Korner J, Savontaus E, Chua S C, Leibel R L, Wardlaw S L
Department of Medicine, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
J Neuroendocrinol. 2001 Nov;13(11):959-66. doi: 10.1046/j.1365-2826.2001.00716.x.
Agouti-related protein (AGRP) is synthesized in the same neurones in the arcuate nucleus as neuropeptide Y (NPY), another potent orexigenic peptide. AGRP antagonizes the action of alpha-melanocyte stimulating hormone, a derivative of pro-opiomelanocortin (POMC) at the hypothalamic MC4 receptor to increase food intake. Although leptin has been shown to regulate Agrp/Npy and Pomc-expressing neurones, there are differences with respect to Agrp regulation in leptin receptor-deficient mice and rats. Unlike the obese leptin receptor-deficient db/db mouse, which exhibits upregulation of Agrp mRNA expression in the medial basal hypothalamus (MBH) compared to lean controls, the obese leptin receptor-deficient (faf; Koletsky) rat does not exhibit upregulation of Agrp expression. To determine whether this represents a general difference between leptin receptor-deficient mice and rats, neuropeptide gene expression was analysed in the MBH of lean and obese rats segregating for a different leptin receptor mutation, Leprfa (Zucker). Fasting in lean rats (+/fa) for 72 h significantly increased Agrp and Npy mRNA expression, and decreased Pomc mRNA expression as detected by a sensitive solution hybridization/S1 nuclease protection assay. Npy mRNA levels were significantly increased in fed obese fa/fa compared to lean rats, and further increased in the obese animals after fasting. In contrast, Agrp mRNA levels did not differ between fed lean and fed obese rats, and fasting did not significantly change Agrp levels in obese rats. To determine whether the change in Agrp expression that occurs with food deprivation in lean rats could be prevented by leptin replacement, Sprague-Dawley rats were fasted and infused via subcutaneous osmotic micropumps for 48 h with either saline or recombinant mouse leptin. Fasting significantly increased Agrp and Npy, and decreased Pomc mRNA levels. Leptin infusion almost completely reversed these changes such that there was no significant difference between the levels in the fasted rats and those that were fed ad libitum. Thus, in fasted lean rats, Agrp and Npy are upregulated in parallel when leptin levels fall and are downregulated by leptin infusion. By contrast, the absence of a functional leptin receptor results in the upregulation of Npy but not Agrp mRNA.
刺鼠相关蛋白(AGRP)与另一种强效促食欲肽神经肽Y(NPY)在弓状核的同一神经元中合成。AGRP在下丘脑促黑素细胞激素4(MC4)受体处拮抗α-黑素细胞刺激素(一种阿片-促黑素皮质素原(POMC)的衍生物)的作用,从而增加食物摄入量。尽管已证明瘦素可调节表达Agrp/Npy和Pomc的神经元,但在瘦素受体缺陷的小鼠和大鼠中,Agrp的调节存在差异。与瘦对照相比,肥胖的瘦素受体缺陷db/db小鼠在内侧基底下丘脑(MBH)中Agrp mRNA表达上调,而肥胖的瘦素受体缺陷(faf;科莱茨基)大鼠则未表现出Agrp表达上调。为了确定这是否代表瘦素受体缺陷小鼠和大鼠之间的普遍差异,对分离出不同瘦素受体突变Leprfa( Zucker)的瘦和肥胖大鼠的MBH中的神经肽基因表达进行了分析。通过灵敏的溶液杂交/S1核酸酶保护试验检测到,瘦大鼠(+/fa)禁食72小时显著增加了Agrp和Npy mRNA表达,并降低了Pomc mRNA表达。与瘦大鼠相比,喂食的肥胖fa/fa大鼠中Npy mRNA水平显著升高,禁食后肥胖动物中进一步升高。相比之下,喂食的瘦大鼠和喂食的肥胖大鼠之间Agrp mRNA水平没有差异,禁食也未显著改变肥胖大鼠中的Agrp水平。为了确定瘦大鼠中食物剥夺时发生的Agrp表达变化是否可以通过补充瘦素来预防,将斯普拉格-道利大鼠禁食,并通过皮下渗透微型泵用生理盐水或重组小鼠瘦素灌注48小时。禁食显著增加了Agrp和Npy,并降低了Pomc mRNA水平。瘦素灌注几乎完全逆转了这些变化,使得禁食大鼠中的水平与自由采食大鼠中的水平之间没有显著差异。因此,在禁食的瘦大鼠中,当瘦素水平下降时,Agrp和Npy平行上调,而通过瘦素灌注下调。相比之下,缺乏功能性瘦素受体会导致Npy上调,但不会导致Agrp mRNA上调。