School of Basic Pharmaceutical and Toxicological Sciences, College of Pharmacy, University of Louisiana Monroe, Monroe, Louisiana 71201, United States.
ACS Chem Neurosci. 2024 Jun 5;15(11):2350-2358. doi: 10.1021/acschemneuro.4c00206. Epub 2024 May 17.
Growth hormone-releasing hormone (Ghrh) neurons in the dorsomedial ventromedial hypothalamic nucleus (VMNdm) express the metabolic transcription factor steroidogenic factor-1 and hypoglycemia-sensitive neurochemicals of diverse chemical structures, transmission modes, and temporal signaling profiles. Ghrh imposes neuromodulatory control of coexpressed transmitters. Multiple metabolic sensory mechanisms are employed in the brain, including screening of the critical nutrient glucose or the energy currency ATP. Here, combinatory laser-catapult-microdissection/single-cell multiplex qPCR tools were used to investigate whether these neurons possess molecular machinery for monitoring cellular metabolic status and if these biomarkers exhibit sex-specific sensitivity to insulin-induced hypoglycemia. Data show that hypoglycemia up- (male) or downregulated (female) Ghrh neuron glucokinase (Gck) mRNA; Ghrh gene silencing decreased baseline and hypoglycemic patterns of Gck gene expression in each sex. Ghrh neuron glucokinase regulatory protein (Gckr) transcript levels were respectively diminished or augmented in hypoglycemic male vs female rats; this mRNA profile was decreased by Ghrh siRNA in both sexes. Gene transcripts encoding catalytic alpha subunits of the energy monitor 5-AMP-activated protein kinase (AMPK), i.e., Prkaa1 and 2, were increased by hypoglycemia in males, yet only the former mRNA was hypoglycemia-sensitive in females. Ghrh siRNA downregulated baseline and hypoglycemia-associated Prkaa subunit mRNAs in males but elicited divergent changes in Prkaa2 transcripts in eu- vs hypoglycemic females. Results provide unique evidence that VMNdm Ghrh neurons express the characterized metabolic sensor biomarkers glucokinase and AMPK and that the corresponding gene profiles exhibit distinctive sex-dimorphic transcriptional responses to hypoglycemia. Data further document Ghrh neuromodulation of baseline and hypoglycemic transcription patterns of these metabolic gene profiles.
生长激素释放激素 (Ghrh) 神经元位于下丘脑腹内侧核背内侧 (VMNdm),表达代谢转录因子甾醇生成因子 1 和具有不同化学结构、传递方式和时间信号特征的低血糖敏感神经化学物质。Ghrh 对共表达递质施加神经调节控制。大脑中采用了多种代谢感觉机制,包括筛选关键营养物质葡萄糖或能量货币 ATP。在这里,使用组合式激光弹射微切割/单细胞多重 qPCR 工具来研究这些神经元是否具有监测细胞代谢状态的分子机制,以及这些生物标志物是否表现出对胰岛素诱导的低血糖的性别特异性敏感性。数据表明,低血糖上调 (雄性) 或下调 (雌性) Ghrh 神经元葡萄糖激酶 (Gck) mRNA;Ghrh 基因沉默降低了两性的基础水平和低血糖模式的 Gck 基因表达。Ghrh 神经元葡萄糖激酶调节蛋白 (Gckr) 转录本水平分别在低血糖雄性和雌性大鼠中降低或增加;这种 mRNA 谱在两性中都被 Ghrh siRNA 降低。编码能量监测 5-AMP 激活蛋白激酶 (AMPK) 催化α亚基的基因转录物,即 Prkaa1 和 2,在雄性中被低血糖增加,但只有前者的 mRNA 在雌性中对低血糖敏感。Ghrh siRNA 下调了雄性的基础水平和与低血糖相关的 Prkaa 亚基 mRNA,但在血糖正常和低血糖雌性大鼠中引发了 Prkaa2 转录物的不同变化。结果提供了独特的证据,表明 VMNdm Ghrh 神经元表达了特征代谢传感器生物标志物葡萄糖激酶和 AMPK,并且相应的基因谱对低血糖表现出独特的性别二态转录反应。数据进一步记录了 Ghrh 对这些代谢基因谱的基础水平和低血糖转录模式的神经调节作用。