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Developmental control of plasma leptin and adipose leptin messenger ribonucleic acid in the ovine fetus during late gestation: role of glucocorticoids and thyroid hormones

Developmental control of plasma leptin and adipose leptin messenger ribonucleic acid in the ovine fetus during late gestation: role of glucocorticoids and thyroid hormones
Developmental control of plasma leptin and adipose leptin messenger ribonucleic acid in the ovine fetus during late gestation: role of glucocorticoids and thyroid hormones
In developed countries, the increasing incidence of obesity is a serious health problem. Leptin exposure in the perinatal period affects long-term regulation of appetite and energy expenditure, but control of leptin production in utero is unclear. This study investigated perirenal adipose tissue (PAT) and placental leptin expression in ovine fetuses during late gestation and after manipulation of plasma glucocorticoid and thyroid hormone concentrations. Between 130 and 144 d of gestation (term at 145 ± 2 d), plasma leptin and PAT leptin mRNA levels increased in association with increments in plasma cortisol and T3. Fetal adrenalectomy prevented these developmental changes, and exposure of intact 130 d fetuses to glucocorticoids, by cortisol infusion or maternal dexamethasone treatment, caused premature elevations in plasma leptin and PAT leptin gene expression. Fetal thyroidectomy increased plasma leptin and PAT leptin mRNA abundance, whereas intravenous T3 infusion to intact 130 d fetuses had no effect on circulating or PAT leptin. Leptin mRNA expression was low in the ovine placenta. Therefore, in the sheep fetus, PAT appears to be a primary source of leptin in the circulation, and leptin gene expression is regulated by both glucocorticoids and thyroid hormones. Developmental changes in circulating and PAT leptin may mediate the maturational effects of cortisol in utero and have long-term consequences for appetite regulation and the development of obesity.
0013-7227
3750-3757
O’Connor, Deirdre M.
f152d74e-cfb8-452c-a441-2c87efbb7c4f
Blache, Dominique
733e6794-0388-42c1-b8a6-031782a26aa1
Hoggard, Nigel
31e830c3-71d7-4657-ae05-6ca22a829c3d
Brookes, Emily
425dafc2-111b-4f6c-9336-f720c4ef8cac
Wooding, F. B. Peter
25d35c07-7813-4dec-b8e4-a7f52982c190
Fowden, Abigail L.
78847bb7-4d2d-4e79-93c8-a90e0131c1d6
Forhead, Alison J.
8ad02d28-a814-4b74-93ff-9c29a254019c
O’Connor, Deirdre M.
f152d74e-cfb8-452c-a441-2c87efbb7c4f
Blache, Dominique
733e6794-0388-42c1-b8a6-031782a26aa1
Hoggard, Nigel
31e830c3-71d7-4657-ae05-6ca22a829c3d
Brookes, Emily
425dafc2-111b-4f6c-9336-f720c4ef8cac
Wooding, F. B. Peter
25d35c07-7813-4dec-b8e4-a7f52982c190
Fowden, Abigail L.
78847bb7-4d2d-4e79-93c8-a90e0131c1d6
Forhead, Alison J.
8ad02d28-a814-4b74-93ff-9c29a254019c

O’Connor, Deirdre M., Blache, Dominique, Hoggard, Nigel, Brookes, Emily, Wooding, F. B. Peter, Fowden, Abigail L. and Forhead, Alison J. (2007) Developmental control of plasma leptin and adipose leptin messenger ribonucleic acid in the ovine fetus during late gestation: role of glucocorticoids and thyroid hormones. Endocrinology, 148 (8), 3750-3757. (doi:10.1210/en.2007-0310).

Record type: Article

Abstract

In developed countries, the increasing incidence of obesity is a serious health problem. Leptin exposure in the perinatal period affects long-term regulation of appetite and energy expenditure, but control of leptin production in utero is unclear. This study investigated perirenal adipose tissue (PAT) and placental leptin expression in ovine fetuses during late gestation and after manipulation of plasma glucocorticoid and thyroid hormone concentrations. Between 130 and 144 d of gestation (term at 145 ± 2 d), plasma leptin and PAT leptin mRNA levels increased in association with increments in plasma cortisol and T3. Fetal adrenalectomy prevented these developmental changes, and exposure of intact 130 d fetuses to glucocorticoids, by cortisol infusion or maternal dexamethasone treatment, caused premature elevations in plasma leptin and PAT leptin gene expression. Fetal thyroidectomy increased plasma leptin and PAT leptin mRNA abundance, whereas intravenous T3 infusion to intact 130 d fetuses had no effect on circulating or PAT leptin. Leptin mRNA expression was low in the ovine placenta. Therefore, in the sheep fetus, PAT appears to be a primary source of leptin in the circulation, and leptin gene expression is regulated by both glucocorticoids and thyroid hormones. Developmental changes in circulating and PAT leptin may mediate the maturational effects of cortisol in utero and have long-term consequences for appetite regulation and the development of obesity.

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Published date: 1 August 2007

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Local EPrints ID: 472132
URI: http://eprints.soton.ac.uk/id/eprint/472132
ISSN: 0013-7227
PURE UUID: 33c76154-7c87-4c18-8190-c7a6a0968b9c
ORCID for Emily Brookes: ORCID iD orcid.org/0000-0003-2175-4349

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Date deposited: 28 Nov 2022 17:40
Last modified: 17 Mar 2024 04:14

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Contributors

Author: Deirdre M. O’Connor
Author: Dominique Blache
Author: Nigel Hoggard
Author: Emily Brookes ORCID iD
Author: F. B. Peter Wooding
Author: Abigail L. Fowden
Author: Alison J. Forhead

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