Vaccari A
Br J Pharmacol. 1985 Mar;84(3):773-8. doi: 10.1111/j.1476-5381.1985.tb16160.x.
The action of the antithyroid, sulphydryl reagent methimazole (MMI) on the specific binding of [3H]-imipramine in the cerebral cortex and corpus striatum of immature and mature rats has been examined. Chronic administration of MMI through the first 30 days of life decreased the number of imipramine binding sites in cortical but not striatal membranes, as assessed 48 h after the last injection of goitrogen. A similar treatment did not affect the binding profile of [3H]-imipramine in mature rats. Acute administration of MMI to 30 day-old rats increased the number of imipramine binding sites shortly after the injection, an effect no longer evident 48 h later. MMI in vitro increased the binding of [3H]-imipramine. It is concluded that maturational impairment of the hypothyroid cortex, rather than any alteration of membrane bound thiol groups, was a major cause for the diminished binding of [3H]-imipramine in MMI-treated, immature rats.
已研究了抗甲状腺巯基试剂甲巯咪唑(MMI)对未成熟和成熟大鼠大脑皮质及纹状体中[3H] - 丙咪嗪特异性结合的作用。在出生后的前30天持续给予MMI,在最后一次注射致甲状腺肿物质48小时后评估发现,其减少了皮质膜而非纹状体膜中丙咪嗪结合位点的数量。类似的处理对成熟大鼠中[3H] - 丙咪嗪的结合情况没有影响。对30日龄大鼠急性给予MMI后,注射后不久丙咪嗪结合位点数量增加,48小时后这种效应不再明显。MMI在体外增加了[3H] - 丙咪嗪的结合。得出的结论是,甲状腺功能减退的皮质成熟受损,而非膜结合巯基基团的任何改变,是MMI处理的未成熟大鼠中[3H] - 丙咪嗪结合减少的主要原因。