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Inflammation ; 37(2): 486-94, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24158570

RESUMO

Although assist ventilation with FIO2 0.21 is the preferable mode of ventilation in the intensive care unit, sometimes controlled ventilation with hyperoxia is needed. But the impact of this setting has not been extensively studied in elderly subjects. We hypothesized that a high fraction of inspired oxygen (FiO(2)) and controlled mechanical ventilation (CMV) is associated with greater deleterious effects in old compared to adult subjects. Adult and old rats were submitted to CMV with low tidal volume (6 ml/kg) and FiO(2) 1 during 3 or 6 h. Arterial blood gas samples were measured at 0, 60 and 180 min (four groups: old and adult rats, 3 or 6 h of CMV), and additionally at 360 min (two groups: old and adult rats, 6 h of CMV). Furthermore, total protein content (TPC) and tumor necrosis factor-alpha (TNF-α) in bronchoalveolar lavage were assessed; lung tissue was used for malondialdehyde and histological analyses, and the diaphragm for measurement of contractile function. Arterial blood gas analysis showed an initial (60 min) greater PaO(2) in elderly versus adult animals; after that time, elderly animals had lowers pH and PaO(2), and greater PaCO(2). After 3 h of CMV, TPC and TNF-α levels were higher in the old compared with the adult group (P < 0.05). After 6 h of MV, malondialdehyde was significantly higher in elderly compared with the adult animals (P < 0.05). Histological analysis showed leukocyte infiltration and edema, greater in old animals. In diaphragm, twitch contraction with caffeine significantly declined after 6 h of CMV only for the elderly group. These data support the hypothesis that relatively short-term CMV with low tidal volume and hyperoxia has greatest impact in elderly rats, decreasing diaphragmatic contractile function and increasing lung inflammation.


Assuntos
Diafragma/fisiopatologia , Hiperóxia/complicações , Pulmão/fisiopatologia , Pneumonia Associada à Ventilação Mecânica/etiologia , Respiração Artificial/efeitos adversos , Fatores Etários , Animais , Gasometria , Líquido da Lavagem Broncoalveolar/química , Modelos Animais de Doenças , Hiperóxia/sangue , Hiperóxia/imunologia , Hiperóxia/patologia , Hiperóxia/fisiopatologia , Mediadores da Inflamação/metabolismo , Pulmão/imunologia , Pulmão/patologia , Masculino , Malondialdeído/metabolismo , Contração Muscular , Pneumonia Associada à Ventilação Mecânica/sangue , Pneumonia Associada à Ventilação Mecânica/imunologia , Pneumonia Associada à Ventilação Mecânica/patologia , Pneumonia Associada à Ventilação Mecânica/fisiopatologia , Ratos , Ratos Wistar , Fatores de Risco , Volume de Ventilação Pulmonar , Fatores de Tempo , Fator de Necrose Tumoral alfa/metabolismo
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