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Published on: February 20, 2019
Dorsolateral prefrontal and orbitofrontal cortex interactions during self-control of cigarette craving
Takuya Hayashi1, Ji Hyun Ko, Antonio P Strafella
1McConnell Brain Imaging Center, Montreal Neurological Institute, McGill University, Montreal, QC, Canada H3A 2B4. takuya.hayashi@riken.jp
The dorsolateral prefrontal cortex (DLPFC) regulates drug craving by integrating drug availability information. Inactivating the DLPFC reduces craving, suggesting its crucial role in addiction.
Area of Science:
- Neuroscience
- Addiction Research
Background:
- Drug cues trigger craving, perpetuating use and relapse.
- Frontal lobe activity influences cue reactivity, but specific regions remain unclear.
Purpose of the Study:
- To investigate frontal lobe contributions to drug craving under varying drug availability.
- To determine the role of the dorsolateral prefrontal cortex (DLPFC) in regulating craving based on intertemporal availability.
Main Methods:
- Combined transcranial magnetic stimulation (TMS) and functional magnetic resonance imaging (fMRI) in smokers.
- Transiently inactivated the DLPFC using TMS to assess its causal role.
- Examined brain activity in relation to subjective craving and drug availability.
Main Results:
- Subjective craving increased when cigarettes were immediately available; this effect was abolished by DLPFC inactivation.
- Medial orbitofrontal cortex (mOFC) activity correlated with craving, while DLPFC encoded availability information.
- DLPFC inactivation attenuated mOFC craving signals, particularly when drugs were readily available, and reduced signals in the anterior cingulate and ventral striatum.
Conclusions:
- The DLPFC integrates drug availability information to modulate craving.
- Aberrant connectivity between DLPFC and mOFC may underlie addiction.
- DLPFC plays a key role in linking drug availability to craving and subsequent actions.
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