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21. |
Alteration of n-3 fatty acid composition in lung tissue after short-term infusion of fish oil emulsion attenuates inflammatory vascular reaction |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1893-1902
Irmingard Breil,
Thea Koch,
Axel Heller,
Ewald Schlotzer,
Adolf Grunert,
Klaus van Ackern,
Heinz Neuhof,
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摘要:
ObjectivesTo investigate whether modulation of the fatty acid profile can be achieved by the short-term infusion of a fish oil emulsion which may attenuate the pulmonary response to inflammatory stimulation. Changes of fatty acid pattern in lung tissue and perfusate were analyzed and correlated with physiologic data after a 3-hr infusion of fish oil in comparison with a soybean oil preparation.DesignProspective, randomized, controlled trial.SettingExperimental laboratory in a university teaching hospital.SubjectsForty standard breed rabbits of either gender.InterventionsIsolated lungs from anesthetized rabbits were ventilated and recirculation-perfused (200 mL/min) with 200 mL of cell-free buffer solution to which either 2 mL of saline (control, n = 6), 2 mL of a 10% soybean oil preparation (n = 6), or 2 mL of a 10% fish oil emulsion (n = 6) were added. Samples of perfusate and lung tissue were collected for analysis of fatty acid composition. Tissue and perfusate fatty acid composition were analyzed by capillary gas chromatography. To study metabolic alterations in states of inflammatory stimulation, lungs of each group were stimulated with small doses of the calcium ionophore, A23187 (10 sup -8 M), during the 180-min lipid perfusion period and again after washing out the lipids by exchanging the perfusion fluid. Pulmonary arterial pressure and lung weight gain were monitored, and eicosanoids were analyzed in the perfusate.Measurements and Main ResultsFree eicosapentaenoic acids increased several-fold in lung tissue and perfusate during a 3-hr infusion with fish oil. The intravenously administered n-3 fatty acids were rapidly hydrolyzed, as indicated by the appearance of substantial quantities of eicosapentaenoic acid in the perfusate free fatty acid fraction. This increase of perfusion levels of eicosapentaenoic acid was paralleled by an attenuated pressure increase and edema formation due to calcium ionophore challenge and an altered eicosanoid spectrum determined in the perfusate compared with soybean oil-treated lungs.ConclusionShort-term n-3 lipid application (fish oil emulsion) exerts anti-inflammatory effects on lung vasculature, which may be due to the metabolism of eicosapentaenoic acid resulting in the generation of less potent inflammatory eicosanoids.(Crit Care Med 1996; 24:1893-1902)
ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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22. |
Protective effects of human urinary trypsin inhibitor against trypsin-induced relaxation in rat aorta |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1903-1907
Takuji Ooka,
Yoshio Hatano,
Manabu Yamamoto,
Kohji Ogawa,
Shizuya Saika,
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摘要:
ObjectivesTo investigate the vasodilatory responses induced by trypsin, and to determine the antitrypsin effects of human urinary trypsin inhibitor on blood vessels.DesignProspective, randomized, controlled study, with repeated measurements.SettingUniversity research laboratory.InterventionsThe isometric tension of the aortic rings isolated from male Wistar rats was recorded. The vasodilatory responses to varying amounts of trypsin (0.01 to 10 U/mL) were examined under pretreatment with human urinary trypsin inhibitor (1 to 10 U/mL), chicken-egg-white trypsin inhibitor (0.1 to 10 mg/mL), Nomega-nitro-L-arginine (3 times 10 sup -5 M), and denudation of the endothelium. In addition, with the scanning electron microscopy, the endothelium of aorta was examined under treatment with trypsin alone (10 U/mL), and with trypsin plus human urinary trypsin inhibitor (10 U/mL each).4Measurements and Main ResultsThe addition of trypsin produced dose-dependent relaxation in aortic rings with an intact endothelium, which was abolished by denudation and treatment with Nomega-nitro-L-arginine. Pretreatment with human urinary trypsin inhibitor and with chicken-egg-white trypsin inhibitor caused dose-dependent inhibition against trypsin-induced vasorelaxation. On the repeated trials of the response to trypsin, the responses gradually developed tachyphylaxis in control aortic rings, whereas no tachyphylaxis developed in rings pretreated with human urinary trypsin inhibitor (10 U/mL). Scanning electron microscopy demonstrated endothelial disruption in aorta exposed to trypsin alone, whereas the endothelium was intact in strips treated with trypsin plus human urinary trypsin inhibitor.ConclusionsThe data indicate that relaxation induced by trypsin is attributable to nitric oxide released from the endothelium, and that human urinary trypsin inhibitor protects vessels against trypsin-induced endothelial injury. It appears that the clinical antishock effect of human urinary trypsin inhibitor is ascribable in part to its antitrypsin activity on the endothelium of vascular smooth muscle.(Crit Care Med 1996; 24:1903-1907)
ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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23. |
Role of granulocyte elastase in ischemia/reperfusion injury of rat liver |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1908-1912
Shigeki Kushimoto,
Kenji Okajima,
Mitsuhiro Uchiba,
Kazunori Murakami,
Naoaki Harada,
Hiroaki Okabe,
Kiyoshi Takatsuki,
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摘要:
ObjectiveTo investigate the role of granulocyte elastase in ischemia/reperfusion injury of liver, the effect of ONO-5046, a granulocyte elastase inhibitor, was examined in ischemia/reperfusion-induced liver injury in rats.DesignProspective, randomized, controlled study.SettingResearch laboratory at a university medical center.SubjectsMale Wistar rats, weighing 220 to 280 g.InterventionsAnimals receiving continuous intravenous infusion of ONO-5046 (50 mg/kg/hr) were subjected to hepatic ischemia/reperfusion. Hepatic damage was evaluated by effects on bile formation capacity, plasma clearance of indocyanine green, and serum aminotransferase concentrations after ischemia/reperfusion.Measurements and Main ResultsHepatic dysfunction, observed after 60 mins of ischemia/reperfusion, led to a reduction in bile flow and to a decrease in the plasma clearance of indocyanine green. These indicators of hepatic dysfunction were prevented, to a large extent, by administration of ONO-5046. Serum concentrations of aminotransferases increased after hepatic ischemia/reperfusion, peaking at 12 hrs of reperfusion. Increases in serum concentrations of aminotransferases were significantly inhibited by ONO-5046.ConclusionGranulocyte elastase derived from activated leukocytes may play a critical role in hepatic dysfunction and the subsequent hepatic injury induced by ischemia/reperfusion.(Crit Care Med 1996; 24:1908-1912)
ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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24. |
Inhaled nitric oxide in neonatal and pediatric acute respiratory distress syndromeDose response, prolonged inhalation, and weaning |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1913-1919
Sueha Demirakca,
Joerg Dotsch,
Christoph Knothe,
Juergen Magsaam,
Hans Ludwig Reiter,
Juergen Bauer,
Peter Gonne Kuehl,
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摘要:
ObjectiveInhaled nitric oxide is a potent and selective pulmonary artery vasodilator. We studied the effects of nitric oxide inhalation in neonatal and pediatric acute respiratory distress syndrome (ARDS) patients with respect to dosage, prolonged inhalation, and weaning.DesignProspective, open-label study.SettingNeonatal and pediatric intensive care units of a level three university hospital.Patients20 cm H2O/torr) were enrolled.InterventionsTo identify the optimal dosage for continuous nitric oxide inhalation, doses between 1 and 80 parts per million (ppm) of nitric oxide were tested after the patients had stabilized. Daily withdrawals of nitric oxide were made, according to predetermined criteria.Measurements and Main ResultsNine neonatal and eight pediatric ARDS patients (mean Pediatric Risk of Mortality score 28.4 +/- 6.1; mortality risk 54 +/- 15%) were studied. The following variables changed within 24 hrs of nitric oxide inhalation: mean oxygenation index decreased by 56% (from 34 +/- 12 to 15 +/- 7 cm H2O/torr, p = .0004); alveolar-arterial O2gradient decreased by 31% (from 579 +/- 71 to 399 +/- 102 torr (77.2 +/- 9.5 to 53.2 +/- 13.6 kPa), p = .0004); and mean systemic arterial pressure increased by 15% (from 49 +/- 10 to 57 +/- 12 mm Hg, p = .0029). The optimal dose of nitric oxide was 20 ppm in neonates (with additional persistent pulmonary hypertension of the newborn) and 10 ppm in pediatric patients. Prolonged inhalation (4 to 21 days) was associated with continuous improvement of oxygenation. An oxygenation index of <5 cm H2O/torr predicted successful withdrawal, with a sensitivity of 75% and a specificity of 89%. None of the patients had to be rescued with extracorporeal membrane oxygenation and 16 of the 17 patients survived.ConclusionsInhaled nitric oxide enhances pulmonary gas exchange, with concomitant hemodynamic stabilization, in neonatal and pediatric ARDS. Best effective doses were 10 ppm of nitric oxide in pediatric ARDS and 20 ppm in neonates. Treatment should be continued until an oxygenation index of <or=to5 cm H2O/torr is achieved. Effects on outcome need verification in larger controlled trials.(Crit Care Med 1996; 24:1913-1919)
ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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25. |
Relationship between the humidity and temperature of inspired gas and the function of the airway mucosa |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1920-1929
Robin Williams,
Nigel Rankin,
Tony Smith,
David Galler,
Paul Seakins,
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摘要:
ObjectiveTo review the available literature on the relationship between the humidity and temperature of inspired gas and airway mucosal function.Data SourcesInternational computerized databases and published indices, experts in the field, conference proceedings, bibliographies.Study Selection/Data ExtractionTwo hundred articles/texts on respiratory tract physiology and humidification were reviewed. Seventeen articles were selected from 40 articles for inclusion in the published data verification of the model. Selection was by independent reviewers. Extraction was by consensus, and was based on finding sufficient data.Data SynthesisA relationship exists between inspired gas humidity and temperature, exposure time to a given humidity level, and mucosal function. This relationship can be modeled and represented as an inspired humidity magnitude vs. exposure time map. The model is predictive of mucosal function and can be partially verified by the available literature. It predicts that if inspired humidity deviates from an optimal level, a progressive mucosal dysfunction begins. The greater the humidity deviation, the faster the mucosal dysfunction progresses.ConclusionsA model for the relationship between airway mucosal dysfunction and the combination of the humidity of inspired gas and the duration over which the airway mucosa is exposed to that humidity is proposed. This model suggests that there is an optimal temperature and humidity above which, and below which, there is impaired mucosal function. This optimal level of temperature and humidity is core temperature and 100% relative humidity. However, existing data are only sufficient to test this model for gas conditions below core temperature and 100% relative humidity. These data concur with the model in that region. No studies have yet looked at this relationship beyond 24 hrs. Longer exposure times to any given level of inspired humidity and inspired gas temperatures and humidities above core temperature and 100% relative humidity need to be studied to fully verify the proposed model.(Crit Care Med 1996; 24:1920-1929)
ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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26. |
Acute Renal Failure in Intensive Care Units |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1930-1931
Andreas Mayr,
Engelbert Deusch,
Walter Hasibeder,
Norbert Mutz,
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ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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27. |
Acute Renal Failure in Intensive Care Units |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1931-1931
Francois G. Brivet,
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ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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28. |
Use of Phosphate Buffered Solution in Gastric Tonometry |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1932-1933
Gisbert Knichwitz,
Thomas Brussel,
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ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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29. |
Hypertonic Saline and Cerebral Oxygen Delivery in Head-Injured Cats |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1933-1934
Steven R. Shackford,
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ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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30. |
Hypertonic Saline and Cerebral Oxygen Delivery in Head-Injured Cats |
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Critical Care Medicine,
Volume 24,
Issue 11,
1996,
Page 1934-1936
Douglas S. DeWitt,
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ISSN:0090-3493
出版商:OVID
年代:1996
数据来源: OVID
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