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関: metabotropic glutamate receptor

関: Metabotropic glutamate receptors

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/04/05 04:16:23」(JST)

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fluorescent micrographs of cells expressing mGluR1 labeled with green fluorescent protein^[1]

The metabotropic glutamate receptors, or mGluRs, are a type of glutamate receptor that are active through an indirect metabotropic process. They are members of the group C family of G-protein-coupled receptors, or GPCRs.^[2] Like all glutamate receptors, mGluRs bind with glutamate, an amino acid that functions as an excitatory neurotransmitter.

Glutamic acid

Function and structure

The mGluRs perform a variety of functions in the central and peripheral nervous systems: For example, they are involved in learning, memory, anxiety, and the perception of pain.^[3] They are found in pre- and postsynaptic neurons in synapses of the hippocampus, cerebellum,^[4] and the cerebral cortex, as well as other parts of the brain and in peripheral tissues.^[5]

Like other metabotropic receptors, mGluRs have seven transmembrane domains that span the cell membrane.^[6] Unlike ionotropic receptors, metabotropic glutamate receptors are not ion channels. Instead, they activate biochemical cascades, leading to the modification of other proteins, as for example ion channels.^[7] This can lead to changes in the synapse's excitability, for example by presynaptic inhibition of neurotransmission,^[8] or modulation and even induction of postsynaptic responses.^[2]^[5]^[6]^[9]

Classification

Eight different types of mGluRs, labeled mGluR₁ to mGluR₈ (GRM1 to GRM8), are divided into groups I, II, and III.^[2]^[4]^[5]^[9] Receptor types are grouped based on receptor structure and physiological activity.^[3] The mGluRs are further divided into subtypes, such as mGluR_7a and mGluR_7b.

Overview

Overview of glutamate receptors
Family	Receptors ^[10]^[11]	Gene	Mechanism^[10]	Function	Agonists & Activators	Antagonists	Synapse site
Group I	mGluR₁	GRM1	G_q, ↑Na⁺,^[5] ↑K⁺,^[5] ↓glutamate^[9]	Increase^[12]^[13] NMDA receptor activity and risk of excitotoxicity	3,5-dihydroxyphenylglycine		mainly postsynaptic^[14]
Group I	mGluR₅	GRM5	G_q, ↑Na⁺,^[5] ↑K⁺,^[5] ↓glutamate^[9]		3,5-dihydroxyphenylglycine		mainly postsynaptic^[14]
Group II	mGluR₂	GRM2	G_i/G₀	Decrease^[15] NMDA receptor activity and risk of excitotoxicity Attenuate schizophrenia	eglumegad Biphenylindanone A DCG-IV	APICA EGLU LY-341,495	mainly presynaptic^[14]
Group II	mGluR₃	GRM3	G_i/G₀		eglumegad Biphenylindanone A DCG-IV	APICA EGLU LY-341,495	mainly presynaptic^[14]
Group III	mGluR₄	GRM4	G_i/G₀	Decrease^[15] NMDA receptor activity and risk of excitotoxicity	L-AP4		mainly presynaptic^[14]
	mGluR₆	GRM6	G_i/G₀
	mGluR₇	GRM7	G_i/G₀
	mGluR₈	GRM8	G_i/G₀

Group I

Quisqualic acid

The mGluRs in group I, including mGluR₁ and mGluR₅, are stimulated most strongly by the excitatory amino acid analog L-quisqualic acid.^[5]^[16] Stimulating the receptors causes the associated enzyme phospholipase C to hydrolyze phosphoinositide phospholipids in the cell's plasma membrane.^[2]^[5]^[9] This leads to the formation of inositol 1,4,5-trisphosphate (IP3) and diacyl glycerol. Due to its hydrophilic character, IP3 can travel to the endoplasmic reticulum, where it induces, via fixation on its receptor, the opening of calcium channels increasing in this way the cytosolic calcium concentrations. The lipophilic diacylglycerol remains in the membrane, acting as a cofactor for the activation of protein kinase C.

These receptors are also associated with Na⁺ and K⁺ channels.^[5] Their action can be excitatory, increasing conductance, causing more glutamate to be released from the presynaptic cell, but they also increase inhibitory postsynaptic potentials, or IPSPs.^[5] They can also inhibit glutamate release and can modulate voltage-dependent calcium channels.^[9]

Group I mGluRs, but not other groups, are activated by 3,5-dihydroxyphenylglycine (DHPG),^[14] a fact that is useful to experimenters because it allows them to isolate and identify them.

Group II & Group III

The receptors in group II, including mGluRs 2 and 3, and group III, including mGluRs 4, 6, 7, and 8, (with some exceptions) prevent the formation of cyclic adenosine monophosphate, or cAMP, by activating a G protein that inhibits the enzyme adenylyl cyclase, which forms cAMP from ATP.^[2]^[4]^[5]^[17] These receptors are involved in presynaptic inhibition,^[9] and do not appear to affect postsynaptic membrane potential by themselves. Receptors in groups II and III reduce the activity of postsynaptic potentials, both excitatory and inhibitory, in the cortex.^[5]

The chemicals 2-(2,3-dicarboxycyclopropyl)glycine (DCG-IV) and eglumegad activate only group II mGluRs, while 2-amino-4-phosphonobutyrate (L-AP4) activates only group III mGluRs.^[14] Several subtype-selective positive allosteric modulators that activate only the mGlu2 subtype, such as Biphenylindanone A, have also now been developed.

LY-341,495 and MGS-0039 are drugs that act as a selective antagonist blocking both of the group II metabotropic glutamate receptors, mGluR₂ and mGluR₃.^[18] RO4491533 acts as a negative allosteric modulator of mGluR₂ and mGluR₃.^[19]

Localization

Different types of mGluRs are distributed differently in cells. For example, one study found that Group I mGluRs are located mostly on postsynaptic parts of cells, while groups II and III are mostly located on presynaptic elements,^[14] though they have been found on both pre- and postsynaptic membranes.^[9]

Also, different mGluR subtypes are found predominantly in different parts of the body. For example, mGluR₄ is located only in the brain, in locations such as the thalamus, hypothalamus and caudate nucleus.^[20] All mGluRs except mGluR₆ are thought to exist in the hippocampus and entorhinal cortex.^[14]

Roles

It is thought that mGluRs play a role in a variety of different functions.

Modulation of other receptors

Metabotropic glutamate receptors are known to act as modulators of (affect the activity of) other receptors. For example, group I mGluRs are known to increase the activity of N-methyl-D-aspartate receptors (NMDARs),^[12]^[13] a type of ion channel-linked receptor that is central in a neurotoxic process called excitotoxicity. Proteins called PDZ proteins frequently anchor mGluRs near enough to NMDARs to modulate their activity.^[21]

It has been suggested that mGluRs may act as regulators of neurons' vulnerability to excitotoxicity (a deadly neurochemical process involving glutamate receptor overactivation) through their modulation of NMDARs, the receptor most involved in that process.^[22] Excessive amounts of N-methyl-D-aspartate (NMDA), the selective specific agonist of NMDARs, has been found to cause more damage to neurons in the presence of group I mGluR agonists.^[23] On the other hand, agonists of group II^[24] and III mGluRs reduce NMDAR activity.^[15]

Group II^[25] and III^[23] mGluRs tend to protect neurons from excitotoxicity,^[15]^[26]^[27] possibly by reducing the activity of NMDARs.

Metabotropic glutamate receptors are also thought to affect dopaminergic and adrenergic neurotransmission.^[28]

Role in plasticity

Like other glutamate receptors, mGluRs have been shown to be involved in synaptic plasticity^[2]^[9] and in neurotoxicity and neuroprotection.^[29]^[30]

They participate in long term potentiation and long term depression, and they are removed from the synaptic membrane in response to agonist binding.^[17]

Roles in disease

Since metabotropic glutamate receptors are involved in a variety of functions, abnormalities in their expression can contribute to disease. For example, studies with mutant mice have suggested that mutations in expression of mGluR₁ may be involved in the development of certain types of cancer.^[31] In addition, manipulating mGluRs can be useful in treating some conditions. For example, clinical trial suggested that an mGlu_2/3 agonist, LY354740, was effective in the treatment of generalized anxiety disorder.^[32] Also, some researchers have suggested that activation of mGluR₄ could be used as a treatment for Parkinson's disease.^[33] Most recently, Group I mGluRs, have been implicated in the pathogenesis of Fragile X, a type of autism,^[34] and a number of studies are currently testing the therapeutic potential of drugs that modify these receptors.^[35] There is also growing evidence that group II metabotropic glutamate receptor agonists may play a role in the treatment of schizophrenia. Schizophrenia is associated with deficits in cortical inhibitory interneurons that release GABA and synaptic abnormalities associated with deficits in NMDA receptor function.^[36] These inhibitory deficits may impair cortical function via cortical disinhibition and asynchrony.^[37] An mGluR_2/3 agonist was shown to attenuate physiologic and cognitive abnormalities in animal and human studies of NMDA receptor antagonist and serotonergic hallucinogen effects,^[38]^[39]^[40]^[41] supporting the subsequent clinical evidence of efficacy for an mGluR_2/3 agonist in the treatment of schizophrenia.^[42]

History

The first demonstration that glutamate could induce the formation of molecules belonging to a major second messenger system was in 1985, when it was shown that it could stimulate the formation of inositol phosphates.^[43] This finding allowed in 1987 to yield an explanation for oscillatory ionic glutamate responses and to provide further evidence for the existence of metabotropic glutamate receptors.^[44] In 1991 the first metabotropic glutamate receptor of the seven transmembrane domain family was cloned.^[45] More recent reports on ionotropic glutamate receptors able to couple to metabotropic transduction systems^[46]^[47] suggest that metabotropic responses of glutamate might not be limited to seven transmembrane domain metabotropic glutamate receptors. Currently, Dr. Mark Schmidt has worked on the most mGlu receptors of anyone in the world (mGlu2 and mGlu8).

References

^ Kammermeier PJ (2006). "Surface clustering of metabotropic glutamate receptor 1 induced by long Homer proteins". BMC Neurosci 7: 1. doi:10.1186/1471-2202-7-1. PMC 1361788. PMID 16393337.
^ ^a ^b ^c ^d ^e ^f Bonsi P, Cuomo D, De Persis C, Centonze D, Bernardi G, Calabresi P, Pisani A (2005). "Modulatory action of metabotropic glutamate receptor (mGluR) 5 on mGluR1 function in striatal cholinergic interneurons". Neuropharmacology. 49. Suppl 1: 104–13. doi:10.1016/j.neuropharm.2005.05.012. PMID 16005029.
^ ^a ^b Ohashi H, Maruyama T, Higashi-Matsumoto H, Nomoto T, Nishimura S, Takeuchi Y (2002). "A novel binding assay for metabotropic glutamate receptors using [3H] L-quisqualic acid and recombinant receptors" (subscription required). Z. Naturforsch., C, J. Biosci. 57 (3-4): 348–55. PMID 12064739.
^ ^a ^b ^c Hinoi E, Ogita K, Takeuchi Y, Ohashi H, Maruyama T, Yoneda Y (2001). "Characterization with [3H]quisqualate of group I metabotropic glutamate receptor subtype in rat central and peripheral excitable tissues". Neurochem. Int. 38 (3): 277–85. doi:10.1016/S0197-0186(00)00075-9. PMID 11099787.
^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j ^k ^l ^m Chu Z, Hablitz JJ (2000). "Quisqualate induces an inward current via mGluR activation in neocortical pyramidal neurons". Brain Res. 879 (1-2): 88–92. doi:10.1016/S0006-8993(00)02752-9. PMID 11011009.
^ ^a ^b Platt SR (2007). "The role of glutamate in central nervous system health and disease--a review". Vet. J. 173 (2): 278–86. doi:10.1016/j.tvjl.2005.11.007. PMID 16376594.
^ Gabriel L, Lvov A, Orthodoxou D, Rittenhouse A, Kobertz W, Melikian H (2012). "The Acid-sensitive, Anesthetic-activated Potassium Leak Channel, KCNK3, Is Regulated by 14-3-3β-dependent, Protein Kinase C (PKC)-mediated Endocytic Trafficking". JBC 287 (39): 32354–32366. doi:10.1074/jbc.M112.391458. PMID 22846993.
^ Sladeczek F., Momiyama A.,Takahashi T. (1992). "Presynaptic inhibitory action of metabotropic glutamate receptor agonist on excitatory transmission in visual cortical neurons". Proc. Roy. Soc. Lond. B 1993 253, 297-303.
^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ Endoh T (2004). "Characterization of modulatory effects of postsynaptic metabotropic glutamate receptors on calcium currents in rat nucleus tractus solitarius". Brain Res. 1024 (1-2): 212–24. doi:10.1016/j.brainres.2004.07.074. PMID 15451384.
^ ^a ^b If not otherwise specified in table:TABLE 1 Classification of the metabotropic glutamate (mGlu) receptors From the following article:
^ Swanson CJ, Bures M, Johnson MP, Linden AM, Monn JA, Schoepp DD (2005). "Metabotropic glutamate receptors as novel targets for anxiety and stress disorders". Nat Rev Drug Discov 4 (2): 131–44. doi:10.1038/nrd1630. PMID 15665858.
^ ^a ^b Skeberdis VA, Lan J, Opitz T, Zheng X, Bennett MV, Zukin RS (2001). "mGluR1-mediated potentiation of NMDA receptors involves a rise in intracellular calcium and activation of protein kinase C". Neuropharmacology 40 (7): 856–65. doi:10.1016/S0028-3908(01)00005-3. PMID 11378156.
^ ^a ^b Lea PM, Custer SJ, Vicini S, Faden AI (2002). "Neuronal and glial mGluR5 modulation prevents stretch-induced enhancement of NMDA receptor current". Pharmacol. Biochem. Behav. 73 (2): 287–98. doi:10.1016/S0091-3057(02)00825-0. PMID 12117582.
^ ^a ^b ^c ^d ^e ^f ^g Shigemoto R, Kinoshita A, Wada E, Nomura S, Ohishi H, Takada M, Flor PJ, Neki A, Abe T, Nakanishi S, Mizuno N (1997). "Differential presynaptic localization of metabotropic glutamate receptor subtypes in the rat hippocampus" (abstract). J. Neurosci. 17 (19): 7503–22. PMID 9295396.
^ ^a ^b ^c ^d Ambrosini A, Bresciani L, Fracchia S, Brunello N, Racagni G (1995). "Metabotropic glutamate receptors negatively coupled to adenylate cyclase inhibit N-methyl-D-aspartate receptor activity and prevent neurotoxicity in mesencephalic neurons in vitro" (abstract). Mol. Pharmacol. 47 (5): 1057–64. PMID 7746273.
^ Bates B, Xie Y, Taylor N, Johnson J, Wu L, Kwak S, Blatcher M, Gulukota K, Paulsen JE (2002). "Characterization of mGluR5R, a novel, metabotropic glutamate receptor 5-related gene". Brain Res. Mol. Brain Res. 109 (1-2): 18–33. doi:10.1016/S0169-328X(02)00458-8. PMID 12531512.
^ ^a ^b MRC (Medical Research Council), Glutamate receptors: Structures and functions., University of Bristol Centre for Synaptic Plasticity (2003). Retrieved January 20, 2008.
^ Koike H, Iijima M, Chaki S. Involvement of the mammalian target of rapamycin signaling in the antidepressant-like effect of group II metabotropic glutamate receptor antagonists. Neuropharmacology. 2011 Dec;61(8):1419-23. PMID 21903115
^ Campo, B.; Kalinichev, M.; Lambeng, N.; Yacoubi, M. E.; Royer-Urios, I.; Schneider, M.; Legrand, C.; Parron, D. et al. (2011). "Characterization of an mGluR2/3 Negative Allosteric Modulator in Rodent Models of Depression". Journal of Neurogenetics 25 (4): 152–166. doi:10.3109/01677063.2011.627485. PMID 22091727. edit
^ InterPro. InterPro: IPR001786 Metabotropic glutamate receptor 4. Retrieved on January 20, 2008.
^ Tu JC, Xiao B, Naisbitt S, Yuan JP, Petralia RS, Brakeman P, Doan A, Aakalu VK, Lanahan AA, Sheng M, Worley PF (1999). "Coupling of mGluR/Homer and PSD-95 complexes by the Shank family of postsynaptic density proteins". Neuron 23 (3): 583–92. doi:10.1016/S0896-6273(00)80810-7. PMID 10433269.
^ Baskys A, Blaabjerg M (2005). "Understanding regulation of nerve cell death by mGluRs as a method for development of successful neuroprotective strategies". J. Neurol. Sci. 229-230: 201–9. doi:10.1016/j.jns.2004.11.028. PMID 15760640.
^ ^a ^b Bruno V, Copani A, Knöpfel T, Kuhn R, Casabona G, Dell'Albani P, Condorelli DF, Nicoletti F (1995). "Activation of metabotropic glutamate receptors coupled to inositol phospholipid hydrolysis amplifies NMDA-induced neuronal degeneration in cultured cortical cells". Neuropharmacology 34 (8): 1089–98. doi:10.1016/0028-3908(95)00077-J. PMID 8532158.
^ Buisson A, Yu SP, Choi DW (1996). "DCG-IV selectively attenuates rapidly triggered NMDA-induced neurotoxicity in cortical neurons". Eur. J. Neurosci. 8 (1): 138–43. doi:10.1111/j.1460-9568.1996.tb01174.x. PMID 8713457.
^ Bruno V, Battaglia G, Copani A, Giffard RG, Raciti G, Raffaele R, Shinozaki H, Nicoletti F (1995). "Activation of class II or III metabotropic glutamate receptors protects cultured cortical neurons against excitotoxic degeneration". Eur. J. Neurosci. 7 (9): 1906–13. doi:10.1111/j.1460-9568.1995.tb00712.x. PMID 8528465.
^ Allen JW, Ivanova SA, Fan L, Espey MG, Basile AS, Faden AI (1999). "Group II metabotropic glutamate receptor activation attenuates traumatic neuronal injury and improves neurological recovery after traumatic brain injury" (abstract). J. Pharmacol. Exp. Ther. 290 (1): 112–20. PMID 10381766.
^ Faden AI, Ivanova SA, Yakovlev AG, Mukhin AG (1997). "Neuroprotective effects of group III mGluR in traumatic neuronal injury". J. Neurotrauma 14 (12): 885–95. doi:10.1089/neu.1997.14.885. PMID 9475370.
^ Wang J-Q, Brownell A-L (2007). Development of metabotropic glutamate receptor ligands for neuroimaging. Current Medical Imaging Reviews 3 (3): 186-205. Retrieved on January 20, 2008.
^ Siliprandi R, Lipartiti M, Fadda E, Sautter J, Manev H (1992). "Activation of the glutamate metabotropic receptor protects retina against N-methyl-D-aspartate toxicity". Eur. J. Pharmacol. 219 (1): 173–4. doi:10.1016/0014-2999(92)90598-X. PMID 1397046.
^ Baskys A, Fang L, Bayazitov I (2005). "Activation of neuroprotective pathways by metabotropic group I glutamate receptors: a potential target for drug discovery?". Ann. N. Y. Acad. Sci. 1053 (1): 55–73. doi:10.1196/annals.1344.006. PMID 16179509.
^ Namkoong J, Shin SS, Lee HJ, Marín YE, Wall BA, Goydos JS, Chen S (2007). "Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma". Cancer Res. 67 (5): 2298–305. doi:10.1158/0008-5472.CAN-06-3665. PMID 17332361.
^ Dunayevich E, Erickson J, Levine L, Landbloom R, Schoepp DD, Tollefson GD (2007). "Efficacy and Tolerability of an mGlu_2/3 Agonist in the Treatment of Generalized Anxiety Disorder". Neuropsychopharmacology 33 (7): 1603. doi:10.1038/sj.npp.1301531. PMID 17712352.
^ Marino MJ, Williams DL, O'Brien JA, Valenti O, McDonald TP, Clements MK, Wang R, DiLella AG, Hess JF, Kinney GG, Conn PJ (2003). "Allosteric modulation of group III metabotropic glutamate receptor 4: a potential approach to Parkinson's disease treatment". Proc. Natl. Acad. Sci. U.S.A. 100 (23): 13668–73. doi:10.1073/pnas.1835724100. PMC 263871. PMID 14593202.
^ Dölen G, Osterweil E, Rao BS, Smith GB, Auerbach BD, Chattarji S, Bear MF (2007). "Correction of fragile X syndrome in mice". Neuron 56 (6): 955–62. doi:10.1016/j.neuron.2007.12.001. PMC 2199268. PMID 18093519.
^ Dölen G, Carpenter RL, Ocain TD, Bear MF (2010). "Mechanism-based approaches to treating fragile X". Pharmacol Ther 127 (1): 78–93. doi:10.1016/j.pharmthera.2010.02.008. PMID 20303363.
^ Krystal JH, D'Souza DC, Mathalon D, Perry E, Belger A, Hoffman R (2003). "NMDA receptor antagonist effects, cortical glutamatergic function, and schizophrenia: toward a paradigm shift in medication development". Psychopharmacology (Berl.) 169 (3-4): 215–33. doi:10.1007/s00213-003-1582-z. PMID 12955285.
^ Ford JM, Krystal JH, Mathalon DH (2007). "Neural synchrony in schizophrenia: from networks to new treatments". Schizophr Bull 33 (4): 848–52. doi:10.1093/schbul/sbm062. PMC 2632315. PMID 17567628.
^ Homayoun H, Jackson ME, Moghaddam B (2005). "Activation of metabotropic glutamate 2/3 receptors reverses the effects of NMDA receptor hypofunction on prefrontal cortex unit activity in awake rats". J. Neurophysiol. 93 (4): 1989–2001. doi:10.1152/jn.00875.2004. PMID 15590730.
^ Moghaddam B, Adams BW (1998). "Reversal of phencyclidine effects by a group II metabotropic glutamate receptor agonist in rats". Science 281 (5381): 1349–52. doi:10.1126/science.281.5381.1349. PMID 9721099.
^ Krystal JH, Abi-Saab W, Perry E, D'Souza DC, Liu N, Gueorguieva R, McDougall L, Hunsberger T, Belger A, Levine L, Breier A (2005). "Preliminary evidence of attenuation of the disruptive effects of the NMDA glutamate receptor antagonist, ketamine, on working memory by pretreatment with the group II metabotropic glutamate receptor agonist, LY354740, in healthy human subjects". Psychopharmacology (Berl.) 179 (1): 303–9. doi:10.1007/s00213-004-1982-8. PMID 15309376.
^ Aghajanian GK, Marek GJ (2000). "Serotonin model of schizophrenia: emerging role of glutamate mechanisms". Brain Res. Brain Res. Rev. 31 (2-3): 302–12. doi:10.1016/S0165-0173(99)00046-6. PMID 10719157.
^ Patil ST, Zhang L, Martenyi F, Lowe SL, Jackson KA, Andreev BV, Avedisova AS, Bardenstein LM, Gurovich IY, Morozova MA, Mosolov SN, Neznanov NG, Reznik AM, Smulevich AB, Tochilov VA, Johnson BG, Monn JA, Schoepp DD (2007). "Activation of mGlu2/3 receptors as a new approach to treat schizophrenia: a randomized Phase 2 clinical trial". Nat. Med. 13 (9): 1102–7. doi:10.1038/nm1632. PMID 17767166.
^ Sladeczek F, Pin JP, Récasens M, Bockaert J, Weiss S (1985). "Glutamate stimulates inositol phosphate formation in striatal neurones". Nature 317 (6039): 717–9. doi:10.1038/317717a0. PMID 2865680.
^ Sugiyama H, Ito I, Hirono C (1987). "A new type of glutamate receptor linked to inositol phospholipid metabolism". Nature 325 (6104): 531–3. doi:10.1038/325531a0. PMID 2880300.
^ Masu M, Tanabe Y, Tsuchida K, Shigemoto R, Nakanishi S (February 1991). "Sequence and expression of a metabotropic glutamate receptor". Nature 349 (6312): 760–5. doi:10.1038/349760a0. PMID 1847995.
^ Dingledine R, Borges K, Bowie D, Traynelis SF (March 1999). "The glutamate receptor ion channels". Pharmacol. Rev. 51 (1): 7–61. PMID 10049997.
^ Wang Y, Small DL, Stanimirovic DB, Morley P, Durkin JP (October 1997). "AMPA receptor-mediated regulation of a Gi-protein in cortical neurons". Nature 389 (6650): 502–4. doi:10.1038/39062. PMID 9333240.

External links

Metabotropic Glutamate Receptors at the US National Library of Medicine Medical Subject Headings (MeSH)

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1. 脆弱X症候群：小児および思春期におけるマネージメント fragile x syndrome management in children and adolescents

English Journal

Epileptic stimulus increases Homer 1a expression to modulate endocannabinoid signaling in cultured hippocampal neurons.

Li Y, Krogh KA, Thayer SA.SourceDepartment of Pharmacology, University of Minnesota Medical School, 6-120 Jackson Hall, 321 Church Street, Minneapolis, MN 55455, USA.
Neuropharmacology.Neuropharmacology.2012 Nov;63(6):1140-9. Epub 2012 Jul 16.
Endocannabinoid (eCB) signaling serves as an on-demand neuroprotective system. eCBs are produced postsynaptically in response to depolarization or activation of metabotropic glutamate receptors (mGluRs) and act on presynaptic cannabinoid receptor-1 to suppress synaptic transmission. Here, we examine
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β-Estradiol unmasks metabotropic receptor-mediated metaplasticity of NMDA receptor transmission in the female rat dentate gyrus.

Nebieridze N, Zhang XL, Chachua T, Velíšek L, Stanton PK, Velíšková J.SourceDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY, USA.
Psychoneuroendocrinology.Psychoneuroendocrinology.2012 Nov;37(11):1845-54. doi: 10.1016/j.psyneuen.2012.03.023. Epub 2012 Apr 27.
Loss of estrogen in women following menopause is associated with increased risk for cognitive decline, dementia and depression, all of which can be prevented by estradiol replacement. The dentate gyrus plays an important role in cognition, learning and memory. The gatekeeping function of the dentate
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Japanese Journal

Ca(2+)-dependent binding of calcium-binding protein 1 to presynaptic group III metabotropic glutamate receptors and blockage by phosphorylation of the receptors.

Nakajima Yoshiaki
Biochemical and biophysical research communications 412(4), 602-605, 2011-09-09
Presynaptic group III metabotropic glutamate receptors (mGluRs) and Ca(2+) channels are the main neuronal activity-dependent regulators of synaptic vesicle release, and they use common molecules in th …
NAID 80021990000

神経系前駆細胞における機能的グルタミン酸シグナリング

中道範隆
薬学雑誌 131(9), 1311-1316, 2011
… In this review, we have summarized our recent studies on the functionality of ionotropic (iGluR) and metabotropic (mGluR) glutamate receptors expressed by undifferentiated neural progenitor cells (NPC) isolated from embryonic rat and mouse brains. … Reverse transcription polymerase chain reaction analyses revealed expression of mRNA for particular iGluR and mGluR subtypes in NPC. …
NAID 40018967174

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