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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container_end_page 1173
container_issue 7
container_start_page 1167
container_title Critical care medicine
container_volume 22
creator Tanigaki, Toshimori
Suzuki, Yukio
Heimer, Dov
Wang, Weizheng
Sussman, Howard H
Ross, William G
Murphy, Gloria A
Ikeda, Hiroshi
Raffin, Thomas A
description 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
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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 &lt; .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 &lt; .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 stimulate neutrophil chemiluminescence; it decreased chemiluminescence. CONCLUSIONSa) Protein kinase C inhibition with high-dose H-7 increased wet/dry weight and albumin in lung/plasma and bronchoalveolar lavage/plasma ratios in guinea pigs; b) the H-7 high-dose group demonstrated damaged pulmonary endothelium by electron microscopy; and c) since neutrophil oxygen radical production was not increased by H-7 as assessed by flow cytometry and chemiluminescence, it appears that H-7-induced acute lung injury and endothelial damage are not mediated by increased neutrophil oxygen radical production. (Crit Care Med 1994; 22:1167–1173)</description><identifier>ISSN: 0090-3493</identifier><identifier>EISSN: 1530-0293</identifier><identifier>DOI: 10.1097/00003246-199407000-00020</identifier><identifier>PMID: 8026208</identifier><identifier>CODEN: CCMDC7</identifier><language>eng</language><publisher>Hagerstown, MD: Williams &amp; Wilkins</publisher><subject>1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine ; Animals ; Biological and medical sciences ; Bronchoalveolar Lavage Fluid - cytology ; Cell Membrane Permeability - drug effects ; Endothelium - drug effects ; Endothelium - ultrastructure ; Flow Cytometry ; Guinea Pigs ; Humans ; Isoquinolines - pharmacology ; Luminescent Measurements ; Lung - drug effects ; Lung - physiopathology ; Lung - ultrastructure ; Medical sciences ; Microscopy, Electron ; Neutrophils - drug effects ; Neutrophils - metabolism ; Oxygen - blood ; Piperazines - pharmacology ; Pneumology ; Protein Kinase C - antagonists &amp; inhibitors ; Random Allocation ; Respiratory Distress Syndrome, Adult - chemically induced ; Respiratory Distress Syndrome, Adult - pathology ; Respiratory Distress Syndrome, Adult - physiopathology ; Respiratory system : syndromes and miscellaneous diseases ; Specific Pathogen-Free Organisms</subject><ispartof>Critical care medicine, 1994-07, Vol.22 (7), p.1167-1173</ispartof><rights>Williams &amp; Wilkins 1994. All Rights Reserved.</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3840-b2c9907a180ef4c2324cb5caa8cb9a6d0a29786722cb85af8d926ca571da26d03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4126634$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8026208$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tanigaki, Toshimori</creatorcontrib><creatorcontrib>Suzuki, Yukio</creatorcontrib><creatorcontrib>Heimer, Dov</creatorcontrib><creatorcontrib>Wang, Weizheng</creatorcontrib><creatorcontrib>Sussman, Howard H</creatorcontrib><creatorcontrib>Ross, William G</creatorcontrib><creatorcontrib>Murphy, Gloria A</creatorcontrib><creatorcontrib>Ikeda, Hiroshi</creatorcontrib><creatorcontrib>Raffin, Thomas A</creatorcontrib><title>The protein kinase C inhibitor, H-7, induces acute lung injury in guinea pigs</title><title>Critical care medicine</title><addtitle>Crit Care Med</addtitle><description>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 &lt; .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 &lt; .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 stimulate neutrophil chemiluminescence; it decreased chemiluminescence. CONCLUSIONSa) Protein kinase C inhibition with high-dose H-7 increased wet/dry weight and albumin in lung/plasma and bronchoalveolar lavage/plasma ratios in guinea pigs; b) the H-7 high-dose group demonstrated damaged pulmonary endothelium by electron microscopy; and c) since neutrophil oxygen radical production was not increased by H-7 as assessed by flow cytometry and chemiluminescence, it appears that H-7-induced acute lung injury and endothelial damage are not mediated by increased neutrophil oxygen radical production. (Crit Care Med 1994; 22:1167–1173)</description><subject>1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bronchoalveolar Lavage Fluid - cytology</subject><subject>Cell Membrane Permeability - drug effects</subject><subject>Endothelium - drug effects</subject><subject>Endothelium - ultrastructure</subject><subject>Flow Cytometry</subject><subject>Guinea Pigs</subject><subject>Humans</subject><subject>Isoquinolines - pharmacology</subject><subject>Luminescent Measurements</subject><subject>Lung - drug effects</subject><subject>Lung - physiopathology</subject><subject>Lung - ultrastructure</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - metabolism</subject><subject>Oxygen - blood</subject><subject>Piperazines - pharmacology</subject><subject>Pneumology</subject><subject>Protein Kinase C - antagonists &amp; inhibitors</subject><subject>Random Allocation</subject><subject>Respiratory Distress Syndrome, Adult - chemically induced</subject><subject>Respiratory Distress Syndrome, Adult - pathology</subject><subject>Respiratory Distress Syndrome, Adult - physiopathology</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Specific Pathogen-Free Organisms</subject><issn>0090-3493</issn><issn>1530-0293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kV9PwjAUxRujQUQ_gkkffGR6-2db-2iIignGF3xe7roOCmOQdgvh21sFebNJc3N6zmnSXwmhDB4Z6PwJ4hJcZgnTWkIeVRI3hwsyZKmIgmtxSYYAGhIhtbgmNyGsAJhMczEgAwU846CG5GO-tHTnt511LV27FoOlE-rapStdt_VjOk3ycdRVb2ygaPrO0qZvF_Fo1ftDHHTRu9Yi3blFuCVXNTbB3p3miHy9vswn02T2-fY-eZ4lRigJScmN1pAjU2BraXh8iSlTg6hMqTGrALnOVZZzbkqVYq0qzTODac4q5NEWI6KO9xq_DcHbuth5t0F_KBgUP4CKP0DFGVDxCyhW74_VXV9ubHUunohE_-HkYzDY1B5b48I5JhnPMiFjTB5j-23TWR_WTb-3vlhabLpl8d_3iG_I5nu3</recordid><startdate>199407</startdate><enddate>199407</enddate><creator>Tanigaki, Toshimori</creator><creator>Suzuki, Yukio</creator><creator>Heimer, Dov</creator><creator>Wang, Weizheng</creator><creator>Sussman, Howard H</creator><creator>Ross, William G</creator><creator>Murphy, Gloria A</creator><creator>Ikeda, Hiroshi</creator><creator>Raffin, Thomas A</creator><general>Williams &amp; Wilkins</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199407</creationdate><title>The protein kinase C inhibitor, H-7, induces acute lung injury in guinea pigs</title><author>Tanigaki, Toshimori ; Suzuki, Yukio ; Heimer, Dov ; Wang, Weizheng ; Sussman, Howard H ; Ross, William G ; Murphy, Gloria A ; Ikeda, Hiroshi ; Raffin, Thomas A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3840-b2c9907a180ef4c2324cb5caa8cb9a6d0a29786722cb85af8d926ca571da26d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bronchoalveolar Lavage Fluid - cytology</topic><topic>Cell Membrane Permeability - drug effects</topic><topic>Endothelium - drug effects</topic><topic>Endothelium - ultrastructure</topic><topic>Flow Cytometry</topic><topic>Guinea Pigs</topic><topic>Humans</topic><topic>Isoquinolines - pharmacology</topic><topic>Luminescent Measurements</topic><topic>Lung - drug effects</topic><topic>Lung - physiopathology</topic><topic>Lung - ultrastructure</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - metabolism</topic><topic>Oxygen - blood</topic><topic>Piperazines - pharmacology</topic><topic>Pneumology</topic><topic>Protein Kinase C - antagonists &amp; inhibitors</topic><topic>Random Allocation</topic><topic>Respiratory Distress Syndrome, Adult - chemically induced</topic><topic>Respiratory Distress Syndrome, Adult - pathology</topic><topic>Respiratory Distress Syndrome, Adult - physiopathology</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Specific Pathogen-Free Organisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tanigaki, Toshimori</creatorcontrib><creatorcontrib>Suzuki, Yukio</creatorcontrib><creatorcontrib>Heimer, Dov</creatorcontrib><creatorcontrib>Wang, Weizheng</creatorcontrib><creatorcontrib>Sussman, Howard H</creatorcontrib><creatorcontrib>Ross, William G</creatorcontrib><creatorcontrib>Murphy, Gloria A</creatorcontrib><creatorcontrib>Ikeda, Hiroshi</creatorcontrib><creatorcontrib>Raffin, Thomas A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanigaki, Toshimori</au><au>Suzuki, Yukio</au><au>Heimer, Dov</au><au>Wang, Weizheng</au><au>Sussman, Howard H</au><au>Ross, William G</au><au>Murphy, Gloria A</au><au>Ikeda, Hiroshi</au><au>Raffin, Thomas A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The protein kinase C inhibitor, H-7, induces acute lung injury in guinea pigs</atitle><jtitle>Critical care medicine</jtitle><addtitle>Crit Care Med</addtitle><date>1994-07</date><risdate>1994</risdate><volume>22</volume><issue>7</issue><spage>1167</spage><epage>1173</epage><pages>1167-1173</pages><issn>0090-3493</issn><eissn>1530-0293</eissn><coden>CCMDC7</coden><abstract>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 &lt; .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 &lt; .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 stimulate neutrophil chemiluminescence; it decreased chemiluminescence. CONCLUSIONSa) Protein kinase C inhibition with high-dose H-7 increased wet/dry weight and albumin in lung/plasma and bronchoalveolar lavage/plasma ratios in guinea pigs; b) the H-7 high-dose group demonstrated damaged pulmonary endothelium by electron microscopy; and c) since neutrophil oxygen radical production was not increased by H-7 as assessed by flow cytometry and chemiluminescence, it appears that H-7-induced acute lung injury and endothelial damage are not mediated by increased neutrophil oxygen radical production. (Crit Care Med 1994; 22:1167–1173)</abstract><cop>Hagerstown, MD</cop><pub>Williams &amp; Wilkins</pub><pmid>8026208</pmid><doi>10.1097/00003246-199407000-00020</doi><tpages>7</tpages></addata></record>
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subjects 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
Animals
Biological and medical sciences
Bronchoalveolar Lavage Fluid - cytology
Cell Membrane Permeability - drug effects
Endothelium - drug effects
Endothelium - ultrastructure
Flow Cytometry
Guinea Pigs
Humans
Isoquinolines - pharmacology
Luminescent Measurements
Lung - drug effects
Lung - physiopathology
Lung - ultrastructure
Medical sciences
Microscopy, Electron
Neutrophils - drug effects
Neutrophils - metabolism
Oxygen - blood
Piperazines - pharmacology
Pneumology
Protein Kinase C - antagonists & inhibitors
Random Allocation
Respiratory Distress Syndrome, Adult - chemically induced
Respiratory Distress Syndrome, Adult - pathology
Respiratory Distress Syndrome, Adult - physiopathology
Respiratory system : syndromes and miscellaneous diseases
Specific Pathogen-Free Organisms
title The protein kinase C inhibitor, H-7, induces acute lung injury in guinea pigs
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