Hooked on benzodiazepines: GABAA receptor subtypes and addiction

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Název: Hooked on benzodiazepines: GABAA receptor subtypes and addiction
Autoři: Christian Lüscher, Kelly R. Tan, Uwe Rudolph
Zdroj: Trends in Neurosciences, Vol. 34, No 4 (2011) pp. 188-97
Trends in neurosciences
Informace o vydavateli: Elsevier BV, 2011.
Rok vydání: 2011
Témata: 0301 basic medicine, 616.8, Substance-Related Disorders, Dopamine, Neurons/metabolism, Ventral Tegmental Area/metabolism, Substance-Related Disorders/physiopathology, Benzodiazepines, 03 medical and health sciences, GABA Modulators/adverse effects/metabolism/therapeutic use, Reward, Animals, Humans, Protein Subunits/metabolism, GABA Modulators, Anxiety Disorders/drug therapy, Neurons, 0303 health sciences, Receptors, GABA-A/metabolism, Ventral Tegmental Area, Receptors, GABA-A, Anxiety Disorders, ddc:616.8, Benzodiazepines/adverse effects/metabolism/therapeutic use, 3. Good health, Dopamine/metabolism, Behavior, Addictive, Protein Subunits
Popis: Benzodiazepines are widely used clinically to treat anxiety and insomnia. They also induce muscle relaxation, control epileptic seizures, and can produce amnesia. Moreover, benzodiazepines are often abused after chronic clinical treatment and also for recreational purposes. Within weeks, tolerance to the pharmacological effects can develop as a sign of dependence. In vulnerable individuals with compulsive drug use, addiction will be diagnosed. Here we review recent observations from animal models regarding the cellular and molecular basis that might underlie the addictive properties of benzodiazepines. These data reveal how benzodiazepines, acting through specific GABA(A) receptor subtypes, activate midbrain dopamine neurons, and how this could hijack the mesolimbic reward system. Such findings have important implications for the future design of benzodiazepines with reduced or even absent addiction liability.
Druh dokumentu: Article
Popis souboru: application/pdf
Jazyk: English
ISSN: 0166-2236
DOI: 10.1016/j.tins.2011.01.004
Přístupová URL adresa: https://europepmc.org/articles/pmc4020178?pdf=render
https://pubmed.ncbi.nlm.nih.gov/21353710
http://www.cell.com/trends/neurosciences/fulltext/S0166-2236(11)00005-1
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020178
http://europepmc.org/articles/PMC4020178
https://www.cell.com/trends/neurosciences/fulltext/S0166-2236(11)00005-1
https://archive-ouverte.unige.ch/unige:26928
http://www.cell.com/trends/neurosciences/abstract/S0166-2236(11)00005-1
https://archive-ouverte.unige.ch/unige:26928
https://doi.org/10.1016/j.tins.2011.01.004
https://archive-ouverte.unige.ch/unige:26928
Rights: Elsevier TDM
Přístupové číslo: edsair.doi.dedup.....1c1fa50e649cb9c6e7ffa7f29d2fb7da
Databáze: OpenAIRE
Popis
Abstrakt:Benzodiazepines are widely used clinically to treat anxiety and insomnia. They also induce muscle relaxation, control epileptic seizures, and can produce amnesia. Moreover, benzodiazepines are often abused after chronic clinical treatment and also for recreational purposes. Within weeks, tolerance to the pharmacological effects can develop as a sign of dependence. In vulnerable individuals with compulsive drug use, addiction will be diagnosed. Here we review recent observations from animal models regarding the cellular and molecular basis that might underlie the addictive properties of benzodiazepines. These data reveal how benzodiazepines, acting through specific GABA(A) receptor subtypes, activate midbrain dopamine neurons, and how this could hijack the mesolimbic reward system. Such findings have important implications for the future design of benzodiazepines with reduced or even absent addiction liability.
ISSN:01662236
DOI:10.1016/j.tins.2011.01.004