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1.
Pulm Pharmacol Ther ; 14(1): 47-53, 2001.
Article in English | MEDLINE | ID: mdl-11162419

ABSTRACT

To determine whether the severity of the pulmonary edema in sheep models of cardiogenic and non-cardiogenic pulmonary edema correlate with concomitant alterations in airway responsiveness using three separate measures of pulmonary edema: post-mortem wet-to-dry lung weight ratio (W/D), chest radiograph (CXR) scores, and small airway wall area. Cardiogenic pulmonary edema was induced by increasing left atrial pressure (increase PLA) and non-cardiogenic pulmonary edema was induced by intravenous administration of Perilla ketone (PK). There was a significant negative correlation between changes in airway responsiveness and changes in CXR grade (r=-0.749, P<0.05), W/D (r=-0.662, P<0.05), airway wall areas (r=0.784, P<0.05) after increases in both PLA and PK. Chest radiograph score, W/D, and airway wall area correlated with each other (CXR score and W/D r=0.657, P<0.05; CXR score and airway wall area r=0.678, P<0.05; airway wall area and W/D r=0.704, P<0.05). We speculate that the increased airway responsiveness observed during pulmonary edema may result from the mechanical effects of edema formation within the airways.


Subject(s)
Airway Resistance/physiology , Bronchi/physiology , Pulmonary Edema/physiopathology , Animals , Asthma/physiopathology , Autopsy/veterinary , Biometry , Bronchi/anatomy & histology , Disease Models, Animal , Female , Male , Pulmonary Edema/drug therapy , Radiography, Thoracic , Respiratory Distress Syndrome , Severity of Illness Index , Sheep
2.
Respiration ; 66(6): 522-7, 1999.
Article in English | MEDLINE | ID: mdl-10575338

ABSTRACT

BACKGROUND: Though it is well known that cardiogenic and noncardiogenic pulmonary edema can cause changes in lung mechanics, actual alterations in tracheal diameter have not been described. OBJECTIVE: To evaluate the effects of pulmonary edema induced by increased left atrial pressure (cardiogenic) and Perilla ketone (PK; noncardiogenic) on tracheal diameter in chronically instrumented awake sheep. METHODS: We investigated the effects of two mechanistically distinct types of pulmonary edema on tracheal diameter in chronically instrumented awake sheep. Cardiogenic pulmonary edema (analogous to congestive heart failure in humans) was induced by increasing left atrial pressure ( upward arrowP(LA)) by inflating the balloon on a Foley catheter positioned in the mitral valve annulus to cause partial obstruction to flow across the valve (n = 18). Noncardiogenic pulmonary edema (increased pulmonary microvascular permeability pulmonary edema analogous to the acute respiratory distress syndrome in humans) was produced by the intravenous administration of PK (n = 11). Lateral chest radiographs (CXRs) were scored by a standardized 5-point scoring system for the severity of pulmonary edema, and tracheal diameter was measured at a fixed location in the carina. Three radiologists, blinded to sheep identification number and experimental protocol, evaluated the radiographs independently at different points in time for edema severity and tracheal diameter. The sheep were sacrificed immediately after the final CXR, and wet/dry lung weight ratio (W/D ratio) was determined. RESULTS: Both upward arrowP(LA) and PK were associated with statistically significant tracheal narrowing ( upward arrowP(LA): 20.3 +/- 0.6 to 15.1 +/- 0.9 mm; PK: 20.2 +/- 0.6 to 14.1 +/- 1.4 mm). Tracheal narrowing correlated with the severity of the pulmonary edema determined radiographically ( upward arrowP(LA): r = -0.69, p < 0.01; PK: r = -0.62, p < 0.01) and by W/D ratio ( upward arrowP(LA): r = -0.64, p < 0.05; PK: r = -0.54, p < 0. 05). CONCLUSIONS: We conclude that tracheal narrowing occurs in sheep models of both cardiogenic and noncardiogenic pulmonary edema and that the degree of narrowing correlates with the severity of the edema.


Subject(s)
Edema, Cardiac/complications , Monoterpenes , Pulmonary Edema/complications , Trachea/diagnostic imaging , Tracheal Diseases/diagnostic imaging , Tracheal Diseases/etiology , Animals , Constriction, Pathologic/diagnostic imaging , Constriction, Pathologic/physiopathology , Disease Models, Animal , Edema, Cardiac/diagnostic imaging , Linear Models , Lung/pathology , Organ Size , Pulmonary Edema/diagnostic imaging , Pulmonary Edema/pathology , Radiography , Reference Values , Severity of Illness Index , Sheep , Terpenes , Trachea/physiopathology
3.
J Appl Physiol (1985) ; 85(5): 1635-42, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9804563

ABSTRACT

We compared the effects of cardiogenic pulmonary edema, brief pulmonary vascular congestion without frank edema, and noncardiogenic pulmonary edema on responsiveness to inhaled histamine in chronically instrumented awake sheep. Histamine responsiveness was measured before and after 1) cardiogenic pulmonary edema induced by raising left atrial pressure to 35 cmH2O (Pla) for 3.5 h by partial obstruction of flow across the mitral valve, 2) brief cardiogenic congestion via Pla for 0.5 h, 3) noncardiogenic pulmonary edema induced by 25 mg/kg intravenous perilla ketone (PK), and 4) 3.5 h of monitoring without Pla or PK (controls). Treatment for 3.5 h with Pla (n = 9) and PK (n = 11) each significantly lessened the histamine dose required to cause a fall to 65% of baseline dynamic lung compliance (ED65Cdyn), i.e., increased responsiveness. Sheep treated for 0.5 h with Pla (n = 7) and controls (n = 5) showed no significant change in ED65Cdyn. Intravenous atropine (0.1 mg/kg) before the second histamine challenge altered neither the reduction of ED65Cdyn in Pla (n = 8) and PK (n = 9) sheep nor the ED65Cdyn level of controls (n = 9). These data imply that the local effects of edema, rather than bronchial vascular hemodynamics, cholinergic reflexes, and permeability changes, are germane to lung hyperresponsiveness during pulmonary edema in sheep.


Subject(s)
Heart Diseases/complications , Heart Diseases/physiopathology , Histamine/pharmacology , Monoterpenes , Pulmonary Edema/etiology , Pulmonary Edema/physiopathology , Aerosols , Animals , Atropine/pharmacology , Blood Pressure/drug effects , Dose-Response Relationship, Drug , Female , Histamine/administration & dosage , Histamine Release/drug effects , Male , Muscarinic Agonists/pharmacology , Pulmonary Circulation/drug effects , Pulmonary Circulation/physiology , Sheep , Terpenes/toxicity , Toxins, Biological/toxicity
4.
J Appl Physiol (1985) ; 84(5): 1610-4, 1998 May.
Article in English | MEDLINE | ID: mdl-9572806

ABSTRACT

To further define the role of platelet-activating factor (PAF) in endotoxin-induced lung dysfunction, we examined the effect of ABT-299, a specific and potent PAF-receptor antagonist, on the response to endotoxemia in six chronically instrumented awake sheep. We administered Escherichia coli endotoxin (0.5 microg/kg) intravenously with or without pretreatment with ABT-299 while monitoring mean pulmonary arterial pressure (Ppa), mean systemic arterial pressure (Psa), dynamic compliance of the lungs (Cdyn), and functional residual capacity (FRC). Endotoxin administration caused pulmonary hypertension, reduced Cdyn, leukopenia, and hypoxemia while having no significant effect on Psa or FRC. Administration of ABT-299 did not affect any of the measured variables at baseline. Pretreatment with ABT-299 attenuated the peak Ppa seen after endotoxin administration but had minimal effects on endotoxin-induced changes in Cdyn, white blood cell count, or alveolar-to-arterial oxygen difference. ABT-299 was shown to completely block the pulmonary hypertension and reduction in Cdyn seen after intravenous administration of exogenous PAF. We conclude that PAF does not play an essential role in the sheep's response to endotoxin.


Subject(s)
Endotoxins/pharmacology , Lung/drug effects , Platelet Activating Factor/physiology , Platelet Membrane Glycoproteins/antagonists & inhibitors , Receptors, Cell Surface , Receptors, G-Protein-Coupled , Animals , Blood Pressure/drug effects , Humans , Infant, Newborn , Leukocyte Count/drug effects , Lung/physiopathology , Oxygen/blood , Platelet Aggregation Inhibitors/pharmacology , Prodrugs/pharmacology , Pyridinium Compounds/pharmacology , Respiratory Distress Syndrome, Newborn/drug therapy , Respiratory Function Tests , Sheep , Thiazoles/pharmacology
5.
J Orthop Trauma ; 12(3): 169-75; discussion 175-6, 1998.
Article in English | MEDLINE | ID: mdl-9553857

ABSTRACT

OBJECTIVES/HYPOTHESIS: At present, the optimal treatment for appropriately resuscitated, multiply injured patients includes fixation of long bone fractures within twenty-four hours of injury. This management approach has been shown to decrease the incidence of pulmonary complications, multiple organ failure, and death. Some investigators have hypothesized that acute reamed intramedullary nailing of the femur (RIMNF) may result in pulmonary dysfunction as a result of the pulmonary fat embolization generated during this procedure. Patients with concomitant thoracic trauma may be at particular risk for this potentially severe complication. In an attempt to determine whether RIMNF can be safely carried out regardless of the severity of a pulmonary injury, we monitored the pulmonary effects of RIMNF in sheep in which an acute respiratory disorder (ARDS)-like state had been induced. Our hypothesis was that, if the pulmonary fat embolization that occurs as a result of RIMNF has a clinically significant effect, it would be detectable in an animal model in which a severe lung injury had been induced prior to the start of RIMNF. STUDY DESIGN: This was an acute experimental procedure performed on yearling sheep. METHODS: Reamed intramedullary nailing of the femur was performed in two groups of instrumented sheep. The first group had no pulmonary injuries. The second group had an ARDS-like state induced by intravenous infusion of perilla ketone prior to RIMNF. Perilla ketone increases pulmonary microvascular permeability without changing filling pressures and is used to induce a model of human ARDS. Hemodynamic and oximetric parameters were measured or calculated, as was pulmonary dynamic compliance during the experiment. RESULTS: Infusion of perilla ketone caused a significant pulmonary injury. RIMNF caused no additional significant effect on intrapulmonary shunt, mixed venous oxygen saturation, or dynamic compliance, which are clinically used to assess the severity of pulmonary dysfunction in injured patients. CONCLUSIONS: The fat embolization that occurs during RIMNF in an appropriately resuscitated sheep has no clinically significant effect on pulmonary function, even in the setting of a severe pulmonary dysfunction.


Subject(s)
Embolism, Fat/etiology , Fracture Fixation, Intramedullary/adverse effects , Monoterpenes , Respiratory Distress Syndrome/complications , Animals , Disease Models, Animal , Fracture Fixation, Intramedullary/methods , Hemodynamics , Oxygen/blood , Respiratory Distress Syndrome/chemically induced , Sheep , Terpenes , Toxins, Biological
6.
Am J Respir Crit Care Med ; 157(1): 81-8, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9445282

ABSTRACT

BMS182874, an endothelin receptor antagonist, blocks the effects of exogenously administered endothelins in chronically instrumented awake sheep. A possible role for endothelin in endotoxin-induced pulmonary hypertension in sheep was investigated by studying animals given intravenous endotoxin with and without pretreatment with BMS182874. BMS182874 administration alone caused a reduction in pulmonary artery pressure (P[PA]) and systemic arterial pressure (P[SA]). Endotoxin alone caused an acute, nearly threefold increase in P(PA) which was followed, from 2-5 h after endotoxin, by a sustained but less severe increase in P(PA). These changes were accompanied by a threefold increase in lung lymph flow and dramatic increases in plasma and lung lymph thromboxane B2 concentrations. Pretreatment with BMS182874 significantly attenuated the early endotoxin-induced acute increase in P(PA) and completely blocked the late sustained pulmonary hypertension (p < 0.05), while having no affect on the increases in thromboxane levels. BMS182874 shifts the dose response curve for U46619, a prostaglandin H2 analogue, to the right. BMS182874, in addition to functioning as an endothelium receptor antagonist, appears to counteract the action of thromboxane at the receptor level. We theorize that BMS182874 attenuates the early endotoxin-induced pulmonary hypertension by counteracting the effects of thromboxane, since previous studies demonstrated that the early acute rise in P(PA) is caused by thromboxane. The late sustained pulmonary hypertension of endotoxemia, on the other hand, appears to be mediated by endothelin.


Subject(s)
Antihypertensive Agents/pharmacology , Dansyl Compounds/pharmacology , Disease Models, Animal , Endothelin Receptor Antagonists , Endothelins/physiology , Endotoxemia/complications , Hypertension, Pulmonary/drug therapy , Hypertension, Pulmonary/physiopathology , Premedication , Animals , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Female , Hypertension, Pulmonary/blood , Hypertension, Pulmonary/etiology , Lymph/physiology , Male , Pulmonary Wedge Pressure/drug effects , Sheep , Thromboxane B2/blood
7.
Pulm Pharmacol Ther ; 10(2): 111-8, 1997.
Article in English | MEDLINE | ID: mdl-9425643

ABSTRACT

Endothelins have potent biological effect in vivo which may, in part, be mediated by stimulation of cyclooxygenase metabolism of arachidonic acid. We administered endothelins (ETs) intravenously to chronically instrumented awake sheep with and without pretreatment with meclofenamate (n = 8). 30 micrograms doses of ET-1, ET-2, and ET-3 caused similar degrees of acute elevation of pulmonary artery pressure (PPA), reduction of the dynamic compliance of the lungs (Cdyn), and increases in lung lymph flow. Pretreatment with meclofenamate inhibited the rise in PPA and reduction in Cdyn, but had no effect on lung lymph flow. We conclude that the biological effects of the endothelins on PPA and Cdyn, but not lung fluid balance, are mediated in part by cyclooxygenase products of arachidonic acid metabolism.


Subject(s)
Cyclooxygenase Inhibitors/therapeutic use , Endothelins/toxicity , Hypertension, Pulmonary/chemically induced , Lung/drug effects , Meclofenamic Acid/therapeutic use , Animals , Blood Pressure , Endothelin-1/toxicity , Endothelin-2/toxicity , Endothelin-3/toxicity , Female , Hypertension, Pulmonary/physiopathology , Lung/physiopathology , Lung Compliance , Lymph/physiology , Male , Sheep
8.
J Orthop Trauma ; 10(2): 75-80, 1996.
Article in English | MEDLINE | ID: mdl-8932664

ABSTRACT

We have recently developed an open-chest sheep model to monitor and study the effects of major orthopedic procedures on pulmonary physiology. In this pilot study, we focused on reamed intramedullary femoral nailing in animals without pulmonary injury. Details of the model are described herein. The control group consisted of sheep that underwent thoracotomy and invasive monitoring only, while the study group also underwent femoral osteotomy, reaming, and intramedullary nailing. Baseline, postthoracotomy, and post-reaming/nailing values were recorded for mean pulmonary arterial pressure, central venous pressure, left arterial pressure, dynamic compliance, arterial blood gas, mixed venous O2, cardiac index, and mean arterial pressure so that hemodynamic and oxygen transport data could be calculated. Postprocedure values were recorded at hourly intervals for 4 h. A physiologically stable, reproducible model was created. No statistically significant differences were found between the control and experimental groups, indicating no adverse effect of femoral reaming/nailing. In one animal, using echocardiography, pulmonary embolization was documented while reaming and inserting the intramedullary nail. Reamed femoral intramedullary nailing is not detrimental to sheep with otherwise normal lungs. This finding suggests that femoral reaming and nailing in trauma patients without associated pulmonary injuries and otherwise normal lungs may be carried out without risk of inducing significant respiratory complications.


Subject(s)
Femoral Fractures/surgery , Fracture Fixation, Intramedullary , Lung/physiology , Postoperative Complications/physiopathology , Pulmonary Embolism/etiology , Analysis of Variance , Animals , Disease Models, Animal , Fracture Fixation, Intramedullary/adverse effects , Osteotomy , Pilot Projects , Respiratory Function Tests , Sheep , Thoracotomy
9.
Chest ; 108(3): 798-803, 1995 Sep.
Article in English | MEDLINE | ID: mdl-7656636

ABSTRACT

We designed a series of experiments to compare the pulmonary dysfunction observed in models of cardiogenic and noncardiogenic pulmonary edema in chronically instrumented awake sheep. Cardiogenic pulmonary edema was induced by inflating the balloon of a Foley catheter surgically positioned in the mitral valve orifice causing increased left atrial pressure (increases PLA). Noncardiogenic pulmonary edema was induced by intravenous infusion of Perilla ketone (PK). Calculated microvascular pressure remained constant during PK infusion but increased from 9.4 +/- 0.7 to 42.8 +/- 2.4 cm H2O during increases PLA. Comparable increases in lung lymph flow (QL) were observed in the two protocols (five to seven times baseline). Pulmonary edema as quantified by chest radiograph scores increased from 0 (normal) to 2.9 +/- 0.5 and 3.4 +/- 0.1 in the PK and increases PLA groups, respectively. Room air alveolar to arterial oxygen pressure difference (P[A-a]O2) increased from 24 +/- 3 to 46 +/- 7 mm Hg in the PK group and from 23 +/- 4 to 56 +/- 6 mm Hg in the increases PLA group. Dynamic compliance of the lungs (Cdyn) expressed as the percentage of the baseline value decreased to 53 +/- 7 and 50 +/- 7% in the PK and increases PLA groups, respectively. Resistance to airflow across the lungs (RL) increased from 2.5 +/- 0.6 to 3.3 +/- 0.8 cm H2O.L-1.sec-1 in the PK group and from 1.4 +/- 0.3 to 4.2 +/- 1.1 in the increases PLA group. Significant correlations were observed between changes in the severity of pulmonary edema observed on chest radiographs, Cdyn, delta P(A-a)O2, and QL in both the increases PLA groups. We conclude that similar degrees of pulmonary edema, regardless of the mechanism, are associated with similar changes in QL, Cdyn, and delta P(A-a)O2. Hydrostatic pulmonary edema appeared to cause greater changes in RL than that resulting from increased microvascular permeability.


Subject(s)
Lung/physiopathology , Monoterpenes , Pulmonary Edema/etiology , Pulmonary Edema/physiopathology , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/physiopathology , Animals , Atrial Function, Left/physiology , Capillary Permeability/physiology , Hemodynamics/physiology , Hydrostatic Pressure , Lung/diagnostic imaging , Pulmonary Gas Exchange/physiology , Radiography , Respiratory Mechanics/physiology , Sheep , Terpenes , Toxins, Biological
10.
J Clin Invest ; 95(6): 2749-56, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7769115

ABSTRACT

Hormonal activation of protein kinase C (PKC) is a major signaling mechanism regulating salt and water transport in the distal nephron. We used antisense DNA to down-regulate a PKC isoform in the rabbit cortical collecting duct (CCD) and examined its role in mediating arginine vasopressin's (AVP) effect on salt transport in the CCD. Immunoblots demonstrate that PKC-epsilon (diacylglycerol sensitive) and PKC-zeta (diacylglycerol insensitive) are the major PKC isoforms in both freshly isolated and primary cultures of rabbit CCDs. Rabbit CCDs grown on semi-permeable supports, displayed a positive baseline short circuit current (Isc), which was abolished by amiloride, demonstrating active Na+ absorption. Both AVP and 8-chloro-phenylthio-cAMP (8CPTcAMP) transiently increased Isc, however, within 40 min Isc fell below baseline. Down-regulation of PKC-epsilon, as confirmed by immunoblot, was achieved either by treatment with a PKC-epsilon-specific antisense oligonucleotide or 48 h of 1 microM PMA. In PKC-epsilon down-regulated cells, 8CPTcAMP produced a sustained, rather than transient, increase in Isc. We suggest cAMP stimulates Na+ transport, but secondary activation of PKC-epsilon results in the sustained inhibition of Na+ transport seen in response to vasopressin in the CCD.


Subject(s)
Isoenzymes/metabolism , Kidney Tubules, Collecting/metabolism , Protein Kinase C/metabolism , Sodium/metabolism , Vasopressins/pharmacology , Animals , Base Sequence , Cells, Cultured , Cyclic AMP/pharmacology , DNA, Antisense/chemistry , Electric Conductivity , Female , Hydrogen-Ion Concentration , In Vitro Techniques , Isoenzymes/genetics , Molecular Sequence Data , Protein Kinase C/genetics , Protein Kinase C-epsilon , Rabbits , Tetradecanoylphorbol Acetate/pharmacology
11.
J Clin Invest ; 95(5): 2150-60, 1995 May.
Article in English | MEDLINE | ID: mdl-7738183

ABSTRACT

Cytochrome P450 metabolizes arachidonic acid to several unique and biologically active compounds in rabbit liver and kidney. Microsomal fractions prepared from rabbit lung homogenates metabolized arachidonic acid through cytochrome P450 pathways, yielding cis-epoxyeicosatrienoic acids (EETs) and their hydration products, vic-dihydroxyeicosatrienoic acids, mid-chain cis-trans conjugated dienols, and 19- and 20-hydroxyeicosatetraenoic acids. Inhibition studies using polyclonal antibodies prepared against purified CYP2B4 demonstrated 100% inhibition of arachidonic acid epoxide formation. Purified CYP2B4, reconstituted in the presence of NADPH-cytochrome P450 reductase and cytochrome b5, metabolized arachidonic acid, producing primarily EETs. EETs were detected in lung homogenate using gas chromatography/mass spectroscopy, providing evidence for the in vivo pulmonary cytochrome P450 epoxidation of arachidonic acid. Chiral analysis of these lung EETs demonstrated a preference for the 14(R),15(S)-, 11(S),12(R)-, and 8(S),9(R)-EET enantiomers. Both EETs and vic-dihydroxyeicosatrienoic acids were detected in bronchoalveolar lavage fluid. At micromolar concentrations, methylated 5,6-EET and 8,9-EET significantly relaxed histamine-contracted guinea pig hilar bronchi in vitro. In contrast, 20-hydroxyeicosatetraenoic acid caused contraction to near maximal tension. We conclude that CYP2B4, an abundant rabbit lung cytochrome P450 enzyme, is the primary constitutive pulmonary arachidonic acid epoxygenase and that these locally produced, biologically active eicosanoids may be involved in maintaining homeostasis within the lung.


Subject(s)
Arachidonic Acids/metabolism , Aryl Hydrocarbon Hydroxylases , Cytochrome P-450 Enzyme System/metabolism , Lung/enzymology , Microsomes/enzymology , Steroid Hydroxylases/metabolism , Animals , Arachidonic Acids/pharmacology , Base Sequence , Blotting, Northern , Bronchi/drug effects , Bronchi/physiology , Bronchoalveolar Lavage Fluid , Chromatography, High Pressure Liquid , Cytochrome P-450 Enzyme System/biosynthesis , Cytochrome P-450 Enzyme System/isolation & purification , Cytochromes b5/metabolism , Gene Expression , Guinea Pigs , Kidney/enzymology , Kinetics , Liver/enzymology , Male , Molecular Sequence Data , Muscle Tonus/drug effects , Muscle, Smooth/drug effects , Muscle, Smooth/physiology , NADPH-Ferrihemoprotein Reductase/metabolism , Oligonucleotide Probes , Organ Specificity , RNA, Messenger/analysis , RNA, Messenger/biosynthesis , Rabbits , Steroid Hydroxylases/biosynthesis , Steroid Hydroxylases/isolation & purification
12.
Arch Biochem Biophys ; 316(1): 443-51, 1995 Jan 10.
Article in English | MEDLINE | ID: mdl-7840649

ABSTRACT

The metabolism of cis-epoxyeicosatrienoic acids (EETs), methyl cis-epoxyeicosatrienoates, and cis-epoxyeicosanoic acids by cytosolic epoxide hydrolase was studied to identify substrate structural features important for stereoselective metabolism and chiral diol formation. 14(R), 15(S)-, 11(S),12(R)-, and 8(S),9(R)-EET, the predominant enantiomers present endogenously in rat organs, were metabolized at substantially higher rates than their antipodes. With the exception of 8(R),9(S)-EET (Km = 41 microM), differences in enantiomer hydration rates appear to be caused by Km-independent factors since the apparent Km values for the enantiomers of 14,15-, 11,12-, and 8(S),9(R)-EET were similar (between 3 and 5 microM). Chiral analysis of the diols resulting from enzymatic hydration of homochiral EETs showed that the regio and/or stereochemistry of water addition was EET regioisomer dependent. For the 11,12-EET enantiomers, water addition was nonregioselective; whereas, with both 8,9-EET antipodes water addition occurred predominantly at C9. Importantly, for 14,15-EET the regiochemistry of water addition was enantiomer-dependent. Only with 14(R),15(S)-EET did enzymatic hydration result in regiospecific addition at C15. Hence, enantioselective EET hydration is determined, principally, by enantiomer specific differences in rates of catalytic turnover and/or substrate binding parameters. On the other hand, the chirality of the diol products is determined by EET enantiomer-dependent differences in the regiochemistry of enzymatic oxirane cleavage and water addition. Esterification resulted in an overall reduction in the rates of epoxide hydration for all three EET-methyl esters (59, 89, and 68% of the EET rate for 8,9-, 11,12-, and 14,15-EET-methyl ester, respectively) and in the loss of regioselectivity during methyl 8(S),9(R)-EET oxirane cleavage. Catalytic EET hydrogenation reduced the rates of EET hydration (56, 45, and 23% of the EET rates for 8,9-, 11,12-, and 14,15-epoxyeicosanoic acids, respectively). Compared to 14,15-EET, enzyme catalyzed hydration of 14,15-epoxyeicosanoic acid was less regioselective and yielded products with a substantially lower chiral purity. Based on these data, as well as on the documentation of 14(R),15(R)-dihydroxyeicosatrienoic acid as an endogenous constituent of rat urine we concluded that: (1) cytosolic epoxide hydrolase plays a significant role in the regio- and stereoselective metabolism of endogenous EETs; (2) differences in the affinities and/or turnover rates of the enzyme for the individual EET antipodes may be responsible for enantioselective EET metabolism; and (3) for 14,15- and 8,9-EET, regioselective and/or enantioselective oxirane water addition is responsible for asymmetric diol formation.(ABSTRACT TRUNCATED AT 400 WORDS)


Subject(s)
8,11,14-Eicosatrienoic Acid/analogs & derivatives , Epoxide Hydrolases/metabolism , Epoxy Compounds/metabolism , Fatty Acids, Unsaturated/metabolism , Liver/enzymology , Animals , Binding Sites , Catalysis , Cytosol/enzymology , Fatty Acids, Unsaturated/urine , Kinetics , Male , Mice , Stereoisomerism , Substrate Specificity , Water/metabolism
13.
Am Rev Respir Dis ; 147(6 Pt 1): 1371-9, 1993 Jun.
Article in English | MEDLINE | ID: mdl-8503548

ABSTRACT

Neutrophils have been implicated as important cellular mediators of the pulmonary dysfunction observed following endotoxemia in chronically instrumented awake sheep. Several areas of research suggest that neutrophil-derived proteases may be mediators of this dysfunction. We hypothesized that neutrophil elastase inhibitors would attenuate the effects of endotoxemia in sheep. To test this hypothesis, we studied the effects of two putative neutrophil elastase inhibitors, SC-37698 and SC-39026 (Searle, Skokie, IL), on endotoxin-induced lung dysfunction in awake sheep. Sheep were given intravenous neutrophil elastase inhibitor alone (20 mg/kg/h for 6 h), intravenous endotoxin (E. coli endotoxin, 0.5 microgram/kg over 20 min) 1 h after beginning the 6-h infusion of elastase inhibitor, or endotoxin 1 h after beginning a 6-h infusion of elastase inhibitor vehicle. SC-37698 attenuated the increase in lung lymph flow and lung lymph protein clearance, the alterations in lung mechanics, and the fall in white blood count. Qualitatively similar effects were seen with SC-39026. These data suggest the need for further research examining the role of protease-antiprotease interactions and the potential utility of neutrophil elastase inhibitors in acute lung injury like that observed in the adult respiratory distress syndrome (ARDS) in the human.


Subject(s)
Chlorobenzoates/pharmacology , Endotoxins/toxicity , Escherichia coli , Lung/drug effects , Neutrophils/enzymology , Pancreatic Elastase/antagonists & inhibitors , Wakefulness/drug effects , Analysis of Variance , Animals , Drug Interactions , Hemodynamics/drug effects , Lung/physiopathology , Lymph/drug effects , Respiratory Mechanics/drug effects , Sheep , Time Factors , Wakefulness/physiology
14.
J Biol Chem ; 268(9): 6402-7, 1993 Mar 25.
Article in English | MEDLINE | ID: mdl-8454612

ABSTRACT

The hydration of cis-epoxyeicosatrienoic acids to the corresponding vic-dihydroxyeicosatrienoic acids by cytosolic epoxide hydrolase demonstrates moderate regioselectivity with rates of hydration highest for the 14,15-epoxide and lower for the 11,12- and 8,9-epoxide (4.5, 1.6, and 1.5 mumol of product/mg of protein/min, respectively). Incubations of the 8,9- and 14,15-epoxides with cytosolic epoxide hydrolase show stereoselective formation of diols (7:3 and 4:1 ratio of antipodes, respectively) and concomitant chiral enrichment of the remaining unmetabolized substrate. In contrast, hydration of the 11,12-epoxide is nonenantioselective. The Km value of the enzyme for the 14(R),15(S)-epoxide is 3 microM. Incubations of the enantiomerically pure 8,9- and 14,15-epoxides with lung or liver cytosol, followed by chiral analysis of the resulting diols demonstrate selective cleavage of the oxirane ring at C9 and C15, respectively. On the other hand, cleavage of the 11,12- oxirane ring was less selective. The stereochemical preference of the cytosolic epoxide hydrolase, together with the known chiral composition of the endogenous arachidonate epoxide pools, suggests a functional role for this enzyme in the metabolism of these important compounds.


Subject(s)
8,11,14-Eicosatrienoic Acid/metabolism , Cytosol/enzymology , Epoxide Hydrolases/metabolism , 8,11,14-Eicosatrienoic Acid/analogs & derivatives , Animals , Chromatography, High Pressure Liquid , Ethylene Oxide/metabolism , Hydroxyeicosatetraenoic Acids/metabolism , Male , Molecular Structure , Rabbits , Water/metabolism
15.
J Appl Physiol (1985) ; 74(2): 596-605, 1993 Feb.
Article in English | MEDLINE | ID: mdl-8384614

ABSTRACT

We studied the effects of a 5-lipoxygenase inhibitor, SC-45662, on endotoxin-induced pulmonary dysfunction in chronically instrumented unanesthetized sheep. Each sheep was studied with endotoxin alone, SC-45662 alone, and endotoxin after SC-45662 pretreatment. Endotoxin did not cause consistent increases in plasma or lung lymph concentrations of leukotriene B4 (LTB4). Ex vivo stimulation of whole blood from sheep before and after treatment with SC-45662 demonstrated no inhibition of cyclooxygenase metabolism but an approximately 80% inhibition of LTB4 production. At drug concentrations obtained in vivo, SC-45662 did not significantly inhibit in vitro A23187-stimulated whole blood thromboxane B2 production but did inhibit LTB4 production from ionophore-stimulated sheep granulocytes. SC-45662 attenuated the early changes in lung mechanics and pulmonary hypertension but did not attenuate the later increase in lung fluid and solute exchange observed after endotoxemia. We conclude that 5-lipoxygenase products are not measurably involved in the later increase in lung fluid and solute exchange observed after endotoxemia in sheep.


Subject(s)
Acetates , Endotoxins/toxicity , Lipoxygenase Inhibitors/therapeutic use , Lung Diseases/prevention & control , Phenols , 6-Ketoprostaglandin F1 alpha/metabolism , Animals , Arachidonate 5-Lipoxygenase/pharmacology , Blood Pressure/drug effects , Dinoprostone/metabolism , Female , Gas Chromatography-Mass Spectrometry , Granulocytes/drug effects , Granulocytes/metabolism , Hemodynamics/drug effects , Leukotriene B4/pharmacology , Lung Diseases/chemically induced , Lymphatic System/drug effects , Male , Phenothiazines/pharmacology , Respiratory Mechanics/drug effects , Sheep , Superoxides/metabolism , Thromboxane B2/metabolism
16.
Anal Biochem ; 207(2): 236-40, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1481976

ABSTRACT

A chromatographic method is described for the direct enantiomeric characterization of 5,6-, 8,9-, 11,12-, and 14,15-vic-dihydroxyeicosatrienoic acids (DHETs), metabolites of the cytochrome P-450 arachidonate epoxygenase pathway, and of their corresponding saturated vic-dihydroxyeicosanoic acids. Following esterification, the individual methyl or pentafluorobenzyl esters are resolved by chiral-phase chromatography utilizing a Chiralcel OC or OD column. This methodology will find analytical and preparative applications since it is simple and efficient and preserves, intact, the diol functionality.


Subject(s)
8,11,14-Eicosatrienoic Acid/analogs & derivatives , 8,11,14-Eicosatrienoic Acid/isolation & purification , 8,11,14-Eicosatrienoic Acid/chemistry , Chromatography, High Pressure Liquid/methods , Cytochrome P-450 CYP2J2 , Cytochrome P-450 Enzyme System/metabolism , Indicators and Reagents , Isomerism , Mass Spectrometry/methods , Oxygenases/metabolism
17.
Prostaglandins ; 44(6): 555-77, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1475377

ABSTRACT

PAF was administered as an intravenous bolus (0.1 micrograms/kg) to eight chronically instrumented awake sheep. The effects of pretreatment with an inhibitor of cyclooxygenase (meclofenamate) on PAF-induced changes in lung function were compared to those observed with a specific inhibitor of thromboxane synthase (DP1904). Each animal was studied four times in varied order: PAF alone, PAF + DP1904, PAF + meclofenamate, and DP1904 alone. Saline alone (control), DP1904 alone, and meclofenamate alone did not cause changes in any of the measured variables. DP1904 and meclofenamate significantly attenuated the PAF-induced fall in lung compliance, elevation in peak pulmonary artery pressure, and increased lung lymph flow. Both drugs abolished the PAF-induced increases in lung lymph thromboxane B2 concentrations. Meclofenamate, but not DP1904, blocked the rise in lymph 6-keto-PGF1 alpha. Although meclofenamate blocked the rise in lymph PGE2, DP1904 resulted in levels 2.7 times higher than PAF alone. We conclude that: (1) inhibition of thromboxane synthase is as effective as inhibition of cyclooxygenase in attenuating PAF-induced changes in lung function, and (2) thromboxane synthase inhibition results in augmented production of PGE2 following PAF administration in vivo.


Subject(s)
Arachidonic Acid/metabolism , Lung/drug effects , Platelet Activating Factor/antagonists & inhibitors , Prostaglandin-Endoperoxide Synthases/metabolism , Thromboxane-A Synthase/metabolism , Animals , Body Fluids/metabolism , Imidazoles/pharmacology , Lung/metabolism , Meclofenamic Acid/pharmacology , Pilot Projects , Respiratory Mechanics/drug effects , Sheep , Tetrahydronaphthalenes/pharmacology
18.
Am Rev Respir Dis ; 146(4): 997-1002, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1416431

ABSTRACT

We studied the effects of two structurally unrelated sulfidopeptide leukotriene receptor antagonists on endotoxin-induced pulmonary dysfunction in chronically instrumented unanesthetized sheep. The agents employed were L-660,711 (MK-571) (Merck-Frosst, Canada) and SK&F 104,353 (Smith Kline and French, King of Prussia, PA). The efficacy and specificity of the agents were verified in sheep by administering boluses of exogenous leukotrienes (LTB4, LTC4, LTD4, and LTE4) in doses as great as 100 micrograms while monitoring lung mechanics and vascular pressures. The antagonists blocked the changes in lung mechanics and pulmonary hemodynamics induced by the sulfidopeptide leukotrienes (LTC4, LTD4, and LTE4) while having no effect on the animals' responses to LTB4. The endotoxin studies were performed by administering endotoxin alone (Escherichia coli endotoxin 0.75 microgram/kg) or endotoxin after pretreatment with one of the sulfidopeptide leukotriene receptor antagonists. In control studies, each animal received a continuous infusion of one of the receptor antagonists for a duration identical to that of the endotoxin studies. Neither L-660,711 nor SK&F 104,353 significantly altered the endotoxin-induced changes in pulmonary hemodynamics, lung mechanics, lung fluid and solute exchange, oxygenation, or leukopenia. Peak lung lymph thromboxane B2 levels were significantly lower in sheep pretreated with L-660,711. When the antagonists were given alone, no effects were seen. We conclude that (1) sulfidopeptide leukotrienes do not measurably contribute to endotoxin-induced pulmonary dysfunction in chronically instrumented sheep; (2) sulfidopeptide leukotrienes may contribute to thromboxane release after endotoxin.


Subject(s)
Dicarboxylic Acids/pharmacology , Endotoxins/adverse effects , Escherichia coli , Propionates/pharmacology , Quinolines/pharmacology , Respiratory Distress Syndrome/physiopathology , SRS-A/antagonists & inhibitors , SRS-A/physiology , Animals , Consciousness , Female , Lymph/chemistry , Male , Pulmonary Circulation/drug effects , Respiratory Distress Syndrome/etiology , Respiratory Mechanics/drug effects , Sheep , Thromboxane B2/metabolism
19.
Infect Immun ; 60(9): 3489-96, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1500155

ABSTRACT

The in vivo responses to staphylococcal alpha toxin are reported for 15 chronically instrumented awake yearling sheep. The data obtained from a total of 30 experiments are grouped into four categories of response: no response, noted in seven experiments done on 5 sheep; pressor response, obtained seven times in 4 sheep; fluid and solute exchange, noted on six occasions in 3 sheep; and acute heart failure and death, which occurred in 10 of the 15 sheep. "No response" denoted no change in any of the measured outcome variables. The group of sheep labeled as showing "pressor response" responded to alpha toxin infusion with an increase in pulmonary artery pressure, unaccompanied by changes either in lung lymph flow or in lung mechanics. "Changes in lung fluid and solute exchange" involve increases in lung lymph flow. The harbinger of the last category, acute left heart failure leading to death, was a marked elevation in left atrial pressure. The threshold response dose in sheep is approximately 21 micrograms/kg. A very steep dose-response curve is observed, with only a narrow window of doses, 15 to 25 micrograms/kg, between the group showing no response and the group showing death from acute heart failure. The data obtained in these studies indicate that the lethal effects of alpha toxin in sheep include acute heart failure, which may be due to direct toxicity to heart muscle and/or the coronary vasculature endothelium.


Subject(s)
Bacterial Toxins/toxicity , Hemolysin Proteins/toxicity , Staphylococcus aureus/pathogenicity , Animals , Antibodies, Bacterial/analysis , Blood Pressure/drug effects , Catheters, Indwelling/adverse effects , Female , Heart Failure/chemically induced , Lung/drug effects , Lung/metabolism , Male , Permeability , Sheep
20.
Am Rev Respir Dis ; 143(3): 578-84, 1991 Mar.
Article in English | MEDLINE | ID: mdl-2001069

ABSTRACT

We studied the pulmonary effects of repetitive bolus injections of autologous zymosan-activated plasma (ZAP) in nine chronically instrumented awake sheep. Aerosol histamine responsiveness was determined 1 h before and 4.5 h after the first bolus injection of ZAP. Each sheep received in the pulmonary artery a total of eight 5-ml bolus injections of ZAP separated by 30 min. On a separate day, with the order of experimentation varied to avoid sequential bias, six of the nine sheep also received "control" plasma (plasma prepared in the identical fashion as ZAP but not incubated with zymosan). "Control" plasma caused reproducible transient increases in pulmonary artery pressure, but it did not cause alterations in any of the other measured variables. Repetitive bolus injections of ZAP caused reproducible alterations in lung mechanics, pulmonary hemodynamics, lung fluid and solute exchange, oxygenation, and peripheral leukocyte counts. The increases in thromboxane-B2 concentrations in lung lymph and plasma were greatest after the first bolus injection of ZAP, with the magnitude of these changes diminishing on succeeding injections of ZAP. Aerosol histamine responsiveness did not increase after the eight bolus injections of ZAP.


Subject(s)
Plasma , Respiratory Mechanics , Zymosan , 6-Ketoprostaglandin F1 alpha/analysis , 6-Ketoprostaglandin F1 alpha/blood , Animals , Blood Pressure , Dose-Response Relationship, Drug , Extravascular Lung Water/metabolism , Female , Histamine/pharmacology , Injections, Intra-Arterial , Lung/metabolism , Lung Compliance , Lymph/chemistry , Lymph/metabolism , Male , Oxygen/blood , Pulmonary Artery/physiology , Respiratory Mechanics/drug effects , Sheep , Thromboxane B2/analysis , Thromboxane B2/blood
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