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Newly Synthesized Dopamine as the Precursor for Norepinephrine Synthesis in Bovine Adrenomedullary Chromaffin Cells
Author(s) -
Menniti Frank S.,
Diliberto Emanuel J.
Publication year - 1989
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1989.tb11788.x
Subject(s) - dopamine , norepinephrine , catecholamine , chemistry , medicine , endocrinology , tyrosine hydroxylase , chromaffin cell , intracellular , biology , adrenal medulla , biochemistry
The precursor pool of dopamine for norepinephrine synthesis was investigated in cultured bovine adrenomedullary chromaffin cells incubated with [ 14 C]tyrosine. Under conditions where the intracellular [ 14 C]tyrosine specific activity was constant and [ 14 C]dopamine synthesis was maximal, [ 14 C]dopamine and [ 14 C]norepinephrine accumulated over time, and the total intracellular dopamine content more than doubled within 120 min. When [ 14 C]norepinephrine synthesis was calculated at different times based on the specific activity of [ 14 C]dopamine, this rate was approximately equal to the rate of [ l4 C]dopamine synthesis and was, thus, inconsistent with the observed dopamine accumulation. However, the rate of [ 14 C]norepinephrine synthesis based on the [ l4 C]tyrosine specific activity accounted for the dopamine accumulation, an observation suggesting that newly synthesized dopamine, i.e., dopamine with a specific activity equivalent to that of its precursor, [ 14 C]tyrosine, is preferentially utilized for norepinephrine synthesis. Further studies showed that the subcellular distribution of [ 14 C]dopamine was identical to that of norepinephrine and epinephrine and that the accumulated [ 14 C]dopamine could be converted to norepinephrine within the chromaffin vesicle if dopamine uptake was blocked. Taken together, these results suggest that a small intravesicular dopamine pool, rapidly replenished by newly synthesized dopamine, serves as the substrate for dopamine β‐hydroxylase. Several mechanisms to account for this observation are discussed.