ABSTRACT Here, we evaluated whether the exposure of rats to a cafeteria diet pre- and/or post-weaning, alters histological characteristics in the White Adipose Tissue (WAT), Brown Adipose Tissue (BAT), and liver of adult male offspring. Female Wistar rats were divided into Control (CTL; fed on standard rodent chow) and Cafeteria (CAF; fed with the cafeteria diet throughout life, including pregnancy and lactation). After birth, only male offspring (F1) were maintained and received the CTL or CAF diets; originating four experimental groups: CTL-CTLF1; CTL-CAFF1; CAF-CTLF1; CAF-CAFF1. Data of biometrics, metabolic parameters, liver, BAT and WAT histology were assessed and integrated using the Principal Component Analysis (PCA). According to PCA analysis worse metabolic and biometric characteristics in adulthood are associated with the post-weaning CAF diet compared to pre and post weaning CAF diet. Thus, the CTL-CAFF1 group showed obesity, higher deposition of fat in the liver and BAT and high fasting plasma levels of glucose, triglycerides and cholesterol. Interestingly, the association between pre and post-weaning CAF diet attenuated the obesity and improved the plasma levels of glucose and triglycerides compared to CTL-CAFF1 without avoiding the higher lipid accumulation in BAT and in liver, suggesting that the impact of maternal CAF diet is tissue-specific.

OBJETIVO: Analisar as alterações histológicas pulmonares de quatro casos fatais de influenza pandêmica H1N1, correlacionando-os a características clínico-epidemiológicas. MÉTODOS: Estudo retrospectivo e descritivo de dados de prontuários de quatro pacientes que faleceram por influenza H1N1 na Unidade de Terapia Intensiva de um hospital universitário, em 2009. Os pacientes haviam sido submetidos a aspirado de nasofaringe e as amostras foram analisadas pelo método de reação em cadeia da polimerase em tempo real. Biópsia pulmonar foi realizada no dia do óbito; um escore de intensidade das alterações histopatológica foi aplicado. RESULTADOS: Três pacientes apresentaram reação em cadeia da polimerase em tempo real com resultado positivo (embora todos tivessem diagnóstico de influenza H1N1). As principais alterações histológicas identificadas foram: dano alveolar difuso exsudativo, com atelectasia de alvéolos; graus variáveis de hemorragia e edema alveolar; necrose e descamação do epitélio respiratório de vários bronquíolos; e formação de trombos. Uma das pacientes (gestante) apresentou, à histopatologia, achado de inclusão citomegálica. CONCLUSÃO: Os achados histopatológicos pulmonares em pacientes com influenza H1N1 fatal revelaram dano alveolar grave, com hemorragia alveolar e bronquiolite. Foi descrita uma coinfecção com citomegalovírus em paciente gestante.

OBJECTIVE: To analyze the histopathological lung findings of four fatal cases of the 2009 H1N1 influenza pandemic and their correlation with clinical and epidemiological characteristics. METHODS: Descriptive data from medical records of four patients who died in the Intensive Care Unit of a university hospital in 2009. Nasopharyngeal aspirate specimens were collected from the patients and were analyzed by real-time polymerase chain reaction. Lung biopsy was performed post mortem; a score of intensity for pathological changes was applied. RESULTS: Three patients had positive real-time polymerase chain reaction (although all of them had a clinical diagnose of influenza H1N1). The main histopathological changes were: exudative diffuse alveolar damage with atelectasis; varying degrees of alveolar hemorrhage and edema, necrosis and sloughing of the respiratory epithelium in several bronchioli; and thrombus formation. One of the patients (the pregnant one) presented histopathological findings of cytomegalic inclusion. CONCLUSION: The pulmonary histopathological findings in patients with fatal 2009 H1N1 influenza pandemic disclosed intense alveolar damage and hemorrhage and severe bronchiolitis. A co-infection with cytomegalovirus was described in the pregnant patient.