Kato S, Negishi K, Teranishi T
J Neurochem. 1985 Mar;44(3):893-9. doi: 10.1111/j.1471-4159.1985.tb12900.x.
Kainic acid (KA) at micromolar concentrations stimulated the release of gamma-[3H]aminobutyric acid [( 3H]GABA) from a particulate fraction of the carp (Cyprinus carpio) retina. The KA action was dose-dependent but Ca2+-independent. A similar response was elicited by another glutamate receptor agonist, quisqualic acid, and high K+, but not by an aspartate agonist, N-methyl-D-aspartic acid. The stimulatory action of KA on the [3H]GABA release was selectively blocked by the KA blockers gamma-D-glutamylglycine and cis-2,3-piperidine dicarboxylic acid. Dopamine (DA), which is contained in DA interplexiform cells in the carp retina, inhibited the [3H]GABA release induced by KA and high K+ in a dose-dependent manner. 5-Hydroxytryptamine and two well-known GABA antagonists, bicuculline (Bic) and picrotoxin (Pic), also mimicked the DA effect on the GABA release at a comparable concentration. This inhibitory effect of DA as well as Bic and Pic on the [3H]GABA release evoked by KA was clearly antagonized by a DA blocker, haloperidol. The action of these agents (KA, DA, GABA antagonist) belonging to three different receptor categories on the GABAergic neurons (possibly external horizontal cells; H1 cells) is discussed in relation to other electrophysiological studies on the lateral spread of S-potentials between H1 cells.
微摩尔浓度的海人酸(KA)刺激了鲤鱼(Cyprinus carpio)视网膜微粒体部分γ-[3H]氨基丁酸[(3H)GABA]的释放。KA的作用呈剂量依赖性,但不依赖于Ca2+。另一种谷氨酸受体激动剂喹啉酸和高钾也引发了类似反应,但天冬氨酸激动剂N-甲基-D-天冬氨酸未引发此反应。KA对[3H]GABA释放的刺激作用被KA拮抗剂γ-D-谷氨酰甘氨酸和顺式-2,3-哌啶二羧酸选择性阻断。鲤鱼视网膜多巴胺(DA)中间神经元中含有的多巴胺以剂量依赖性方式抑制KA和高钾诱导的[3H]GABA释放。5-羟色胺以及两种著名的GABA拮抗剂荷包牡丹碱(Bic)和印防己毒素(Pic)在相当浓度下也模拟了DA对GABA释放的作用。DA以及Bic和Pic对KA诱发的[3H]GABA释放的这种抑制作用被DA拮抗剂氟哌啶醇明显拮抗。结合其他关于H1细胞间S电位横向传播的电生理研究,讨论了属于三种不同受体类别的这些药剂(KA、DA、GABA拮抗剂)对GABA能神经元(可能是外水平细胞;H1细胞)的作用。