CRF-CRF1 system activation mediates withdrawal-induced increases in nicotine self-administration in nicotine-dependent rats

Proc Natl Acad Sci U S A. 2007 Oct 23;104(43):17198-203. doi: 10.1073/pnas.0707585104. Epub 2007 Oct 5.

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

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amygdala / drug effects
  • Amygdala / metabolism
  • Animals
  • Anxiety
  • Behavior, Addictive
  • Behavior, Animal / drug effects
  • Corticotropin-Releasing Hormone / metabolism*
  • Feeding Behavior / drug effects
  • Male
  • Mecamylamine / pharmacology
  • Nicotine / administration & dosage*
  • Nicotine / adverse effects
  • Nicotine / pharmacology*
  • Rats
  • Rats, Wistar
  • Receptors, Corticotropin-Releasing Hormone / antagonists & inhibitors
  • Receptors, Corticotropin-Releasing Hormone / metabolism*
  • Self Administration
  • Substance Withdrawal Syndrome / metabolism*

Substances

  • Receptors, Corticotropin-Releasing Hormone
  • CRF receptor type 1
  • Mecamylamine
  • Nicotine
  • Corticotropin-Releasing Hormone