Low-protein diet in adult male rats has long-term effects on metabolism.

Nutritional insults during developmental plasticity have been linked with metabolic diseases such as diabetes in adulthood. We aimed to investigate whether a low-protein (LP) diet at the beginning of adulthood is able to program metabolic disruptions in rats. While control rats ate a normal-protein (23%; NP group) diet, treated rats were fed a LP (4%; LP group) diet from 60 to 90 days of age, after which an NP diet was supplied until they were 150 days old. Plasma levels of glucose and insulin, autonomous nervous system (ANS), and pancreatic islet function were then evaluated. Compared with the NP group, LP rats exhibited unchanged body weight and reduced food intake throughout the period of protein restriction; however, after the switch to the NP diet, hyperphagia of 10% (P<0.05), and catch-up growth of 113% (P<0.0001) were found. The LP rats showed hyperglycemia, insulin resistance, and higher fat accretion than the NP rats. While the sympathetic tonus from LP rats reduced by 28%, the vagus tonus increased by 21% (P<0.05). Compared with the islets from NP rats, the glucose insulinotropic effect as well as cholinergic and adrenergic actions was unaltered in the islets from LP rats. Protein restriction at the beginning of adulthood induced unbalanced ANS activity and fat tissue accretion later in life, even without functional disturbances in the pancreatic islets.

Moderate exercise restores pancreatic beta-cell function and autonomic nervous system activity in obese rats induced by high-fat diet.

BACKGROUND/AIMS: Metabolic syndrome has been identified as one of the most significant threats to human health in the 21(st) century. Exercise training has been shown to counteract obesity and metabolic syndrome. The present study aimed to investigate the effects of moderate exercise training on pancreatic beta-cell function and autonomic nervous system (ANS) activity in rats fed a high-fat diet (HFD). METHODS: Weaning rats were divided into four groups: rats fed a standard chow or HFD (sedentary, Control-SED and HFD-SED; or exercised, Control-EXE and HFD-EXE, respectively). Exercised rats ran (from 21- to 91-days-old) for 60 minutes (3 times/week) over a 10-week period. Glucose and insulin tolerance tests were performed. Pancreatic islets were isolated to study glucose-induced insulin secretion (GIIS). Parasympathetic and sympathetic nerve electrical signals were measured, and liver samples were processed and histologically analyzed. RESULTS: Exercise prevented obesity, insulin resistance, and liver steatosis as well as improved total cholesterol, ALT, and AST levels. Islets from HFD rats showed insulin hypersecretion which was ameliorated by exercise. Exercise decreased vagal nerve activity in the HFD-EXE group and increased the activity of the sympathetic nervous system in both exercised groups. CONCLUSION: Exercise prevents obesity and liver steatosis and restores pancreatic beta-cell function and ANS activity in HFD-obese rats.

Use of the anabolic steroid nandrolone decanoate associated to strength training in Wistar rats / Uso do esteróide anabólico decanoato de nandrolona associado ao treinamento de força em ratos Wistar

Anabolic steroids have been constantly used among athletes and physically active individuals. Adverse effects of such use are reported in the literature. However, little is known about the effects of anabolic steroid use associated with strength training. Thus, this research aimed to identify possible morphophysiological alterations in Wistar rats treated with the anabolic steroid nandrolone decanoate and submitted to strength training. Twenty Wistar rats were divided in four groups: sedentary control (SC), sedentary hormone (SH), trained control (TC) and trained hormone (TH). After the experimental protocol period, animals were killed and body weight, adiposity, renal and hepatic injury markers, plasmatic lipid profile, glycemia, and insulinemia were determined. The experimental conditions strength training and nandrolone decanoate (isolated or associated) were positively correlated to a reduction on visceral and subcutaneous adipose tissue. The association of strength training with nandrolone decanoate was the most effective condition to increase muscle mass. Heart and kidneys weights, aspartate aminotransferase (AST) and high density lipoprotein (HDL) concentration were also negatively modified. The data demonstrated effects of anabolic steroids in body composition, with better results when associated with strength training, but collateral effects were observed.

Os esteróides anabólicos são usados indiscriminadamente entre atletas e praticantes de atividades físicas sendo que os efeitos adversos desse uso constam na literatura. Contudo, pouco se sabe dos efeitos do uso de esteróides anabólicos associados ao treinamento de força. Assim, este estudo objetivou identificar possíveis alterações morfofisiológicas em ratos Wistar tratados com decanoato de nandrolona e submetidos ao treinamento de força. Para atingir tal propósito, vinte ratos Wistar foram divididos em quatro grupos: sedentário controle (SC), sedentário hormônio (SH), treinado controle (TC) e treinado hormônio (TH). Após o período experimental, foram analisados o peso corporal, a adiposidade, marcadores de lesões hepáticas e renais, o perfil lipídico, a glicemia e a insulinemia. Foram observados efeitos do treinamento de força e do uso de decanoato de nandrolona (isolados ou associados) nos tecidos adiposos viscerais e subcutâneo. A associação de treinamento de força e uso de decanoato de nandrolona foi mais efetiva para aumentar a massa muscular. Os pesos dos rins e coração, e concentrações de aspartato aminotransferase (AST) e lipoproteína de alta densidade (HDL) foram negativamente modificados. Os dados demonstram efeitos do esteróide anabólico sobre a composição corporal, com melhores resultados obtidos com a associação ao treinamento de força, contudo efeitos colaterais foram observados.

Poor pubertal protein nutrition disturbs glucose-induced insulin secretion process in pancreatic islets and programs rats in adulthood to increase fat accumulation.

Similar to gestation/lactation, puberty is also a critical phase in which neuronal connections are still being produced and during which metabolic changes may occur if nutrition is disturbed. In the present study we aimed to determine whether peripubertal protein restriction induces metabolic programming. Thirty-day-old male rats were fed either a low protein (LP group) diet (4% w/w protein) or a normal protein (NP group) diet (23%) until 60 days of age, when they received the NP diet until they were 120 days old. Body weight (BW), food intake, fat tissue accumulation, glucose tolerance, and insulin secretion were evaluated. The nerve electrical activity was recorded to evaluate autonomous nervous system (ANS) function. Adolescent LP rats presented hypophagia and lower BW gain during the LP diet treatment (P<0.001). However, the food intake and BW gain by the LP rats were increased (P<0.001) after the NP diet was resumed. The LP rats presented mild hyperglycemia, hyperinsulinemia, severe hyperleptinemia upon fasting, peripheral insulin resistance and increased fat tissue accumulation and vagus nerve activity (P<0.05). Glucose-induced insulin secretion was greater in the LP islets than in the NP islets; however, the cholinergic response was decreased (P<0.05). Compared with the islets from the NP rats, the LP islets showed changes in the activity of muscarinic receptors (P<0.05); in addition, the inhibition of glucose-induced insulin secretion by epinephrine was attenuated (P<0.001). Protein restriction during adolescence caused high-fat tissue accumulation in adult rats. Islet dysfunction could be related to an ANS imbalance.

Efeito da redução de ninhada sobre as respostas autonômicas e metabólicas de ratos Wistar / Effect of small litter size on the autonomic and metabolic responses of Wistar rats

OBJETIVO: Este estudo investigou o perfil lipídico e a atividade elétrica dos nervos parassimpático (vago superior) e simpático (localizado na região esplâncnica) de ratos obesos oriundos de ninhada reduzida. MÉTODOS: Foram pesquisados dois grupos distintos, com 12 animas cada um: ninhada padrão, padronizado em nove filhotes por ninhada, e ninhada reduzida, três filhotes por ninhada. O consumo de ração e peso corporal foi acompanhado do desmame até o final do protocolo experimental. Aos 90 dias de idade, os animais foram anestesiados com (Thiopental®) e submetidos ao registro da atividade elétrica dos nervos simpático (vago) e parassimpático (da região esplâncnica); em seguida, foram sacrificados e retiradas e pesadas as gorduras retroperitoneal e periepididimal. Amostras de sangue foram coletadas para dosagens de glicemia, insulinemia, colesterol total, triglicerídeos e lipoproteína de alta densidade colesterol. RESULTADOS: Os ratos de ninhada reduzida apresentaram aumento da ingestão alimentar, peso corporal e tecido adiposo branco, quadros de hiperglicemia, hiperinsulinemia e hipercolesterolemia, aumento dos triglicérides e redução do lipoproteína de alta densidade colesterol. CONCLUSÃO: Quanto à atividade do nervo vago, os ratos ninhada reduzida apresentaram um aumento significativo em relação aos ratos ninhada padrão, e mesmo não havendo diferença na atividade simpática, o modelo ninhada reduzida mostrou-se eficaz para indução da obesidade, dislipidemia, hipercolesterolemia, hiperinsulinemia, hiperglicemia e desequilíbrio autonômico em roedores.

OBJECTIVE: This study investigated the lipid profile and electric activity of the parasympathetic (vagus nerve) and sympathetic (located in the splanchnic region) nerves of obese rats from small litters. METHODS: Two distinct groups were studied, each with 12 animals: normal litter with nine pups per litter and small litter, with three pups per litter. Chow intake and body weight were monitored from weaning until the end of the experimental protocol. At age 90 days, the animals were anesthetized with Thiopental® for investigation of the electric activity of the sympathetic and parasympathetic nerves. They were then sacrificed for removal and weighing of the retroperitoneal and epididymal fat pads. Blood samples were collected for determination of blood glucose, insulin, total cholesterol, triglycerides and high-density lipoprotein cholesterol. RESULTS: The small litters rats had high food intake, body weight, white fat tissue, blood glucose, blood insulin, total cholesterol and triglycerides, and low high-density lipoprotein cholesterol levels. CONCLUSION: The vagus nerve of the small litters rats was significantly more active than that of the normal litter rats. Sympathetic activity did not differ between the groups but the small litters model effectively promoted obesity, dyslipidemia, hypercholesterolemia, hyperinsulinemia, hyperglycemia and autonomic imbalance in rats.