Leptin Predicts Bone and Fat Mass after Accounting for the Effects of Diet and Glucocorticoid Treatment in Piglets 1
Abstract
The role of leptin in neonatal growth and bone metabolism has been investigated, but not simultaneously. The objectives of this study were to determine if leptin relates to bone mass during rapid growth; if consumption of maternal milk is related to elevated circulating concentrations of leptin resulting in higher fat mass; and if glucocorticoids result in higher fat mass and reduced bone mass due to elevated leptin. Thirty-two piglets were randomized to either a suckling or milk substitute plus either dexamethasone (DEX) or placebo injection for 15 days beginning at 5 days of age. Milk and blood samples were obtained at baseline, and after 15 days, blood was sampled again for measurement of leptin and bone biochemistry. Weight at baseline plus weight and length after 15 days were recorded, followed by measurement of whole body bone mineral content, bone area, and fat mass using dual energy x-ray absorptiometry. At baseline, plasma leptin was elevated in suckled piglets. Piglets that suckled had elevated fat mass as did those who received DEX. However, DEX resulted in suppressed weight and length, bone mass, and bone metabolism. Leptin was similar among groups after the 15 days. After accounting for body size and treatment effects, piglet plasma leptin was predictive of bone and fat mass. Leptin circulating early postnatally is linked to body composition, specifically fat and bone mass. Elevations in fat mass and reductions in bone mass observed after 15 days of DEX treatment are not related to leptin metabolism. Both human and porcine neonates share similar characteristics with respect to relationships of leptin with fat and bone mass.
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In animal studies, excess glucocorticoid exposure in utero consistently programmes the offspring for increased adiposity.
“In animal studies, excess glucocorticoid exposure in utero was consistently shown to programme the offspring for increased adiposity (Table 6 and [119–123]).”
From Developmental programming of offspring adipose tissue biology and obesity risk (2021) · cites this paper as [123]
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- Authors
- Weiler, H. A., Kovacs, H., Murdock, C., Adolphe, J., & Wong, S. F.
- Affiliations
- University of Manitoba (CA)
- Corresponding author
- Weiler, Hope A.
- Venue
- Experimental Biology and Medicine
- Publisher
- Frontiers Media SA
- Published
- 2002-09
- Volume
- 227
- Issue
- 8
- Pages
- 639-644
- ISSN
- 0071-3384 (ISSN-L)
- 1535-3702
- 1535-3699
- OpenAlex
- W2166042314
- Cited by
- 11
- References
- 38
- Citations by year
- 2023: 1 · 2021: 1 · 2012: 2
- FWCI
- 0.21
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental Biology and Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Keywords
- leptin, bone mass, fat mass, neonatal growth, piglets, dexamethasone, glucocorticoids, suckling, dairy alternatives, bone mineral content, body composition, bone metabolism
- MeSH terms
- Adipose Tissue, Animals, Animal Feed, Body Composition, Body Weight, Bone and Bones, Dexamethasone, Male, Milk, Minerals, Organ Size, Random Allocation, Species Specificity, Swine, Weight Gain, Bone Density, Leptin, Models, Animal
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