Document Detail


Leptin is not necessary for gestation and parturition but regulates maternal nutrition via a leptin resistance state.
MedLine Citation:
PMID:  9832467     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Leptin levels are significantly elevated in pregnant mice, rats and humans suggesting a critical role for leptin during gestation. To address whether leptin plays a putative role in the physiology of pregnancy, we asked whether a mouse pregnancy would be affected by the complete absence of leptin from both the mother and fetuses. Thus, leptin-deficient ob/ob females were first treated with exogenous leptin and then mated to similarly treated ob/ob males. All resulting fetuses have an ob/ob genotype and lack like their mothers any endogenous leptin production. Withdrawal of leptin treatment at 0.5, 6.5, 10.5 and 19.5 days p.c. did not affect any stage of the pregnancy despite a gradual return of the mothers to an obese state. However, some mice had delayed gestation periods of 21-23 days which were associated with prolonged parturition. The pups were normally delivered with no obvious signs of deformities although none survived beyond a day after delivery due to failure of lactation. Monitoring daily food intake of pregnant ob/ob females treated throughout gestation with leptin revealed significantly elevated levels of food intake from day 10 p.c. and onward demonstrating an attenuation of a leptin response during pregnancy and a leptin resistance effect. These studies demonstrate that in the mouse, leptin is not a critical molecule for implantation, gestation, fetal growth and parturition but that the leptin resistance effect at mid-gestation aims to stimulate food intake thus providing sustained energy resources for pregnancy.
Authors:
K Mounzih; J Qiu; A Ewart-Toland; F F Chehab
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Endocrinology     Volume:  139     ISSN:  0013-7227     ISO Abbreviation:  Endocrinology     Publication Date:  1998 Dec 
Date Detail:
Created Date:  1998-12-24     Completed Date:  1998-12-24     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  5259-62     Citation Subset:  AIM; IM    
Affiliation:
Univ. of California, Department of Laboratory Medicine, San Francisco 94143, USA.
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MeSH Terms
Descriptor/Qualifier:
Animal Nutritional Physiological Phenomena*
Animals
Drug Resistance / physiology
Eating / physiology
Female
Humans
Labor, Obstetric / physiology*
Leptin
Male
Mice
Nutritional Physiological Phenomena / physiology*
Pregnancy
Pregnancy, Animal / physiology*
Proteins / metabolism,  physiology*
Grant Support
ID/Acronym/Agency:
HD35142/HD/NICHD NIH HHS; HL53762/HL/NHLBI NIH HHS; T32DK 07636/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Leptin; 0/Proteins

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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