Perinatal Western-style Diet Exposure associated with Decreased Microglial Counts throughout the Arcuate Nucleus of the Hypothalamus in Japanese Macaques.

arcuate nucleus of the hypothalamus high-fat high-sugar western-style diet microglia neuroinflammation non-human primates

Journal

Journal of neurophysiology
ISSN: 1522-1598
Titre abrégé: J Neurophysiol
Pays: United States
ID NLM: 0375404

Informations de publication

Date de publication:
10 Jan 2024
Historique:
medline: 10 1 2024
pubmed: 10 1 2024
entrez: 10 1 2024
Statut: aheadofprint

Résumé

Perinatal exposure to a high-fat, high-sugar, Western-style diet (WSD) is associated with altered neural circuitry in the melanocortin system. This association may have an underlying inflammatory component, as consumption of a WSD during pregnancy can lead to an elevated inflammatory environment. Our group previously demonstrated that prenatal WSD exposure was associated with increased markers of inflammation in the placenta and fetal hypothalamus in Japanese macaques. In this follow-up study, we sought to determine whether this heightened inflammatory state persisted into the postnatal period, as prenatal exposure to inflammation has been shown to reprogram offspring immune function, and long-term neuroinflammation would present a potential means for prolonged disruptions to microglia-mediated neuronal circuit formation. Neuroinflammation was approximated in one-year-old offspring by counting resident microglia and peripherally-derived macrophages in the region of the hypothalamus examined in the fetal study, the arcuate nucleus (ARC). Microglia and macrophages were immunofluorescently stained with their shared marker, ionized calcium-binding adaptor protein-1 (Iba1), and quantified in eleven regions along the rostral-caudal axis of the ARC. A mixed effects model revealed main effects of perinatal diet (

Identifiants

pubmed: 38197176
doi: 10.1152/jn.00213.2023
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : ODCDC CDC HHS
ID : P51 OD011092
Pays : United States

Auteurs

Samantha Papadakis (S)

Behavioral Neuroscience, Oregon Health and Science University Hospital, Portland, OR, United States.

Jacqueline R Thompson (JR)

Neuroscience, Oregon National Primate Research Center, Beaverton, OR, United States.

Eric Feczko (E)

University of Minnesota, Minneapolis, MN, United States.

Oscar Miranda-Dominguez (O)

Oregon Health and Science University Hospital, Portland, OR, United States.

Geoffrey A Dunn (GA)

Department of Human Physiology, University of Oregon, Eugene, OR, United States.

Matthew Selby (M)

Department of Human Physiology, University of Oregon, Eugene, OR, United States.

A J Mitchell (AJ)

Behavioral Neuroscience, Oregon Health and Science University Hospital, Portland, OR, United States.

Elinor L Sullivan (EL)

Neuroscience, Oregon National Primate Research Center, Beaverton, OR, United States.

Damien A Fair (DA)

Masonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, United States.

Classifications MeSH