SOME OBSERVATIONS ON THE INCORPORATION OF PRECURSORS INTO RIBONUCLEIC ACID OF RAT BRAIN

IN COMMON with other organs, brain utilises precursors such as [14C]formate (MANELL and ROSSITER, 1955), [14C]adenine and [14C]orotic acid (KOENIG, 1958) and [14C]glycine (HENDERSON and LEPAGE, 1959) for the synthesis of acid-soluble nucleotides and RNA. More recently, during an investigation into the effects of 6-azauridine on pyrimidine metabolism in the central nervous system, WELLS, GAINES and KOENIG (1963) suggested that the orotic acid pathway provided a significant portion of the pyrimidine nucleotides in the neuraxis of the cat. They also suggested that the maintenance of the RNA concentration in azauridine-treated brain indicated that preformed pyrimidines derived from the blood stream may supplement the in situ biogenesis of pyrimidines under certain conditions. So far, however, there appears to have been little direct study of the relative efficiencies of the de nouo and the preformed base pathways for the production of brain RNA or of possible effects of the blood-brain barrier on the availability of such precursors. This paper represents an effort to answer some of the questions as a preliminary to studies on the metabolic effects of the incorporation of abnormal bases into cerebral nucleic acid.

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