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Ann N Y Acad Sci ; 1070: 5-9, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16888146

ABSTRACT

We have taken advantage of the availability of vasoactive intestinal polypeptide (VIP) knockout (KO) mice to examine the possible influence of deletion of the VIP gene on: (a) airway reactivity and airway inflammation, as indicators of bronchial asthma; (b) mortality from endotoxemia, a model of septic shock; and (c) the pulmonary circulation. VIP KO mice showed: (a) airway hyperresponsiveness to the cholinergic agonist methacholine, as well as peribronchial and perivascular inflammation; (b) a greater susceptibility to death from endotoxemia; and (c) evidence suggestive of pulmonary hypertension.


Subject(s)
Vasoactive Intestinal Peptide/deficiency , Vasoactive Intestinal Peptide/metabolism , Animals , Bronchitis/chemically induced , Bronchitis/genetics , Bronchitis/metabolism , Disease Susceptibility , Endotoxemia/genetics , Endotoxemia/metabolism , Endotoxemia/pathology , Female , Lipopolysaccharides/pharmacology , Male , Methacholine Chloride/pharmacology , Mice , Mice, Inbred C57BL , Mice, Knockout , Survival Rate , Vasoactive Intestinal Peptide/genetics
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