4.2 Article

Role of α7-and β4-Containing Nicotinic Acetylcholine Receptors in the Affective and Somatic Aspects of Nicotine Withdrawal: Studies in Knockout Mice

期刊

BEHAVIOR GENETICS
卷 42, 期 3, 页码 423-436

出版社

SPRINGER
DOI: 10.1007/s10519-011-9511-0

关键词

Intracranial self-stimulation; Somatic signs; Reward deficit; Anhedonia; Mecamylamine; nAChR

资金

  1. NIH [R01DA023209]
  2. University of Colorado, Boulder [P30 DA015663]

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To assess which nicotinic acetylcholine receptors (nAChRs) are involved in the aversive aspects of nicotine withdrawal, brain reward function and the somatic signs of nicotine withdrawal were assessed in mice that lack alpha 7 and beta 4 nAChR subunits. Brain reward function was assessed with the intracranial self-stimulation (ICSS) procedure, in which elevations in ICSS thresholds reflect an anhedonic mood state. At 3-6 h of spontaneous nicotine/saline withdrawal, thresholds were elevated in nicotine-withdrawing alpha 7(+/+) and beta 4(+/+), but not alpha 7(-/-) or beta 4(-/-), mice compared with saline-withdrawing mice, indicating a delay in the onset of withdrawal in the knockout mice. From 8 to 100 h of withdrawal, thresholds in alpha 7(+/+) and alpha 7(-/-) mice were equally elevated, whereas thresholds in beta 4(+/+) and beta 4(-/-) mice returned to baseline levels. Somatic signs were attenuated in nicotine-withdrawing beta 4(-/-), but not alpha 7(-/-), mice. Administration of a low dose of the nAChR antagonist mecamylamine induced threshold elevations in alpha 7(-/-), but not alpha 7(+/+), mice, whereas the highest dose tested only elevated thresholds in alpha 7(+/+) mice. Mecamylamine-induced threshold elevations were similar in beta 4(-/-) and beta 4(+/+) mice. In conclusion, null mutation of the alpha 7 and beta 4 nAChR subunits resulted in a delayed onset of the anhedonic aspects of the spontaneous nicotine withdrawal syndrome. Previous findings of attenuated somatic signs of nicotine withdrawal in beta 4(-/-), but not alpha 7(-/-), mice were confirmed in the present study, indicating an important role for beta 4-containing nAChRs in the somatic signs of nicotine withdrawal. The mecamylamine-precipitated withdrawal data suggest that compensatory adaptations may occur in constitutive alpha 7(-/-) mice or that mecamylamine may interact with other receptors besides nAChRs in these mice. In summary, the present results indicate an important role for alpha 7 and beta 4-containing nAChRs in the anhedonic or somatic signs of nicotine withdrawal.

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