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The importance of corticosterone in mediating restraint-induced weight loss in rats

  • Isabell J. Scherer
    ,
  • Philip V. Holmes
    ,
  • Ruth B.S. Harris(corresponding author)
*Corresponding author for this work
  • University of Georgia
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

I. J. Scherer, P. V. Holmes, R. B.S. Harris. The importance of corticosterone in mediating restraint-induced weight loss in rats. PHYSIOL BEHAV 00 (0) 000-000, 2010. Rats restrained for 3. h/day for 3. days (RR) lose weight and do not return to the weight of non-restrained controls once restraint has ended. This study tested the importance of restraint-induced corticosterone release in mediating the change in body weight by injecting ADX rats with 2.0. mg corticosterone/kg before each restraint to replicate the restraint-induced surge in circulating corticosterone. Restrained adrenalectomized (ADX) rats injected with corticosterone had the same initial weight loss as intact restrained rats, whereas corticosterone injection in non-restrained ADX rats and restraint of ADX rats injected with saline each produced only half as much initial weight loss. Sustained weight loss, measured for 14. days after the end of RR, was the same for restrained intact rats and restrained ADX rats injected with corticosterone whereas restrained ADX rats injected with saline achieved the same weight gain as their controls. Corticosterone injections had no effect on weight gain of non-restrained intact rats. In situ hybridization showed that corticotropin releasing factor (CRF) mRNA expression in the paraventricular nucleus of the hypothalamus (PVN) was increased by the same degree in ADX rats and restrained intact rats and was not modified by corticosterone injections. There was no significant effect of restraint, ADX or corticosterone injection on PVN arginine vasopressin (AVP) mRNA expression. These data indicate that a surge in corticosterone causes sustained weight loss in ADX rats through a mechanism that can be compensated for in intact rats and is independent of changes in PVN CRF or AVP mRNA expression.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 225-233 (9 pages)

Journal (Volume, Issue Number)

Physiology and Behavior (Volume 102, Issue 2)

Publication milestones

  • Published - 02/01/2011

Publication status

Published - 02/01/2011

ISSN

0031-9384

Publication IDs

  • Scopus: 78649583865
  • PubMed: 21092743

Publication metrics

Metrics

SciVal
FWCI
0.21
SciVal
Author count
3
SciVal
citations
17
SciVal
Paper percentile
74
Scopus
citations
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1

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Citation count
24
Captures
40

Funding Details

This work was supported by NIH grant MH068281 awarded to RBSH. The authors thank Samantha Haring, Rachel Doyle and Hayden Kramer for their assistance with this project.
FundersFunding number
National Institutes of Health
-
NIMH
R01MH068281