The Effect of Adrenocorticotropin and Nucleotides on Ca2+Uptake in Adrenal Cortical Microsomal Vesicles*

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Abstract
Rat and bovine adrenal cortical microsomal fractions isolated at 27,000 .times. g and 105,000 .times. g accumulated Ca2+ by a nonmitochondrial, ATP-dependent uptake system that was stimulated by ammonium oxalate. ACTH (2 mU[units]/ml) significantly increased Ca2+ uptake in bovine adrenal cortical microsomes and in adrenal microsomes from acutely hypophysectomized rats, but only when the hormone was preincubated with intact tissue and not when it was added after homogenization. ACTH did not stimulate Ca2+ uptake in adrenal microsomes isolated from nonhypophysectomized, ether-stressed rats, in which basal Ca2+ uptake was higher than that observed in microsomes from hypophysectomized animals. The peptides oxytocin, insulin and TSH [thyrotropin] did not stimulate Ca2+ uptake by adrenal cortical microsomes. ACTH preincubated with intact tissue had no effect on Ca2+ uptake in microsomes from liver, kidney, esophagus, or aorta. c[cyclic]AMP, 5''-AMP and several other nucleotides, nucleosides and related compounds stimulated adrenal cortical microsomal Ca2+ uptake by as much as 540% of control. The stimulatory effects of nucleotides, unlike those of ACTH, were apparent even when the agents were added after homogenization. Like ACTH, the nucleotides were unable to stimulate Ca2+ uptake when they were added to isolated membrane vesicles during Ca2+ uptake measurements. The microsomal Ca2+ uptake system may respond to physiological stimulants and regulate Ca2+ availability in the intact cell.