LEPTIN GENE-EXPRESSION INCREASES WITH AGE INDEPENDENT OF INCREASING ADIPOSITY IN RATS

Citation
H. Li et al., LEPTIN GENE-EXPRESSION INCREASES WITH AGE INDEPENDENT OF INCREASING ADIPOSITY IN RATS, Diabetes, 46(12), 1997, pp. 2035-2039
Citations number
26
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00121797
Volume
46
Issue
12
Year of publication
1997
Pages
2035 - 2039
Database
ISI
SICI code
0012-1797(1997)46:12<2035:LGIWAI>2.0.ZU;2-W
Abstract
Humans and rats tend to gain weight as they age. Leptin is one regulat or of food intake and energy expenditure. To determine if the increase in adiposity with age is related to altered leptin gene expression, w e assessed adiposity levels, leptin mRNA levels in epididymal and ingu inal white adipose tissue (EWAT and IWAT), and uncoupling protein (UCP I) mRNA levels in interscapular brown adipose tissue (IBAT) from F344 x BN rats ages 3, 12, 18, 24, and 30 months (n = 8/age). Levels of adi posity determined by the adiposity index and the Lee index increased b etween ages 3 and 24 months, with a decrease at age 30 months. There m ere parallel increases with age in body weight, EWAT, and IWAT depot s ize up to age 24 months, followed by a non-significant decrease at age 30 months. Daily food intake was unchanged with age. In EWAT, leptin mRNA per microgram of RNA was unchanged with age, whereas in IWAT, it increased up to 24 months, then declined at 30 months. Total leptin mR NA levels in both IWAT and EWAT depots increased with age, peaking at age 24 months, and were correlated with adiposity. Serum leptin levels increased with age, also peaking at age 24 months, and were correlate d with total leptin mRNA in WAT pads and adiposity. The rate of increa se in serum leptin was greater than the increase in adiposity with age , suggesting contributions from both the increase in leptin expression per unit of WAT and the increase in WAT depot size. In addition, UCPI mRNA levels in IBAT did not change with age. These data suggest that adiposity increases with age and cannot be attributed to increased foo d intake, impaired leptin gene expression, or decreased UCP1 mRNA leve l in IBAT. Furthermore, leptin gene expression in IWAT increases with age independent of increasing adiposity.