Cirone J, Pothecary C A, Turner J P, Salt T E
Department of Visual Science, Institute of Ophthalmology, University College London, 11-43 Bath Street, UK.
J Physiol. 2002 Jun 15;541(Pt 3):895-903. doi: 10.1113/jphysiol.2002.016618.
Group I metabotropic glutamate receptors (mGluRs) are expressed in cells in the superficial layers of the rat superior colliculus (SSC) and SSC afferents. The purpose of this study was to investigate the physiological effect of Group I mGluR activation on visual responses of SSC neurones using both in vivo and in vitro techniques. In the in vivo preparation, agonists and antagonists were applied by iontophoresis and single neurone activity was recorded extracellularly in anaesthetised rats. Application of the Group I agonist (S)-3,5-dihydroxyphenylglycine (DHPG) resulted in a reversible inhibition of the visual response. The effect of DHPG could be blocked by concurrent application of the Group I (mGluR1/mGluR5) antagonist (S)-4-carboxyphenylglycine (4CPG) or mGluR1 antagonist (+)-2-methyl-4-carboxyphenylglycine (LY367385). Application of 4CPG alone resulted in a facilitation of the visual response and this effect was not changed when the visual stimulus contrast was varied. Response habituation was observed when visual stimuli were presented at 0.5 s intervals, but this was not affected by DHPG or 4CPG. In slices of the superior colliculus, stimulation of the optic tract resulted in a field EPSP recorded from the SSC whose duration was increased in the presence of the GABA antagonists picrotoxin and CGP55845. Application of DHPG (5-100 microM) reduced the field EPSP, and this effect could be reversed by the mGluR1 antagonist LY367385 (200 microM), but not by the mGluR5 antagonist MPEP (5 microM). These data show that activation of mGluR1, but probably not mGluR5, can modulate visual responses of SSC neurones in vivo, and that this could be via presynaptic inhibition of glutamate release from either retinal or, possibly, cortical afferents.
I 型代谢型谷氨酸受体(mGluRs)表达于大鼠上丘浅层(SSC)的细胞及 SSC 传入神经中。本研究旨在运用体内和体外技术,探究 I 型 mGluR 激活对 SSC 神经元视觉反应的生理作用。在体内实验中,通过离子电泳施加激动剂和拮抗剂,并在麻醉大鼠中细胞外记录单个神经元的活动。施加 I 型激动剂(S)-3,5-二羟基苯甘氨酸(DHPG)导致视觉反应出现可逆性抑制。同时施加 I 型(mGluR1/mGluR5)拮抗剂(S)-4-羧基苯甘氨酸(4CPG)或 mGluR1 拮抗剂(+)-2-甲基-4-羧基苯甘氨酸(LY367385)可阻断 DHPG 的作用。单独施加 4CPG 会促进视觉反应,且当视觉刺激对比度变化时,这种作用不变。当以 0.5 秒的间隔呈现视觉刺激时,观察到反应习惯化,但这不受 DHPG 或 4CPG 的影响。在上丘切片中,刺激视束会在 SSC 记录到一个场兴奋性突触后电位(EPSP),其持续时间在存在 GABA 拮抗剂印防己毒素和 CGP55845 时会增加。施加 DHPG(5 - 100 μM)会降低场 EPSP,且这种作用可被 mGluR1 拮抗剂 LY367385(200 μM)逆转,但不能被 mGluR5 拮抗剂 MPEP(5 μM)逆转。这些数据表明,mGluR1 的激活而非 mGluR5 的激活,可能在体内调节 SSC 神经元的视觉反应,并且这可能是通过对视网膜或可能的皮质传入神经释放谷氨酸的突触前抑制来实现的。