Photoperiod regulates arcuate nucleus POMC, AGRP, and leptin receptor mRNA in Siberian hamster hypothalamus

被引:144
作者
Mercer, JG
Moar, KM
Ross, AW
Hoggard, N
Morgan, PJ
机构
[1] Rowett Res Inst, Mol Neuroendocrinol Unit, Aberdeen AB21 9SB, Scotland
[2] Rowett Res Inst, Mol Physiol Grp, Aberdeen Ctr Energy Regulat & Obes, Aberdeen AB21 9SB, Scotland
关键词
Phodopus; agouti-related protein; proopiomelanocortin; orexins; melanin-concentrating hormone;
D O I
10.1152/ajpregu.2000.278.1.R271
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Siberian hamsters decreased body weight by 30% during 18 wk in short day (SD) vs. long day (LD) controls. Subsequent imposed food deprivation (FD; 24 h) caused a further 10% decrease. In the hypothalamic arcuate nucleus (ARC), SDs reduced proopiomelanocortin (POMC) gene expression and agouti-related protein (AGRP) mRNA was elevated, changes that summate to reduced catabolic drive through the melanocortin receptors. There was no effect of photoperiod on neuropeptide Y (NPY), melanin concentrating hormone, orexin, or corticotropin-releasing factor mRNAs. Superimposed FD increased AGRP gene expression and caused a localized elevation of NPY mRNA in the ARC. Both adipose tissue leptin and ARC leptin receptor (OB-Rb) mRNAs were downregulated in SDs, whereas FD increased OB-Rb gene expression. Thus OB-Rb mRNA is differentially regulated by acute and chronic changes in plasma leptin in this species. In a separate experiment in LDs, AGRP gene expression was increased by 24 or 48 h FD, whereas POMC mRNA was downregulated in the caudal ARC. AGRP and NPY mRNAs were extensively coexpressed in the ARC, and their differential regulation by photoperiod and FD is suggestive of transcript-specific regulation at the level of individual neurons.
引用
收藏
页码:R271 / R281
页数:11
相关论文
共 45 条
[1]   PHOTOPERIODIC CONTROL OF BODY-WEIGHT AND ENERGY-METABOLISM IN SYRIAN-HAMSTERS (MESOCRICETUS-AURATUS) - ROLE OF PINEAL-GLAND, MELATONIN, GONADS, AND DIET [J].
BARTNESS, TJ ;
WADE, GN .
ENDOCRINOLOGY, 1984, 114 (02) :492-498
[2]   Increased expression of mRNA for the long form of the leptin receptor in the hypothalamus is associated with leptin hypersensitivity and fasting [J].
Baskin, DG ;
Seeley, RJ ;
Kuijper, JL ;
Lok, S ;
Weigle, DS ;
Erickson, JC ;
Palmiter, RD ;
Schwartz, MW .
DIABETES, 1998, 47 (04) :538-543
[3]   Effects of photoperiod and androgen on proopiomelanocortin gene expression in the arcuate nucleus of golden hamsters [J].
Bittman, EL ;
Tubbiola, ML ;
Foltz, G ;
Hegarty, CM .
ENDOCRINOLOGY, 1999, 140 (01) :197-206
[4]  
Boss-Williams Katherine A., 1996, Physiology and Behavior, V59, P157, DOI 10.1016/0031-9384(95)02037-3
[5]   RECOMBINANT MOUSE OB PROTEIN - EVIDENCE FOR A PERIPHERAL SIGNAL LINKING ADIPOSITY AND CENTRAL NEURAL NETWORKS [J].
CAMPFIELD, LA ;
SMITH, FJ ;
GUISEZ, Y ;
DEVOS, R ;
BURN, P .
SCIENCE, 1995, 269 (5223) :546-549
[6]   Evidence that the diabetes gene encodes the leptin receptor: Identification of a mutation in the leptin receptor gene in db/db mice [J].
Chen, H ;
Charlat, O ;
Tartaglia, LA ;
Woolf, EA ;
Weng, X ;
Ellis, SJ ;
Lakey, ND ;
Culpepper, J ;
Moore, KJ ;
Breitbart, RE ;
Duyk, GM ;
Tepper, RI ;
Morgenstern, JP .
CELL, 1996, 84 (03) :491-495
[7]   Proopiomelanocortin neurons are direct targets for leptin in the hypothalamus [J].
Cheung, CC ;
Clifton, DK ;
Steiner, RA .
ENDOCRINOLOGY, 1997, 138 (10) :4489-4492
[8]   The hypocretins: Hypothalamus-specific peptides with neuroexcitatory activity [J].
De Lecea, L ;
Kilduff, TS ;
Peyron, C ;
Gao, XB ;
Foye, PE ;
Danielson, PE ;
Fukuhara, C ;
Battenberg, ELF ;
Gautvik, VT ;
Bartlett, FS ;
Frankel, WN ;
van den Pol, AN ;
Bloom, FE ;
Gautvik, KM ;
Sutcliffe, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :322-327
[9]   Leptin activates hypothalamic CART neurons projecting to the spinal cord [J].
Elias, CF ;
Lee, C ;
Kelly, J ;
Aschkenasi, C ;
Ahima, RS ;
Couceyro, PR ;
Kuhar, MJ ;
Saper, CB ;
Elmquist, JK .
NEURON, 1998, 21 (06) :1375-1385
[10]   Sensitivity to leptin and susceptibility to seizures of mice lacking neuropeptide Y [J].
Erickson, JC ;
Clegg, KE ;
Palmiter, RD .
NATURE, 1996, 381 (6581) :415-418