Effects of cold exposure on rat adrenal tyrosine hydroxylase: an analysis of RNA, protein, enzyme activity, and cofactor levels

A Baruchin, EP Weisberg, LL Miner… - Journal of …, 1990 - Wiley Online Library
A Baruchin, EP Weisberg, LL Miner, D Ennis, LK Nisenbaum, E Naylor, EM Stricker
Journal of neurochemistry, 1990Wiley Online Library
Long‐term cold exposure (5–7 days) is known to induce concomitant increases in the levels
of adrenomedullary tyrosine hydroxylase (TH) RNA, protein, and enzyme activity. In this
report, we compare the time courses of these changes and investigate the effects of cold
exposure on the levels of biopterin, the cofactor required for tyrosine hydroxylation. After
only 1 h of cold exposure, TH mRNA abundance increased 71% compared with nonstressed
controls. Increases in total cellular TH RNA levels were maximal (threefold over control …
Abstract
Long‐term cold exposure (5–7 days) is known to induce concomitant increases in the levels of adrenomedullary tyrosine hydroxylase (TH) RNA, protein, and enzyme activity. In this report, we compare the time courses of these changes and investigate the effects of cold exposure on the levels of biopterin, the cofactor required for tyrosine hydroxylation. After only 1 h of cold exposure, TH mRNA abundance increased 71% compared with nonstressed controls. Increases in total cellular TH RNA levels were maximal (threefold over control values) within 3–6 h of cold exposure and remained elevated throughout the duration of the experiment (72 h). TH protein levels increased rapidly after 24 h of cold exposure and reached a maximal value threefold above that of controls at 48–72 h. Despite the relatively rapid and large elevations in TH RNA and protein content, only modest increases in TH activity were detected during the initial 48 h of cold exposure. Adrenomedullary biopterin increased rapidly after the onset of cold exposure, rising to a level approximately twofold that of the nonstressed controls at 24 h, and remained at this level throughout the duration of the stress period. Taken together, the results of this time course study indicate that cold‐induced alterations in adrenal TH activity are mediated by multiple cellular control mechanisms, which may include pre‐ and posttranslational regulation. Our findings also suggest that cold stress‐induced increases in the levels of the TH cofactor may represent another key event in the sympathoadrenal system's response to cold stress.
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