Jaspers R M, de Vries T J, Cools A R
Psychoneuropharmacological Research Unit, University of Nijmegen, The Netherlands.
Behav Brain Res. 1990 Mar 26;37(3):247-54. doi: 10.1016/0166-4328(90)90136-3.
Bilateral intracaudate application of the glutamate agonist DL-alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid (AMPA), viz. an agonist of quisqualate receptors, is known to produce the following effects in cats that had to climb on a small wooden bar and, subsequently, to switch to distinct patterns: it produces increases in switching from one pattern to another pattern (1) and it induces limb deficits, i.e. unilateral deficient placing of the fore- and/or hindlimb. In the present study, the effect of stimulating striatal dopamine receptors on behavioural changes induced by intracaudate injections of AMPA was investigated. Therefore, the dopamine agonist apomorphine was injected into the caudate nucleus 5 min before the striatal injection of 1.0 micrograms AMPA. AMPA-induced increases in switching behaviour were prevented by 0.6 micrograms, but not 0.3 micrograms, apomorphine. In contrast, AMPA-induced limb deficits were not prevented by pretreatment of apomorphine. In view of the notion that the dopaminergic caudate nucleus, its output station the substantia nigra, pars reticulata and the nigral output station the deeper layers of the colliculus superior are essential for switching behaviour, but not for the display of disturbances like AMPA-induced limb deficits, the present data strongly suggest that only AMPA-induced changes in switching, but not AMPA-induced limb deficits, are mediated by the caudato-nigro-collicular circuitry. The glutamate receptor-selectivity of the modulatory action of dopamine is discussed.
已知在猫身上双侧尾状核内应用谷氨酸激动剂DL-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA),即quisqualate受体激动剂,会在猫爬上一根小木条并随后切换到不同模式时产生以下效应:它会增加从一种模式切换到另一种模式的频率(1),并且会诱发肢体缺陷,即前肢和/或后肢单侧放置不足。在本研究中,研究了刺激纹状体多巴胺受体对尾状核内注射AMPA所诱导的行为变化的影响。因此,在纹状体注射1.0微克AMPA前5分钟,将多巴胺激动剂阿扑吗啡注入尾状核。0.6微克阿扑吗啡可阻止AMPA诱导的切换行为增加,但0.3微克则不能。相反,阿扑吗啡预处理并不能阻止AMPA诱导的肢体缺陷。鉴于多巴胺能尾状核、其输出站黑质网状部以及黑质输出站中脑上丘深层对于切换行为至关重要,但对于像AMPA诱导的肢体缺陷这样的干扰表现并非如此,目前的数据强烈表明,只有AMPA诱导的切换变化,而不是AMPA诱导的肢体缺陷,是由尾状核-黑质-中脑上丘回路介导的。文中还讨论了多巴胺调节作用的谷氨酸受体选择性。