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Appetite regulatory mechanisms and food intake in mice are sensitive to mismatch in diets between pregnancy and postnatal periods

Appetite regulatory mechanisms and food intake in mice are sensitive to mismatch in diets between pregnancy and postnatal periods
Appetite regulatory mechanisms and food intake in mice are sensitive to mismatch in diets between pregnancy and postnatal periods
Human and animal studies suggest that obesity in adulthood may have its origins partly during prenatal development. One of the underlying causes of obesity is the perturbation of hypothalamic mechanisms controlling appetite. We determined mRNA levels of genes that regulate appetite, namely neuropeptide Y (NPY), pro-opiomelanocortin (POMC) and the leptin receptor isoform Ob-Rb, in the hypothalamus of adult mouse offspring from pregnant dams fed a protein-restricted diet, and examined whether mismatched post-weaning high-fat diet altered further expression of these gene transcripts. Pregnant MF1 mice were fed either normal protein (C, 18% casein) or protein-restricted (PR, 9% casein) diet throughout pregnancy. Weaned offspring were fed to adulthood a high-fat (HF; 45% kcal fat) or standard chow (21% kcal fat) diet to generate the C/HF, C/C, PR/HF and PR/C groups. Food intake and body weight were monitored during this period. Hypothalamic tissues were collected at 16 weeks of age for analysis of gene expression by real time RT-PCR. All HF-fed offspring were observed to be heavier vs. C groups regardless of the maternal diet during pregnancy. In the PR/HF males, but not in females, daily energy intake was reduced by 20% vs. the PR/C group (p<0.001). In PR/HF males, hypothalamic mRNA levels were lower vs. the PR/C group for NPY (p<0.001) and Ob-Rb (p<0.05). POMC levels were similar in all groups. In females, mRNA levels for these transcripts were similar in all groups. Our results suggest that adaptive changes during prenatal development in response to maternal dietary manipulation may have long-term sex-specific consequences on the regulation of appetite and metabolism following post-weaning exposure to an energy-rich nutritional environment
human, female, gene expression, developmental origins, mice, obesity, exposure, health, analysis, weight, diet, development, metabolism, disease, body weight, energy intake, maternal, environment, expression, pregnancy, male, leptin, gene-expression, protein, adult
0006-8993
146-152
Sellayah, D.
e4670170-eedd-46db-bd0f-44d3aeac4b06
Sek, K.
84ac9342-1986-4652-9905-b027119ae755
Anthony, F. W.
5ff8af5d-96db-435d-a98b-05cb07a0c791
Watkins, A. J.
4be0819a-e658-4f49-9872-5c882e78ec57
Osmond, C.
2677bf85-494f-4a78-adf8-580e1b8acb81
Fleming, T. P.
2abf761a-e5a1-4fa7-a2c8-12e32d5d4c03
Hanson, M. A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Cagampang, F. R.
7cf57d52-4a65-4554-8306-ed65226bc50e
Sellayah, D.
e4670170-eedd-46db-bd0f-44d3aeac4b06
Sek, K.
84ac9342-1986-4652-9905-b027119ae755
Anthony, F. W.
5ff8af5d-96db-435d-a98b-05cb07a0c791
Watkins, A. J.
4be0819a-e658-4f49-9872-5c882e78ec57
Osmond, C.
2677bf85-494f-4a78-adf8-580e1b8acb81
Fleming, T. P.
2abf761a-e5a1-4fa7-a2c8-12e32d5d4c03
Hanson, M. A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Cagampang, F. R.
7cf57d52-4a65-4554-8306-ed65226bc50e

Sellayah, D., Sek, K., Anthony, F. W., Watkins, A. J., Osmond, C., Fleming, T. P., Hanson, M. A. and Cagampang, F. R. (2008) Appetite regulatory mechanisms and food intake in mice are sensitive to mismatch in diets between pregnancy and postnatal periods. Brain Research, 1237, 146-152. (doi:10.1016/j.brainres.2008.07.126).

Record type: Article

Abstract

Human and animal studies suggest that obesity in adulthood may have its origins partly during prenatal development. One of the underlying causes of obesity is the perturbation of hypothalamic mechanisms controlling appetite. We determined mRNA levels of genes that regulate appetite, namely neuropeptide Y (NPY), pro-opiomelanocortin (POMC) and the leptin receptor isoform Ob-Rb, in the hypothalamus of adult mouse offspring from pregnant dams fed a protein-restricted diet, and examined whether mismatched post-weaning high-fat diet altered further expression of these gene transcripts. Pregnant MF1 mice were fed either normal protein (C, 18% casein) or protein-restricted (PR, 9% casein) diet throughout pregnancy. Weaned offspring were fed to adulthood a high-fat (HF; 45% kcal fat) or standard chow (21% kcal fat) diet to generate the C/HF, C/C, PR/HF and PR/C groups. Food intake and body weight were monitored during this period. Hypothalamic tissues were collected at 16 weeks of age for analysis of gene expression by real time RT-PCR. All HF-fed offspring were observed to be heavier vs. C groups regardless of the maternal diet during pregnancy. In the PR/HF males, but not in females, daily energy intake was reduced by 20% vs. the PR/C group (p<0.001). In PR/HF males, hypothalamic mRNA levels were lower vs. the PR/C group for NPY (p<0.001) and Ob-Rb (p<0.05). POMC levels were similar in all groups. In females, mRNA levels for these transcripts were similar in all groups. Our results suggest that adaptive changes during prenatal development in response to maternal dietary manipulation may have long-term sex-specific consequences on the regulation of appetite and metabolism following post-weaning exposure to an energy-rich nutritional environment

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More information

Published date: October 2008
Keywords: human, female, gene expression, developmental origins, mice, obesity, exposure, health, analysis, weight, diet, development, metabolism, disease, body weight, energy intake, maternal, environment, expression, pregnancy, male, leptin, gene-expression, protein, adult

Identifiers

Local EPrints ID: 70533
URI: http://eprints.soton.ac.uk/id/eprint/70533
ISSN: 0006-8993
PURE UUID: d708dbc2-b674-4e0a-a218-67b9afca7572
ORCID for C. Osmond: ORCID iD orcid.org/0000-0002-9054-4655
ORCID for M. A. Hanson: ORCID iD orcid.org/0000-0002-6907-613X
ORCID for F. R. Cagampang: ORCID iD orcid.org/0000-0003-4404-9853

Catalogue record

Date deposited: 03 Feb 2010
Last modified: 14 Mar 2024 02:47

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Contributors

Author: D. Sellayah
Author: K. Sek
Author: F. W. Anthony
Author: A. J. Watkins
Author: C. Osmond ORCID iD
Author: T. P. Fleming
Author: M. A. Hanson ORCID iD
Author: F. R. Cagampang ORCID iD

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