1
40
2
-
Text
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URL Address
<a href="http://doi.org/10.1152/jappl.1992.73.1.50" target="_blank" rel="noreferrer noopener">http://doi.org/10.1152/jappl.1992.73.1.50</a>
Pages
50–58
Issue
1
Volume
73
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Pulmonary vascular protein sieving capability after exposure to high vascular pressures.
Publisher
An entity responsible for making the resource available
Journal of applied physiology (Bethesda, Md. : 1985)
Date
A point or period of time associated with an event in the lifecycle of the resource
1992
1992-07
Subject
The topic of the resource
Animals; Barotrauma/physiopathology; Blood Pressure/physiology; Blood Proteins/chemistry/*metabolism; Chemical; Dogs; Electrophoresis; Hypertension; Lymph/cytology/metabolism; Male; Models; Muscle; Permeability; Polyacrylamide Gel; Pulmonary Circulation/*physiology; Pulmonary Edema/physiopathology; Pulmonary/*physiopathology; Smooth; Vascular/*physiology
Creator
An entity primarily responsible for making the resource
Bosso F J; Maron M B; Pilati C F; Jarjoura D G
Description
An account of the resource
We evaluated the ability of the canine in situ left lower lobe (LLL) vasculature to sieve endogenous plasma proteins of various molecular radii (34-124 A) after LLL arterial pressure had been transiently elevated to 23.8 +/- 0.9 (control group, n = 5) or 92.3 +/- 1.4 (SE) Torr (high-pressure group, n = 9) by restricting LLL venous outflow under conditions of constant flow. After LLL flow was returned to natural perfusion, left atrial pressure was elevated in step increments, and LLL lymph and blood samples were collected until filtration-independent lymph-to-plasma protein concentration ratios (CL/CP) were obtained. The osmotic reflection coefficients (sigma d) for total proteins and seven protein fractions (separated by gradient gel electrophoresis) were calculated. The average total protein sigma d of the high-pressure group [0.51 +/- 0.06 (SE)] was significantly lower than that of the control group (0.68 +/- 0.03). Several LLLs of the high-pressure group, however, exhibited normal sigma d's. Protein fraction CL/CP's decreased with increasing molecular radius in both groups, but the CL/CP-molecular radius relationship was displaced upward in the high-pressure group. Pore analysis suggested that the decreases in sigma d could be explained by increases in the fractional flow through a large-pore system.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1152/jappl.1992.73.1.50" target="_blank" rel="noreferrer noopener">10.1152/jappl.1992.73.1.50</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
1992
Animals
Barotrauma/physiopathology
Blood Pressure/physiology
Blood Proteins/chemistry/*metabolism
Bosso F J
Chemical
Dogs
Electrophoresis
Hypertension
Jarjoura D G
Journal of applied physiology (Bethesda, Md. : 1985)
Lymph/cytology/metabolism
Male
Maron M B
Models
Muscle
Permeability
Pilati C F
Polyacrylamide Gel
Pulmonary Circulation/*physiology
Pulmonary Edema/physiopathology
Pulmonary/*physiopathology
Smooth
Vascular/*physiology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.1139/y94-098" target="_blank" rel="noreferrer noopener">http://doi.org/10.1139/y94-098</a>
Pages
693–700
Issue
6
Volume
72
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Temporal changes in left ventricular function after massive sympathetic nervous system activation.
Publisher
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Canadian journal of physiology and pharmacology
Date
A point or period of time associated with an event in the lifecycle of the resource
1994
1994-06
Subject
The topic of the resource
Acidosis/physiopathology; Anesthesia; Animals; Blood Pressure/physiology; Cardiac Output/physiology; Catecholamines/blood; Dogs; Electron; Female; Heart Rate/physiology; Heart Ventricles/anatomy & histology/ultrastructure; Hypertension/physiopathology; Left/*physiology; Male; Microscopy; Sympathetic Nervous System/drug effects/*physiology; Ventricular Function; Veratrine/pharmacology
Creator
An entity primarily responsible for making the resource
Lang S A; Maron M B; Bosso F J; Pilati C F
Description
An account of the resource
Intense activation of the sympathetic nervous system (SNS) decreases the contractile state of the rabbit left ventricle (LV). In this study, we determined the time course of LV dysfunction after massive central activation of the SNS in dogs. Veratrine (40-80 micrograms/kg) was injected intracisternally to activate the SNS in six chloralose-anesthetized dogs, and LV end-diastolic pressure (LVEDP), cardiac output, heart rate, and aortic pressure (Pa) were measured at
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1139/y94-098" target="_blank" rel="noreferrer noopener">10.1139/y94-098</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
1994
Acidosis/physiopathology
Anesthesia
Animals
Blood Pressure/physiology
Bosso F J
Canadian journal of physiology and pharmacology
Cardiac Output/physiology
Catecholamines/blood
Dogs
Electron
Female
Heart Rate/physiology
Heart Ventricles/anatomy & histology/ultrastructure
Hypertension/physiopathology
Lang S A
Left/*physiology
Male
Maron M B
Microscopy
Pilati C F
Sympathetic Nervous System/drug effects/*physiology
Ventricular Function
Veratrine/pharmacology