Opioid Receptor-Mediated Regulation of Neurotransmission in the Brain
Опосредованная опиоидными рецепторами регуляция нейротрансмиссии в головном мозге
2022-06-15
SCID: 54.1/urvbk684
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brain regionsneural circuitsneurotransmitter releaseopioid receptorssynaptic transmission
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Abstract (AI)
opioid receptors: mu, delta, and kappa. At the neuronal level, opioid receptors are generally inhibitory, presynaptically reducing neurotransmitter release and postsynaptically hyperpolarizing neurons. However, opioid receptor-mediated regulation of neuronal function and synaptic transmission is not uniform in expression pattern and mechanism across the brain. The localization of receptors within specific cell types and neurocircuits determine the effects that endogenous and exogenous opioids have on brain function. In this review we will explore the similarities and differences in opioid receptor-mediated regulation of neurotransmission across different brain regions. We discuss how future studies can consider potential cell-type, regional, and neural pathway-specific effects of opioid receptors in order to better understand how opioid receptors modulate brain function.
Key Findings
1
Mu, delta, and kappa opioid receptors generally inhibit neuronal activity by presynaptically reducing neurotransmitter release and postsynaptically hyperpolarizing neurons.
2
Opioid receptor-mediated regulation of neurotransmission varies across brain regions in both receptor expression patterns and underlying mechanisms.
3
Receptor localization within specific neuronal cell types and neural circuits determines how endogenous and exogenous opioids affect brain function.
4
Understanding opioid modulation requires consideration of cell-type-, regional-, and pathway-specific effects across distinct brain networks.
Research Object
opioid receptor-mediated neurotransmission in the brain
Research Subject
the cell-type-, brain-region-, and neural-pathway-specific mechanisms and effects of mu, delta, and kappa opioid receptor regulation of neurotransmitter release, neuronal excitability, and synaptic transmission
Publication Details
Publication Date
2022-06-15
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