Abstract

Recent studies have linked gestational exposure to highly caloric diets with a disrupted endogenous cannabinoid system (ECS). In the present study, we have extended these studies by analyzing the impact of the exposure to a palatable diet during gestation and lactation on a) the adult expression of endocannabinoid-related behaviors, b) the metabolic profile of adult offspring and c) the mRNA expression of the signaling machinery of the ECS in the hypothalamus, the liver and the adipose tissue of adult offspring of both sexes. Exposure to a palatable diet resulted in a) sex-dimorphic and perinatal diet specific feeding behaviors, including the differential response to the inhibitory effects of the cannabinoid receptor inverse agonist AM251, b) features of metabolic syndrome including increased adiposity, hyperleptinemia, hypertriglyceridemia and hypercholesterolemia and c) tissue and sex-specific changes in the expression of both CB1 and CB2 receptors and in that of the endocannabinoid-degrading enzymes FAAH and MAGL, being the adipose tissue the most affected organ analyzed. Since the effects were observed in adult animals that were weaned while consuming a normal diet, the present results indicate that the ECS is one of the targets of maternal programming of the offspring energy expenditure. These results clearly indicate that the maternal diet has long-term effects on the development of pups through multiple alterations of signaling homeostatic pathways that include the ECS. The potential relevance of these alterations for the current obesity epidemic is discussed.

Highlights

  • Obesity and metabolic syndrome prevalence are increasing worldwide [1,2]

  • The data demonstrate that exposure to a maternal palatable diet since the preconception period predisposes animals to develop features of metabolic syndrome, and affect the feeding behavior, including the differential response to the inverse cannabinonid agonist AM251, and the expression of genes involved in cannabinoid and lipid metabolism of the offspring in a sexspecific manner, even though the animals are weaned on standard chow diet

  • The increased expression of Cnr1 in the hypothalamus and perirenal adipose tissue (PAT) of PC female offspring suggest a hyposensitization of the cannabinoid activity, which may result in a reduction in chocolate preference, leptinemia and body weight at adulthood

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Summary

Introduction

Lifestyle factors contribute to this epidemic, it is becoming clear that nutritional conditions during critical windows of development, including the perinatal period, could impact the future health of offspring and increase the risk of metabolic diseases [3,4,5]. This phenomenon has been defined as nutritional programming [6]. It is well-known that maternal and postnatal nutrition tends to be excessive in Western societies. A maternal high-fat diet or perinatal exposure to junk food modifies the metabolic outcomes and the gene expression profile of several metabolism-related genes in a sex-specific manner [12,13,14]

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