Cabanillas A M, Masini-Repiso A M, Costamagna M E, Pellizas C, Coleoni A H
Departamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina.
J Endocrinol. 1994 Nov;143(2):303-8. doi: 10.1677/joe.0.1430303.
The present work was addressed to study a possible relationship between monoamine oxidase (MAO) and the thyroid iodide transport mechanism. Normal rats treated with clorgyline (a selective MAO-A inhibitor) or tranylcypromine (a non-selective MAO inhibitor) showed a significantly diminished thyroid MAO activity, while deprenyl and pargyline (MAO-B inhibitors) did not modify the thyroidal enzyme activity with respect to the control group. Under these conditions, in vivo iodide transport was reduced both by clorgyline and tranylcypromine administration whereas it remained unchanged after treatment with MAO-B inhibitors. The effect of MAO inhibitors on thyroid MAO activity and in vivo iodide transport was also evaluated in rats treated with exogenous thyrotrophin (TSH) after endogenous TSH secretion blockade produced by T4 administration. In this condition, thyroid MAO activity was significantly lowered by clorgyline and was not modified by deprenyl. In contrast to the results observed in normal rats, in vivo iodide transport in TSH-treated rats remained unaltered after treatment either with clorgyline or deprenyl. MAO activity evaluated in bovine thyroid follicles in primary culture was highly sensitive to low concentrations of clorgyline (< 10 nmol/l) and relatively insensitive to deprenyl, a finding that indicates a predominance of the MAO-A isoform in the follicular cells in culture. When clorgyline (0.1 and 1 mumol/l) or deprenyl (1 mumol/l) were added to the culture medium, no modifications in the active transport of iodide were observed. These results indicate the absence of a direct linkage between thyroid MAO activity and the active iodide transport.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在探讨单胺氧化酶(MAO)与甲状腺碘转运机制之间可能存在的关系。用氯吉兰(一种选择性MAO - A抑制剂)或反苯环丙胺(一种非选择性MAO抑制剂)处理的正常大鼠,其甲状腺MAO活性显著降低,而司来吉兰和帕吉林(MAO - B抑制剂)对甲状腺酶活性的影响与对照组相比无变化。在这些条件下,氯吉兰和反苯环丙胺给药均降低了体内碘转运,而MAO - B抑制剂处理后碘转运保持不变。在用T4阻断内源性促甲状腺激素(TSH)分泌后,对外源性TSH处理的大鼠也评估了MAO抑制剂对甲状腺MAO活性和体内碘转运的影响。在此条件下,氯吉兰显著降低了甲状腺MAO活性,而司来吉兰对其无影响。与正常大鼠的结果相反,氯吉兰或司来吉兰处理后,TSH处理大鼠的体内碘转运未发生改变。在原代培养的牛甲状腺滤泡中评估的MAO活性对低浓度氯吉兰(<10 nmol/l)高度敏感,对司来吉兰相对不敏感,这一发现表明培养的滤泡细胞中MAO - A同工型占优势。当向培养基中添加氯吉兰(0.1和1 μmol/l)或司来吉兰(1 μmol/l)时,未观察到碘的主动转运有变化。这些结果表明甲状腺MAO活性与碘的主动转运之间不存在直接联系。(摘要截短于250字)