Neuronal deletion of Lepr elicits diabesity in mice without affecting cold tolerance or fertility - PubMed (original) (raw)
. 2005 Sep;289(3):E403-11.
doi: 10.1152/ajpendo.00535.2004. Epub 2005 May 3.
Affiliations
- PMID: 15870101
- DOI: 10.1152/ajpendo.00535.2004
Free article
Neuronal deletion of Lepr elicits diabesity in mice without affecting cold tolerance or fertility
Julie E McMinn et al. Am J Physiol Endocrinol Metab. 2005 Sep.
Free article
Abstract
Leptin signaling in the brain regulates energy intake and expenditure. To test the degree of functional neuronal leptin signaling required for the maintenance of body composition, fertility, and cold tolerance, transgenic mice expressing Cre in neurons (CaMKIIalpha-Cre) were crossed to mice carrying a floxed leptin receptor (Lepr) allele to generate mice with neuron-specific deletion of Lepr in approximately 50% (C F/F mice) and approximately 75% (C Delta17/F mice) of hypothalamic neurons. Leptin receptor (LEPR)-deficient mice (Delta17/Delta17) with heat-shock-Cre-mediated global Lepr deletion served as obese controls. At 16 wk, male C F/F, C Delta17/F, and Delta17/Delta17 mice were 13.2 (P < 0.05), 45.0, and 55.9% (P < 0.001) heavier, respectively, than lean controls, whereas females showed 31.6, 68.8, and 160.7% increases in body mass (P < 0.001). Significant increases in total fat mass (C F/F: P < 0.01; C Delta17/F and Delta17/Delta17:P < 0.001 vs. sex-matched, lean controls), and serum leptin concentrations (P < 0.001 vs. controls) were present in proportion to Lepr deletion. Male C Delta17/F mice had significant elevations in basal serum insulin concentrations (P < 0.001 vs. controls) and were glucose intolerant, as measured by glucose tolerance test (AUC P < 0.01 vs. controls). In contrast with previous observations in mice null for LEPR signaling, C F/F and C Delta17/F mice were fertile and cold tolerant. These findings support the hypothesis that body weight, adiposity, serum leptin concentrations, and glucose intolerance are proportional to hypothalamic LEPR deficiency. However, fertility and cold tolerance remain intact unless hypothalamic LEPR deficiency is complete.
Similar articles
- Transgenic complementation of leptin receptor deficiency. II. Increased leptin receptor transgene dose effects on obesity/diabetes and fertility/lactation in lepr-db/db mice.
Chua SC Jr, Liu SM, Li Q, Sun A, DeNino WF, Heymsfield SB, Guo XE. Chua SC Jr, et al. Am J Physiol Endocrinol Metab. 2004 Mar;286(3):E384-92. doi: 10.1152/ajpendo.00349.2003. Epub 2003 Nov 4. Am J Physiol Endocrinol Metab. 2004. PMID: 14600075 - Complete rescue of obesity, diabetes, and infertility in db/db mice by neuron-specific LEPR-B transgenes.
de Luca C, Kowalski TJ, Zhang Y, Elmquist JK, Lee C, Kilimann MW, Ludwig T, Liu SM, Chua SC Jr. de Luca C, et al. J Clin Invest. 2005 Dec;115(12):3484-93. doi: 10.1172/JCI24059. Epub 2005 Nov 10. J Clin Invest. 2005. PMID: 16284652 Free PMC article. - Increased expression of hypothalamic leptin receptor and adiponectin accompany resistance to dietary-induced obesity and infertility in female C57BL/6J mice.
Tortoriello DV, McMinn JE, Chua SC. Tortoriello DV, et al. Int J Obes (Lond). 2007 Mar;31(3):395-402. doi: 10.1038/sj.ijo.0803392. Epub 2006 Jul 25. Int J Obes (Lond). 2007. PMID: 16865100 - Genetic dissection of neuronal pathways controlling energy homeostasis.
Balthasar N. Balthasar N. Obesity (Silver Spring). 2006 Aug;14 Suppl 5:222S-227S. doi: 10.1038/oby.2006.313. Obesity (Silver Spring). 2006. PMID: 17021371 Review. - Hypothalamic neuronal histamine regulates body weight through the modulation of diurnal feeding rhythm.
Yoshimatsu H. Yoshimatsu H. Nutrition. 2008 Sep;24(9):827-31. doi: 10.1016/j.nut.2008.06.014. Nutrition. 2008. PMID: 18725079 Review.
Cited by
- Ablation of LMO4 in glutamatergic neurons impairs leptin control of fat metabolism.
Zhou X, Gomez-Smith M, Qin Z, Duquette PM, Cardenas-Blanco A, Rai PS, Harper ME, Tsai EC, Anisman H, Chen HH. Zhou X, et al. Cell Mol Life Sci. 2012 Mar;69(5):819-28. doi: 10.1007/s00018-011-0794-3. Epub 2011 Aug 27. Cell Mol Life Sci. 2012. PMID: 21874351 Free PMC article. - Role of Astrocytes in Leptin Signaling.
Wang Y, Hsuchou H, He Y, Kastin AJ, Pan W. Wang Y, et al. J Mol Neurosci. 2015 Aug;56(4):829-839. doi: 10.1007/s12031-015-0518-5. Epub 2015 Feb 17. J Mol Neurosci. 2015. PMID: 25687329 Free PMC article. - Selective deletion of leptin receptors in gonadotropes reveals activin and GnRH-binding sites as leptin targets in support of fertility.
Akhter N, CarlLee T, Syed MM, Odle AK, Cozart MA, Haney AC, Allensworth-James ML, Beneš H, Childs GV. Akhter N, et al. Endocrinology. 2014 Oct;155(10):4027-42. doi: 10.1210/en.2014-1132. Epub 2014 Jul 24. Endocrinology. 2014. PMID: 25057790 Free PMC article. - A Tale of Three Systems: Toward a Neuroimmunoendocrine Model of Obesity.
O'Brien CJO, Haberman ER, Domingos AI. O'Brien CJO, et al. Annu Rev Cell Dev Biol. 2021 Oct 6;37:549-573. doi: 10.1146/annurev-cellbio-120319-114106. Annu Rev Cell Dev Biol. 2021. PMID: 34613819 Free PMC article. Review. - Central nervous control of energy and glucose balance: focus on the central melanocortin system.
Xu Y, Elmquist JK, Fukuda M. Xu Y, et al. Ann N Y Acad Sci. 2011 Dec;1243:1-14. doi: 10.1111/j.1749-6632.2011.06248.x. Ann N Y Acad Sci. 2011. PMID: 22211889 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
- F32-DK-61229/DK/NIDDK NIH HHS/United States
- P01-DK-56687/DK/NIDDK NIH HHS/United States
- P30-DK-63608/DK/NIDDK NIH HHS/United States
- R01-DK-57621/DK/NIDDK NIH HHS/United States
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous