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1.
Pediatr Res ; 53(2): 302-8, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12538790

ABSTRACT

The present study examined the extent to which abundance of the prolactin receptor (PRLR) and a range of primary mitochondrial proteins are influenced by either maternal nutrition and/or fetal number in adipose tissue. Pregnant sheep were control fed [consuming 100% of total metabolizable energy (ME) requirements (taking into account requirements for both ewe maintenance and growth of the conceptus to produce a 4.5-kg lamb at term) for that stage of gestation] or were nutrient restricted (consuming 60% of total ME requirements). All ewes lambed normally at term and both perirenal adipose and hepatic tissues were sampled within 6 h of birth. Plasma membranes and mitochondria were prepared and analyzed using immunoblotting for abundance of PRLR and/or cytochrome c, voltage-dependent anion channel (VDAC), and uncoupling protein-1 (UCP1). Irrespective of maternal nutrition, abundance of specific isoforms of PRLR were significantly higher in adipose tissue sampled from twins compared with singletons and total UCP1 concentration per milligram of tissue was increased (p < 0.05). There was no effect of fetal number on PRLR abundance in the liver. Maternal nutrient restriction resulted in an increased abundance of both cytochrome c (p < 0.001) and VDAC in adipose tissue of twins but not singletons. This occurred despite maternal nutrition having no effect on either lamb body or adipose tissue weights, although both were lower (p < 0.05) in twins compared with singletons. In conclusion, fetal adipose tissue development is highly sensitive to nutritionally mediated changes in late gestation. An increase in fetal number results in greater PRLR abundance, which, in conjunction with a decrease in maternal nutrition, results in up-regulation of specific mitochondrial proteins.


Subject(s)
Adipose Tissue/growth & development , Adipose Tissue/metabolism , Animals, Newborn/growth & development , Embryonic and Fetal Development/physiology , Maternal Nutritional Physiological Phenomena/physiology , Receptors, Prolactin/metabolism , Animals , Birth Weight/physiology , Female , Gestational Age , Mitochondrial Proteins/metabolism , Pregnancy , Sheep , Twinning, Monozygotic
2.
FASEB J ; 16(11): 1438-40, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12205040

ABSTRACT

As the role of leptin in energy balance in neonate is unknown, we investigated the effect of acute (2 h) and chronic (7 days) administration of leptin (100 microg/day) on thermoregulation and mitochondrial protein abundance in adipose tissue. The concentration of uncoupling protein (UCP)1 and voltage-dependent anion channel (VDAC) located on the inner and outer mitochondrial membranes, respectively, were measured. Administration of leptin prevented the normal decline in colonic temperature over the first few hours and days after birth. It subsequently accelerated the loss of both mRNA and protein for UCP1 but had no effect on VDAC abundance. At seven days of age, colonic temperature was correlated strongly with both mRNA abundance and thermogenic potential of UCP1 in leptin-treated but not control lambs, indicating more effective use of UCP1 for heat production following leptin administration. Leptin had no effect on weight gain or adipose tissue deposition; at one day of age only, leptin mRNA was correlated positively with adipose tissue weight. In conclusion, leptin administration to neonatal lambs improves thermoregulation and promotes the loss of UCP1 in brown adipose tissue.


Subject(s)
Adipose Tissue, Brown/metabolism , Body Temperature Regulation , Carrier Proteins/biosynthesis , Leptin/pharmacology , Membrane Proteins/biosynthesis , Adipose Tissue, Brown/drug effects , Adipose Tissue, Brown/growth & development , Animals , Animals, Newborn , Body Temperature Regulation/drug effects , Carrier Proteins/genetics , Carrier Proteins/physiology , Colon/physiology , Ion Channels , Membrane Proteins/genetics , Membrane Proteins/physiology , Mitochondrial Proteins , Models, Biological , RNA, Messenger/biosynthesis , Sheep , Uncoupling Protein 1
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