Abstract

Ample evidence from epidemiological studies has linked maternal obesity with metabolic disorders such as obesity, cardiovascular disease, and diabetes in the next generation. Recently, it was also shown that maternal obesity has long-term effects on the progeny’s central nervous system. However, very little is known regarding how maternal overnutrition may affect, in particular, the cognitive abilities of the offspring. We reported that first-generation offspring exposed to a maternal high-fat diet (MHFD) displayed age-dependent cognitive deficits. These deficits were associated with attenuations of amino acid levels in the medial prefrontal cortex and the hippocampus regions of MHFD offspring. Here, we tested the hypothesis that MHFD in mice may induce long-term cognitive impairments and neurochemical dysfunctions in the second and third generations. We found that MHFD led to cognitive disabilities and an altered response to a noncompetitive receptor antagonist of the N-Methyl-D-aspartic acid (NMDA) receptor in adult MHFD offspring in both second and third generations in a sex-specific manner. Our results suggest that maternal overnutrition leads to an increased risk of developing obesity in subsequent generations as well as to cognitive impairments, affecting learning and memory processes in adulthood. Furthermore, MHFD exposure may facilitate pathological brain aging which is not a consequence of obesity. Our findings shed light on the long-term effects of maternal overnutrition on the development of the central nervous system and the underlying mechanisms which these traits relate to disease predisposition.

Highlights

  • The prevalence of obesity is increasing worldwide and has reached epidemic proportions posing a major problem for healthcare [1]

  • Our results suggest that maternal overnutrition leads to an increased risk of developing obesity in subsequent generations as well as to cognitive impairments, affecting learning and memory processes in adulthood

  • Offspring born to high-fat diet (HFD) ancestors did not show any difference in spontaneous locomotor activity compared to the control diet (CTR) offspring (F1,36 = 0.277; P = 0.60, Figure 1B)

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Summary

Introduction

The prevalence of obesity is increasing worldwide and has reached epidemic proportions posing a major problem for healthcare [1]. Obesity is associated with an increased incidence of comorbidities like dyslipidemia, hypertension, and type 2 diabetes mellitus (T2DM) [1]. A particular concern emerged in the past two decades, namely obesity during pregnancy [3,4,5,6]. Two-thirds of women of childbearing age (19–44) are overweight, and 36.5% are obese. It is not surprising that this epidemic affects children of all ages with nearly 41 million children under the age of five years classified as overweight or obese [2]. It is already known that the obesity epidemic cannot be explained only as a result of an affluent lifestyle, reduced physical activity, or a genetic predisposition

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