Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
1739462
Reference Type
Journal Article
Title
A small animal model for direct respiratory and hemodynamic measurements in toxicokinetic studies of volatile chemicals
Author(s)
Dallas, C; Weir, F; Bruckner, J
Year
1983
Is Peer Reviewed?
Yes
Journal
Developments in Toxicology and Environmental Science
ISSN:
0165-2214
Report Number
NIOSH/00148328
Volume
11
Page Numbers
419-422
Language
English
PMID
6677479
Abstract
A method for direct respiratory and hemodynamic measurements after exposure to volatile organics was examined in rats. Male Sprague-Dawley-rats were anesthetized for monitoring hemodynamic parameters in blood samples. One rat received a 100 milligram oral dose of 1,1-dichloroethylene (75354) (DCE) and another was exposed by inhaling 200 parts per million (ppm) DCE for 3 hours. Blood samples were withdrawn periodically from the femoral vein for blood content of test compounds. For inhalation exposures, a tracheostomy was performed and a miniaturized one way breathing valve was inserted into the trachea. For oral administration, test compounds were administered by gavage. Exhaled breath samples were taken from an exhalation sampling port located immediately adjacent to the breathing valve. Respiratory rate and minute volume were monitored with a pneumotachograph connected to a physiograph. Blood pressure, cardiac rate, and core temperature were continuously monitored by other physiograph channels. Alveolar concentrations of the test compound were calculated from the data generated from measurements of exhaled breath concentrations, respiratory rate, and minute volume. Concentrations of DCE in the blood, exhaled breath, and alveolar air simultaneously reached a steady state 45 minutes after initiation of inhalation exposure. DCE was eliminated very rapidly from the exhaled breath and bloodstream following cessation of exposures. Alveolar and exhaled breath concentrations of DCE peaked several minutes after maximum blood concentrations were achieved in the orally dosed animal. The authors conclude that the small animal model can be used to conduct toxicokinetic studies that require simultaneous collection of sequential samples of exhaled breath and blood during exposures.
Keywords
DCN-135072
;
Medical research
;
Animal studies
;
Quantitative analysis
;
Toxicology
;
Analytical methods
;
Laboratory techniques
;
Physiological measurements
;
Analytical models
;
Respiratory gas analysis
;
Blood analysis
;
Cardiopulmonary function
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity