Acute nicotine abstinence amplifies subjective withdrawal symptoms and threat-evoked fear and anxiety, but not extended amygdala reactivity

PLoS One. 2023 Jul 20;18(7):e0288544. doi: 10.1371/journal.pone.0288544. eCollection 2023.

Abstract

Tobacco smoking imposes a staggering burden on public health, underscoring the urgency of developing a deeper understanding of the processes that maintain addiction. Clinical and experience-sampling data highlight the importance of anxious withdrawal symptoms, but the underlying neurobiology has remained elusive. Mechanistic work in animals implicates the central extended amygdala (EAc)-including the central nucleus of the amygdala and the neighboring bed nucleus of the stria terminalis-but the translational relevance of these discoveries remains unexplored. Here we leveraged a randomized trial design, well-established threat-anticipation paradigm, and multidimensional battery of assessments to understand the consequences of 24-hour nicotine abstinence. The threat-anticipation paradigm had the expected consequences, amplifying subjective distress and arousal, and recruiting the canonical threat-anticipation network. Abstinence increased smoking urges and withdrawal symptoms, and potentiated threat-evoked distress, but had negligible consequences for EAc threat reactivity, raising questions about the translational relevance of prominent animal and human models of addiction. These observations provide a framework for conceptualizing nicotine abstinence and withdrawal, with implications for basic, translational, and clinical science.

Publication types

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

MeSH terms

  • Amygdala / physiology
  • Anxiety
  • Fear / physiology
  • Humans
  • Nicotine / adverse effects
  • Septal Nuclei* / physiology
  • Substance Withdrawal Syndrome*

Substances

  • Nicotine

Grants and funding

This work was supported by the California National Primate Center, National Institutes of Health (AA031261, DA040717, MH107444, MH121409, MH121735, MH131264, MH129851, MH018921, OD011107, Awarded: Dr. Alexander Shackman), National Science Foundation (DGE-1632976, Awarded: Hyung Cho Kim), and University of Maryland. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.