Effects of activated protein C on coagulation and fibrinolysis in rabbits with endotoxin induced acute lung injury

Background Sepsis induced acute lung injury (ALI) as a common syndrome in clinical practice has a high mortality. Recombinant human activated protein C (APC) can significantly reduce the mortality of patients with severe sepsis. Several studies have implicated that APC may be protective in ALI. Meth...

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Veröffentlicht in:Chinese medical journal 2008-12, Vol.121 (24), p.2561-2565
Hauptverfasser: He, Hang-yong, Wang, Chen, Pang, Bao-sen
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description Background Sepsis induced acute lung injury (ALI) as a common syndrome in clinical practice has a high mortality. Recombinant human activated protein C (APC) can significantly reduce the mortality of patients with severe sepsis. Several studies have implicated that APC may be protective in ALI. Methods Twenty-one rabbits were operatively prepared and randomly divided into sham, control, or APC groups (n=7 in each group). After a tracheotomy had been performed, ALI was produced in the control and APC groups by infusion of Escherichia coil endotoxin 100 μg/kg per hour intravenously for 1 hour. The sham group received only the vehicle, infusion of 20 ml of 0.9% saline. The rabbits were studied under anesthesia for 6 hours and were ventilated with 40% oxygen. Bovine APC (25 μg·kg^-1·h^-1) was intravenously administered. The infusion was initiated half an hour post-injury and lasted for 4 hours. The animals were resuscitated with Ringer's lactate solution. Results In comparison with nontreatment in the control group, the infusion of APC significantly reduced the increase of thrombomodulin level (TM; control group was (0.68±0.06) ng/ml, vs APC group of (0.62±0.07) ng/ml at 6 hours, P 〈0.05), and significantly attenuated the fall in protein S (PS; control group was (2.32±0.03) μg/ml at 2 hours, (2.24±0.06) μg/ml at 4 hours and (2.21±0.09)μg/ml at 6 hours, vs APC group (2.46±0.04) μg/ml at 2 hours, (2.40±0.05) μg/ml at 4 hours and (2.39±0.07) μg/ml at 6 hours, P 〈0.01). In addition, APC limited the increase in plasminogen activator inhibitor-1 (PAI-1) both in plasma (control group was (0.68±0.12) ng/ml at 1 hour, (0.84±0.06) ng/ml at 2 hours, (0.87±0.08) ng/ml at 4 hours and (0.91±0.05) ng/ml at 6 hours, vs APC group (0.42±0.16) ng/ml at 1 hour, (0.43±0.04) ng/ml at 2 hours, (0.45±0.09) ng/ml at 4 hours and (0.45±0.14) ng/ml at 6 hours, P 〈0.01) and in bronchoalveolar lavage fluid (at 6 hours: sham, (1.05±0.05) ng/ml; control, (1.13±0.06) ng/ml; APC, (1.06±0.06) ng/ml; P 〈0.05). However, APC failed to prevent the decrease in PaO2/FiO2 ratio. APC-treated rabbits showed no significant difference in platelet count and antithrombin but exhibited less D-dimer production than did the controls. Moreover, APC limited the histopathological score of lung injury (2.6±0.8 in control, vs 1.4±0.6 in APC group, P〈0.01). Conclusion Anti-coagulation and pro-fibrinolysis activity may be two of the possible mechanisms by which activated protein C attenuated endotoxin-induced ALI.
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Recombinant human activated protein C (APC) can significantly reduce the mortality of patients with severe sepsis. Several studies have implicated that APC may be protective in ALI. Methods Twenty-one rabbits were operatively prepared and randomly divided into sham, control, or APC groups (n=7 in each group). After a tracheotomy had been performed, ALI was produced in the control and APC groups by infusion of Escherichia coil endotoxin 100 μg/kg per hour intravenously for 1 hour. The sham group received only the vehicle, infusion of 20 ml of 0.9% saline. The rabbits were studied under anesthesia for 6 hours and were ventilated with 40% oxygen. Bovine APC (25 μg·kg^-1·h^-1) was intravenously administered. The infusion was initiated half an hour post-injury and lasted for 4 hours. The animals were resuscitated with Ringer's lactate solution. Results In comparison with nontreatment in the control group, the infusion of APC significantly reduced the increase of thrombomodulin level (TM; control group was (0.68±0.06) ng/ml, vs APC group of (0.62±0.07) ng/ml at 6 hours, P 〈0.05), and significantly attenuated the fall in protein S (PS; control group was (2.32±0.03) μg/ml at 2 hours, (2.24±0.06) μg/ml at 4 hours and (2.21±0.09)μg/ml at 6 hours, vs APC group (2.46±0.04) μg/ml at 2 hours, (2.40±0.05) μg/ml at 4 hours and (2.39±0.07) μg/ml at 6 hours, P 〈0.01). In addition, APC limited the increase in plasminogen activator inhibitor-1 (PAI-1) both in plasma (control group was (0.68±0.12) ng/ml at 1 hour, (0.84±0.06) ng/ml at 2 hours, (0.87±0.08) ng/ml at 4 hours and (0.91±0.05) ng/ml at 6 hours, vs APC group (0.42±0.16) ng/ml at 1 hour, (0.43±0.04) ng/ml at 2 hours, (0.45±0.09) ng/ml at 4 hours and (0.45±0.14) ng/ml at 6 hours, P 〈0.01) and in bronchoalveolar lavage fluid (at 6 hours: sham, (1.05±0.05) ng/ml; control, (1.13±0.06) ng/ml; APC, (1.06±0.06) ng/ml; P 〈0.05). However, APC failed to prevent the decrease in PaO2/FiO2 ratio. APC-treated rabbits showed no significant difference in platelet count and antithrombin but exhibited less D-dimer production than did the controls. Moreover, APC limited the histopathological score of lung injury (2.6±0.8 in control, vs 1.4±0.6 in APC group, P〈0.01). Conclusion Anti-coagulation and pro-fibrinolysis activity may be two of the possible mechanisms by which activated protein C attenuated endotoxin-induced ALI.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.1097/00029330-200812020-00017</identifier><identifier>PMID: 19187596</identifier><language>eng</language><publisher>China: Beijing Institute of Respiratory Medicine, Beijing Chaoyang Hospital Capital Medical University, Beijing 100020, China</publisher><subject>Acute Lung Injury - blood ; Acute Lung Injury - chemically induced ; Animals ; Antithrombin III - metabolism ; Blood Coagulation - drug effects ; Blood Pressure - drug effects ; Endotoxins - pharmacology ; Fibrinolysis - drug effects ; Male ; Plasminogen Activator Inhibitor 1 - blood ; Protein C - pharmacology ; Protein S - metabolism ; Rabbits ; Random Allocation ; Thrombomodulin - blood ; 凝固作用 ; 急性肺损伤 ; 活性蛋白C ; 纤维蛋白溶解 ; 脓血症</subject><ispartof>Chinese medical journal, 2008-12, Vol.121 (24), p.2561-2565</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-e5bb48778d43311a97824ac7613891137b05b472842d1031c4040ee79d48ce843</citedby><cites>FETCH-LOGICAL-c421t-e5bb48778d43311a97824ac7613891137b05b472842d1031c4040ee79d48ce843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19187596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>He, Hang-yong</creatorcontrib><creatorcontrib>Wang, Chen</creatorcontrib><creatorcontrib>Pang, Bao-sen</creatorcontrib><title>Effects of activated protein C on coagulation and fibrinolysis in rabbits with endotoxin induced acute lung injury</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background Sepsis induced acute lung injury (ALI) as a common syndrome in clinical practice has a high mortality. Recombinant human activated protein C (APC) can significantly reduce the mortality of patients with severe sepsis. Several studies have implicated that APC may be protective in ALI. Methods Twenty-one rabbits were operatively prepared and randomly divided into sham, control, or APC groups (n=7 in each group). After a tracheotomy had been performed, ALI was produced in the control and APC groups by infusion of Escherichia coil endotoxin 100 μg/kg per hour intravenously for 1 hour. The sham group received only the vehicle, infusion of 20 ml of 0.9% saline. The rabbits were studied under anesthesia for 6 hours and were ventilated with 40% oxygen. Bovine APC (25 μg·kg^-1·h^-1) was intravenously administered. The infusion was initiated half an hour post-injury and lasted for 4 hours. The animals were resuscitated with Ringer's lactate solution. Results In comparison with nontreatment in the control group, the infusion of APC significantly reduced the increase of thrombomodulin level (TM; control group was (0.68±0.06) ng/ml, vs APC group of (0.62±0.07) ng/ml at 6 hours, P 〈0.05), and significantly attenuated the fall in protein S (PS; control group was (2.32±0.03) μg/ml at 2 hours, (2.24±0.06) μg/ml at 4 hours and (2.21±0.09)μg/ml at 6 hours, vs APC group (2.46±0.04) μg/ml at 2 hours, (2.40±0.05) μg/ml at 4 hours and (2.39±0.07) μg/ml at 6 hours, P 〈0.01). In addition, APC limited the increase in plasminogen activator inhibitor-1 (PAI-1) both in plasma (control group was (0.68±0.12) ng/ml at 1 hour, (0.84±0.06) ng/ml at 2 hours, (0.87±0.08) ng/ml at 4 hours and (0.91±0.05) ng/ml at 6 hours, vs APC group (0.42±0.16) ng/ml at 1 hour, (0.43±0.04) ng/ml at 2 hours, (0.45±0.09) ng/ml at 4 hours and (0.45±0.14) ng/ml at 6 hours, P 〈0.01) and in bronchoalveolar lavage fluid (at 6 hours: sham, (1.05±0.05) ng/ml; control, (1.13±0.06) ng/ml; APC, (1.06±0.06) ng/ml; P 〈0.05). However, APC failed to prevent the decrease in PaO2/FiO2 ratio. APC-treated rabbits showed no significant difference in platelet count and antithrombin but exhibited less D-dimer production than did the controls. Moreover, APC limited the histopathological score of lung injury (2.6±0.8 in control, vs 1.4±0.6 in APC group, P〈0.01). Conclusion Anti-coagulation and pro-fibrinolysis activity may be two of the possible mechanisms by which activated protein C attenuated endotoxin-induced ALI.</description><subject>Acute Lung Injury - blood</subject><subject>Acute Lung Injury - chemically induced</subject><subject>Animals</subject><subject>Antithrombin III - metabolism</subject><subject>Blood Coagulation - drug effects</subject><subject>Blood Pressure - drug effects</subject><subject>Endotoxins - pharmacology</subject><subject>Fibrinolysis - drug effects</subject><subject>Male</subject><subject>Plasminogen Activator Inhibitor 1 - blood</subject><subject>Protein C - pharmacology</subject><subject>Protein S - metabolism</subject><subject>Rabbits</subject><subject>Random Allocation</subject><subject>Thrombomodulin - blood</subject><subject>凝固作用</subject><subject>急性肺损伤</subject><subject>活性蛋白C</subject><subject>纤维蛋白溶解</subject><subject>脓血症</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE9PGzEQxS3UCgLlKyCrh962Hf_ZtX1EEYVKSL3A2bK93sRhYwevt5B--hqStqcZPb33ZvRDCBP4SkCJbwBAFWPQUABJKFBoqkTECVrQltOm7Tj5gBbAuq7plFJn6HyaNjXUtqI7RWdEESla1S1QvhkG78qE04CNK-GXKb7Hu5yKDxEvcYrYJbOaR1NC3U3s8RBsDjGN-ylMuJqysTbUhpdQ1tjHPpX0WuUQ-9nVLuPm4vE4x1WVNnPef0IfBzNO_vI4L9Dj95uH5V1z__P2x_L6vnGcktL41louhZA9Z4wQo4Sk3DjRESYVIUxYaC0XVHLaE2DEceDgvVA9l85Lzi7Ql0Pvi4mDiSu9SXOO9aL-vXbbzRs6yiu0apQHo8tpmrIf9C6Hrcl7TUC_8dZ_eet_vPU77xq9OkR3s936_n_wCLgaPh-71ymunkN9wxr3NITRa6qAAVOU_QGKqIZi</recordid><startdate>20081220</startdate><enddate>20081220</enddate><creator>He, Hang-yong</creator><creator>Wang, Chen</creator><creator>Pang, Bao-sen</creator><general>Beijing Institute of Respiratory Medicine, Beijing Chaoyang Hospital Capital Medical University, Beijing 100020, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</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><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20081220</creationdate><title>Effects of activated protein C on coagulation and fibrinolysis in rabbits with endotoxin induced acute lung injury</title><author>He, Hang-yong ; Wang, Chen ; Pang, Bao-sen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-e5bb48778d43311a97824ac7613891137b05b472842d1031c4040ee79d48ce843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acute Lung Injury - blood</topic><topic>Acute Lung Injury - chemically induced</topic><topic>Animals</topic><topic>Antithrombin III - metabolism</topic><topic>Blood Coagulation - drug effects</topic><topic>Blood Pressure - drug effects</topic><topic>Endotoxins - pharmacology</topic><topic>Fibrinolysis - drug effects</topic><topic>Male</topic><topic>Plasminogen Activator Inhibitor 1 - blood</topic><topic>Protein C - pharmacology</topic><topic>Protein S - metabolism</topic><topic>Rabbits</topic><topic>Random Allocation</topic><topic>Thrombomodulin - blood</topic><topic>凝固作用</topic><topic>急性肺损伤</topic><topic>活性蛋白C</topic><topic>纤维蛋白溶解</topic><topic>脓血症</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Hang-yong</creatorcontrib><creatorcontrib>Wang, Chen</creatorcontrib><creatorcontrib>Pang, Bao-sen</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Hang-yong</au><au>Wang, Chen</au><au>Pang, Bao-sen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of activated protein C on coagulation and fibrinolysis in rabbits with endotoxin induced acute lung injury</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2008-12-20</date><risdate>2008</risdate><volume>121</volume><issue>24</issue><spage>2561</spage><epage>2565</epage><pages>2561-2565</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Sepsis induced acute lung injury (ALI) as a common syndrome in clinical practice has a high mortality. Recombinant human activated protein C (APC) can significantly reduce the mortality of patients with severe sepsis. Several studies have implicated that APC may be protective in ALI. Methods Twenty-one rabbits were operatively prepared and randomly divided into sham, control, or APC groups (n=7 in each group). After a tracheotomy had been performed, ALI was produced in the control and APC groups by infusion of Escherichia coil endotoxin 100 μg/kg per hour intravenously for 1 hour. The sham group received only the vehicle, infusion of 20 ml of 0.9% saline. The rabbits were studied under anesthesia for 6 hours and were ventilated with 40% oxygen. Bovine APC (25 μg·kg^-1·h^-1) was intravenously administered. The infusion was initiated half an hour post-injury and lasted for 4 hours. The animals were resuscitated with Ringer's lactate solution. Results In comparison with nontreatment in the control group, the infusion of APC significantly reduced the increase of thrombomodulin level (TM; control group was (0.68±0.06) ng/ml, vs APC group of (0.62±0.07) ng/ml at 6 hours, P 〈0.05), and significantly attenuated the fall in protein S (PS; control group was (2.32±0.03) μg/ml at 2 hours, (2.24±0.06) μg/ml at 4 hours and (2.21±0.09)μg/ml at 6 hours, vs APC group (2.46±0.04) μg/ml at 2 hours, (2.40±0.05) μg/ml at 4 hours and (2.39±0.07) μg/ml at 6 hours, P 〈0.01). In addition, APC limited the increase in plasminogen activator inhibitor-1 (PAI-1) both in plasma (control group was (0.68±0.12) ng/ml at 1 hour, (0.84±0.06) ng/ml at 2 hours, (0.87±0.08) ng/ml at 4 hours and (0.91±0.05) ng/ml at 6 hours, vs APC group (0.42±0.16) ng/ml at 1 hour, (0.43±0.04) ng/ml at 2 hours, (0.45±0.09) ng/ml at 4 hours and (0.45±0.14) ng/ml at 6 hours, P 〈0.01) and in bronchoalveolar lavage fluid (at 6 hours: sham, (1.05±0.05) ng/ml; control, (1.13±0.06) ng/ml; APC, (1.06±0.06) ng/ml; P 〈0.05). However, APC failed to prevent the decrease in PaO2/FiO2 ratio. APC-treated rabbits showed no significant difference in platelet count and antithrombin but exhibited less D-dimer production than did the controls. Moreover, APC limited the histopathological score of lung injury (2.6±0.8 in control, vs 1.4±0.6 in APC group, P〈0.01). Conclusion Anti-coagulation and pro-fibrinolysis activity may be two of the possible mechanisms by which activated protein C attenuated endotoxin-induced ALI.</abstract><cop>China</cop><pub>Beijing Institute of Respiratory Medicine, Beijing Chaoyang Hospital Capital Medical University, Beijing 100020, China</pub><pmid>19187596</pmid><doi>10.1097/00029330-200812020-00017</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute Lung Injury - blood
Acute Lung Injury - chemically induced
Animals
Antithrombin III - metabolism
Blood Coagulation - drug effects
Blood Pressure - drug effects
Endotoxins - pharmacology
Fibrinolysis - drug effects
Male
Plasminogen Activator Inhibitor 1 - blood
Protein C - pharmacology
Protein S - metabolism
Rabbits
Random Allocation
Thrombomodulin - blood
凝固作用
急性肺损伤
活性蛋白C
纤维蛋白溶解
脓血症
title Effects of activated protein C on coagulation and fibrinolysis in rabbits with endotoxin induced acute lung injury
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