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1.
Braz. j. biol ; 78(4): 615-618, Nov. 2018. graf
Article in English | LILACS | ID: biblio-951590

ABSTRACT

Abstract Aim Obesity during pregnancy is one of the most established risk factors for negative long-term programming. The aim of the present study was to investigate the effects of maternal consumption of a high-fat diet during pregnancy and lactation on the weight gain, visceral adipose tissue and cholesterolemia in neonatal rats. Methods Wistar rats were divided into two groups according to the mother's diet during pregnancy and lactation: Control group (CG, n = 12) were the offspring of rats fed a standard diet (4% lipid) and the Test group (TG, n = 12) were pups rats fed on a high fat diet (23% lipid). The weight of the animals was measured on alternate days until the 22nd day of life, when collected visceral adipose tissue and blood were collected for biochemical analysis. For statistical analysis the Student t test, Sidak´s teste and two way ANOVA was used, with p <0.05. Results the test group showed differences in weight gain, visceral adipose tissue and higher cholesterol. Conclusion a maternal exposure to a high-fat diet during pregnancy and lactation can promote changes in weight gain, hypercholesterolemia and an increase in adipose tissue in neonatal rats.


Resumo Objetivo A obesidade durante a gestação é um dos fatores de risco mais estabelecidos para uma programação negativa em longo prazo. O objetivo do presente estudo foi investigar os efeitos do consumo materno de uma dieta hiperlipídica durante a gestação e lactação no aumento do peso, do tecido adiposo visceral e colesterolemia em ratos neonatos. Métodos Ratos Wistar foram divididos em dois grupos de acordo com a dieta da mãe durante a gestação e lactação: grupo controle (GC, n=12) composto por filhotes de ratas alimentadas com uma dieta padrão (lipídios 4%) e o grupo teste (GT, n=12) composto de filhotes de ratas alimentadas com dieta hiperlipídica (lipídios 23%). O peso dos animais foi aferido em dias alternados até o 22° dia de vida, quando foi coletado sangue para análises bioquímicas. Para a análise estatística utilizou-se os seguintes testes: two way ANOVA, teste de Sidak e teste t de Student, com p< 0,05. Resultados O grupo teste mostrou diferença no ganho de peso, no tecido adiposo visceral e nos níveis de colesterol. Conclusão Uma exposição materna a uma dieta hiperlipídica durante a gestação e lactação pode promover maior ganho ponderal, hipercolesterolemia e um aumento do tecido adiposo em ratos neonatos.


Subject(s)
Animals , Female , Pregnancy , Rats , Prenatal Exposure Delayed Effects/metabolism , Lactation/physiology , Adipose Tissue/pathology , Cholesterol/blood , Diet, High-Fat/adverse effects , Animals, Newborn/metabolism , Prenatal Exposure Delayed Effects/physiopathology , Pregnancy, Animal/physiology , Rats, Wistar , Disease Models, Animal , Lipids/blood , Animals, Newborn/growth & development , Obesity/pathology
2.
An. acad. bras. ciênc ; 89(1): 223-230, Jan,-Mar. 2017. tab, graf
Article in English | LILACS | ID: biblio-886620

ABSTRACT

ABSTRACT The aim of this study was to compare two models of swimming applied to pregnant rats born small for pregnancy age (SPA). Diabetes was chemically induced in adult female rats to develop an inadequate intrauterine environment, leading to birth of a SPA offspring. In adulthood, the female SPA rats were mated and submitted to different swimming programs. The exercise program 1 (Ex1) consisted of swimming for 15 minutes, followed by 15 minutes of rest and another 15 minutes of swimming, 3 days a week before and during pregnancy. Another program (Ex2) was applied during 60 minutes uninterrupted a day, 6 days/week during pregnancy. The pregnant rats presented no interference on body weight and glycemia. The rats submitted to Ex2 model showed decreased insulin and blood glucose levels by oral glucose tolerance test, and reduction in area under curve values. The offspring from dams submitted to both exercise protocols presented an increased rate of newborns SPA. However, the offspring from Ex2 dams showed percentage twice higher of newborns SPA than Ex1 offspring. Our data suggests that continuous exercise of 60 min/day ameliorated the enhanced peripheral insulin sensitivity in growth-restricted females. However, this protocol employed at pregnancy leads to intrauterine growth restriction.


Subject(s)
Animals , Male , Female , Pregnancy , Physical Conditioning, Animal/physiology , Physical Conditioning, Animal/methods , Swimming/physiology , Fetal Development/physiology , Prenatal Exposure Delayed Effects/physiopathology , Prenatal Exposure Delayed Effects/metabolism , Reference Values , Time Factors , Blood Glucose/analysis , Blood Glucose/metabolism , Body Weight/physiology , Random Allocation , Rats, Wistar , Models, Animal , Diabetes Mellitus, Experimental/physiopathology , Diabetes Mellitus, Experimental/metabolism , Fetal Growth Retardation/physiopathology , Fetal Growth Retardation/metabolism , Glucose Tolerance Test , Animals, Newborn/physiology
3.
CoDAS ; 28(5): 640-645, Sept.-Oct. 2016. tab, graf
Article in Portuguese | LILACS | ID: biblio-828568

ABSTRACT

RESUMO Objetivo Identificar os efeitos da ingestão de álcool na gestação sobre o sistema nervoso auditivo central em relação aos seus possíveis diagnósticos, Síndrome Fetal do Álcool, Síndrome Fetal do Álcool Parcial, Distúrbios ao Nascimento Relacionados ao Álcool e Distúrbio do Neurodesenvolvimento Relacionado ao Álcool, sua extensão e o método de avaliação auditiva. Estratégia de pesquisa Busca sistemática e integrativa nas bases de dados PubMed, LILACS e SciELO, com os termos em português e inglês “síndrome fetal do álcool”, “desordens relacionadas ao uso do álcool” associadas a “audição”. Critérios de seleção Dos 123 resumos identificados, foram seis selecionados, publicados até maio de 2015. Análise dos dados Foram elencados tópicos a serem respondidos, caracterização da casuística; o diagnóstico decorrente da exposição fetal nas crianças; método de avaliação auditiva; e resultados descritos. Resultados Entre as avaliações comportamentais, foram utilizados os testes dicóticos verbais com sílabas e com sentenças e o teste fala com ruído. Entre os testes eletrofisiológicos, no Potencial Evocado Auditivo de Tronco Encefálico, foi detectada alteração de sincronia neural, e no Potencial Evocado Auditivo de Longa Latência – P300, valores de latência precoces. Conclusão Existem evidências de que as crianças e adultos jovens expostos ao álcool na gestação apresentam sinais de comprometimento do sistema nervoso auditivo central, mas não foi possível caracterizar essas alterações nos diferentes subtipos diagnósticos do espectro. As vias auditivas corticais foram as mais investigadas e o método eletrofisiológico o mais utilizado, com um resultado inesperado em dois deles, a latência precoce da N2 e da P300.


ABSTRACT Purpose To identify the effects of alcohol intake during pregnancy on the central auditory nervous system in relation to their possible diagnosis, Fetal Alcohol Syndrome, partial Fetal Alcohol Syndrome, Alcohol-Related Birth Defects and Alcohol-Related Neurodevelopmental Disorder, his extension and the hearing assessment method. Research strategy Systematic and integrative review searched the databases PubMed, LILACS and SciELO, with terms in Portuguese and English “fetal alcohol syndrome”, “alcohol-related disorders” associated with “hearing”. Selection criteria: We identified 123 abstracts, six were selected and published until May 2015. Data analysis Were listed topics to be answered, characterization of the sample; the diagnosis result of fetal exposure; method of hearing assessment and described results. Results Among the behavioral assessments, Verbal Dichotic Tests with syllables and sentences and Speech in Noise Test, were used. Among the electrophysiological tests, the Brainstem Auditory Evoked Potential was detected change neural synchrony, and Long-Latency Auditory Evoked Potential – P300, early latency values. Conclusion There is evidence that children exposed to alcohol in utero present central auditory nervous system involvement signals, but it was not possible to identify the influence of different subtypes and their losses. Cortical auditory pathways were the most investigated and the electrophysiological method as used with an unexpected result in two of them, early N2 and P300 latency.


Subject(s)
Humans , Female , Pregnancy , Child , Prenatal Exposure Delayed Effects/etiology , Alcohol Drinking/adverse effects , Fetal Diseases/etiology , Hearing Disorders/chemically induced , Prenatal Exposure Delayed Effects/diagnosis , Prenatal Exposure Delayed Effects/physiopathology , Auditory Perception , Evoked Potentials, Auditory, Brain Stem , Electrophysiology , Evoked Potentials, Auditory , Fetal Diseases/diagnosis , Fetal Diseases/physiopathology , Hearing Disorders/diagnosis , Hearing Disorders/physiopathology
4.
Clinics ; 71(9): 521-527, Sept. 2016. tab, graf
Article in English | LILACS | ID: lil-794641

ABSTRACT

OBJECTIVES: Considering that changes in the maternal environment may result in changes in progeny, the aim of this study was to investigate the influence of sleep restriction during the last week of pregnancy on renal function and autonomic responses in male descendants at an adult age. METHODS: After confirmation of pregnancy, female Wistar rats were randomly assigned to either a control or a sleep restriction group. The sleep-restricted rats were subjected to sleep restriction using the multiple platforms method for over 20 hours per day between the 14th and 20th day of pregnancy. After delivery, the litters were limited to 6 offspring that were designated as offspring from control and offspring from sleep-restricted mothers. Indirect measurements of systolic blood pressure (BPi), renal plasma flow, glomerular filtration rate, glomerular area and number of glomeruli per field were evaluated at three months of age. Direct measurements of cardiovascular function (heart rate and mean arterial pressure), cardiac sympathetic tone, cardiac parasympathetic tone, and baroreflex sensitivity were evaluated at four months of age. RESULTS: The sleep-restricted offspring presented increases in BPi, glomerular filtration rate and glomerular area compared with the control offspring. The sleep-restricted offspring also showed higher basal heart rate, increased mean arterial pressure, increased sympathetic cardiac tone, decreased parasympathetic cardiac tone and reduced baroreflex sensitivity. CONCLUSIONS: Our data suggest that reductions in sleep during the last week of pregnancy lead to alterations in cardiovascular autonomic regulation and renal morpho-functional changes in offspring, triggering increases in blood pressure.


Subject(s)
Animals , Female , Pregnancy , Prenatal Exposure Delayed Effects/etiology , Sleep Deprivation/complications , Hypertension/etiology , Kidney Diseases/etiology , Prenatal Exposure Delayed Effects/physiopathology , Sleep Deprivation/physiopathology , Autonomic Nervous System/physiopathology , Time Factors , Blood Pressure/physiology , Random Allocation , Risk Factors , Rats, Wistar , Baroreflex/physiology , Fetal Development/physiology , Disease Models, Animal , Fourier Analysis , Glomerular Filtration Rate , Heart Rate/physiology , Hypertension/physiopathology , Kidney/physiopathology , Kidney Diseases/physiopathology
5.
Biol. Res ; 49: 1-10, 2016. ilus, graf
Article in English | LILACS | ID: biblio-950843

ABSTRACT

Schizophrenia is a severe psychiatric disorder that results in a significant disability for the patient. The disorder is characterized by impairment of the adaptive orchestration of actions, a cognitive function that is mainly dependent on the prefrontal cortex. This behavioral deficit, together with cellular and neurophysiological alterations in the prefrontal cortex, as well as reduced density of GABAergic cells and aberrant oscillatory activity, all indicate structural and functional deficits of the prefrontal cortex in schizophrenia. Among the several risk factors for the development of schizophrenia, stress during the prenatal period has been identified as crucial. Thus, it is proposed that prenatal stress induces neurodevelopmental alterations in the prefrontal cortex that are expressed as cognitive impairment observed in schizophrenia. However, the precise mechanisms that link prenatal stress with the impairment of prefrontal cortex function is largely unknown. Reelin is an extracellular matrix protein involved in the development of cortical neural connectivity at embryonic stages, and in synaptic plasticity at postnatal stages. Interestingly, down-regulation of reelin expression has been associated with epigenetic changes in the reelin gene of the prefrontal cortex of schizophrenic patients. We recently showed that, similar to schizophrenic patients, prenatal stress induces down-expression of reelin associated with the methylation of its promoter in the rodent prefrontal cortex. These alterations were paralleled with altered prefrontal cortex functional connectivity and impairment in prefrontal cortex-dependent behavioral tasks. Therefore, considering molecular, cellular, physiological and behavioral evidence, we propose a unifying framework that links prenatal stress and prefrontal malfunction through epigenetic alterations of the reelin gene.


Subject(s)
Humans , Female , Pregnancy , Prenatal Exposure Delayed Effects/physiopathology , Schizophrenia/etiology , Schizophrenia/physiopathology , Stress, Physiological/physiology , Brain/embryology , Serine Endopeptidases/genetics , Cell Adhesion Molecules, Neuronal/genetics , Extracellular Matrix Proteins/genetics , Epigenesis, Genetic/physiology , Nerve Tissue Proteins/genetics , Social Behavior Disorders/physiopathology , Brain/physiopathology , Gene Expression , Risk Factors , Cognition Disorders/physiopathology , DNA Methylation
6.
Int. braz. j. urol ; 41(1): 110-115, jan-feb/2015. tab, graf
Article in English | LILACS | ID: lil-742883

ABSTRACT

Introduction Non-androgenic growth factors are involved in the growth regulation of prostate cancer (PCa). Objective This is the first Brazilian study to correlate, in a population of patients operated for PCa, PSA, total testosterone, insulin-like growth factor-I (IGF-I) and insulin-like growth factor-binding protein-3 (IGFBP-3) with Gleason score and to compare with a control group with benign prostate hyperplasia (BPH). Materials and Methods This retrospective single-center study included 49 men with previously diagnosed PCa and 45 with previously diagnosed BPH. PSA, testosterone, IGF-I, IGFBP-3 were determined in both groups. Results PSA and IGFBP-3 levels were significantly higher in the PCa group as compared to the BPH group (p<0.001 and p=0.004, respectively). There was a significant difference when we compared the PSA before surgery (p<0.001) and at the inclusion in the study (p<0.001) and IGFBP3 (0.016) among patients with Gleason <7, ≥7 and BPH. In the PCa group, PSA, testosterone, IGF-I and IGFBP-3 levels were comparable between Gleason <7 and ≥7. Conclusions Our data suggest that in localized PCa, the quantification of PSA and, not of IGF-1, may provide independent significant information in the aggressiveness. IGFBP-3 could be a biochemical marker of disease control in PCa patients. .


Subject(s)
Animals , Female , Humans , Male , Mice , Pregnancy , Air Pollutants/toxicity , Cell Differentiation/drug effects , Depressive Disorder/physiopathology , Nanoparticles/toxicity , Prenatal Exposure Delayed Effects/physiopathology , Animals, Newborn , Blotting, Western , Cells, Cultured , Cities , Depressive Disorder/etiology , Hippocampus/metabolism , JNK Mitogen-Activated Protein Kinases/metabolism , Maze Learning/drug effects , Neurites/drug effects , Neurites/physiology , Neurons/cytology , Neurons/drug effects , Pilot Projects , Particulate Matter/toxicity , Prenatal Exposure Delayed Effects/etiology
7.
Rev. saúde pública (Online) ; 49: 41, 2015. tab, graf
Article in English | LILACS | ID: biblio-962125

ABSTRACT

OBJECTIVE Investigate the effect of exposure to smoking during pregnancy and early childhood on changes in the body mass index (BMI) from birth to adolescence.METHODS A population-based cohort of children (0-5 years old) from Cuiabá, Midwest Brazil, was assessed in 1999-2000 (n = 2,405). Between 2009 and 2011, the cohort was re-evaluated. Information about birth weight was obtained from medical records, and exposure to smoking during pregnancy and childhood was assessed at the first interview. Linear mixed effects models were used to estimate the association between exposure to maternal smoking during pregnancy and preschool age, and the body mass index of children at birth, childhood and adolescence.RESULTS Only 11.3% of the mothers reported smoking during pregnancy, but most of them (78.2%) also smoked during early childhood. Among mothers who smoked only during pregnancy (n = 59), 97.7% had smoked only in the first trimester. The changes in body mass index at birth and in childhood were similar for children exposed and those not exposed to maternal smoking. However, from childhood to adolescence the rate of change in the body mass index was higher among those exposed only during pregnancy than among those who were not exposed.CONCLUSIONS Exposure to smoking only during pregnancy, especially in the first trimester, seems to affect changes in the body mass index until adolescence, supporting guidelines that recommend women of childbearing age to stop smoking.


OBJETIVO Analisar se a exposição ao tabagismo materno durante a gravidez e no início da infância afeta as mudanças no índice de massa corporal entre o nascimento e a adolescência.MÉTODOS Realizado estudo de coorte de base populacional com 2.405 crianças (0 a 5 anos) nascidas em Cuiabá, Brasil, e avaliadas de 1999 a 2000. De 2009 a 2011, esse grupo foi reavaliado. Peso ao nascer foi obtido a partir de registros médicos e a exposição ao tabagismo durante a gravidez e infância foi avaliada na primeira entrevista. Modelos lineares de efeitos mistos foram utilizados para estimar a associação entre a exposição ao tabagismo materno, durante a gravidez e a fase pré-escolar, e o índice de massa corporal das crianças ao nascer e durante a infância e adolescência.RESULTADOS Apenas 11,3% das mães relataram fumar durante a gravidez, sendo que a maioria delas (78,2%) também fumou durante a fase pré-escolar da criança. Entre as mães que fumaram exclusivamente durante a gravidez (n = 59), 97,7% fumaram somente no primeiro trimestre. As mudanças de índice de massa corporal entre o nascimento e a infância foram semelhantes entre as crianças expostas e não expostas ao tabagismo materno. Entretanto, entre a infância e a adolescência, a taxa de variação do índice de massa corporal foi maior entre os expostos ao tabagismo materno apenas durante a gravidez quando comparado aos não expostos.CONCLUSÕES A exposição ao fumo apenas durante a gravidez, especialmente no primeiro trimestre, pode afetar as mudanças no índice de massa corporal até a adolescência, apoiando a recomendação de cessação do tabagismo entre as mulheres em idade fértil.


Subject(s)
Humans , Male , Female , Pregnancy , Child , Adolescent , Prenatal Exposure Delayed Effects/physiopathology , Smoking/physiopathology , Body Mass Index , Socioeconomic Factors , Birth Weight , Body Height , Cohort Studies
8.
Einstein (Säo Paulo) ; 12(4): 413-419, Oct-Dec/2014. tab, graf
Article in English | LILACS | ID: lil-732452

ABSTRACT

Objective To evaluate the effect of maternal diabetes on the blood pressure and kidney function of female offspring, as well as if such changes exacerbate during pregnancy. Methods Diabetes mellitus was induced in female rats with the administration of streptozotocin in a single dose, one week before mating. During pregnancy, blood pressure was measured through plethysmography. On the 20th day of pregnancy, the animals were placed for 24 hours in metabolic cages to obtain urine samples. After the animals were removed from the cages, blood samples were withdrawn. One month after pregnancy, new blood and urine sample were collected. Kidney function was evaluated through proteinuria, plasma urea, plasma creatinine, creatinine excretion rate, urinary flow, and creatinine clearance. Results The female offspring from diabetic mothers showed an increase in blood pressure, and a decrease in glomerular filtration rate in relation to the control group. Conclusion Hyperglycemia during pregnancy was capable of causing an increase in blood pressure and kidney dysfunction in the female offspring. .


Objetivo Avaliar o efeito do diabetes materno sobre a pressão arterial e a função renal da prole feminina, bem como verificar se as alterações observadas se exacerbam durante a prenhez. Métodos O diabetes mellitus foi induzido em ratas com a administração de estreptozocina em dose única, uma semana antes do cruzamento. Durante a prenhez, foram feitas medidas da pressão arterial por pletismografia. No 20o dia da prenhez, os animais foram colocados durante 24 horas em gaiolas metabólicas para obtenção de amostras de urina. Após a retirada dos animais das gaiolas, foram obtidas amostras de sangue. Um mês após a prenhez, foram obtidas novas amostras de sangue e urina para as determinações. A função renal foi avaliada por meio de proteinúria, ureia plasmática, creatinina plasmática, carga excretada de creatinina, fluxo urinário e clearance de creatinina. Resultados As fêmeas da prole de mães diabéticas apresentaram elevação da pressão arterial e redução do ritmo de filtração glomerular em relação ao grupo controle. Conclusão A hiperglicemia durante a gestação foi capaz de causar elevação da pressão arterial e disfunção renal na prole de sexo feminino. .


Subject(s)
Animals , Female , Pregnancy , Diabetes Mellitus, Experimental/complications , Diabetic Nephropathies/etiology , Hypertension/etiology , Pregnancy in Diabetics , Prenatal Exposure Delayed Effects/etiology , Creatinine/blood , Disease Models, Animal , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/metabolism , Diabetic Nephropathies/physiopathology , Gestational Age , Glomerular Filtration Rate , Hyperglycemia/complications , Hypertension/physiopathology , Kidney/physiopathology , Pregnancy in Diabetics/metabolism , Prenatal Exposure Delayed Effects/physiopathology , Proteinuria/urine , Rats, Wistar , Reference Values , Streptozocin , Time Factors , Urea/blood
9.
Arq. neuropsiquiatr ; 72(2): 136-144, 02/2014. tab, graf
Article in English | LILACS | ID: lil-702549

ABSTRACT

The maternal exposure to high fat diet (HFD) during pregnancy and breastfeeding have been considered an important inducer of alterations in offspring normal programming, both in animals and humans, and may disturb brain development. In the present study we investigated the somatic and sensory-motor development of the offspring from rat dams fed a HFD, compared with dams fed a control diet, during pregnancy or lactation. Indicators of the body growth, physical maturation, and reflex ontogeny were evaluated. Offspring of dams fed a HFD showed reduced weight and body growth, delayed physical maturation, and delayed maturation of the physiological reflexes, such as vibrissa placing, auditory startle response, and free-fall righting. Our findings suggest that maternal HFD during pregnancy or lactation modifies somatic and neurological development of the offspring, possibly increasing the risk of neuroendocrine and neuropsychiatric disorders later in life.


A exposição materna a dieta rica em gordura (DRG) durante a gravidez e a amamentação tem sido considerada um importante indutor de alterações da programação normal da prole, em animais e humanos, e pode atrapalhar o desenvolvimento do cérebro. No presente estudo, investigamos o desenvolvimento somático e sensório-motor da prole de ratas alimentadas com uma DRG, em comparação com ratas alimentadas com uma dieta controle, durante a gravidez ou lactação. Foram avaliados indicadores de crescimento corporal, maturação física e ontogênese de reflexos. A prole de ratas alimentadas com DRG mostrou redução de peso e crescimento do corpo, atraso da maturação física e maturação tardia de reflexos fisiológicos, tais como colocação pelas vibrissas, resposta ao susto e reação de aceleração. Nossos resultados sugerem que DRG materna durante a gravidez ou lactação modifica desenvolvimento somático e neurológico da prole, possivelmente aumentando o risco para distúrbios neuroendócrinos e neuropsiquiátricos mais tarde na vida.


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Avoidance Learning/physiology , Behavior, Animal/physiology , Diet, High-Fat/adverse effects , Prenatal Exposure Delayed Effects/physiopathology , Reflex/physiology , Animals, Newborn/growth & development , Body Weight , Lactation , Rats, Wistar
10.
Arq. bras. endocrinol. metab ; 56(2): 96-103, Mar. 2012. graf, tab
Article in English | LILACS | ID: lil-622529

ABSTRACT

OBJECTIVES: The objective of this study was to evaluate physical and sexual development and reproductive physiology in female rat offspring that developed in hyperglycemia conditions in utero and during lactation. MATERIALS AND METHODS: Maternal diabetes was induced in female rats by a single IV injection of streptozotocin before mating. Female offspring development was evaluated by means of the following parameters: physical development; age of vaginal opening and first estrus; weight and histological evaluation of uterus and ovaries; duration of the estrous cycle, sexual behavior, and fertility after natural mating. RESULTS: In the female offspring, maternal diabetes caused delays in initial physical development; diminution in ovary weight and number of follicles; and inferior reproductive performance compared with the control group. CONCLUSIONS: The exposure to hyperglycemia in uterus and during lactation caused delays in physical and sexual development, and affected the reproductive physiology of female rats negatively.


OBJETIVOS: O objetivo deste estudo foi avaliar o desenvolvimento físico e sexual e a fisiologia reprodutiva de ratas que se desenvolveram em condições hiperglicêmicas in utero e lactação. MATERIAIS E METODOS: Para induzir o diabetes nas ratas, foi utilizada estreptozotocina em dose única via intravenosa antes do acasalamento. A prole feminina foi avaliada por meio dos seguintes parâmetros: o desenvolvimento físico; a idade de abertura vaginal e do primeiro estro, peso e avaliação histológica do útero e ovários; a duração do ciclo estral, o comportamento sexual e a fertilidade após acasalamentos naturais. RESULTADOS: O diabetes materno provocou, na prole feminina, retardo no desenvolvimento físico; diminuição do peso dos ovários e do número de folículos; a performance reprodutiva foi inferior à do grupo controle. CONCLUSÕES: Concluiu-se que a exposição aos meios intrauterino e lactacional hiperglicêmicos provocou retardo no desenvolvimento físico e sexual e prejudicou a fisiologia reprodutiva de ratas.


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Diabetes Mellitus, Experimental/chemically induced , Lactation/drug effects , Prenatal Exposure Delayed Effects/physiopathology , Reproduction/drug effects , Sexual Development/drug effects , Animals, Newborn/growth & development , Disease Models, Animal , Fertility/drug effects , Ovary/drug effects , Ovary/growth & development , Random Allocation , Streptozocin , Sexual Behavior, Animal/drug effects
11.
Biol. Res ; 45(1): 87-92, 2012. ilus, tab
Article in English | LILACS | ID: lil-626752

ABSTRACT

The effect of prenatal malnutrition on the anatomy of the corpus callosum was assessed in adult rats (45-52 days old). In the prenatally malnourished animals we observed a significant reduction of the corpus callosum total area, partial areas, and perimeter, as compared with normal animals. In addition, the splenium of corpus callosum (posterior fifth) showed a significant decrease of fiber diameters in the myelinated fibers without changing density. There was also a significant decrease in diameter and a significant increase in density of unmyelinated fibers. Measurements of perimeter's fractal dimensions from sagittal sections of the brain and corpus callosum did not show significant differences between malnourished and control animals. These findings indicate that cortico-cortical connections are vulnerable to the prenatal malnutrition, and suggest this may affect interhemispheric conduction velocity, particulary in visual connections (splenium).


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Corpus Callosum/anatomy & histology , Malnutrition/pathology , Nerve Fibers/ultrastructure , Prenatal Exposure Delayed Effects/pathology , Body Weight/physiology , Control Groups , Corpus Callosum/physiology , Malnutrition/physiopathology , Nerve Fibers, Myelinated/ultrastructure , Prenatal Exposure Delayed Effects/physiopathology , Rats, Sprague-Dawley
12.
Rio de Janeiro; s.n; 2012. 69 f p.
Thesis in Portuguese | LILACS | ID: lil-756246

ABSTRACT

Dieta materna hiperlipídica (HF) em roedores ocasiona o desenvolvimento de resistência à insulina e o diabetes mellitus tipo 2 na prole adulta. Camundongos fêmeas foram alimentadas com dieta SC (standard chow) ou HF (hiperlipídica) durante oito semanas anteriores ao acasalamento, durante o período gestacional e metade da lactação. Os filhotes machos foram avaliados ao nascimento (0 dia) e aos 10 dias de idade. Nas progenitoras, foram avaliados o ganho de massa corporal (MC), a pressão arterial (PA), a eficiência alimentar (EA) e o teste oral de tolerância à glicose (TOTG). Na prole, foram avaliadas a evolução da massa corporal (MC), a glicemia, a estrutura da ilhota do pâncreas e a massa de célula-beta. Nas progenitoras, a ganho de massa corporal (MC) e a eficiência alimentar (EA) do grupo HF apresentaram um aumento de 50% em relação ao grupo SC durante o período pré-gestacional e um aumento de 70% do ganho de MC e 250% na EA, durante a gestação (P<0,0001). A pressão arterial e os níveis de corticosterona foram maiores no grupo HF quando comparados ao grupo SC (P=0,001). Em relação à massa corporal das proles, não houve diferença ao nascimento, contudo aos 10 dias de idade o grupo HF apresentou um aumento neste parâmetro, assim como um aumento dos níveis de glicemia e aumento do diâmetro da ilhota em relação ao grupo SC (P<0,001). Ao nascimento, a razão da massa de célula-beta/massa do pâncreas (MCB/MP), foi menor no grupo HF quando comparado ao grupo SC (-54%, P<0,0001), no entanto essa diferença não foi observada aos 10 dias de idade. A MCB/MP foi maior no grupo HF aos 10 dias de idade em relação ao grupo SC (+146%, P<0,0001)...


Subject(s)
Animals , Male , Female , Mice , Diet, High-Fat , Prenatal Exposure Delayed Effects/physiopathology , Insulin Resistance , Maternal Nutritional Physiological Phenomena , Pancreas/physiopathology , Body Composition , Prenatal Exposure Delayed Effects/metabolism , Dietary Fats/metabolism , Pregnancy/metabolism , Lactation/metabolism , Adipose Tissue/physiology
13.
Int. j. morphol ; 29(2): 496-500, June 2011. ilus, mapas, tab
Article in English | LILACS | ID: lil-597481

ABSTRACT

Considering the size of some nuclei and area, sex hormones control the sexual development of the brain. The sexual development of the brain can also be influenced by environmental stress. This study aimed to clear the effect of prenatal water deprivation on the development of sexual dimorphic nucleus (SDN) of the brain. In this research, pregnant rats were divided into two groups (control and treated). For the treated animals, water was removed from the ewes for 48 h at the end of third trimester of gestation (19-21 days). TUNEL staining was used for detection of apoptosis in paraffin embedded diencephalon selected sections. The ratio of apoptotic cells to non- apoptotic ones was calculated as apoptotic index. Differences of apoptotic index and serum testosterone were examined for statistical significance using Paired T- test (p<0.05). The apoptotic index was 0.0160±.01174 percent for control and 0.1870±.02541 percent for treated groups. The concentration of serum testosterone was 22.4±1.3 for control and 13.37±3.3 for treated groups. Prenatal water deprivation induces apoptosis in developing SDN nucleus of male rats that is derived by reducing the concentration of serum testosterone. The study shows the importance of low concentration acting testosterone for development of SDN nucleus that can be affected by environmental stress.


Considerando el tamaño de algunos núcleos y áreas, las hormonas sexuales controlan el desarrollo sexual del cerebro. El desarrollo sexual del cerebro también puede verse influido por el estrés ambiental. Este estudio tuvo como objetivo establecer el efecto de la privación prenatal de agua en el desarrollo del núcleo dimórfico sexual (NDS) del cerebro. Las ratas preñadas fueron divididas en dos grupos (control y tratados). Para los animales tratados, el agua se retiró de los bebederos durante 48h al final del tercer trimestre de gestación (días 19-21). La técnica TUNEL se utilizó para detectar apoptosis en secciones del diencéfalo incluidas en parafina. La proporción de células apoptóticas y no-apoptóticas fue calculada como índice de apoptosis. Las diferencias del índice de apoptosis y testosterona sérica fueron examinadas para observar significación estadística mediante t de Student pareado (p <0,05). El índice de apoptosis fue 0,0160±0,01174 por ciento para el control y 0,1870±0,02541 por ciento para los grupos tratados. La concentración de testosterona en suero fue de 22,4±1,3 para el grupo control y 13,37±3,3 para los grupos tratados. La privación de agua prenatal indujo la apoptosis en el desarrollo del NDS de las ratas macho derivadas por la reducción de concentración de testosterona sérica. El estudio muestra la importancia de una baja concentración de testosterona para el desarrollo de los NDS, que pueden verse afectados por el estrés ambiental.


Subject(s)
Animals , Male , Female , Pregnancy , Rats , Prenatal Exposure Delayed Effects/physiopathology , Sex Differentiation , Water Deprivation , Apoptosis , Preoptic Area , Stress, Physiological , Testosterone/blood , Rats, Sprague-Dawley , In Situ Nick-End Labeling , Genitalia, Male/physiopathology , Animals, Newborn
14.
Braz. j. med. biol. res ; 43(11): 1010-1018, Nov. 2010. ilus, tab
Article in English | LILACS | ID: lil-564138

ABSTRACT

Maternal dietary protein restriction during pregnancy is associated with low fetal birth weight and leads to renal morphological and physiological changes. Different mechanisms can contribute to this phenotype: exposure to fetal glucocorticoid, alterations in the components of the renin-angiotensin system, apoptosis, and DNA methylation. A low-protein diet during gestation decreases the activity of placental 11ß-hydroxysteroid dehydrogenase, exposing the fetus to glucocorticoids and resetting the hypothalamic-pituitary-adrenal axis in the offspring. The abnormal function/expression of type 1 (AT1R) or type 2 (AT2R) AngII receptors during any period of life may be the consequence or cause of renal adaptation. AT1R is up-regulated, compared with control, on the first day after birth of offspring born to low-protein diet mothers, but this protein appears to be down-regulated by 12 days of age and thereafter. In these offspring, AT2R expression differs from control at 1 day of age, but is also down-regulated thereafter, with low nephron numbers at all ages: from the fetal period, at the end of nephron formation, and during adulthood. However, during adulthood, the glomerular filtration rate is not altered, due to glomerulus and podocyte hypertrophy. Kidney tubule transporters are regulated by physiological mechanisms; Na+/K+-ATPase is inhibited by AngII and, in this model, the down-regulated AngII receptors fail to inhibit Na+/K+-ATPase, leading to increased Na+ reabsorption, contributing to the hypertensive status. We also considered the modulation of pro-apoptotic and anti-apoptotic factors during nephrogenesis, since organogenesis depends upon a tight balance between proliferation, differentiation and cell death.


Subject(s)
Animals , Female , Humans , Pregnancy , Hypertension/etiology , Kidney/physiopathology , Pregnancy Complications/physiopathology , Prenatal Exposure Delayed Effects/physiopathology , Protein Deficiency/physiopathology , Animals, Newborn , /metabolism , Apoptosis/physiology , Birth Weight , Diet, Protein-Restricted/adverse effects , Glucocorticoids/metabolism , Hypertension/physiopathology , Kidney Glomerulus/metabolism , Kidney Glomerulus/physiopathology , Kidney/metabolism , Maternal Nutritional Physiological Phenomena , Receptors, Angiotensin/metabolism , Renin-Angiotensin System/physiology
15.
Rev. méd. Chile ; 138(3): 366-372, mar. 2010.
Article in Spanish | LILACS | ID: lil-548175

ABSTRACT

Epigenetics refers to the study of how genes produce their effect on the phenotype of the organism. This article is a review on the scope and importance of recently discovered epigenetic mechanisms on human development and their relationship to perinatal epidemiological issues. It shows a general view and present concepts about epigenetics and its contribution to the comprehension of several physiologic and pathological conditions of human beings. Secondly, it analyzes the evidence coming from epidemiological and animal studies, about the influence of events that occur in the perinatal and early postnatal periods on adult life and the possible epigenetic mechanisms involved. Lastly, it underscores the implications ofthese results of future research and the design of public policies that take into account the importance of events in early life in thefuture development of individuals.


Subject(s)
Animals , Female , Humans , Pregnancy , Epigenesis, Genetic/genetics , Human Development/physiology , Prenatal Exposure Delayed Effects/genetics , Epigenesis, Genetic/physiology , Phenotype , Prenatal Exposure Delayed Effects/physiopathology
16.
Clinics ; 65(2): 209-219, 2010. tab, ilus
Article in English | LILACS | ID: lil-539839

ABSTRACT

OBJECTIVES: Although schizophrenia affects both human genders, there are gender-dependent differences with respect to age of onset, clinical characteristics, course and prognosis of the disease. METHODS: To investigate sex-dependent differences in motor coordination and activity as well as in cognitive and social behavior, we repeatedly tested female (n = 14) and male (n = 12) Fisher rats (postnatal days, PD 56-174) that had received intracerebroventricular injections of kainic acid as well as female (n = 15) and male (n = 16) control animals. The hippocampus was examined histologically. RESULTS: Compared to male controls, in the alcove test both female controls and female animals with prenatal intervention spent less time in a dark box before entering an unknown illuminated area. Again, animals that received prenatal injection (particularly females) made more perseveration errors in the T-maze alternation task compared to controls. Female rats exhibited a higher degree of activity than males, suggesting these effects to be sex-dependent. Finally, animals that received prenatal intervention maintained longer lasting social contacts. Histological analyses showed pyramidal cells in the hippocampal area CA3 (in both hemispheres) of control animals to be longer than those found in treated animals. Sex-dependent differences were found in the left hippocampi of control animals and animals after prenatal intervention. CONCLUSION: These results demonstrate important differences between males and females in terms of weight gain, response to fear, working memory and social behavior. We also found sex-dependent differences in the lengths of hippocampal neurons. Further studies on larger sample sets with more detailed analyses of morphological changes are required to confirm our data.


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Hippocampus/drug effects , Motor Activity/drug effects , Prenatal Exposure Delayed Effects/physiopathology , Social Behavior , Schizophrenia/physiopathology , Disease Models, Animal , Excitatory Amino Acid Agonists , Hippocampus/embryology , Hippocampus/physiopathology , Injections, Intraventricular , Kainic Acid , Maze Learning/drug effects , Sex Factors , Schizophrenia/chemically induced
17.
Rio de Janeiro; s.n; 2010. 85 p. ilus.
Thesis in Portuguese | LILACS | ID: lil-665409

ABSTRACT

A dieta hiperlipídica (high-fat, HF) materna durante a gestação e/ou lactação aumenta a susceptibilidade da prole para o desenvolvimento de doenças crônicas na fase adulta. Verificar a hipótese que a ingestão materna de dieta HF nos períodos críticos de desenvolvimento (gestação e/ou lactação) predispõe à doença não alcoólica do fígado gorduroso e alterações pancreáticas e no tecido adiposo de camundongos machos adultos. Camundongos C57BL/6 fêmeas receberam durante a gestação e/ou lactação dieta padrão (standard chow, SC) ou HF. Filhotes machos foram divididos em cinco grupos: SC - provenientes de mães SC; G - provenientes de mães HF durante a gestação; L - provenientes de mães HF durante a lactação; GL/HF - provenientes de mães HF durante a gestação/lactação, mantendo a mesma dieta HF no período pós-natal (do desmame aos 3 meses de idade); GL - provenientes de mães HF durante a gestação/lactação trocando a dieta para SC no período pós-natal (do desmame aos 3 meses de idade). Foi analisada ao longo do experimento a massa corporal da prole. No sacrifício (3 meses), o fígado, o pâncreas e a gordura epididimária foram removidos, pesados e processados e o sangue foi coletado para análise bioquímica. Ao nascimento e ao desmame, filhotes GL/HF foram mais pesados (+6% e +44%, p<0,05, respectivamente) que os filhotes SC. Os filhotes G apresentaram resistência à insulina e menor expressão do transportador de glicose no fígado (GLUT-2). A esteatose hepática foi observada nos grupos G, L, GL e principalmente nos filhotes do grupo GL/HF. A expressão hepática da proteína ligante de elementos regulatórios de esteróis (SREBP-1c) estava aumentada nos filhotes G, GL e GL/HF. Os filhotes G, GL e GL/HF apresentaram hipertrofia da ilhota pancreática e dos adipócitos quando comparados com o grupo SC. O consumo de dieta HF durante a gestação mostra-se ser o período mais prejudicial para os filhotes adultos de camundongos. A programação metabólica por dieta HF ...


Maternal high-fat diet (HF) during gestation and/or lactation period increases the susceptibility to development of chronic disease in offspring adult life. This work aimed to verify the hypothesis that maternal intake of high-fat diet in critical periods of pregnancy and/or suckling period predisposes to non alcoholic fatty liver disease, pancreatic and adipose tissue alterations in adulthood mice offspring. C57BL/6 female mice were fed, during gestation and/or lactation phases, with standard chow (SC) of HF diet. Male pups were divided into 5 groups: SC - from SC fed dam; G - from HF fed dam during gestation period; L - from HF fed dam during lactation period; GL - from HF fed dam during gestation and lactation periods and GL/HF - from HF fed dam during gestation and lactation, maintaining HF diet from post-weaning to adulthood. We analyzed body mass in all experiment, and at the euthanasia (3 mo-old), liver, pancreas and adipose tissue were removed, weighted and embedded. Blood was collected to biochemical analyses. At birth and at weaning, GL/HF pups were heavier than SC pups (+6% and +44%, p<0.05, respectively). G offspring showed insulin resistance and lower glucose transporter-2 expression (GLUT-2). Hepatic steatosis was present in G, L, GL and mainly in GL/HF offspring. Sterol regulatory element-binding protein-1c (SREBP-1c) expression was higher in G, GL and GL/HF offspring. It is important to mention that pancreatic islet hyperthophy and adipocyte hypertrophy were affected in G, GL and GL/HF offspring in comparison to SC. HF diet administration during gestation period is worse than lactation period. Furthermore, this type of programming by HF predisposes to adverse remodeling in liver, pancreas and adipose tissue in adult mice offspring


Subject(s)
Animals , Male , Female , Pregnancy , Mice , Dietary Fats/adverse effects , Dietary Fats/metabolism , Maternal Nutritional Physiological Phenomena , Prenatal Exposure Delayed Effects/physiopathology , Prenatal Exposure Delayed Effects/metabolism , Fatty Liver/physiopathology , Liver Diseases/etiology , Pancreas/physiopathology , Adipose Tissue/physiopathology
18.
Clinics ; 65(12): 1363-1369, 2010. graf, tab
Article in English | LILACS | ID: lil-578578

ABSTRACT

OBJECTIVES: The aim of the study was to investigate the effect of fetal undernutrition on the passive mechanical properties of skeletal muscle of weaned and young adult rats. INTRODUCTION: A poor nutrition supply during fetal development affects physiological functions of the fetus. From a mechanical point of view, skeletal muscle can be also characterized by its resistance to passive stretch. METHODS: Male Wistar rats were divided into two groups according to their mother's diet during pregnancy: a control group (mothers fed a 17 percent protein diet) and an isocaloric low-protein group (mothers fed a 7.8 percent protein diet). At birth, all mothers received a standardized meal ad libitum. At the age of 25 and 90 days, the soleus muscle and extensor digitorum longus (EDL) muscles were removed in order to test the passive mechanical properties. A first mechanical test consisted of an incremental stepwise extension test using fast velocity stretching (500 mm/s) enabling us to measure, for each extension stepwise, the dynamic stress (σd) and the steady stress (σs). A second test consisted of a slow velocity stretch in order to calculate normalized stiffness and tangent modulus from the stress-strain relationship. RESULTS: The results for the mechanical properties showed an important increase in passive stiffness in both the soleus and EDL muscles in weaned rat. In contrast, no modification was observed in young adult rats. CONCLUSIONS: The increase in passive stiffness in skeletal muscle of weaned rat submitted to intrauterine undernutrition it is most likely due to changes in muscle passive stiffness.


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Elasticity/physiology , Fetal Development/physiology , Malnutrition/complications , Muscle, Skeletal/physiopathology , Prenatal Exposure Delayed Effects/physiopathology , Reflex, Stretch/physiology , Analysis of Variance , Animals, Newborn , Diet, Protein-Restricted/adverse effects , Models, Animal , Muscle Contraction/physiology , Prenatal Nutritional Physiological Phenomena/physiology , Rats, Wistar , Weaning
19.
J. pediatr. (Rio J.) ; 84(3): 264-271, May-June. 2008. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-485285

ABSTRACT

OBJETIVO: Estudar características morfológicas, metabolismo e habilidades contráteis do músculo submetido a desnutrição protéica pré e pós-natal. MÉTODOS: Distribuição dos animais em dois grupos: controle, dieta normoprotéica (GC; n = 15; 5/5/5) e desnutrido, dieta hipoprotéica (GD; n = 15; 5/5/5), observados respectivamente no sétimo, 14º e 28º dia do período experimental. Foram avaliados massa corporal total, peso, habilidades contráteis e a morfologia do músculo tibial anterior. Amostras de tecidos com 8 m de espessura de ratos com idades de 7, 14 e 28 dias, corados por hematoxilina e eosina, e outros submetidos aos métodos histoquímicos nicotinamida adenina tetrazólio redutase (NADH-TR) e miofibrilar (m-ATPase) (pH = 4,4). RESULTADOS: Os pesos corporal e muscular apresentaram-se menores nos grupos desnutridos. Aos 7 dias de desnutrição, o músculo apresentou fibras com menor diâmetro, maior polimorfismo e maior teor de tecido conjuntivo endomisial. Nas histoquímicas, tipos de fibras sem delimitação segura. Aos 14 dias de desnutrição, fibras menores, mais polimórficas, muitas com núcleos centrais e moderado teor de tecido conjuntivo endomisial. Quanto à contração, a reação m-ATPase evidenciou fibras lentas e rápidas. A reação NADH-TR revelou os tipos de fibras slow oxidative, fast oxidative glycolytic e fast glycolytic. Aos 28 dias de desnutrição, fibras menores, agrupadas com contornos variáveis. Quanto ao tipo de contração e metabolismo, os três tipos de fibras apresentaram limites de reconhecimento indistinto. CONCLUSÃO: Os resultados experimentais sugerem que, além da redução no número de fibras, a desnutrição promove um retardamento na diferenciação das características morfológicas, metabólicas e contráteis dos tipos de fibras musculares esqueléticas em ratos na fase de crescimento.


OBJECTIVE: To study the contractile properties, metabolism and morphological characteristics of muscles submitted to prenatal and postnatal protein malnutrition. METHODS: Animals were distributed into two groups: Control, normoprotein diet (CG; n = 15; 5/5/5), and Malnourished, hypoprotein diet (MG; n = 15; 5/5/5), and examined on the 7th, 14th, and 28th days of the experiment. Total body mass, weight, and the contractile properties and morphology of the anterior tibial muscle were assessed. Several 8 µm-thick tissue samples were taken from 7, 14, and 28 day old rats and stained with HE or subjected to NADH-TR or m-ATPase (pH = 4.4) techniques. RESULTS: Body and muscle weight were lower in the malnourished group. On the 7th day of malnutrition, muscle samples exhibited fibers with smaller diameter, higher polymorphism and higher endomysial conjunctive tissue content. Histochemical methods were unable to precisely determine the types of fiber present. On the 14th day, there were smaller muscle fibers, more polymorphism, many of them with central nuclei and moderate endomysial conjunctive tissue content. With reference to contractile properties, the m-ATPase reaction identified both slow and fast fibers. The NADH-TR reaction revealed the following types of fiber: slow oxidative (SO), fast oxidative glycolytic (FOG) and fast glycolytic (FG). On the 28th day smaller, bunched muscle fibers varying shapes. All three types of fiber exhibited unclear recognition limits with respect to contraction and metabolism. CONCLUSION: Our experimental results suggest that, in addition to the reduction in numbers of fibers, malnutrition retards the differentiation of the morphological, metabolic, and contractile characteristics of skeletal muscle fibers in growing rats.


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Muscle Fibers, Skeletal , Muscle, Skeletal , Muscle Contraction/physiology , Muscle Development/physiology , Prenatal Exposure Delayed Effects/metabolism , Protein-Energy Malnutrition/metabolism , Animals, Newborn , Glycolysis/physiology , Muscle Fibers, Skeletal/metabolism , Muscle Fibers, Skeletal/pathology , Muscle, Skeletal/metabolism , Muscle, Skeletal/pathology , Muscle, Skeletal/physiopathology , Oxidation-Reduction , Prenatal Exposure Delayed Effects/pathology , Prenatal Exposure Delayed Effects/physiopathology , Protein-Energy Malnutrition/pathology , Protein-Energy Malnutrition/physiopathology , Rats, Wistar
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