Document Detail


Roles of dorsomedial hypothalamic cholecystokinin signaling in the controls of meal patterns and glucose homeostasis.
MedLine Citation:
PMID:  21871472     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A role for dorsomedial hypothalamus (DMH) cholecystokinin (CCK) signaling in feeding control has been proposed. Administration of CCK into the DMH reduces food intake and OLETF rats lacking CCK1 receptors (CCK1R) become hyperphagic and obese. We hypothesized that site specific replenishment of CCK1R in the DMH of OLETF rats would attenuate aspects of their feeding deficits. Recombinant vectors of adeno-associated viral (AAV)-mediated expression of CCK1R (AAVCCK1R) were bilaterally delivered into the DMH of OLETF. OLETF rats with AAVCCK1R injections demonstrated a 65% replenishment of Cck1r mRNA expression in the DMH relative to lean LETO control rats. Although this level of replenishment did not significantly affect overall food intake or body weight through 14 weeks following viral injections, meal patterns were partially normalized in OLETF rats receiving AAVCCK1R with a significant decrease in dark cycle meal size and a small but significant decrease in daily food intake in the meal analysis chambers. Importantly, the elevation in blood glucose level of OLETF rats was attenuated by the AAVCCK1R injections (p=0.03), suggesting a role for DMH CCK signaling in glucose homeostasis. In support of this role, administration of CCK into the DMH of intact rats enhanced glucose tolerance, as this occurred through activation of CCK1R but not CCK2R signaling. In conclusion, partial replenishment of CCK1R in the DMH of OLETF rats, although insufficient for altering overall food intake and body weight, normalizes meal pattern changes and reduces blood glucose levels. Our study also shows a novel role of DMH CCK signaling in glucose homeostasis.
Authors:
Guangjing Zhu; Jianqun Yan; Wanli W Smith; Timothy H Moran; Sheng Bi
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2011-08-17
Journal Detail:
Title:  Physiology & behavior     Volume:  105     ISSN:  1873-507X     ISO Abbreviation:  Physiol. Behav.     Publication Date:  2012 Jan 
Date Detail:
Created Date:  2011-11-28     Completed Date:  2012-03-26     Revised Date:  2014-09-14    
Medline Journal Info:
Nlm Unique ID:  0151504     Medline TA:  Physiol Behav     Country:  United States    
Other Details:
Languages:  eng     Pagination:  234-41     Citation Subset:  IM    
Copyright Information:
Copyright © 2011 Elsevier Inc. All rights reserved.
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MeSH Terms
Descriptor/Qualifier:
Analysis of Variance
Animals
Blood Glucose / drug effects
Cholecystokinin / genetics,  metabolism*,  pharmacology
Dorsomedial Hypothalamic Nucleus / drug effects,  metabolism*
Feeding Behavior / drug effects,  physiology*
Glucose / metabolism*
Glucose Tolerance Test
Green Fluorescent Proteins / genetics
Male
Microinjections
Motor Activity / genetics
RNA, Messenger / metabolism
Rats
Rats, Inbred OLETF
Rats, Long-Evans
Receptors, Cholecystokinin / genetics,  metabolism
Signal Transduction / genetics,  physiology*
Transduction, Genetic / methods
Grant Support
ID/Acronym/Agency:
DK057609/DK/NIDDK NIH HHS; R01 DK057609/DK/NIDDK NIH HHS; R01 DK057609-09/DK/NIDDK NIH HHS; R01 DK057609-10/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Blood Glucose; 0/RNA, Messenger; 0/Receptors, Cholecystokinin; 147336-22-9/Green Fluorescent Proteins; 9011-97-6/Cholecystokinin; IY9XDZ35W2/Glucose
Comments/Corrections

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


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