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The impact of sex on brain responses to smoking cues: a perfusion fMRI study

BACKGROUND: Anecdotal and clinical theories purport that females are more responsive to smoking cues, yet few objective, neurophysiological examinations of these theories have been conducted. The current study examines the impact of sex on brain responses to smoking cues. METHODS: Fifty-one (31 male...

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Autores principales: Wetherill, Reagan R, Young, Kimberly A, Jagannathan, Kanchana, Shin, Joshua, O’Brien, Charles P, Childress, Anna Rose, Franklin, Teresa R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643879/
https://www.ncbi.nlm.nih.gov/pubmed/23628003
http://dx.doi.org/10.1186/2042-6410-4-9
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author Wetherill, Reagan R
Young, Kimberly A
Jagannathan, Kanchana
Shin, Joshua
O’Brien, Charles P
Childress, Anna Rose
Franklin, Teresa R
author_facet Wetherill, Reagan R
Young, Kimberly A
Jagannathan, Kanchana
Shin, Joshua
O’Brien, Charles P
Childress, Anna Rose
Franklin, Teresa R
author_sort Wetherill, Reagan R
collection PubMed
description BACKGROUND: Anecdotal and clinical theories purport that females are more responsive to smoking cues, yet few objective, neurophysiological examinations of these theories have been conducted. The current study examines the impact of sex on brain responses to smoking cues. METHODS: Fifty-one (31 males) cigarette-dependent sated smokers underwent pseudo-continuous arterial spin-labeled perfusion functional magnetic resonance imaging during exposure to visual smoking cues and non-smoking cues. Brain responses to smoking cues relative to non-smoking cues were examined within males and females separately and then compared between males and females. Cigarettes smoked per day was included in analyses as a covariate. RESULTS: Both males and females showed increased responses to smoking cues compared to non-smoking cues with males exhibiting increased medial orbitofrontal cortex and ventral striatum/ventral pallidum responses, and females showing increased medial orbitofrontal cortex responses. Direct comparisons between male and female brain responses revealed that males showed greater bilateral hippocampal/amygdala activation to smoking cues relative to non-smoking cues. CONCLUSIONS: Males and females exhibit similar responses to smoking cues relative to non-smoking cues in a priori reward-related regions; however, direct comparisons between sexes indicate that smoking cues evoke greater bilateral hippocampal/amygdalar activation among males. Given the current literature on sex differences in smoking cue neural activity is sparse and incomplete, these results contribute to our knowledge of the neurobiological underpinnings of drug cue reactivity.
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spelling pubmed-36438792013-05-04 The impact of sex on brain responses to smoking cues: a perfusion fMRI study Wetherill, Reagan R Young, Kimberly A Jagannathan, Kanchana Shin, Joshua O’Brien, Charles P Childress, Anna Rose Franklin, Teresa R Biol Sex Differ Research BACKGROUND: Anecdotal and clinical theories purport that females are more responsive to smoking cues, yet few objective, neurophysiological examinations of these theories have been conducted. The current study examines the impact of sex on brain responses to smoking cues. METHODS: Fifty-one (31 males) cigarette-dependent sated smokers underwent pseudo-continuous arterial spin-labeled perfusion functional magnetic resonance imaging during exposure to visual smoking cues and non-smoking cues. Brain responses to smoking cues relative to non-smoking cues were examined within males and females separately and then compared between males and females. Cigarettes smoked per day was included in analyses as a covariate. RESULTS: Both males and females showed increased responses to smoking cues compared to non-smoking cues with males exhibiting increased medial orbitofrontal cortex and ventral striatum/ventral pallidum responses, and females showing increased medial orbitofrontal cortex responses. Direct comparisons between male and female brain responses revealed that males showed greater bilateral hippocampal/amygdala activation to smoking cues relative to non-smoking cues. CONCLUSIONS: Males and females exhibit similar responses to smoking cues relative to non-smoking cues in a priori reward-related regions; however, direct comparisons between sexes indicate that smoking cues evoke greater bilateral hippocampal/amygdalar activation among males. Given the current literature on sex differences in smoking cue neural activity is sparse and incomplete, these results contribute to our knowledge of the neurobiological underpinnings of drug cue reactivity. BioMed Central 2013-04-29 /pmc/articles/PMC3643879/ /pubmed/23628003 http://dx.doi.org/10.1186/2042-6410-4-9 Text en Copyright © 2013 Wetherill et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wetherill, Reagan R
Young, Kimberly A
Jagannathan, Kanchana
Shin, Joshua
O’Brien, Charles P
Childress, Anna Rose
Franklin, Teresa R
The impact of sex on brain responses to smoking cues: a perfusion fMRI study
title The impact of sex on brain responses to smoking cues: a perfusion fMRI study
title_full The impact of sex on brain responses to smoking cues: a perfusion fMRI study
title_fullStr The impact of sex on brain responses to smoking cues: a perfusion fMRI study
title_full_unstemmed The impact of sex on brain responses to smoking cues: a perfusion fMRI study
title_short The impact of sex on brain responses to smoking cues: a perfusion fMRI study
title_sort impact of sex on brain responses to smoking cues: a perfusion fmri study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643879/
https://www.ncbi.nlm.nih.gov/pubmed/23628003
http://dx.doi.org/10.1186/2042-6410-4-9
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