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Difference between revisions of "Role of Metabotropic Glutamate Receptors in Pain"
Role of Metabotropic Glutamate Receptors in Pain (view source)
Revision as of 17:34, 19 October 2024
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{{ArtBy|||autore=Silvia Natoli|autore2=Cesare Iani|autore3=Massimo Tolu|autore4=Antonio Pisani}} | {{ArtBy|||autore=Silvia Natoli|autore2=Cesare Iani|autore3=Massimo Tolu|autore4=Antonio Pisani}} | ||
Glutamic acid is the most widespread excitatory neurotransmitter in the Central Nervous System (CNS), playing a critical role in numerous physiological and pathological processes. The discovery of metabotropic glutamate receptors (mGlu), a class of G-protein-coupled receptors, has led to extensive research exploring their function in both normal and diseased states. These receptors are divided into ionotropic and metabotropic types, with the latter being further subdivided into three groups based on their structure and function. | '''Abstract:''' Glutamic acid is the most widespread excitatory neurotransmitter in the Central Nervous System (CNS), playing a critical role in numerous physiological and pathological processes. The discovery of metabotropic glutamate receptors (mGlu), a class of G-protein-coupled receptors, has led to extensive research exploring their function in both normal and diseased states. These receptors are divided into ionotropic and metabotropic types, with the latter being further subdivided into three groups based on their structure and function. | ||
Group I mGlu receptors (mGlu1 and mGlu5) are involved in modulating neuronal excitability by activating ion channels, contributing to the pathogenesis of various CNS disorders such as epilepsy, ischemia, and neurodegenerative diseases. Recent studies highlight their involvement in nociceptive transmission, showing that they play a crucial role in pain signaling at both spinal and cortical levels. Their activation can influence both ionotropic and metabotropic receptor pathways, leading to excitotoxicity, a key factor in neuronal injury during conditions like stroke, Parkinson’s, and Alzheimer’s disease. | Group I mGlu receptors (mGlu1 and mGlu5) are involved in modulating neuronal excitability by activating ion channels, contributing to the pathogenesis of various CNS disorders such as epilepsy, ischemia, and neurodegenerative diseases. Recent studies highlight their involvement in nociceptive transmission, showing that they play a crucial role in pain signaling at both spinal and cortical levels. Their activation can influence both ionotropic and metabotropic receptor pathways, leading to excitotoxicity, a key factor in neuronal injury during conditions like stroke, Parkinson’s, and Alzheimer’s disease. | ||