Hippocampal insulin resistance links maternal obesity with impaired neuronal plasticity in adult offspring. (March 2018)

• Record Type: Journal Article
• Authors: Schmitz, Lisa; Kuglin, Rebecca; Bae-Gartz, Inga; Janoschek, Ruth; Appel, Sarah; Mesaros, Andrea; Jakovcevski, Igor; Vohlen, Christina; Handwerk, Marion; Ensenauer, Regina; Dötsch, Jörg; Hucklenbruch-Rother, Eva
• Is Part Of: Psychoneuroendocrinology. Volume 89(2018)
• Page Start: 46
• Page End: 52
• Publication Date: 2018-03
• Subjects: Insulin resistance -- Hippocampus -- Maternal obesity -- Synapse; Psychoneuroendocrinology -- Periodicals; Endocrinology -- Periodicals; Neurology -- Periodicals; Psychiatry -- Periodicals; Neuropsychoendocrinologie -- Périodiques; 616.8
• DOI: 10.1016/j.psyneuen.2017.12.023
• Languages: English
• ISSNs: 0306-4530

Abstract

Highlights: Maternal obesity results in hippocampal insulin resistance in the adult offspring. Neuronal insulin resistance affects hippocampal neurogenesis, synaptic plasicity, and transmitter trafficking. Hippocampal long-term effects of maternal obesity are independent of the offspring's own body weight or glucose metabolism. Abstract: Objective: Maternal obesity and a disturbed metabolic environment during pregnancy and lactation have been shown to result in many long-term health consequences for the offspring. Among them, impairments in neurocognitive development and performance belong to the most dreaded ones. So far, very few mechanistic approaches have aimed to determine the responsible molecular events. Methods: In a mouse model of maternal diet-induced obesity and perinatal hyperinsulinemia, we assessed adult offspring's hippocampal insulin signaling as well as concurrent effects on markers of hippocampal neurogenesis, synaptic plasticity and function using western blotting and immunohistochemistry. In search for a potential link between neuronal insulin resistance and hippocampal plasticity, we additionally quantified protein expression of key molecules of synaptic plasticity in an in vitro model of acute neuronal insulin resistance. Results: Maternal obesity and perinatal hyperinsulinemia result in adult hippocampal insulin resistance with subsequently reduced hippocampal mTor signaling and altered expression of markers of neurogenesis (doublecortin), synaptic plasticity (FoxO1, pSynapsin) and function (vGlut, vGAT) in the offspring. The observed effects are independent of the offspring's adult metabolic phenotype and can be associated with multiple previously reported behavioral abnormalities. Additionally, we demonstrate that induction of insulin resistance in cultured hippocampal neurons reduces mTor signaling, doublecortin and vGAT protein expression. Conclusions: Hippocampal insulin resistance might play a key role in mediating the long-term effects of maternal obesity and perinatal hyperinsulinemia on hippocampal plasticity and the offspring's neurocognitive outcome.