Beley A, Beley P, Bralet J
Arch Int Physiol Biochim. 1975 Aug;83(3):471-80. doi: 10.3109/13813457509071392.
The effect of chronic treatment with tyroxine (T4) or propylthiouracile (PTU) on the turnover of norepinephrine (NE), dopamine (DA) and 5-hydroxytryptamine (5-HT) has been studied in various areas of the rat brain (brain stem, hypothalamus, striatum and "rest of the brain"). The turnover of NE and DA was determined by the decay in endogenous levels after inhibition of tyrosine hydroxylase by alpha-methylparatyrosine and the turnover of 5-HT was evaluated by the initial accumulation of endogenous 5-HT after inhibition of monoamine oxydase by pargyline. T4 treatment accelerated the release of DA from the striatum but had no significant effects on NA release in the various cerebral areas : nevertheless the NE endogenous level was significantly reduced in the brain stem. PTU treatment delayed the release of DA and NA only from the "rest of the brain". Concerning 5-HT, the only significant variation was observed in the hypothalamus of PTU-treated rats and implied increased turnover. The possible relations between the changes in cerebral monoamines turnover and the behavioural alterations which are observed in thyroid disfunction are discussed.
已在大鼠脑的各个区域(脑干、下丘脑、纹状体和“脑的其他部分”)研究了用甲状腺素(T4)或丙硫氧嘧啶(PTU)进行长期治疗对去甲肾上腺素(NE)、多巴胺(DA)和5-羟色胺(5-HT)周转的影响。通过α-甲基对酪氨酸抑制酪氨酸羟化酶后内源性水平的衰减来测定NE和DA的周转,通过帕吉林抑制单胺氧化酶后内源性5-HT的初始积累来评估5-HT的周转。T4治疗加速了DA从纹状体的释放,但对各个脑区的NA释放没有显著影响:然而,脑干中的NE内源性水平显著降低。PTU治疗仅延迟了DA和NA从“脑的其他部分”的释放。关于5-HT,仅在PTU处理的大鼠的下丘脑中观察到显著变化,这意味着周转增加。讨论了脑单胺周转变化与甲状腺功能障碍中观察到的行为改变之间的可能关系。