Akoev G N, Andrianov Iu N, Bromm B, Sabo T, Sherman N O
Neirofiziologiia. 1989;21(2):160-7.
Effects of bath-application of quisqualate (Q), N-methyl-D-aspartate (NMDA) and antagonists of NMDA-receptors: D-amino-adipate (AA), 2-amino-4-phosphonobutyrate (APB), 2-amino-5-phosphonovalerate (APV) and Mg2+ as well as acidic amino acid antagonist: D-glutamylglycine (DGG) on the synapse between the electroreceptor cells and afferent fibres were studied in the ampullae of Lorenzini. Q (threshold concentration 10(-8) M) and NMDA (threshold concentration 10(-5) M) strongly excited afferent fibres. Neither AA nor APB influenced the resting and evoked activities. APV blocked the synaptic transmission. Mg2+ (30-50 mM) blocked the responses to NMDA, while Q-induced responses were not affected, APV preferentially blocked NMDA-induced responses and in lesser degree--L-aspartate (L-ASP)-induced responses. DGG blocked the synaptic transmission. It is supposed that the synaptic receptor could represent a homogeneous receptor with different binding sites to the known agonists.
研究了在洛伦兹尼壶腹中将喹啉酸(Q)、N-甲基-D-天冬氨酸(NMDA)以及NMDA受体拮抗剂:D-氨基己二酸(AA)、2-氨基-4-膦酰丁酸(APB)、2-氨基-5-膦酰戊酸(APV)和Mg2+以及酸性氨基酸拮抗剂:D-谷氨酰甘氨酸(DGG)浴用对电感受器细胞与传入纤维之间突触的影响。Q(阈浓度10(-8) M)和NMDA(阈浓度10(-5) M)强烈兴奋传入纤维。AA和APB均不影响静息和诱发活动。APV阻断突触传递。Mg2+(30 - 50 mM)阻断对NMDA的反应,而Q诱导的反应不受影响,APV优先阻断NMDA诱导的反应,对L-天冬氨酸(L-ASP)诱导的反应阻断程度较小。DGG阻断突触传递。推测突触受体可能代表一种对已知激动剂具有不同结合位点的同质受体。