Govindaiah G, Cox Charles L
Dept. of Pharmacology and Physiology, University of Illinois, 2357 Beckman Institute, 405 N. Mathews Ave., Urbana, IL 61801, USA.
J Neurophysiol. 2009 Apr;101(4):1761-73. doi: 10.1152/jn.91107.2008. Epub 2009 Jan 28.
The ventral lateral geniculate nucleus (vLGN) has been implicated in numerous functions including circadian rhythms, brightness discrimination, pupillary light reflex, and other visuomotor functions. The contribution of inhibitory mechanisms in the regulation of vLGN neuron excitability remains unexplored. We examined the actions of metabotropic glutamate receptor (mGluR) activation on the intrinsic excitability and inhibitory synaptic transmission in different lamina of vLGN. Activation of mGluRs exerts distinct pre- and postsynaptic actions in vLGN neurons. In the lateral magnocellular subdivision of vLGN (vLGNl), the general mGluR agonist (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (ACPD) enhanced the frequency of GABA(A) receptor-mediated spontaneous inhibitory postsynaptic currents (sIPSC) that persisted in the presence of sodium channel blocker tetrodotoxin (TTX) in a subpopulation of neurons (TTX insensitive). This increase is attributed to the increased output of dendritic GABA release from vLGN interneurons. In contrast, in the medial subdivision of vLGN (vLGNm), the mGluR agonist-mediated increase in sIPSC frequency was completely blocked by TTX. The selective Group I mGluR agonist (RS)-3,5-dihydroxyphenylglycine (DHPG) increased sIPSC frequency, whereas the selective Group II mGluR agonist (2R, 4R)-4-aminopyrrolidine-2,4-dicarboxylate (APDC) significantly decreased sIPSC frequency in vLGNl neurons. Optic tract stimulation also produced an mGluR-dependent increase in sIPSC frequency in vLGNl neurons. In contrast, we were unable to synaptically evoke alterations in sIPSC activity in vLGNm neurons. In addition to these presynaptic actions, DHPG depolarized both vLGNl and vLGNm neurons. In vLGN interneurons, mGluR activation produced opposing actions: APDC hyperpolarized the membrane potential, whereas DHPG produced a membrane depolarization. The present findings demonstrate diverse actions of mGluRs on vLGN neurons localized within different vLGN lamina. Considering these different lamina are coupled with distinct functional roles, thus these diverse actions may be involved in distinctive forms of visual and visuomotor information processing.
腹侧外侧膝状体核(vLGN)参与了多种功能,包括昼夜节律、亮度辨别、瞳孔对光反射以及其他视觉运动功能。抑制机制在调节vLGN神经元兴奋性中的作用仍未得到探索。我们研究了代谢型谷氨酸受体(mGluR)激活对vLGN不同层内固有兴奋性和抑制性突触传递的影响。mGluR的激活在vLGN神经元中发挥了不同的突触前和突触后作用。在vLGN的外侧大细胞亚区(vLGNl),一般的mGluR激动剂(1S,3R)-1-氨基环戊烷-1,3-二羧酸(ACPD)增加了GABA(A)受体介导的自发性抑制性突触后电流(sIPSC)的频率,在一部分神经元中(对河豚毒素(TTX)不敏感),这种增加在存在钠通道阻滞剂河豚毒素(TTX)时仍然持续。这种增加归因于vLGN中间神经元树突状GABA释放量的增加。相比之下,在vLGN的内侧亚区(vLGNm),mGluR激动剂介导的sIPSC频率增加被TTX完全阻断。选择性I组mGluR激动剂(RS)-3,5-二羟基苯甘氨酸(DHPG)增加了sIPSC频率,而选择性II组mGluR激动剂(2R, 4R)-4-氨基吡咯烷-2,4-二羧酸(APDC)显著降低了vLGNl神经元中的sIPSC频率。视束刺激也在vLGNl神经元中产生了mGluR依赖性的sIPSC频率增加。相比之下,我们无法在vLGNm神经元中通过突触诱发sIPSC活性的改变。除了这些突触前作用外,DHPG使vLGNl和vLGNm神经元都发生了去极化。在vLGN中间神经元中,mGluR激活产生了相反的作用:APDC使膜电位超极化,而DHPG使膜去极化。目前的研究结果表明mGluRs对位于vLGN不同层内的vLGN神经元有多种作用。考虑到这些不同的层与不同的功能作用相关联,因此这些不同的作用可能参与了独特形式的视觉和视觉运动信息处理。