Melanocortin-3 Receptors Expressed on Agouti-Related Peptide Neurons Inhibit Feeding Behavior in Female Mice.
Melanocortin-3 Receptors Expressed on Agouti-Related Peptide Neurons Inhibit Feeding Behavior in Female Mice.
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DOI:
10.1002/oby.22306
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发表时间:
2018-12
期刊:
影响因子:
--
通讯作者:
Butler AA
中科院分区:
文献类型:
--
作者:
Girardet C;Marks DL;Butler AA
Activation of hypothalamic agouti-related peptide (AgRP)+ve neurons during energy deficit is a negative valence signal, rapidly activating food seeking behaviors. This study examined the roles of MC3Rs expressed by AgRP+ve neurons. AgRP-MC3R mice expressing MC3Rs selectively in AgRP+ve neurons were generated by crossing AgRP-IRES-Cre mice with LoxTBMc3r mice containing a “loxP-STOP-loxP” sequence in the 5’ UTR. Body weight, body composition and feeding behavior were assessed during ad libitum and timed-restricted feeding conditions. In females, food intake of AgRP-IRES-Cre(+ve) (n=7) or AgRP-IRES-Cre(-ve) (n=9) mice was not significantly different; these mice were therefore pooled to form the “control” group. Female AgRP-MC3R mice exhibited lower food intake (25.4±2.4 kJ/12h, n=6) compared to controls (35.3±1.8 kJ/12h, n=16) and LoxTBMc3r mice (32.1±2.1 kJ/12h, n=9) in the active phase during the dark period. Food intake during the rest phase (lights-on) when mice consume less food (9–10 kJ) was normal between genotypes. Body weight and composition of AgRP-MC3R and LoxTBMc3r mice was similar, suggesting compensatory mechanisms for reduced calorie intake. Remarkably, AgRP-MC3R mice continued to consume less food during re-feeding after fasting and timed-restricted feeding. MC3Rs expressed on AgRP+ve neurons appear to exert a strong inhibitory signal on hypothalamic networks governing feeding behavior.
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影响因子:
3.5
作者:
Anderson EJ;Çakir I;Carrington SJ;Cone RD;Ghamari-Langroudi M;Gillyard T;Gimenez LE;Litt MJ
通讯作者:
Litt MJ
影响因子:
8.1
作者:
Lam BYH;Cimino I;Polex-Wolf J;Nicole Kohnke S;Rimmington D;Iyemere V;Heeley N;Cossetti C;Schulte R;Saraiva LR;Logan DW;Blouet C;O'Rahilly S;Coll AP;Yeo GSH
通讯作者:
Yeo GSH
影响因子:
7.7
作者:
Henry FE;Sugino K;Tozer A;Branco T;Sternson SM
通讯作者:
Sternson SM
影响因子:
25
作者:
Dietrich, Marcelo O.;Bober, Jeremy;Horvath, Tamas L.
通讯作者:
Horvath, Tamas L.
DOI:
10.1152/ajpregu.2000.279.1.r47
发表时间:
2000-07-01
影响因子:
2.8
作者:
Hagan, MM;Rushing, PA;Seeley, RJ
通讯作者:
Seeley, RJ