TY - CHAP
T1 - Ethanol-Taurine Interactions in the Brain
T2 - Mechanisms and Pathophysiological Implications
AU - Albrecht, Jan
AU - Zielinska, Magdalena
AU - Allen, J. W.
AU - Soldin, Offie P.
AU - Aschner, Michael
N1 - Funding Information:
This study was supported by Public Health Service Grant AA 11617, ES07331 and ES10563 to M. A., and SCSR grant no 6P05A 00321 to J. A. and M. Z.
Publisher Copyright:
© 2004 Elsevier Ltd. All rights reserved.
PY - 2005
Y1 - 2005
N2 - This chapter discusses the interactions of ethanol and taurine in the brain and the mechanisms and pathophysiology. Taurine is a nonproteinaceous sulfur amino acid present at high concentrations both in neurons and astrocytes in different brain regions. Taurine is a γ-aminobutyric acidA (GABAA) and glycine receptor agonist in distinct regions of cerebral cortex, cerebellum, and hypothalamus. Taurine is also readily released from and taken up by astrocytes and neurons: its intercellular redistribution upon hyper- or hyposomotic challenge suggests that taurine partici- pates in cell volume regulation. In the neuro-endocrine structures of the hypothalamus, taurine released from astrocytes in response to hypotonic stimulus acts on glycine receptors in the adjacent neurons, contributing to hypotonic inhibition of neurosecretion of oxytocin and vasopressin. Exogenously added taurine is neuroprotective by an anti-excitotoxic mechanism, involving direct interaction with GABAA and/or ionotropic glutamate receptors, mostly of the N-methyl D-aspartate type. A plethora of stimuli trigger taurine release from astrocytes or neurons by mechanisms bypassing changes in the intracellular osmotic pressure, thus increasing the extracellular concentration of taurine and facilitating its neuromodulatory function. Ethanol and taurine share molecular targets in the brain.
AB - This chapter discusses the interactions of ethanol and taurine in the brain and the mechanisms and pathophysiology. Taurine is a nonproteinaceous sulfur amino acid present at high concentrations both in neurons and astrocytes in different brain regions. Taurine is a γ-aminobutyric acidA (GABAA) and glycine receptor agonist in distinct regions of cerebral cortex, cerebellum, and hypothalamus. Taurine is also readily released from and taken up by astrocytes and neurons: its intercellular redistribution upon hyper- or hyposomotic challenge suggests that taurine partici- pates in cell volume regulation. In the neuro-endocrine structures of the hypothalamus, taurine released from astrocytes in response to hypotonic stimulus acts on glycine receptors in the adjacent neurons, contributing to hypotonic inhibition of neurosecretion of oxytocin and vasopressin. Exogenously added taurine is neuroprotective by an anti-excitotoxic mechanism, involving direct interaction with GABAA and/or ionotropic glutamate receptors, mostly of the N-methyl D-aspartate type. A plethora of stimuli trigger taurine release from astrocytes or neurons by mechanisms bypassing changes in the intracellular osmotic pressure, thus increasing the extracellular concentration of taurine and facilitating its neuromodulatory function. Ethanol and taurine share molecular targets in the brain.
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U2 - 10.1016/B978-012564370-2/50068-4
DO - 10.1016/B978-012564370-2/50068-4
M3 - Chapter
AN - SCOPUS:84943253187
SN - 9780125643702
VL - 2-3
SP - 845
EP - 854
BT - Comprehensive Handbook of Alcohol Related Pathology
PB - Elsevier Inc.
ER -