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Apoptosis‐Dependent Acute Lung Injury and Repair After Intratracheal Instillation of Noradrenaline in Rats
Author(s) -
Uhal Bruce D.,
Rayford Heather,
Zhuang Jiaju,
Li Xiaopeng,
Laukka Jeremy,
SoledadConrad Valerie
Publication year - 2003
Publication title -
experimental physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 101
eISSN - 1469-445X
pISSN - 0958-0670
DOI - 10.1113/eph8802523
Subject(s) - bronchoalveolar lavage , apoptosis , in vivo , lung , pharmacology , chemistry , caspase 3 , pathology , medicine , programmed cell death , biology , biochemistry , microbiology and biotechnology
Earlier work in this laboratory showed that noradrenaline (NA) induces apoptosis in primary cultures of alveolar epithelial cells (AECs). Apoptosis of alveolar epithelial cells may promote the collapse of lung barrier function. On this basis we hypothesized that exogenous NA, administered by intratracheal (I.T.) instillation, might induce AEC apoptosis in vivo followed by acute lung injury. Delivery of NA (10 μM) I.T. into male Wistar rats increased labelling of both fragmented DNA, measured by in situ end labelling (ISEL), and the active form of caspase 3 (anti‐Casp3) 6 and 20 h after administration (P < 0.05), but instillation of the vehicle alone (PBS) had no effect. Both ISEL and anti‐Casp3 labelling were attenuated by concurrent I.T. delivery of the broad‐spectrum caspase inhibitor ZVADfmk. After 6 h, most ISEL‐ and Casp3‐positive cells were located in the surfaces of alveolar walls, but after 20 h more were found in alveolar spaces (P < 0.05). Instillation of NA also increased the bronchoalveolar lavage (BAL) content of fluorescent albumin (BODIPY‐alb), which had previously been injected intravenously; the increase was reversed by concurrent ZVADfmk administration. These data suggest that NA‐induced apoptosis of AECs in vivo is sufficient to invoke transient collapse of AEC barrier function that is rapidly repaired.