keyword
https://read.qxmd.com/read/38691510/novel-inhibitory-site-revealed-by-xap044-mode-of-action-on-the-metabotropic-glutamate-7-receptor-venus-flytrap-domain
#1
JOURNAL ARTICLE
Nunzia Cristiano, Alexandre Cabayé, Isabelle Brabet, Ralf Glatthar, Amelie Tora, Cyril Goudet, Hugues-Olivier Bertrand, Anne Goupil-Lamy, Peter J Flor, Jean-Philippe Pin, Isabelle McCort-Tranchepain, Francine C Acher
Metabotropic glutamate (mGlu) receptors play a key role in modulating most synapses in the brain. The mGlu7 receptors inhibit presynaptic neurotransmitter release and offer therapeutic possibilities for post-traumatic stress disorders or epilepsy. Screening campaigns provided mGlu7-specific allosteric modulators as the inhibitor XAP044 (Gee et al. J. Biol. Chem. 2014 ). In contrast to other mGlu receptor allosteric modulators, XAP044 does not bind in the transmembrane domain but to the extracellular domain of the mGlu7 receptor and not at the orthosteric site...
May 1, 2024: Journal of Medicinal Chemistry
https://read.qxmd.com/read/38689353/control-of-astrocytic-ca-2-signaling-by-nitric-oxide-dependent-s-nitrosylation-of-ca-2-homeostasis-modulator-1-channels
#2
JOURNAL ARTICLE
Mariela Puebla, Manuel F Muñoz, Mauricio A Lillo, Jorge E Contreras, Xavier F Figueroa
BACKGROUND: Astrocytes Ca2+ signaling play a central role in the modulation of neuronal function. Activation of metabotropic glutamate receptors (mGluR) by glutamate released during an increase in synaptic activity triggers coordinated Ca2+ signals in astrocytes. Importantly, astrocytes express the Ca2+ -dependent nitric oxide (NO)-synthetizing enzymes eNOS and nNOS, which might contribute to the Ca2+ signals by triggering Ca2+ influx or ATP release through the activation of connexin 43 (Cx43) hemichannels, pannexin-1 (Panx-1) channels or Ca2+ homeostasis modulator 1 (CALHM1) channels...
April 30, 2024: Biological Research
https://read.qxmd.com/read/38672234/two-signaling-modes-are-better-than-one-flux-independent-signaling-by-ionotropic-glutamate-receptors-is-coming-of-age
#3
REVIEW
Valentina Brunetti, Teresa Soda, Roberto Berra-Romani, Giovambattista De Sarro, Germano Guerra, Giorgia Scarpellino, Francesco Moccia
Glutamate is the major excitatory neurotransmitter in the central nervous system. Glutamatergic transmission can be mediated by ionotropic glutamate receptors (iGluRs), which mediate rapid synaptic depolarization that can be associated with Ca2+ entry and activity-dependent change in the strength of synaptic transmission, as well as by metabotropic glutamate receptors (mGluRs), which mediate slower postsynaptic responses through the recruitment of second messenger systems. A wealth of evidence reported over the last three decades has shown that this dogmatic subdivision between iGluRs and mGluRs may not reflect the actual physiological signaling mode of the iGluRs, i...
April 16, 2024: Biomedicines
https://read.qxmd.com/read/38664401/dietary-l-glu-sensing-by-enteroendocrine-cells-adjusts-food-intake-via-modulating-gut-pyy-npf-secretion
#4
JOURNAL ARTICLE
Junjun Gao, Song Zhang, Pan Deng, Zhigang Wu, Bruno Lemaitre, Zongzhao Zhai, Zheng Guo
Amino acid availability is monitored by animals to adapt to their nutritional environment. Beyond gustatory receptors and systemic amino acid sensors, enteroendocrine cells (EECs) are believed to directly percept dietary amino acids and secrete regulatory peptides. However, the cellular machinery underlying amino acid-sensing by EECs and how EEC-derived hormones modulate feeding behavior remain elusive. Here, by developing tools to specifically manipulate EECs, we find that Drosophila neuropeptide F (NPF) from mated female EECs inhibits feeding, similar to human PYY...
April 25, 2024: Nature Communications
https://read.qxmd.com/read/38659864/cholesterol-dependence-of-the-conformational-changes-in-metabotropic-glutamate-receptor-1
#5
Ugochi H Isu, Shadi A Badiee, Adithya Polasa, Seyed H Tabari, Mortaza Derakhshani-Molayousefi, Mahmoud Moradi
Metabotropic glutamate receptors (mGluRs) are class C G protein-coupled receptors that function as obligate dimers in regulating neurotransmission and synaptic plasticity in the central nervous system. The mGluR1 subtype has been shown to be modulated by the membrane lipid environment, particularly cholesterol, though the molecular mechanisms remain elusive. In this study, we employed all-atom molecular dynamics simulations to investigate the effects of cholesterol on the conformational dynamics of the mGluR1 seven-transmembrane (7TM) domain in an inactive state model...
April 20, 2024: bioRxiv
https://read.qxmd.com/read/38657042/shp2-regulates-glua2-tyrosine-phosphorylation-required-for-ampa-receptor-endocytosis-and-mglur-ltd
#6
JOURNAL ARTICLE
Sanghyeon Lee, Jungho Kim, Hyun-Hee Ryu, Hanbyul Jang, DoEun Lee, Seungha Lee, Jae-Man Song, Yong-Seok Lee, Young Ho Suh
Posttranslational modifications regulate the properties and abundance of synaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors that mediate fast excitatory synaptic transmission and synaptic plasticity in the central nervous system. During long-term depression (LTD), protein tyrosine phosphatases (PTPs) dephosphorylate tyrosine residues in the C-terminal tail of AMPA receptor GluA2 subunit, which is essential for GluA2 endocytosis and group I metabotropic glutamate receptor (mGluR)-dependent LTD...
April 30, 2024: Proceedings of the National Academy of Sciences of the United States of America
https://read.qxmd.com/read/38653345/s-3-4-dcpg-a-potent-orthosteric-agonist-for-the-mglu8-receptor-facilitates-extinction-and-inhibits-the-reinstatement-of-morphine-induced-conditioned-place-preference-in-male-rats
#7
JOURNAL ARTICLE
Nazanin Kahvandi, Zahra Ebrahimi, Maryam Sharifi, Seyed Asaad Karimi, Siamak Shahidi, Iraj Salehi, Rasool Haddadi, Abdolrahman Sarihi
The limbic system, particularly the NAc, shows a high concentration of metabotropic glutamate receptors (mGluRs). Recent evidence suggests the significant involvement of mGluRs in mental disorders, including substance abuse and addiction. The objective of this study was to examine the involvement of mGlu8 receptors in the NAc in the mechanisms underlying the extinction and reinstatement of conditioned place preference (CPP) induced by morphine. Male Wistar rats underwent surgical implantation of bilateral cannulas in the NAc and were assessed in a CPP protocol...
April 21, 2024: Pharmacology, Biochemistry, and Behavior
https://read.qxmd.com/read/38609494/metabotropic-glutamate-receptor-genetic-variants-and-peripheral-receptor-expression-affects-trait-scores-of-autistic-probands
#8
JOURNAL ARTICLE
Nilanjana Dutta, Mahasweta Chatterjee, Sharmistha Saha, Swagata Sinha, Kanchan Mukhopadhyay
Glutamate (Glu) is important for memory and learning. Hence, Glu imbalance is speculated to affect autism spectrum disorder (ASD) pathophysiology. The action of Glu is mediated through receptors and we analyzed four metabotropic Glu receptors (mGluR/GRM) in Indo-Caucasoid families with ASD probands and controls. The trait scores of the ASD probands were assessed using the Childhood Autism Rating Scale2-ST. Peripheral blood was collected, genomic DNA isolated, and GRM5 rs905646, GRM6 rs762724 & rs2067011, and GRM7 rs3792452 were analyzed by PCR/RFLP or Taqman assay...
April 12, 2024: Scientific Reports
https://read.qxmd.com/read/38566234/synaptopodin-is-required-for-long-term-depression-at-schaffer-collateral-ca1-synapses
#9
JOURNAL ARTICLE
Yanis Inglebert, Pei You Wu, Julia Tourbina-Kolomiets, Cong Loc Dang, R Anne McKinney
Synaptopodin (SP), an actin-associated protein found in telencephalic neurons, affects activity-dependant synaptic plasticity and dynamic changes of dendritic spines. While being required for long-term depression (LTD) mediated by metabotropic glutamate receptor (mGluR-LTD), little is known about its role in other forms of LTD induced by low frequency stimulation (LFS-LTD) or spike-timing dependent plasticity (STDP). Using electrophysiology in ex vivo hippocampal slices from SP-deficient mice (SPKO), we show that absence of SP is associated with a deficit of LTD at Sc-CA1 synapses induced by LFS-LTD and STDP...
April 2, 2024: Molecular Brain
https://read.qxmd.com/read/38566016/multiple-serum-anti-glutamate-receptor-antibody-levels-in-clozapine-treated-na%C3%A3-ve-patients-with-treatment-resistant-schizophrenia
#10
JOURNAL ARTICLE
Jingqi He, Jinguang Li, Yisen Wei, Zhangyin He, Junyu Liu, Ning Yuan, Risheng Zhou, Xingtao He, Honghong Ren, Lin Gu, Yanhui Liao, Xiaogang Chen, Jinsong Tang
BACKGROUND: Glutamatergic function abnormalities have been implicated in the etiology of treatment-resistant schizophrenia (TRS), and the efficacy of clozapine may be attributed to its impact on the glutamate system. Recently, evidence has emerged suggesting the involvement of immune processes and increased prevalence of antineuronal antibodies in TRS. This current study aimed to investigate the levels of multiple anti-glutamate receptor antibodies in TRS and explore the effects of clozapine on these antibody levels...
April 2, 2024: BMC Psychiatry
https://read.qxmd.com/read/38531909/preso-enhances-mglur1-mediated-excitotoxicity-by-modulating-the-phosphorylation-of-mglur1-homer1-complex-and-facilitating-an-er-stress-after-traumatic-brain-injury
#11
JOURNAL ARTICLE
Zhuoyuan Zhang, Xiangyu Gao, Zhicheng Tian, Erwan Yang, Yutao Huang, Dan Liu, Shuhui Dai, Haofuzi Zhang, Mingdong Bao, Xiaofan Jiang, Xin Li, Peng Luo
Glutamate receptor (GluR)-mediated excitotoxicity is an important mechanism causing delayed neuronal injury after traumatic brain injury (TBI). Preso, as a core scaffolding protein of postsynaptic density (PSD), is considered an important regulator during excitotoxicity and TBI and combines with glutamate receptors to form functional units for excitatory glutamatergic neurotransmission, and elucidating the mechanisms of these functional units will provide new targets for the treatment of TBI. As a multidomain scaffolding protein, Preso directly interacts with metabotropic GluR (mGluR) and another scaffold protein, Homer...
March 26, 2024: Cell Death Discovery
https://read.qxmd.com/read/38472268/impairments-in-the-early-consolidation-of-spatial-memories-via-group-ii-mglur-agonism-in-the-mammillary-bodies
#12
JOURNAL ARTICLE
Michal M Milczarek, James C Perry, Eman Amin, Salma Haniffa, Thomas Hathaway, Seralynne D Vann
mGluR2 receptors are widely expressed in limbic brain regions associated with memory, including the hippocampal formation, retrosplenial and frontal cortices, as well as subcortical regions including the mammillary bodies. mGluR2/3 agonists have been proposed as potential therapeutics for neurological and psychiatric disorders, however, there is still little known about the role of these receptors in cognitive processes, including memory consolidation. To address this, we assessed the effect of the mGluR2/3 agonist, eglumetad, on spatial memory consolidation in both mice and rats...
March 12, 2024: Scientific Reports
https://read.qxmd.com/read/38426491/challenges-in-developing-therapies-in-fragile-x-syndrome-how-the-fxlearn-trial-can-guide-research
#13
JOURNAL ARTICLE
Jeffrey L Neul
Fragile X syndrome (FXS), the most common inherited cause of intellectual disability and the single-gene cause of autism, is caused by decreased expression of the fragile X messenger ribonucleoprotein protein (FMRP), a ribosomal-associated RNA-binding protein involved in translational repression. Extensive preclinical work in several FXS animal models supported the therapeutic potential of decreasing metabotropic glutamate receptor (mGluR) signaling to correct translation of proteins related to synaptic plasticity; however, multiple clinical trials failed to show conclusive evidence of efficacy...
March 1, 2024: Journal of Clinical Investigation
https://read.qxmd.com/read/38396013/effect-of-antipsychotic-drugs-on-group-ii-metabotropic-glutamate-receptor-expression-and-epigenetic-control-in-postmortem-brains-of-schizophrenia-subjects
#14
JOURNAL ARTICLE
Jon DelaCuesta-Barrutia, Oihane Martínez-Peula, Guadalupe Rivero, Jon A Santas-Martín, Eva Munarriz-Cuezva, Iria Brocos-Mosquera, Patricia Miranda-Azpiazu, Rebeca Diez-Alarcia, Benito Morentin, William G Honer, Luis F Callado, Amaia M Erdozain, Alfredo Ramos-Miguel
Antipsychotic-induced low availability of group II metabotropic glutamate receptors (including mGlu2 R and mGlu3 R) in brains of schizophrenia patients may explain the limited efficacy of mGlu2/3 R ligands in clinical trials. Studies evaluating mGlu2/3 R levels in well-designed, large postmortem brain cohorts are needed to address this issue. Postmortem samples from the dorsolateral prefrontal cortex of 96 schizophrenia subjects and matched controls were collected. Toxicological analyses identified cases who were (AP+) or were not (AP-) receiving antipsychotic treatment near the time of death...
February 23, 2024: Translational Psychiatry
https://read.qxmd.com/read/38384385/loss-of-synaptopodin-impairs-mglur5-and-protein-synthesis-dependent-mglur-ltd-at-ca3-ca1-synapses
#15
JOURNAL ARTICLE
Pei You Wu, Linjia Ji, Claudia De Sanctis, Anna Francesconi, Yanis Inglebert, R Anne McKinney
Metabotropic glutamate receptor-dependent long-term depression (mGluR-LTD) is an important form of synaptic plasticity that occurs in many regions of the central nervous system and is the underlying mechanism for several learning paradigms. In the hippocampus, mGluR-LTD is manifested by the weakening of synaptic transmission and elimination of dendritic spines. Interestingly, not all spines respond or undergo plasticity equally in response to mGluR-LTD. A subset of dendritic spines containing synaptopodin (SP), an actin-associated protein is critical for mGluR-LTD and protects spines from elimination through mGluR1 activity...
February 2024: PNAS Nexus
https://read.qxmd.com/read/38339206/neuropharmacological-evidence-implicating-drug-induced-glutamate-receptor-dysfunction-in-affective-and-cognitive-sequelae-of-subchronic-methamphetamine-self-administration-in-mice
#16
JOURNAL ARTICLE
Christopher J E Denning, Lauren E Madory, Jessica N Herbert, Ryan A Cabrera, Karen K Szumlinski
Methamphetamine (MA) is a highly addictive drug, and MA use disorder is often comorbid with anxiety and cognitive impairment. These comorbid conditions are theorized to reflect glutamate-related neurotoxicity within the frontal cortical regions. However, our prior studies of MA-sensitized mice indicate that subchronic, behaviorally non-contingent MA treatment is sufficient to dysregulate glutamate transmission in mouse brain. Here, we extend this prior work to a mouse model of high-dose oral MA self-administration (0...
February 5, 2024: International Journal of Molecular Sciences
https://read.qxmd.com/read/38309326/altered-neuronal-group-1-metabotropic-glutamate-receptor-and-endoplasmic-reticulum-mediated-ca-2-signaling-in-two-rodent-models-of-alzheimer-s-disease
#17
JOURNAL ARTICLE
Aidan Kaar, Megan P Weir, Mark G Rae
Calcium mobilization from the endoplasmic reticulum (ER) induced by, for example, IP3 receptor (IP3 R) stimulation, and its subsequent crosstalk with extracellular Ca2+ influx mediated through voltage-gated calcium channels (VGCCs) and neuronal store-operated calcium entry (nSOCE), is essential for normal neuronal signaling and cellular homeostasis. However, several studies suggest that chronic calcium dysregulation may play a key role in the onset and/or progression of neurodegenerative conditions, particularly Alzheimer's disease (AD)...
February 16, 2024: Neuroscience Letters
https://read.qxmd.com/read/38297084/src-family-kinase-inhibition-rescues-molecular-and-behavioral-phenotypes-but-not-protein-interaction-network-dynamics-in-a-mouse-model-of-fragile-x-syndrome
#18
JOURNAL ARTICLE
Vera Stamenkovic, Jonathan D Lautz, Felicia M Harsh, Stephen E P Smith
Glutamatergic synapses encode information from extracellular inputs using dynamic protein interaction networks (PINs) that undergo widespread reorganization following synaptic activity, allowing cells to distinguish between signaling inputs and generate coordinated cellular responses. Here, we investigate how Fragile X Messenger Ribonucleoprotein (FMRP) deficiency disrupts signal transduction through a glutamatergic synapse PIN downstream of NMDA receptor or metabotropic glutamate receptor (mGluR) stimulation...
January 31, 2024: Molecular Psychiatry
https://read.qxmd.com/read/38295164/gamma-oscillation-plasticity-is-mediated-via-parvalbumin-interneurons
#19
JOURNAL ARTICLE
Michael D Hadler, Alexandra Tzilivaki, Dietmar Schmitz, Henrik Alle, Jörg R P Geiger
Understanding the plasticity of neuronal networks is an emerging field of (patho-) physiological research, yet the underlying cellular mechanisms remain poorly understood. Gamma oscillations (30 to 80 hertz), a biomarker of cognitive performance, require and potentiate glutamatergic transmission onto parvalbumin-positive interneurons (PVIs), suggesting an interface for cell-to-network plasticity. In ex vivo local field potential recordings, we demonstrate long-term potentiation of hippocampal gamma power. Gamma potentiation obeys established rules of PVI plasticity, requiring calcium-permeable AMPA receptors (CP-AMPARs) and metabotropic glutamate receptors (mGluRs)...
February 2, 2024: Science Advances
https://read.qxmd.com/read/38278430/a-molecular-perspective-on-mglur5-regulation-in-the-antidepressant-effect-of-ketamine
#20
REVIEW
Ola Sobhy A Elmeseiny, Heidi Kaastrup Müller
Ketamine, a non-competitive N-methyl-D-aspartate receptor (NMDAR) antagonist, has received much attention for its rapid antidepressant effects. A single administration of ketamine elicits rapid and sustained antidepressant effects in both humans and animals. Current efforts are focused on uncovering molecular mechanisms responsible for ketamine's antidepressant activity. Ketamine primarily acts via the glutamatergic pathway, and increasing evidence suggests that ketamine induces synaptic and structural plasticity through increased translation and release of neurotrophic factors, activation of mammalian target of rapamycin (mTOR), and α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor (AMPAR)-mediated synaptic potentiation...
February 2024: Pharmacological Research: the Official Journal of the Italian Pharmacological Society
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