Cimino M, Marini P, Cattabeni F
Institute of Pharmacology and Pharmacognosy, University of Urbino, Italy.
Eur J Pharmacol. 1996 Dec 27;318(1):201-4. doi: 10.1016/s0014-2999(96)00884-9.
Radioreceptor binding assays and receptor autoradiography were used to investigate the activity of thiocolchicoside on strychnine-sensitive binding sites in rat brain and spinal cord using [3H]strychnine as a ligand. Thiocolchicoside displaced the binding of [3H]strychnine with an affinity similar to that of unlabeled glycine, and showed a Hill coefficient and proportionality parameter (P) less than unity. The activity of thiocolchicoside toward [3H]strychnine binding sites was confirmed in autoradiographic studies. The results suggest that thiocolchicoside behaves as an allosteric compound acting on the strychnine-sensitive glycine receptor in rat brainstem and spinal cord, and that this may provide a possible mechanism for the myorelaxant activity of this colchicoside derivative, the first clinically useful drug acting on this receptor.
采用放射性受体结合试验和受体放射自显影技术,以[3H]士的宁作为配体,研究硫代秋水仙碱苷对大鼠脑和脊髓中士的宁敏感结合位点的活性。硫代秋水仙碱苷取代[3H]士的宁结合的亲和力与未标记甘氨酸相似,且希尔系数和比例参数(P)小于1。放射自显影研究证实了硫代秋水仙碱苷对[3H]士的宁结合位点的活性。结果表明,硫代秋水仙碱苷作为一种变构化合物作用于大鼠脑干和脊髓中的士的宁敏感甘氨酸受体,这可能为这种秋水仙碱苷衍生物的肌松活性提供一种可能机制,该衍生物是首个作用于该受体的临床可用药物。