نتایج جستجو برای: glutamatergic transmission

تعداد نتایج: 251772  

Journal: :Molecular pharmacology 2001
S Ahmadi C Kotalla H Gühring H Takeshima A Pahl H U Zeilhofer

Nociceptin/orphanin FQ (N/OFQ) and nocistatin (NST) are two neuropeptides derived from the same precursor protein that exhibit opposing effects on spinal neurotransmission and nociception. Here, we have used whole-cell, patch-clamp recordings from visually identified neurons in spinal cord dorsal horn slices of genetically modified mice to investigate the role of the N/OFQ receptor (N/OFQ-R) in...

2012
John I. Broussard

In the 1934 Dixon lectures, Sir Henry Dale articulated that the chemical nature of each neuron is fixed and unchangeable (Dale, 1935). John Eccles elevated these observations to a principle in 1954 when he and colleagues postulated that “the same chemical transmitting substance is used at all junctions operated by a particular cell” (Eccles et al., 1954). Dale’s Principle had thus been interpre...

Journal: :Cell reports 2017
Ping Zhong Zhixing Hu Houbo Jiang Zhen Yan Jian Feng

Locomotor symptoms in Parkinson's disease (PD) are accompanied by widespread oscillatory neuronal activities in basal ganglia. Here, we show that activation of dopamine D1-class receptors elicits a large rhythmic bursting of spontaneous excitatory postsynaptic currents (sEPSCs) in midbrain neurons differentiated from induced pluripotent stem cells (iPSCs) of PD patients with parkin mutations, b...

Journal: :Journal of neurophysiology 2013
Shuijin He Li-Rong Shao Yu Wang Suzanne B Bausch

Chronic global N-methyl-d-aspartate receptor (NMDAR) blockade leads to changes in glutamatergic transmission. The impact of more subunit-selective NMDAR inhibition on glutamatergic circuits remains incomplete. To this end, organotypic hippocampal slice cultures were treated for 17-21 days with the high-affinity competitive antagonist d-aminophosphonovaleric acid (d-APV), the allosteric GluN2B-s...

2012
Shuijin He Li-Rong Shao Yu Wang Suzanne B. Bausch

36 37 Chronic global N-methyl-D-aspartate receptor (NMDAR) blockade leads to changes in 38 glutamatergic transmission. The impact of more subunit-selective NMDAR inhibition on glutamatergic 39 circuits remains incomplete. To this end organotypic hippocampal slice cultures were treated for 17-21 40 days with the: high-affinity competitive antagonist D-APV, allosteric GluN2B-selective antagonist ...

2015
Ming-fai Fong Jonathan P. Newman Steve M. Potter Peter Wenner

Homeostatic plasticity encompasses a set of mechanisms that are thought to stabilize firing rates in neural circuits. The most widely studied form of homeostatic plasticity is upward synaptic scaling (upscaling), characterized by a multiplicative increase in the strength of excitatory synaptic inputs to a neuron as a compensatory response to chronic reductions in firing rate. While reduced spik...

Journal: :Science 2008
Nathalie Rouach Annette Koulakoff Veronica Abudara Klaus Willecke Christian Giaume

Astrocytes provide metabolic substrates to neurons in an activity-dependent manner. However, the molecular mechanisms involved in this function, as well as its role in synaptic transmission, remain unclear. Here, we show that the gap-junction subunit proteins connexin 43 and 30 allow intercellular trafficking of glucose and its metabolites through astroglial networks. This trafficking is regula...

Journal: :Current opinion in neurobiology 2011
Weifeng Xu

Activity-dependent modification of excitatory synaptic transmission is a fundamental mechanism for developmental plasticity of the neural circuits and experience-dependent plasticity. Synaptic glutamatergic receptors including AMPA receptors and NMDA receptors (AMPARs and NMDARs) are embedded in the postsynaptic density, a highly organized protein network. Overwhelming data have shown that PSD-...

Journal: :Molecular pharmacology 2007
Delany Torres-Salazar Christoph Fahlke

Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system. After release from glutamatergic nerve terminals, glial and neuronal glutamate transporters remove glutamate from the synaptic cleft to terminate synaptic transmission and to prevent neuronal damage by excessive glutamate receptor activation. In this issue of Molecular Pharmacology, Fontana et al. (p. 12...

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