constance L. Chik2, Bing Li2, Edward Karpinski and Anthony K. Ho

Department of Medicine (C.L.C.) and Department of Physiology (B.L., E.K., A.K.H.), University of Alberta, Edmonton, Alberta, Canada

Address all correspondence and requests for reprints to: C.L. Chik, Room 733 MSB, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.

Tyrosine phosphorylation has recently been shown to modulate ion channel activity. In the present study, the effect of growth factors on the L-type Ca2+ channel current in rat pinealocytes was investigated using the whole cell version of the patch clamp technique. Both insulin and insulin-like growth factor-I (IGF-I) inhibited the L-type Ca2+ channel current. This inhibition was dependent on concentration, with median effective concentration (EC50) values of 60 nM for insulin and 0.14 nM for IGF-I. Heat-inactivated insulin or IGF-I had no effect on the L-type Ca2+ channel current. The presence of anti-IGF-I receptor antibodies blocked the inhibitory effect of IGF-I on the L-type Ca2+ channel current. Two other growth factors, nerve growth factor and epidermal growth factor, had no effect on this current. The effects of insulin and IGF-I were blocked by lavendustin A, a tyrosine kinase inhibitor. Calphostin C, a protein kinase C inhibitor, attenuated the effect of insulin and IGF-I, whereas wortmannin, a phosphatidylinositol 3-kinase inhibitor, was ineffective. These observations indicate that insulin and IGF-I inhibit the L-type Ca2+ channel current in rat pinealocytes, and that tyrosine phosphorylation is involved in these effects of insulin and IGF-I.




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