Document Detail


Diverse basal and stress-related phenotypes of Sprague Dawley rats from three vendors.
MedLine Citation:
PMID:  16935312     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Based on observed phenotypic differences in growth and ACTH responses to stress in Sprague Dawley rats obtained from different vendors, we ran head-to-head comparisons on rats obtained from three different vendors, Harlan, Charles River, and Simonsen, with respect to baseline phenotypic differences and a metabolic feedback hypothesis of hypothalamo-pituitary-adrenal (HPA) regulation. Charles River and Harlan rats gained weight faster than Simonsen rats, but chow intake standardized for body weight was not increased, consistent with their greater caloric efficiency. Weight gain was inversely related with mean daily temperatures, without differences in activity levels. Half of the animals given lard and 32% sucrose solutions in addition to chow increased caloric intake and core temperature, decreased caloric efficiency, and increased fat depots, leptin, and in Simonsen rats, insulin. A 5-day regimen of once-daily 2-h restraint decreased feeding and caloric efficiency. Rats from two vendors with the availability of sucrose and lard, Charles River and Simonsen, showed blunted HPA responses to restraint compared to chow controls, whereas the Harlans exhibited no adrenocorticotropin (ACTH) response and an amplified adrenocortical response on the high-energy diet compared to chow controls. Substantial phenotypic differences exist between Sprague Dawley rats from different vendors with respect to metabolism and HPA function. The metabolic feedback hypothesis was supported in two of the three vendors' rats.
Authors:
Norman Pecoraro; Abigail B Ginsberg; James P Warne; Francisca Gomez; Susanne E la Fleur; Mary F Dallman
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, N.I.H., Extramural     Date:  2006-08-28
Journal Detail:
Title:  Physiology & behavior     Volume:  89     ISSN:  0031-9384     ISO Abbreviation:  Physiol. Behav.     Publication Date:  2006 Nov 
Date Detail:
Created Date:  2006-10-30     Completed Date:  2007-01-04     Revised Date:  2007-12-03    
Medline Journal Info:
Nlm Unique ID:  0151504     Medline TA:  Physiol Behav     Country:  United States    
Other Details:
Languages:  eng     Pagination:  598-610     Citation Subset:  IM    
Affiliation:
Department of Physiology, School of Medicine, University of California San Francisco, 94143-0444, United States. norman.pecoraro@ucsf.edu
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adrenocorticotropic Hormone / blood
Animals
Basal Metabolism / physiology*
Body Composition / physiology*
Body Temperature / physiology
Body Weight / physiology
Corticosterone / blood
Energy Intake / physiology
Feeding Behavior / physiology
Hypothalamo-Hypophyseal System / physiology*
Insulin / blood
Leptin / blood
Male
Phenotype
Pituitary-Adrenal System / physiology*
Rats
Rats, Sprague-Dawley / physiology*
Species Specificity
Stress, Psychological / metabolism*
Grant Support
ID/Acronym/Agency:
DA 016944/DA/NIDA NIH HHS; DK 28172/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Leptin; 11061-68-0/Insulin; 50-22-6/Corticosterone; 9002-60-2/Adrenocorticotropic Hormone

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Development of a benthic index to assess sediment quality in the Tampa Bay Estuary.
Next Document:  The effectiveness of human impact assessment in the Finnish Healthy Cities Network.