RESUMO
AIMS: To evaluate the cell proliferation and death, and structural morphology of the pancreatic islet cells of the rats with hyperglycemia in the first month of life and compare to those of the control rats. MAIN METHODS: Female Sprague-Dawley newborn rats received Streptozotocin (a beta-cytotoxic drug) at birth for diabetes induction. Control and hyperglycemic animals were euthanized on different days of life: 5, 10, 15, and 30. The pancreas was collected and processed for immunohistochemical analysis of cleaved Caspase-3 (cell death), Ki-67 (cell proliferation), PDX-1 (transcription factor responsible for insulin synthesis), and endocrine hormones (insulin, glucagon, and somatostatin). KEY FINDINGS: Control females showed a higher percentage (%) of Ki-67-positive(+) cells on D10 and D15, a higher % of insulin+ and somatostatin+ cells on D15 and D30, a lower % of PDX-1+ cells on D10, and a higher % of glucagon+ cells on D10 and D30. Hyperglycemic females showed a lower % of Ki-67+ cells on D15, a higher % of cleaved Caspase-3+ cells on D15, and insulin+ cells on D15 and D30. In the comparison among the experimental groups, the hyperglycemic females showed an increased % of cleaved Caspase-3+ and Ki-67+ cells and a lower % of PDX-1+ cells. SIGNIFICANCE: This study enabled a better understanding of the abnormal pancreas development regarding cellular proliferation, apoptosis, and hormonal synthesis in the neonatal period. Thus, the pancreatic islets of hyperglycemic rats do not reestablish the normal endocrine cell population, and cellular apoptosis overcame the proliferative activity of these cells.
Assuntos
Animais Recém-Nascidos , Proliferação de Células , Hiperglicemia , Ilhotas Pancreáticas , Ratos Sprague-Dawley , Animais , Feminino , Hiperglicemia/metabolismo , Hiperglicemia/patologia , Ratos , Ilhotas Pancreáticas/metabolismo , Ilhotas Pancreáticas/patologia , Diabetes Mellitus Experimental/patologia , Diabetes Mellitus Experimental/metabolismo , Morte Celular , Glucagon/metabolismo , Insulina/metabolismo , Antígeno Ki-67/metabolismo , Caspase 3/metabolismo , Somatostatina/metabolismo , Apoptose , Transativadores , Proteínas de HomeodomínioRESUMO
Maternal diabetes may influence glucose metabolism in adult offspring, an area with limited research on underlying mechanisms. Our study explored the impact of maternal hyperglycemia during pregnancy on insulin resistance development. Adult female Sprague-Dawley rats from control and diabetic mothers were mated, and their female offspring were monitored for 150 days. The rats were euthanized for blood and muscle samples. Maternal diabetes led to heightened insulin levels, increased HOMA-IR, elevated triglycerides, and a raised TyG index in adult offspring. Muscle samples showed a decreased protein expression of AMPK, PI3K, MAPK, DRP1, and MFF. These changes induced intergenerational metabolic programming in female pups, resulting in insulin resistance, dyslipidemia, and glucose intolerance by day 150. Findings highlight the offspring's adaptation to maternal hyperglycemia, involving insulin resistance, metabolic alterations, the downregulation of insulin signaling sensors, and disturbed mitochondrial morphology. Maintaining maternal glycemic control emerges as crucial in mitigating diabetes-associated disorders in adult offspring.
Assuntos
Diabetes Mellitus Experimental , Diabetes Gestacional , Resistência à Insulina , Insulina , Músculo Esquelético , Fenótipo , Efeitos Tardios da Exposição Pré-Natal , Ratos Sprague-Dawley , Transdução de Sinais , Animais , Feminino , Gravidez , Insulina/metabolismo , Insulina/sangue , Músculo Esquelético/metabolismo , Músculo Esquelético/patologia , Diabetes Gestacional/metabolismo , Diabetes Gestacional/patologia , Efeitos Tardios da Exposição Pré-Natal/metabolismo , Diabetes Mellitus Experimental/metabolismo , Diabetes Mellitus Experimental/patologia , Ratos , Mitocôndrias/metabolismo , Glicemia/metabolismoRESUMO
ABSTRACT Several studies present different methodologies and results about intensity exercise, and many of them are performed in male rats. However, the impact of different type, intensity, frequency and duration of exercise on female rats needs more investigation. From the analysis of blood lactate concentration during lactate minimum test (LacMin) in the swimming exercise, the anaerobic threshold (AT) was identified, which parameter is defined as the transition point between aerobic and anaerobic metabolism. LacMin test is considered a good indicator of aerobic conditioning and has been used in prescription of training in different exercise modalities. However, there is no evidence of LacMin test in female rats. The objective was to determine AT in non-pregnant and pregnant Wistar rats. The LacMin test was performed and AT defined for mild exercise intensity was from a load equivalent to 1% of body weight (bw), moderate exercise as carrying 4% bw and severe intensity as carrying 7% bw. In pregnant rats, the AT was reached at a lower loading from 5.0% to 5.5% bw, while in non-pregnant the load was from 5.5% to 6.0% bw. Thus, this study was effective to identify exercise intensities in pregnant and non-pregnant rats using anaerobic threshold by LacMin test.
Assuntos
Animais , Masculino , Feminino , Gravidez , Ratos , Condicionamento Físico Animal , Limiar Anaeróbio/fisiologia , Ácido Láctico/metabolismo , Resistência Física , Natação , Ratos Wistar , Ácido Láctico/sangue , Teste de Esforço/métodosRESUMO
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.
Assuntos
Animais , Masculino , Feminino , Gravidez , Condicionamento Físico Animal/fisiologia , Condicionamento Físico Animal/métodos , Natação/fisiologia , Desenvolvimento Fetal/fisiologia , Efeitos Tardios da Exposição Pré-Natal/fisiopatologia , Efeitos Tardios da Exposição Pré-Natal/metabolismo , Valores de Referência , Fatores de Tempo , Glicemia/análise , Glicemia/metabolismo , Peso Corporal/fisiologia , Distribuição Aleatória , Ratos Wistar , Modelos Animais , Diabetes Mellitus Experimental/fisiopatologia , Diabetes Mellitus Experimental/metabolismo , Retardo do Crescimento Fetal/fisiopatologia , Retardo do Crescimento Fetal/metabolismo , Teste de Tolerância a Glucose , Animais Recém-Nascidos/fisiologiaRESUMO
ABSTRACT Bauhinia holophylla, commonly known as "cow's hoof", is widely used in Brazilian folk medicine for the diabetes treatment. Therefore, the aim of this study was at evaluating the aqueous extract effect of Bauhinia holophylla leaves treatment on the streptozotocin-induced diabetic rats. Diabetes was induced by Streptozotocin (40 mg/Kg) in female Wistar rats. Oral administration of aqueous extract of Bauhinia holophylla leaves was given to non-diabetic and diabetic rats at a dose of 400 mg/kg during 21 days. On day 17 of treatment, the Oral Glucose Tolerance Test was performed to determine the area under the curve. At the end of the treatment, the animals were anesthetized and blood was collected for serum biochemical parameters analysis. After treatment with Bauhinia holophylla extract, non-diabetic and diabetic rats presented no glycemic changes. On the other hand, the plant treatment decreased body weight and increased ALT and AST activities. In conclusion, the treatment with aqueous extract of B. holophylla leaves given to diabetic rats presented no hypoglycemic effect in nondiabetic animals and no antidiabetic effect in diabetic animals with the doses studied. In addition, the diabetic animals treated with the B. holophylla extract showed inconvenient effects and its indiscriminate consumption requires particular carefulness.
Assuntos
Animais , Feminino , Extratos Vegetais/uso terapêutico , Bauhinia/química , Diabetes Mellitus Experimental/tratamento farmacológico , Hipoglicemiantes/uso terapêutico , Fatores de Tempo , Glicemia/análise , Glicemia/efeitos dos fármacos , Peso Corporal , Extratos Vegetais/farmacologia , Reprodutibilidade dos Testes , Resultado do Tratamento , Ratos Wistar , Estreptozocina , Folhas de Planta/química , Ingestão de Líquidos , Ingestão de Alimentos , Teste de Tolerância a Glucose , Hipoglicemiantes/farmacologiaRESUMO
O objetivo deste trabalho foi investigar se os extratos das folhas de jamboläo (Eugenia jambolana) e de carambola (Averrhoa carambola), comercializados em larga escala por farmácias de manipulaçäo, realmente apresentam afeito hipoglicemiante quando testados em ratas com diabete induzido por streptozotocin. Cada extrato foi preparado com as folhas secas de jamboläo e de carambola por decocçäo (5g/1000mL), de forma semelhante ao método de preparaçäo recomendado à populaçäo. Entretanto, as doses utilizadas foram seis vêzes maiores que a consumida popularmente. Foram utilizadas ratas Wistar divididas aleatoriamente em 3 grupos: diabéticas-controle que receberam água destilada (C,n=7), diabéticas tratadas com 105,0mg/kg do extrato aquoso de carambola (DTC, n=7) e com 50,0mg/kg do extrato de jamboläo (DTJ,n=7), via oral (gavage)