Document Detail


Activation of membrane-associated estrogen receptors decreases food and water intake in ovariectomized rats.
MedLine Citation:
PMID:  23183173     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Estradiol (E2) decreases food and water intake in a variety of species, including rats. Available evidence suggests that this is mediated by genomic mechanisms that are most often attributed to nuclear estrogen receptors. More recent studies indicate that membrane-associated estrogen receptors (mERs) also can influence gene expression through the activation of transcription factors, yet it is unclear whether mERs are involved in mediating the hypophagic and antidipsetic effects of E2. In the present experiments, we injected E2 or a membrane-impermeable form of E2 (E2-BSA) into the lateral cerebral ventricle of ovariectomized female rats and evaluated the effect on 23 h food and water intake. First, we found that higher doses of E2 were necessary to reduce water intake than were sufficient to reduce food intake. Analysis of drinking microstructure revealed that the decrease in water intake after E2 treatment was mediated by both a decrease in burst number and burst size. Next, the activation of mERs with E2-BSA decreased both overnight food and water intake and analysis of drinking microstructure indicated that the decreased water intake resulted from a decrease in burst number. Finally, E2-BSA did not condition a taste aversion, suggesting that the inhibitory effects on food and water intake were not secondary to malaise. Together these findings suggest that activation of mERs is sufficient to decrease food and water intake in female rats.
Authors:
Jessica Santollo; Anikó Marshall; Derek Daniels
Related Documents :
1557453 - Nocturnal cyclic versus continuous total parenteral nutrition: food intake and feeding ...
7356043 - Universal eating monitor for continuous recording of solid or liquid consumption in man.
11830273 - Feeding and activity induced by orexin a in the lateral hypothalamus in rats.
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2012-11-26
Journal Detail:
Title:  Endocrinology     Volume:  154     ISSN:  1945-7170     ISO Abbreviation:  Endocrinology     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2012-12-25     Completed Date:  2013-02-22     Revised Date:  2014-01-09    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  320-9     Citation Subset:  AIM; IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Drinking / drug effects*
Eating / drug effects*
Estradiol / administration & dosage,  pharmacology*
Female
Ovariectomy
Rats
Rats, Long-Evans
Receptors, Estrogen / metabolism*
Grant Support
ID/Acronym/Agency:
HL-091911/HL/NHLBI NIH HHS; R01 HL091911/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Receptors, Estrogen; 4TI98Z838E/Estradiol
Comments/Corrections

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


Previous Document:  The Sphingosine-1-Phosphate Analog FTY720 Reduces Muscle Ceramide Content and Improves Glucose Toler...
Next Document:  Glucose intolerance and lipid metabolic adaptations in response to intrauterine and postnatal calori...