Washio Hiroshi
Department of Biotechnology, Ishinomaki Senshu University, Ishinomaki, Miyagi 986-8580, Japan.
Zoolog Sci. 2002 Feb;19(2):153-62. doi: 10.2108/zsj.19.153.
Effects of application of glutamate and glutamatergic ligands were studied to characterize the receptors for glutamate present on the soma membrane of the dorsal unpaired median (DUM) neurons in the thoracic ganglia of the cockroach, Periplaneta americana, using the intracellular recording technique. Application of L-glutamate did not block the GABA-response, and application of beta-guanidino-propionic acid, a competitive antagonist for GABA, failed to block the response to L-glutamate. These results indicate that most of L-glutamate action may not be mediated by a GABA-activated channel. To examine glutamate receptor types on the DUM neurons, glutamate receptor agonists were applied. The ionotropic glutamate receptor (iGluR) agonists evoked depolarizations with the following relative rank of order of potency: kainate > AMPA > quisqualate. Metabotropic glutamate receptor (mGluR) agonists also elicited membrane depolarizations or hyperpolarizations associated with an increase in membrane conductance. The mGluR agonists evoked depolarizations or hyperpolarizations with the following relative rank of order: L-CCG-1 > 1S, 3R-ACPD > L-AP4. Depolarization of the same DUM neuron was detected following exposure of kainate and L-CCG-I, suggesting the coexistence of distinct iGluR and mGluR types. A membrane permeable cAMP analog, CPT-cAMP, could not mimic the effect of mGluR agonists. The mGluR selective antagonists, MCCG and MCPG, failed to antagonize the response to mGluR agonists. The involvement of cAMP in the mGluR response was not confirmed in DUM neurons. Although the functional roles of these receptors are unknown, it might be possible then that these extrasynaptic receptors have a modulatory effect on the excitability of the DUM neurons.
利用细胞内记录技术,研究了谷氨酸和谷氨酸能配体的应用效果,以表征美洲大蠊胸神经节中背侧不成对中间神经元(DUM)胞体膜上存在的谷氨酸受体。L-谷氨酸的应用并未阻断GABA反应,而GABA的竞争性拮抗剂β-胍基丙酸的应用也未能阻断对L-谷氨酸的反应。这些结果表明,L-谷氨酸的大部分作用可能不是由GABA激活的通道介导的。为了研究DUM神经元上的谷氨酸受体类型,应用了谷氨酸受体激动剂。离子型谷氨酸受体(iGluR)激动剂引起去极化,其效力的相对顺序如下:海人酸>AMPA>quisqualate。代谢型谷氨酸受体(mGluR)激动剂也引起与膜电导增加相关的膜去极化或超极化。mGluR激动剂引起去极化或超极化的相对顺序如下:L-CCG-1>1S,3R-ACPD>L-AP4。在暴露于海人酸和L-CCG-I后,检测到同一DUM神经元的去极化,表明存在不同类型的iGluR和mGluR。一种膜通透性cAMP类似物CPT-cAMP不能模拟mGluR激动剂的作用。mGluR选择性拮抗剂MCCG和MCPG未能拮抗对mGluR激动剂的反应。在DUM神经元中未证实cAMP参与mGluR反应。尽管这些受体的功能作用尚不清楚,但这些突触外受体可能对DUM神经元的兴奋性具有调节作用。