4.7 Review

Gray areas: Neuropeptide circuits linking the Edinger-Westphal and Dorsal Raphe nuclei in addiction

Journal

NEUROPHARMACOLOGY
Volume 198, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2021.108769

Keywords

Midbrain; Neuropeptide; Edinger-westphal; Dorsal raphe; Periaqueductal gray; Addiction

Funding

  1. NIH [T32 DA035165, R00 AA025677]
  2. NHMRC [2002830]
  3. Jack Brockhoff Foundation [4658]
  4. Stanford Psychiatry Innovator Grant
  5. National Health and Medical Research Council of Australia [2002830] Funding Source: NHMRC

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This article delves into the importance of midbrain nuclei like EW and DR in the neural circuitry of addiction, emphasizing the contribution of these neurons in affecting addictive behaviors. It also explores the connectivity between EW and DR, as well as their potential roles in addiction-related behaviors.
The circuitry of addiction comprises several neural networks including the midbrain - an expansive region critically involved in the control of motivated behaviors. Midbrain nuclei like the Edinger-Westphal (EW) and dorsal raphe (DR) contain unique populations of neurons that synthesize many understudied neuroactive molecules and are encircled by the periaqueductal gray (PAG). Despite the proximity of these special neuron classes to the ventral midbrain complex and surrounding PAG, functions of the EW and DR remain substantially underinvestigated by comparison. Spanning approximately -3.0 to -5.2 mm posterior from bregma in the mouse, these various cell groups form a continuum of neurons that we refer to collectively as the subaqueductal paramedian zone. Defining how these pathways modulate affective behavioral states presents a difficult, yet conquerable challenge for today's technological advances in neuroscience. In this review, we cover the known contributions of different neuronal subtypes of the subaqueductal paramedian zone. We catalogue these cell types based on their spatial, molecular, connectivity, and functional properties and integrate this information with the existing data on the EW and DR in addiction. We next discuss evidence that links the EW and DR anatomically and functionally, highlighting the potential contributions of an EW-DR circuit to addiction-related behaviors. Overall, we aim to derive an integrated framework that emphasizes the contributions of EW and DR nuclei to addictive states and describes how these cell groups function in individuals suffering from substance use disorders. This article is part of the special Issue on 'Neurocircuitry Modulating Drug and Alcohol Abuse'.

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