Abstract

Neuropeptide Y (NPY) produced by arcuate nucleus (ARC) neurons has a strong orexigenic effect on target neurons. Hypothalamic NPY levels undergo wide-ranging oscillations during the circadian cycle and in response to fasting and peripheral hormones (from 0.25 to 10-fold change). The aim of the present study was to evaluate the impact of a moderate long-term modulation of NPY within the ARC neurons on food consumption, body weight gain and hypothalamic neuropeptides. We achieved a physiological overexpression (3.6-fold increase) and down-regulation (0.5-fold decrease) of NPY in the rat ARC by injection of AAV vectors expressing NPY and synthetic microRNA that target the NPY, respectively. Our work shows that a moderate overexpression of NPY was sufficient to induce diurnal over-feeding, sustained body weight gain and severe obesity in adult rats. Additionally, the circulating levels of leptin were elevated but the immunoreactivity (ir) of ARC neuropeptides was not in accordance (POMC-ir was unchanged and AGRP-ir increased), suggesting a disruption in the ability of ARC neurons to response to peripheral metabolic alterations. Furthermore, a dysfunction in adipocytes phenotype was observed in these obese rats. In addition, moderate down-regulation of NPY did not affect basal feeding or normal body weight gain but the response to food deprivation was compromised since fasting-induced hyperphagia was inhibited and fasting-induced decrease in locomotor activity was absent.These results highlight the importance of the physiological ARC NPY levels oscillations on feeding regulation, fasting response and body weight preservation, and are important for the design of therapeutic interventions for obesity that include the NPY.

Highlights

  • Obesity and overweight are an increasing health problem associated with the risk to develop life threatening conditions such as diabetes, cardiovascular disease and cancer

  • arcuate nucleus (ARC) neurons are divided into two distinct populations acting together to regulate feeding behavior: the orexigenic NPY/AGRP (Neuropeptide Y/Agouti-Related Protein) neurons and the anorexigenic POMC/CART (ProOpioMelanocortin/Cocaine-and-Amphetamine-Regulated-Transcript) neurons

  • Most of the hypothalamic NPY-expressing neurons are located in the ARC and project to different areas of the hypothalamus, including the paraventricular nucleus (PVN), dorsomedial hypothalamus (DMH), ventromedial hypothalamus (VMH) and lateral hypothalamic area (LH) [3]

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Summary

Introduction

Obesity and overweight are an increasing health problem associated with the risk to develop life threatening conditions such as diabetes, cardiovascular disease and cancer. The main cause of obesity in the western society is the elevated consumption of high caloric aliments and beverages, as well as decreased physical activity. Most of the hypothalamic NPY-expressing neurons are located in the ARC and project to different areas of the hypothalamus, including the paraventricular nucleus (PVN), dorsomedial hypothalamus (DMH), ventromedial hypothalamus (VMH) and lateral hypothalamic area (LH) [3]. NPY acts on down-stream target neurons, including neurons in the PVN and LH, to produce feeding response [6,8,9]

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