Abstract

High levels of d-aspartate occur in the brain and endocrine glands, such as pineal, adrenal and pituitary. In the brain, d-aspartate levels are highest in embryonic and early postnatal stages. Notably high levels occur in the early postnatal cortical plate and subventricular zone of the cerebral cortical cultures, implying a role in development. In embryonic neuronal primary culture cells, we detected high levels of endogenous d-aspartate and demonstrated biosynthesis of [ 14C] d-aspartate using [ 14C] l-aspartate as precursor. Synthesis of d-aspartate in cell cultures is inhibited by amino-oxyacetic acid, an inhibitor of pyridoxal phosphate-dependent enzymes. In the rat adrenal medulla, d-aspartate is depleted by treatment of the animals with intraperitoneal nicotine injections. In adrenal slices, d-aspartate is released by depolarization with KCl or acetylcholine, implying physiological release by activation of the cholinergic innervation of the adrenal. Our characterization of d-aspartate ontogeny, biosynthesis and depolarization-induced release implies specific physiological roles for this amino acid.

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