Department of Physiology & Pharmacology, Oregon Health & Science University, Portland, OR 97239, USA.
Neuropharmacology. 2013 Apr;67:88-94. doi: 10.1016/j.neuropharm.2012.09.023. Epub 2012 Nov 16.
To investigate the role of mGluR8 in modulating the synaptic responses of retinal ganglion cells, we used a recently identified positive allosteric modulator of mGluR8, AZ12216052 (AZ) and the mGluR8-specific orthosteric agonist (S)-3,4-dicarboxyphenylglycine (DCPG). These agents were applied to whole-cell voltage-clamped ganglion cells from an isolated, superfused mouse retina preparation. DCPG reduced OFF-ganglion cell excitatory currents, whereas AZ enhanced the peak excitatory currents in ON-, OFF-, and ON-OFF-ganglion cells. The effects on ganglion cell inhibitory currents were more varied. The effects of the allosteric modulator were stronger for bright stimuli than for dim stimuli, consistent with receptor stimulation by endogenous glutamate being stronger during bright light stimulation and with mGluR8 receptors mainly being localized away from glutamate release sites, immuno-labeled with VGLUT1. The differential sensitivity of ganglion cell light responses to DCPG and AZ supports multiple sites where mGluR8 modulates the light responses of ganglion cells.
为了研究 mGluR8 在调节视网膜神经节细胞突触反应中的作用,我们使用了最近鉴定出的 mGluR8 正变构调节剂 AZ12216052(AZ)和 mGluR8 特异性的变构激动剂 (S)-3,4-二羧基苯甘氨酸(DCPG)。这些药物应用于从分离的、超流培养的小鼠视网膜制备物中的全细胞膜片钳记录的神经节细胞。DCPG 减少了 OFF 神经节细胞兴奋性电流,而 AZ 增强了 ON、OFF 和 ON-OFF 神经节细胞的峰值兴奋性电流。对神经节细胞抑制性电流的影响更为多样化。变构调节剂的作用对于亮刺激比暗刺激更强,这与内源性谷氨酸受体在强光刺激下的刺激更强以及 mGluR8 受体主要位于谷氨酸释放位点之外,用 VGLUT1 免疫标记一致。神经节细胞光反应对 DCPG 和 AZ 的敏感性差异支持 mGluR8 调节神经节细胞光反应的多个位点。