Aguirre Carolina, Castillo Valeska, Llanos Miguel
Unidad Docente Asociada, Ciencias de la Salud, Nutrición y Dietética, Pontificia Universidad Católica de Chile, Campus San Joaquín, Chile.
Laboratorio de Nutrición y Regulación Metabólica, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, Santiago, Chile.
J Nutr Metab. 2017;2017:2945010. doi: 10.1155/2017/2945010. Epub 2017 Jul 20.
We have previously shown that administration of the endocannabinoid anandamide (AEA) during lactation leads to overweight, increased body fat accumulation, and insulin resistance in adult mice. This study was designed to elucidate if these effects are due to increased food intake, stimulated by an augmented abundance and binding ability of the hypothalamic cannabinoid type 1 receptor (CB1R). With this aim, male mice pups were treated with a daily oral dose of AEA during lactation. Adult mice were also treated with a single oral dose of AEA, to evaluate acute food intake during 4 h. At 21 and 160 days, CB1R protein abundance was calculated by western blot analysis. Capacity of hypothalamic membranes to specifically bind the radioligand [H]-CP55.940 was also measured. Western blots showed a 72% increase in CB1R abundance in AEA-treated 21-day-old mice, without differences in adult mice. Additionally, specific binding of [H]-CP55.940 to hypothalamic membranes from adult mice was significantly lower in those mice treated with AEA during lactation. Moreover, AEA did not stimulate acute food intake in both, AEA-treated and control mice. Results suggest that metabolic alterations found in adult mice because of AEA treatment during lactation are not associated with hypothalamic CB1R.
我们之前已经表明,哺乳期给予内源性大麻素花生四烯酸乙醇胺(AEA)会导致成年小鼠超重、体脂堆积增加和胰岛素抵抗。本研究旨在阐明这些影响是否归因于下丘脑1型大麻素受体(CB1R)丰度和结合能力增强所刺激的食物摄入量增加。为此,在哺乳期给雄性幼鼠每日口服一剂AEA。成年小鼠也给予单剂口服AEA,以评估4小时内的急性食物摄入量。在21天和160天时,通过蛋白质印迹分析计算CB1R蛋白丰度。还测量了下丘脑膜特异性结合放射性配体[H]-CP55.940的能力。蛋白质印迹显示,AEA处理的21日龄小鼠中CB1R丰度增加了72%,成年小鼠中无差异。此外,哺乳期用AEA处理的成年小鼠下丘脑膜对[H]-CP55.940的特异性结合显著降低。此外,AEA对AEA处理组和对照组小鼠的急性食物摄入量均无刺激作用。结果表明,哺乳期AEA处理导致成年小鼠出现的代谢改变与下丘脑CB1R无关。