TY - JOUR
T1 - Modifying pulmonary ischemia-reperfusion injury by altering ventilatory strategies during ischemia
AU - Hamvas, A.
AU - Park, C. K.
AU - Palazzo, R.
AU - Liptay, M.
AU - Cooper, J.
AU - Schuster, D. P.
PY - 1992
Y1 - 1992
N2 - We used an intact in vivo canine model of pulmonary ischemia-reperfusion (IR) injury to evaluate the differential effects of alveolar hypoxia and ventilation during 2 h of unilateral warm lung ischemia. Serial measurements of regional pulmonary blood flow, extravascular density (EVD), and transcapillary protein flux were made after reperfusion with the quantitative imaging technique of positron emission tomography. Twenty-seven animals were divided into five experimental groups: VENT O2 (n = 5) in which the left lung was ventilated with 40% O2 during ischemia, STATIC O2 (n = 4) in which the left lung was statically inflated with 40% O2 during ischemia, VENT N2 (n = 5) in which the left lung was ventilated with 100% N2 during ischemia, VENT N2/CO2 (n = 5) in which the left lung was ventilated with 95% N2-5% CO2 during ischemia, and STATIC N2 (n = 8) in which the left lung was statically inflated with 100% N2 during ischemia. These groups were compared with a control group (CONT, n = 3) that was studied previously. Protein flux was significantly increased in the previous ischemic lung only for the STATIC N2 group [median 175 x 10-4 min-1 (range 53-1,217) for the STATIC N2 group vs. 50 x 10-4 min-1 (range 40-56) for the CONT group] 0.25 h after reperfusion and did not change over 3 h. EVD also increased but not significantly. Protein flux and EVD in the other groups were not different from CONT. Thus, ventilation per se, regardless of inspired O2 content or static inflation with O2, conferred protection to an ischemic lung, and only a combination of alveolar hypoxia and the absence of ventilation resulted in injury. The differences in response were not explained by differences in O2 content, acid-base balance, or temperature of the lung during ischemia.
AB - We used an intact in vivo canine model of pulmonary ischemia-reperfusion (IR) injury to evaluate the differential effects of alveolar hypoxia and ventilation during 2 h of unilateral warm lung ischemia. Serial measurements of regional pulmonary blood flow, extravascular density (EVD), and transcapillary protein flux were made after reperfusion with the quantitative imaging technique of positron emission tomography. Twenty-seven animals were divided into five experimental groups: VENT O2 (n = 5) in which the left lung was ventilated with 40% O2 during ischemia, STATIC O2 (n = 4) in which the left lung was statically inflated with 40% O2 during ischemia, VENT N2 (n = 5) in which the left lung was ventilated with 100% N2 during ischemia, VENT N2/CO2 (n = 5) in which the left lung was ventilated with 95% N2-5% CO2 during ischemia, and STATIC N2 (n = 8) in which the left lung was statically inflated with 100% N2 during ischemia. These groups were compared with a control group (CONT, n = 3) that was studied previously. Protein flux was significantly increased in the previous ischemic lung only for the STATIC N2 group [median 175 x 10-4 min-1 (range 53-1,217) for the STATIC N2 group vs. 50 x 10-4 min-1 (range 40-56) for the CONT group] 0.25 h after reperfusion and did not change over 3 h. EVD also increased but not significantly. Protein flux and EVD in the other groups were not different from CONT. Thus, ventilation per se, regardless of inspired O2 content or static inflation with O2, conferred protection to an ischemic lung, and only a combination of alveolar hypoxia and the absence of ventilation resulted in injury. The differences in response were not explained by differences in O2 content, acid-base balance, or temperature of the lung during ischemia.
KW - lung water
KW - oxygen free radicals
KW - positron emission tomography
KW - protein flux
KW - pulmonary blood flow
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U2 - 10.1152/jappl.1992.73.5.2112
DO - 10.1152/jappl.1992.73.5.2112
M3 - Article
C2 - 1474092
AN - SCOPUS:0026495702
SN - 0161-7567
VL - 73
SP - 2112
EP - 2119
JO - Journal of applied physiology
JF - Journal of applied physiology
IS - 5
ER -