The protein kinase C inhibitor, H-7, induces acute lung injury in guinea pigs

OBJECTIVESTo determine if the protein kinase C inhibitor, H-7, alone can cause acute lung injury. In cell studies, H-7 inhibited phorbol myristate acetate-induced neutrophil oxygen radical release. Additionally, one animal study demonstrated that H-7 inhibited phorbol myristate acetate-induced lung...

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Veröffentlicht in:Critical care medicine 1994-07, Vol.22 (7), p.1167-1173
Hauptverfasser: Tanigaki, Toshimori, Suzuki, Yukio, Heimer, Dov, Wang, Weizheng, Sussman, Howard H, Ross, William G, Murphy, Gloria A, Ikeda, Hiroshi, Raffin, Thomas A
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Sprache:eng
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Zusammenfassung:OBJECTIVESTo determine if the protein kinase C inhibitor, H-7, alone can cause acute lung injury. In cell studies, H-7 inhibited phorbol myristate acetate-induced neutrophil oxygen radical release. Additionally, one animal study demonstrated that H-7 inhibited phorbol myristate acetate-induced lung injury. There have been no studies on the effect of H-7 alone on lung function or on neutrophil release of oxygen radicals. DESIGNProspective, randomized, laboratory study along with in vitro studies using flow cytometry and lucigenin-dependent chemiluminescence. SETTINGExperimental laboratory. SUBJECTSSpecific, pathogen-free guinea pigs and isolated human peripheral neutrophils. INTERVENTIONSGuinea pigs were randomized into three experimental groupssaline control, H-7 low dose (2 mg/kg bolus + 0.2 mg/kg/hr), and H-7 high dose (6 mg/kg bolus + 0.5 mg/kg/hr). Human neutrophils were randomized into control and experimental groups. The effects of H-7 on pulmonary permeability in guinea pigs were examined over an 8-hr period. MEASUREMENTS AND MAIN RESULTSWe measured the wet/dry weight ratio as an index of pulmonary edema and we measured the concentration ratios of 125I-labeled albumin in lung tissue and in bronchoalveolar lavage fluid and compared the ratios with those values in plasma as indices of pulmonary permeability. We also studied the in vitro effect of H-7 on human neutrophil oxygen radical production, using flow cytometry and lucigenin-dependent chemiluminescence. By flow cytometry, we measured oxygen radical production using the 2,7′-dichlorofluorescin and hydroethidine assays. The 2,7′-dichlorofluorescin assay mainly measures hydrogen peroxide, while the hydroethidine assay measures either superoxide anion alone or in combination with other oxygen intermediaries like hydrogen peroxide. Neutrophils (5 × 105) were obtained by Ficoll-Hypaque gradient centrifugation and were incubated with H-7 (5, 25, 100 uM). In the H-7 high-dose group, wet/dry weight ratio, and 125I-labeled albumin ratios in lung/plasma, and bronchoalveolar lavage/plasma were significantly increased (p < .05 for each ratio). Pulmonary endothelial gap and subendothelial bleb formation were demonstrated in the high-dose group by electron microscopy. One hundred micromols of H-7 caused a small, significant decrease (23.3%, p < .05) in neutrophil oxygen radical production assessed by 2,7′-dichlorofluorescin. H-7 had no other effects on neutrophil oxygen radical production. H-7 did not stimulat
ISSN:0090-3493
1530-0293
DOI:10.1097/00003246-199407000-00020