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1.
J Nutr Biochem ; 86: 108494, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-32920089

RESUMO

Overfeeding and rapid weight gain during early life are risk factors for the development of obesity in adulthood. This metabolic malprogramming may be mediated by endocrine disturbances during critical periods of development. Cholecystokinin (CCK) acts on the central nervous system by elevating thermogenesis and the activity of anorectic neurons, modulating overall energy balance. Therefore, we tested the hypothesis that postnatal overfeeding impaired CCK effects. Pups were raised in either a litter of three (neonatal overnutrition/small litter group) or 12 (controls/normal litter group) pups per dam to study the effects of postnatal overfeeding on the central and peripheral CCK systems in adulthood. Rats raised in small litters became overweight during lactation and remained overweight as adults, with increased adiposity and plasma levels of lipids, glucose, insulin, and leptin. Neonatally over-nourished rats showed attenuation of gastric emptying and anorexigenic response to CCK, suggesting that offspring from the SL group may present CCK resistance as adult male rats. Consistent with this idea, overweight rats displayed impaired central response in c-Fos immunoreactivity on the nucleus tractus solitarius, area postrema, paraventricular nucleus, central amygdala, arcuate nucleus, and dorsomedial hypothalamus in response to peripheral CCK at adulthood. The small litter group of adult male rats also exhibited reduced norepinephrine- and CCK-stimulated thermogenesis. Unresponsiveness to the effects of CCK may contribute to overweight and metabolic dysfunctions observed in postnatally over-nourished adult rats. Thus, the involvement of an impaired CCK system, among other neurohormonal failures, may contribute to the development of obesity.


Assuntos
Adiposidade , Sistema Nervoso Central/fisiopatologia , Colecistocinina/metabolismo , Sistema Endócrino/fisiopatologia , Hipernutrição/fisiopatologia , Tecido Adiposo/metabolismo , Animais , Animais Recém-Nascidos , Mapeamento Encefálico , Metabolismo Energético , Feminino , Esvaziamento Gástrico , Glucose/metabolismo , Homeostase , Hipotálamo , Leptina/sangue , Lipídeos/química , Masculino , Obesidade/metabolismo , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos , Ratos Wistar , Termogênese , Aumento de Peso
2.
J Physiol Sci ; 68(6): 789-798, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29380149

RESUMO

Maternal behavior has a substantial impact on the behavioral, endocrine, and neural development of the pups. This study investigated the effect of altering the neonatal nutritional environment by modifying the litter size on maternal care and anxiety- and fear-like behaviors in rats during adulthood. On postnatal day (PND) 2, litters were adjusted to a small litter (SL) size of three pups per dam or normal litter (NL) size of 12 pups per dam. Maternal behaviors were scored daily during lactation (PND2-21). The weight gain, food intake, adiposity, and biochemical landmarks of offspring rats were evaluated. On PND60, performances in the open field, elevated plus-maze (EPM), and fear conditioning test were measured. The reduction of the litter size enhanced maternal care in lactating rats, increasing the arched-back posture and licking pups. SL offspring exhibited accelerated weight gain, hyperphagia, increased visceral fat mass, dyslipidemia, and hyperleptinemia in adulthood. The SL offspring of both sexes showed an increase in the anti-thigmotactic effect in the open field, an intact anxious-phenotype in the EPM, and a decrease in the time spent freezing during the fear-conditioning test, compared to NL. The neonatal environment as determined by litter size plays a crucial role in programming the adult metabolic phenotype as well as behavioral responses to stressful stimuli, with an impact on anxiety-like and fear behaviors. These behavioral changes in offspring may be, at least in part, a result of increased maternal care.


Assuntos
Comportamento Animal/fisiologia , Tamanho da Ninhada de Vivíparos , Comportamento Materno/fisiologia , Hipernutrição/metabolismo , Tecido Adiposo/metabolismo , Animais , Animais Recém-Nascidos , Glicemia/análise , Peso Corporal/fisiologia , Ingestão de Alimentos/fisiologia , Feminino , Lipídeos/sangue , Masculino , Ratos
3.
Respir Physiol Neurobiol ; 247: 96-102, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-28963087

RESUMO

Many studies have confirmed the merits of metformin to treat type 2 diabetes, but few studies have addressed its effect on the respiratory system. Moreover, vascular endothelial growth factor (VEGF) is critical to many lung functions. In this way, we evaluated the metformin impact on the lung in treated obese Swiss mice, induced by postnatal overnutrition. Glucose and insulin were detected and the insulin resistance index (HOMA) was calculated; inflammatory cells and nitrite/nitrate concentration (NOx) was quantified from bronchoalveolar lavage, collagen and lung VEGF-a was analysed in the lung tissue and lung mechanics were evaluated by methacholine-induced bronchoconstriction. Values of glucose, insulin, HOMA; VEGF-a and collagen demonstrate the partial ability of metformin to improve the effects of obesity. However, metformin is ineffective in re-establishing the inflammation, shows no effects on NOx and does not restore bronchoconstriction in obese mice. In conclusion, metformins beneficial effects on lung are questionable in the postnatal overnutrition model of obesity.


Assuntos
Hipoglicemiantes/farmacologia , Pulmão/efeitos dos fármacos , Metformina/farmacologia , Obesidade/tratamento farmacológico , Respiração/efeitos dos fármacos , Animais , Líquido da Lavagem Broncoalveolar , Dieta , Modelos Animais de Doenças , Pulmão/patologia , Pulmão/fisiopatologia , Masculino , Camundongos , Nitratos/metabolismo , Nitritos/metabolismo , Obesidade/patologia , Obesidade/fisiopatologia , Distribuição Aleatória , Fator A de Crescimento do Endotélio Vascular/metabolismo
4.
J Neuroimmunol ; 289: 75-83, 2015 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-26616874

RESUMO

This study investigated behavioral responses to an immune challenge among animals with fructose-induced metabolic disorders. Adult male Wistar rats were provided either water or a fructose solution (10%) for 5 weeks. Sickness behaviors were assessed 2h following the injection of either a lipopolysaccharide (LPS) or vehicle. The rats were subjected to an open field test, a social interaction test, a food intake test and a fever evaluation. Cytokine expression was assessed in both adipose tissue and hypothalamus samples. The neural response was assessed in the forebrain immunohistochemistry for c-Fos. Compared with the control group, the fructose diet induced dyslipidemia and significantly higher plasma total cholesterol, HDL-cholesterol, triglyceride, and glucose levels as well as both epididymal and retroperitoneal adiposity. Furthermore, in response to LPS (1 mg/kg), the rats subjected to a fructose diet exhibited exacerbated sickness behaviors and accentuated febrile responses. LPS induced Fos protein expression in several areas of the brains of the control rats; however, higher numbers of Fos-positive cells were observed in the brains of the rats that were fed a fructose diet. Moreover, larger increases in cytokine expression were observed in both the hypothalamus and the adipose tissue of the obese rats compared with the control rats in response to LPS. In this study, fructose diets played an important role in both the induction of metabolic disorders and the modulation of sickness behaviors in response to an immunological challenge, most likely through the induction of cytokines in the hypothalamus.


Assuntos
Frutose/toxicidade , Comportamento de Doença/fisiologia , Doenças Metabólicas/induzido quimicamente , Doenças Metabólicas/fisiopatologia , Edulcorantes/toxicidade , Animais , Temperatura Corporal/efeitos dos fármacos , Citocinas/genética , Citocinas/metabolismo , Modelos Animais de Doenças , Ingestão de Alimentos/efeitos dos fármacos , Comportamento Exploratório/efeitos dos fármacos , Regulação da Expressão Gênica/efeitos dos fármacos , Hipotálamo/efeitos dos fármacos , Hipotálamo/metabolismo , Relações Interpessoais , Lipopolissacarídeos/toxicidade , Masculino , Doenças Metabólicas/patologia , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos , Ratos Wistar , Proteínas Ribossômicas/genética , Proteínas Ribossômicas/metabolismo , Fatores de Tempo
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