Galli A, Franchi-Micheli S, Mori F, Luzzi S, Zilletti L
Department of Preclinical and Clinical Pharmacology, University of Florence, Firenze, Italy.
Neuropharmacology. 1990 Feb;29(2):145-50. doi: 10.1016/0028-3908(90)90054-u.
Ten microM glycine, D-serine and D-alanine potentiated L-glutamate (30 microM)-induced contractions of the guinea pig ileum by an average of 35, 53 and 24%, respectively. On the contrary, D-cysteine, at the same concentration, caused a 21% inhibition of the contractile response to L-glutamate. This inhibitory effect of D-cysteine was abolished by 10 microM glycine. The corresponding L-isomers of these amino acids, namely L-serine, L-alanine and L-cysteine and the other amino acids tested, possessed negligible activity or were inactive in this test. The IC50 values of the same compounds for strychnine-insensitive binding of [3H]glycine (20 nM) to cortical membranes from the brain of the rat were: 0.26 microM, glycine; 1.2 microM, D-serine; 2.1 microM, D-alanine; 8.6 microM, D-cysteine; 51 microM, L-serine; 90 microM, L-alanine; greater than 1000 microM, L-cysteine. On the whole, these results point out a strict requirement for stereoselectivity for both of the effects examined. In addition, the results obtained in the ileum preparation suggest that D-cysteine may act as an antagonist, rather than as an agonist at the glycine site which regulates the responses of N-methyl-D-aspartate receptors.
10微摩尔的甘氨酸、D-丝氨酸和D-丙氨酸分别使L-谷氨酸(30微摩尔)诱导的豚鼠回肠收缩平均增强了35%、53%和24%。相反,相同浓度的D-半胱氨酸使对L-谷氨酸的收缩反应受到21%的抑制。10微摩尔的甘氨酸可消除D-半胱氨酸的这种抑制作用。这些氨基酸的相应L-异构体,即L-丝氨酸、L-丙氨酸和L-半胱氨酸以及所测试的其他氨基酸,在此测试中活性可忽略不计或无活性。相同化合物对[3H]甘氨酸(20纳摩尔)与大鼠脑皮质膜上士的宁不敏感结合的IC50值分别为:甘氨酸0.26微摩尔;D-丝氨酸1.2微摩尔;D-丙氨酸2.1微摩尔;D-半胱氨酸8.6微摩尔;L-丝氨酸51微摩尔;L-丙氨酸90微摩尔;L-半胱氨酸大于1000微摩尔。总体而言,这些结果表明所研究的两种效应都严格要求立体选择性。此外,在回肠制备实验中获得的结果表明,D-半胱氨酸可能作为拮抗剂,而不是在调节N-甲基-D-天冬氨酸受体反应的甘氨酸位点上作为激动剂起作用。