Primeaux Stefany D, Blackmon Christine, Barnes Maria J, Braymer H Douglas, Bray George A
Dietary Obesity Laboratory, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, LA 70808, USA.
Peptides. 2008 Nov;29(11):1994-2000. doi: 10.1016/j.peptides.2008.07.024. Epub 2008 Aug 13.
Pyrogultamylated arginine-phenylalanineamide peptide (QRFP) is strongly conserved across species and is a member of the family of RFamide-related peptides, with the motif Arg-Phe-NH(2) at the C-terminal end. The precursor peptide for QRFP generates a 26-amino acid peptide (QRFP-26) and a 43-amino acid peptide (QRFP-43), both of which bind to the G protein-coupled receptor, GPR103. Recently, QRFP has been characterized in rats, mice and humans and has been reported to have orexigenic properties. In rodents, prepro-QRFP mRNA is expressed in localized regions of the mediobasal hypothalamus, a region implicated in feeding behavior. Increased intake of a high fat diet contributes to increased weight gain and obesity. Therefore, the current experiments investigated the effects of QRFP administration in rats and the effects of a high fat diet on prepro-QRFP mRNA and GPR103 receptor mRNA levels. Intracerebroventricular administration of QRFP-26 (3.0nM, 5.0nM) and QRFP-43 (1.0nM, 3.0nM) dose-dependently increased 1h, 2h, and 4h cumulative intake of high fat (55% fat), but not low fat (10% fat) diet. In Experiment 2, hypothalamic prepro-QRFP mRNA levels and GPR103 receptor mRNA levels were measured in rats fed a high fat or a low fat diet for 21 days. Prepro-QRFP mRNA was significantly increased in the ventromedial nucleus/arcuate nucleus of the hypothalamus of rats fed a high fat diet compared to those fed a low fat diet, while GPR103 mRNA levels were unchanged. These findings suggest that QRFP is a regulator of dietary fat intake and is influenced by the intake of a high fat diet.
焦谷氨酸化精氨酸 - 苯丙氨酸酰胺肽(QRFP)在物种间具有高度保守性,是RF酰胺相关肽家族的成员,其C末端具有Arg - Phe - NH₂基序。QRFP的前体肽可产生一个26个氨基酸的肽段(QRFP - 26)和一个43个氨基酸的肽段(QRFP - 43),二者均可与G蛋白偶联受体GPR103结合。最近,QRFP已在大鼠、小鼠和人类中得到鉴定,并被报道具有促食欲特性。在啮齿动物中,前体QRFP mRNA在下丘脑腹内侧核的局部区域表达,该区域与进食行为有关。高脂饮食摄入量的增加会导致体重增加和肥胖。因此,当前实验研究了QRFP给药对大鼠的影响以及高脂饮食对前体QRFP mRNA和GPR103受体mRNA水平的影响。脑室内注射QRFP - 26(3.0nM,5.0nM)和QRFP - 43(1.0nM,3.0nM)剂量依赖性地增加了1小时、2小时和4小时高脂(55%脂肪)饮食的累积摄入量,但对低脂(10%脂肪)饮食无此作用。在实验2中,对喂食高脂或低脂饮食21天的大鼠下丘脑前体QRFP mRNA水平和GPR103受体mRNA水平进行了测量。与喂食低脂饮食的大鼠相比,喂食高脂饮食的大鼠下丘脑腹内侧核/弓状核中的前体QRFP mRNA显著增加,而GPR103 mRNA水平未发生变化。这些发现表明,QRFP是饮食脂肪摄入的调节因子,并受高脂饮食摄入的影响。