Dipartimento di Biologia ed Evoluzione, Università di Ferrara, Sez Fisiologia e Biofisica, Via Borsari 46, 44100 Ferrara, Italy.
Brain Res. 2010 Oct 1;1354:47-63. doi: 10.1016/j.brainres.2010.07.104. Epub 2010 Aug 5.
Effects of activation of metabotropic glutamatergic receptors (mGluR) were investigated in mouse dopaminergic olfactory bulb neurons. After blockage of ionotropic receptors, focal application of glutamate or of group I/II mGluR agonist t-ACPD resulted in a depolarization, paralleled by an inward current in voltage-clamp conditions. The Group I agonist DHPG induced a depolarization, which could be largely blocked by mGluR1 antagonists. The DHPG action i) was prevented by buffering intracellular Ca(2+) with BAPTA and by a phospholipase C inhibitor; ii) was not affected by the block of Ca(2+) entry, and iii) was blocked by inhibitors of the Na(+)/Ca(2+) exchanger. These observations were interpreted as a mGluR1-mediated intracellular Ca(2+) release, followed by the activation of an electrogenic Na(+)/Ca(2+) exchanger. The mGluR5 agonist CHPG induced a hyperpolarization of membrane potential, resulting in a decrease of the spontaneous firing frequency. CHPG induced i) a decrease in membrane resistance; ii) an increase in the action potential repolarization rate, and iii) an increase in the amplitude of the afterhyperpolarization. This was interpreted as a mGluR5-mediated opening of a K(+) conductance. These data suggest that mGluR1 and mGluR5 play different and non-overlapping roles in the regulation of the excitability of bulbar dopaminergic neurons.
研究了代谢型谷氨酸受体(mGluR)的激活对小鼠多巴胺能嗅球神经元的影响。在阻断离子型受体后,在电压钳条件下,局部应用谷氨酸或 I/II 组 mGluR 激动剂 t-ACPD 可导致去极化,并伴有内向电流。I 组激动剂 DHPG 诱导去极化,该去极化可被 mGluR1 拮抗剂大部分阻断。DHPG 作用:i)可通过 BAPTA 缓冲细胞内 Ca(2+)和磷脂酶 C 抑制剂来阻止;ii)不受 Ca(2+)内流阻断的影响;iii)可被 Na(+)/Ca(2+)交换器抑制剂阻断。这些观察结果被解释为 mGluR1 介导的细胞内 Ca(2+)释放,随后激活电致 Na(+)/Ca(2+)交换器。mGluR5 激动剂 CHPG 使膜电位超极化,导致自发放电频率降低。CHPG 诱导:i)膜电阻降低;ii)动作电位复极化率增加;iii)后超极化幅度增加。这被解释为 mGluR5 介导的 K(+)电导开放。这些数据表明,mGluR1 和 mGluR5 在调节嗅球多巴胺能神经元兴奋性方面发挥不同且不重叠的作用。