Miller David W, Harrison Joanne L, Bennett Ellen J, Findlay Patricia A, Adam Clare L
Obesity and Metabolic Health Division, Rowett Research Institute, Bucksburn, Aberdeen, UK.
Endocrinology. 2007 Nov;148(11):5313-22. doi: 10.1210/en.2007-0534. Epub 2007 Aug 16.
This study investigated how changing nutritional status may alter reproductive neuroendocrine (LH) output via circulating leptin and insulin signaling through orexigenic hypothalamic pathways. Thin sheep were given an increasing nutritional plane (INP), sheep with intermediate adiposity a static nutritional plane (SNP), and fat sheep a decreasing nutritional plane (DNP) for 6 wk. Mean group adiposities converged by wk 6, LH output increased in INP, remained unchanged in SNP, and decreased in DNP sheep. Plasma and cerebrospinal fluid (CSF) insulin and plasma leptin concentrations increased in INP but did not change in the SNP and DNP groups. In INP sheep, LH output correlated positively with adiposity and plasma and CSF insulin concentrations and negatively with orexigenic neuropeptide Y gene expression in the hypothalamic arcuate nucleus (ARC). In DNP sheep, LH output correlated positively with adiposity, CSF leptin concentrations, and ARC proopiomelanocortin gene expression and negatively with leptin receptor (OB-Rb) and agouti-related peptide gene expression in the ARC. These data are consistent with the feedback response to an increasing nutritional plane being mediated by increasing circulating insulin entering the brain and stimulating LH via inhibition of hypothalamic neuropeptide Y and the response to a decreasing nutritional plane being mediated by altered hypothalamic leptin signaling brought about by increased OB-Rb expression and decreased melanocortin signaling. Because end point adiposity was similar yet LH output was different, the hypothalamus apparently retains a nutritional memory, based on changes in orexigenic neuropeptide expression, that influences contemporary neuroendocrine responses.
本研究调查了营养状况的改变如何通过循环中的瘦素和胰岛素信号,经促食欲的下丘脑途径,改变生殖神经内分泌(促黄体生成素,LH)的输出。给瘦羊逐渐增加营养水平(INP),给中等肥胖的羊维持静态营养水平(SNP),给肥羊逐渐降低营养水平(DNP),持续6周。到第6周时,各组平均肥胖程度趋于一致,INP组的LH输出增加,SNP组保持不变,DNP组的LH输出减少。INP组血浆和脑脊液(CSF)胰岛素以及血浆瘦素浓度升高,而SNP组和DNP组则无变化。在INP组绵羊中,LH输出与肥胖程度、血浆和脑脊液胰岛素浓度呈正相关,与下丘脑弓状核(ARC)中促食欲神经肽Y基因表达呈负相关。在DNP组绵羊中,LH输出与肥胖程度、脑脊液瘦素浓度以及ARC中阿黑皮素原基因表达呈正相关,与ARC中瘦素受体(OB-Rb)和刺鼠相关肽基因表达呈负相关。这些数据表明,对营养水平增加的反馈反应是由进入大脑的循环胰岛素增加介导的,通过抑制下丘脑神经肽Y来刺激LH;而对营养水平降低的反应是由下丘脑瘦素信号改变介导的,这种改变是由OB-Rb表达增加和黑皮质素信号减少引起的。由于终点肥胖程度相似但LH输出不同,下丘脑显然基于促食欲神经肽表达的变化保留了一种营养记忆,这种记忆会影响当代神经内分泌反应。