Abstract
Nicotine, the main psychoactive ingredient of tobacco, induces negative emotional symptoms during abstinence that contribute to a profound craving for nicotine. However, the neurobiological mechanisms underlying how nicotine produces dependence remains poorly understood. We demonstrate one mechanism for both the anxiety-like symptoms of withdrawal and excessive nicotine intake observed after abstinence, through recruitment of the extrahypothalamic stress peptide corticotropin-releasing factor (CRF) system and activation of CRF(1) receptors. Overactivation of the CRF-CRF(1) system may contribute to nicotine dependence and may represent a prominent target for investigating the vulnerability to tobacco addiction.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Amygdala / drug effects
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Amygdala / metabolism
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Animals
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Anxiety
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Behavior, Addictive
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Behavior, Animal / drug effects
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Corticotropin-Releasing Hormone / metabolism*
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Feeding Behavior / drug effects
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Male
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Mecamylamine / pharmacology
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Nicotine / administration & dosage*
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Nicotine / adverse effects
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Nicotine / pharmacology*
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Rats
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Rats, Wistar
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Receptors, Corticotropin-Releasing Hormone / antagonists & inhibitors
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Receptors, Corticotropin-Releasing Hormone / metabolism*
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Self Administration
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Substance Withdrawal Syndrome / metabolism*
Substances
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Receptors, Corticotropin-Releasing Hormone
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CRF receptor type 1
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Mecamylamine
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Nicotine
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Corticotropin-Releasing Hormone