Pazos A, Hoyer D, Palacios J M
Eur J Pharmacol. 1984 Nov 27;106(3):531-8. doi: 10.1016/0014-2999(84)90056-6.
The kinetic and pharmacological characteristics of the binding of [3H]ketanserin and [3H]mesulergine to frontal cortical brain membranes from rat, pig and human were studied. In the 3 species [3H]ketanserin labeled sites with the characteristics of the 5-HT2 receptors previously described in the rat. In contrast, [3H]mesulergine labeled 5-HT2 receptors in rat, but not in pig and human cortices. The characteristics of the sites labeled by [3H]mesulergine in pig cortex were similar to those of sites in the choroid plexus of rats, pigs and humans. While several reputed 5-HT2 ligands presented a similar affinity for the [3H]ketanserin binding sites in the 3 species, other such ligands, e.g. mesulergine, methysergide, cinanserin and LSD which displaced these sites with high affinity in rat brain, had lower affinities in pig and human brain. These results indicate that 5-HT2 receptors show different pharmacological profiles in different species. Caution should thus be exerted in extrapolating data from laboratory animals to humans.
研究了[3H]酮色林和[3H]美舒麦角与大鼠、猪和人额叶皮质脑膜结合的动力学和药理学特性。在这3个物种中,[3H]酮色林标记的位点具有先前在大鼠中描述的5-HT2受体的特征。相比之下,[3H]美舒麦角在大鼠皮质中标记5-HT2受体,但在猪和人皮质中未标记。[3H]美舒麦角在猪皮质中标记的位点的特征与大鼠、猪和人脉络丛中的位点相似。虽然几种著名的5-HT2配体对这3个物种中[3H]酮色林结合位点表现出相似的亲和力,但其他此类配体,如美舒麦角、甲基麦角新碱、肉桂硫胺和麦角酸二乙酰胺,在大鼠脑中能以高亲和力取代这些位点,而在猪和人脑中的亲和力较低。这些结果表明,5-HT2受体在不同物种中表现出不同的药理学特征。因此,在将实验动物的数据外推至人类时应谨慎。