Skip Navigation

Publication Detail

Title: Early postnatal manganese exposure causes arousal dysregulation and lasting hypofunctioning of the prefrontal cortex catecholaminergic systems.

Authors: Conley, Travis E; Beaudin, Stephane A; Lasley, Stephen M; Fornal, Casimir A; Hartman, Jasenia; Uribe, Walter; Khan, Tooba; Strupp, Barbara J; Smith, Donald R

Published In J Neurochem, (2020 06)

Abstract: Studies have reported associations between environmental manganese (Mn) exposure and impaired cognition, attention, impulse control, and fine motor function in children. Our recent rodent studies established that elevated Mn exposure causes these impairments. Here, rats were exposed orally to 0, 25, or 50 mg Mn kg-1  day-1 during early postnatal life (PND 1-21) or lifelong to determine whether early life Mn exposure causes heightened behavioral reactivity in the open field, lasting changes in the catecholaminergic systems in the medial prefrontal cortex (mPFC), altered dendritic spine density, and whether lifelong exposure exacerbates these effects. We also assessed astrocyte reactivity (glial fibrillary acidic protein, GFAP), and astrocyte complement C3 and S100A10 protein levels as markers of A1 proinflammatory or A2 anti-inflammatory reactive astrocytes. Postnatal Mn exposure caused heightened behavioral reactivity during the first 5-10 min intervals of daily open field test sessions, consistent with impairments in arousal regulation. Mn exposure reduced the evoked release of norepinephrine (NE) and caused decreased protein levels of tyrosine hydroxylase (TH), dopamine (DA) and NE transporters, and DA D1 receptors, along with increased DA D2 receptors. Mn also caused a lasting increase in reactive astrocytes (GFAP) exhibiting increased A1 and A2 phenotypes, with a greater induction of the A1 proinflammatory phenotype. These results demonstrate that early life Mn exposure causes broad lasting hypofunctioning of the mPFC catecholaminergic systems, consistent with the impaired arousal regulation, attention, impulse control, and fine motor function reported in these animals, suggesting that mPFC catecholaminergic dysfunction may underlie similar impairments reported in Mn-exposed children.

PubMed ID: 31811785 Exiting the NIEHS site

MeSH Terms: Age Factors; Animals; Animals, Newborn; Arousal/drug effects; Arousal/physiology*; Dopamine Plasma Membrane Transport Proteins/metabolism*; Glial Fibrillary Acidic Protein/metabolism*; Male; Manganese/administration & dosage; Manganese/toxicity*; Norepinephrine Plasma Membrane Transport Proteins/metabolism*; Prefrontal Cortex/drug effects; Prefrontal Cortex/metabolism*; Rats; Rats, Long-Evans

Back
to Top