Fig. 3. Release of thromboxane (TX) B2(± SD), a stable metabolite of TXA2, into the perfusate of isolated rabbit lungs in which leukocyte activation was performed with 10−6M  N -formyl-Met-Leu-Phe (fMLP) in the absence or in presence of pancreatitis-associated protein (PAP; 260 μg/l, n = 9; 500 μg/l, n = 6). *  P < 0.05  vs. fMLP, **  P < 0.01  vs. fMLP, analysis of variance. PAP reduced TXB2generation in a dose-dependent manner. 

Fig. 3. Release of thromboxane (TX) B2(± SD), a stable metabolite of TXA2, into the perfusate of isolated rabbit lungs in which leukocyte activation was performed with 10−6M  N -formyl-Met-Leu-Phe (fMLP) in the absence or in presence of pancreatitis-associated protein (PAP; 260 μg/l, n = 9; 500 μg/l, n = 6). *  P < 0.05  vs. fMLP, **  P < 0.01  vs. fMLP, analysis of variance. PAP reduced TXB2generation in a dose-dependent manner. 

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