Kosinski C, Gross G, Hanft G
Department of Pharmacology, University of Essen, Federal Republic of Germany.
Br J Clin Pharmacol. 1990;30 Suppl 1(Suppl 1):128S-130S. doi: 10.1111/j.1365-2125.1990.tb05483.x.
The density of calcium channel binding sites as determined by [3H]-nitrendipine binding was found to be decreased in hearts of hyperthyroid rats but hardly altered by hypothyroidism. In contrast, dihydropyridine binding sites in the cerebral cortex were unaffected by dysthyroid states. Myocardial [3H]-nitrendipine binding sites were also decreased after treatment of the animals with isoprenaline but not in spontaneously hypertensive rats. These findings suggest that myocardial hypertrophy is not necessarily accompanied by a loss of calcium channels and that thyroid hormone regulates the density of [3H]-nitrendipine binding sites in a tissue-specific manner.
通过[3H]-尼群地平结合测定发现,甲状腺功能亢进大鼠心脏中钙通道结合位点的密度降低,但甲状腺功能减退几乎未使其改变。相比之下,甲状腺功能紊乱状态对大脑皮质中二氢吡啶结合位点没有影响。用异丙肾上腺素处理动物后,心肌[3H]-尼群地平结合位点也减少,但自发性高血压大鼠未出现这种情况。这些发现表明,心肌肥大不一定伴随着钙通道的丧失,并且甲状腺激素以组织特异性方式调节[3H]-尼群地平结合位点的密度。