Davis S, Laroche S
Laboratoire de Neurobiologie de l' Apprentissage et de la Mémoire, CNRS URA 1491, Université Paris Sud, Orsay, France.
Neuropharmacology. 1996 Mar;35(3):337-46. doi: 10.1016/0028-3908(95)00185-9.
Activation of ACPD-sensitive metabotropic receptors induced differential effects on synaptic transmission and the induction of LTP in CA1 and the dentate gyrus of the hippocampus i.c.v. injections of (1.S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid [(1S,3R)-ACPD] induced enduring potentiation of the fEPSP in CA1, which occluded tetanically induced LTP. In contrast, ACPD induced a dose-dependent biphasic effect on the fEPSP in the dentate gyrus, consisting of an initial short lasting potentiation, followed by enduring depression of the response, and blockade of LTP. These two effects are likely to be mediated by two different classes of the receptor as in the dentate gyrus the selective class I agonist, (RS)-3,5-dihydroxyphenylglycine (DHPG) induced sustained potentiation of the fEPSP, whereas the mixed mGluR2 agonist-mGluR1 antagonist, (S)-4-carboxy-3-hydrophenylglycine((S)-4C3H-PG) induced only depression. Increasing the concentration of calcium directly in the dentate gyrus prior to, and in conjunction with, injections of ACPD induced sustained potentiation rather than depression. The differential effects indicate that the second messenger cascades the subtypes of receptors are linked with, mediate different forms of synaptic plasticity within the hippocampus and have important implications for their role in learning.
对氨基环丙烷-1,3-二羧酸(ACPD)敏感的代谢型受体的激活对海马CA1区和齿状回的突触传递及长时程增强(LTP)的诱导产生了不同影响。脑室内注射(1.S,3R)-1-氨基环丙烷-1,3-二羧酸[(1S,3R)-ACPD]可诱导CA1区场兴奋性突触后电位(fEPSP)的持久增强,这会阻断强直诱导的LTP。相反,ACPD对齿状回的fEPSP产生剂量依赖性双相效应,包括最初短暂的增强,随后是反应的持久抑制以及LTP的阻断。这两种效应可能由两类不同的受体介导,因为在齿状回中,选择性I类激动剂(RS)-3,5-二羟基苯甘氨酸(DHPG)可诱导fEPSP的持续增强,而混合的代谢型谷氨酸受体2(mGluR2)激动剂-代谢型谷氨酸受体1(mGluR1)拮抗剂(S)-4-羧基-3-羟基苯甘氨酸[(S)-4C3H-PG]仅诱导抑制。在注射ACPD之前并与之同时直接增加齿状回中的钙浓度会诱导持续增强而非抑制。这些不同的效应表明,受体亚型所关联的第二信使级联反应介导了海马体内不同形式的突触可塑性,并且对它们在学习中的作用具有重要意义。