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Circadian Genes, the Stress Axis, and Alcoholism

The body’s internal system to control the daily rhythm of the body’s functions (i.e., the circadian system), the body’s stress response, and the body’s neurobiology are highly interconnected. Thus, the rhythm of the circadian system impacts alcohol use patterns; at the same time, alcohol drinking al...

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Autor principal: Sarkar, Dipak K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute on Alcohol Abuse and Alcoholism 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860413/
https://www.ncbi.nlm.nih.gov/pubmed/23134053
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author Sarkar, Dipak K.
author_facet Sarkar, Dipak K.
author_sort Sarkar, Dipak K.
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description The body’s internal system to control the daily rhythm of the body’s functions (i.e., the circadian system), the body’s stress response, and the body’s neurobiology are highly interconnected. Thus, the rhythm of the circadian system impacts alcohol use patterns; at the same time, alcohol drinking also can alter circadian functions. The sensitivity of the circadian system to alcohol may result from alcohol’s effects on the expression of several of the clock genes that regulate circadian function. The stress response system involves the hypothalamus and pituitary gland in the brain and the adrenal glands, as well as the hormones they secrete, including corticotrophin-releasing hormone, adrenocorticotrophic hormone, and glucocorticoids. It is controlled by brain-signaling molecules, including endogenous opioids such as β-endorphin. Alcohol consumption influences the activity of this system and vice versa. Finally, interactions exist between the circadian system, the hypothalamic–pituitary–adrenal axis, and alcohol consumption. Thus, it seems that certain clock genes may control functions of the stress response system and that these interactions are affected by alcohol.
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spelling pubmed-38604132014-01-13 Circadian Genes, the Stress Axis, and Alcoholism Sarkar, Dipak K. Alcohol Res Articles The body’s internal system to control the daily rhythm of the body’s functions (i.e., the circadian system), the body’s stress response, and the body’s neurobiology are highly interconnected. Thus, the rhythm of the circadian system impacts alcohol use patterns; at the same time, alcohol drinking also can alter circadian functions. The sensitivity of the circadian system to alcohol may result from alcohol’s effects on the expression of several of the clock genes that regulate circadian function. The stress response system involves the hypothalamus and pituitary gland in the brain and the adrenal glands, as well as the hormones they secrete, including corticotrophin-releasing hormone, adrenocorticotrophic hormone, and glucocorticoids. It is controlled by brain-signaling molecules, including endogenous opioids such as β-endorphin. Alcohol consumption influences the activity of this system and vice versa. Finally, interactions exist between the circadian system, the hypothalamic–pituitary–adrenal axis, and alcohol consumption. Thus, it seems that certain clock genes may control functions of the stress response system and that these interactions are affected by alcohol. National Institute on Alcohol Abuse and Alcoholism 2012 /pmc/articles/PMC3860413/ /pubmed/23134053 Text en http://creativecommons.org/publicdomain/mark/1.0/ Unless otherwise noted in the text, all material appearing in this journal is in the public domain and may be reproduced without permission. Citation of the source is appreciated.
spellingShingle Articles
Sarkar, Dipak K.
Circadian Genes, the Stress Axis, and Alcoholism
title Circadian Genes, the Stress Axis, and Alcoholism
title_full Circadian Genes, the Stress Axis, and Alcoholism
title_fullStr Circadian Genes, the Stress Axis, and Alcoholism
title_full_unstemmed Circadian Genes, the Stress Axis, and Alcoholism
title_short Circadian Genes, the Stress Axis, and Alcoholism
title_sort circadian genes, the stress axis, and alcoholism
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860413/
https://www.ncbi.nlm.nih.gov/pubmed/23134053
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