Sex-Dimorphic Effects of Hypoglycemia on Metabolic Sensor mRNA Expression in Ventromedial Hypothalamic Nucleus-Dorsomedial Division (VMNdm) Growth Hormone-Releasing Hormone Neurons

IF 4.1 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY ACS Chemical Neuroscience Pub Date : 2024-05-17 DOI:10.1021/acschemneuro.4c00206
Subash Sapkota,  and , Karen P. Briski*, 
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Abstract

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.

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低血糖对中内侧下丘脑核-背内侧分部(VMNdm)生长激素释放激素神经元代谢传感器 mRNA 表达的性别双态效应
下丘脑背内侧腹侧核(VMNdm)中的生长激素释放激素(Ghrh)神经元表达代谢转录因子类固醇生成因子-1和对低血糖敏感的神经化学物质,这些物质具有不同的化学结构、传输模式和时间信号特征。Ghrh 对共表达的递质进行神经调节控制。大脑中采用了多种新陈代谢感觉机制,包括筛选关键营养物质葡萄糖或能量通货 ATP。在这里,研究人员利用激光-弹弓-微切片/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对胰岛素诱导的低血糖表现出性别特异性敏感性。数据显示,低血糖会上调(男性)或下调(女性)Ghrh神经元葡萄糖激酶(Gck)mRNA;Ghrh基因沉默会降低每种性别Gck基因表达的基线和低血糖模式。低血糖雄性大鼠与雌性大鼠的 Ghrh 神经元葡萄糖激酶调节蛋白(Gckr)转录水平分别降低或升高;Ghrh siRNA 可降低雌雄大鼠的这种 mRNA 表达。编码能量监测器 5-AMP激活蛋白激酶(AMPK)催化α亚基的基因转录物,即 Prkaa1 和 2,在雄性大鼠中因低血糖而增加,但在雌性大鼠中只有前者的 mRNA 对低血糖敏感。Ghrh siRNA 下调了雄性的基线和低血糖相关的 Prkaa 亚基 mRNA,但在血糖过高和血糖过低的雌性中引起了 Prkaa2 转录物的不同变化。研究结果提供了独特的证据,证明 VMNdm Ghrh 神经元表达具有特征性的代谢传感器生物标志物葡萄糖激酶和 AMPK,而且相应的基因图谱对低血糖表现出独特的性别二态性转录反应。数据进一步证明了 Ghrh 神经元对这些代谢基因图谱的基线和低血糖转录模式的调节作用。
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来源期刊
ACS Chemical Neuroscience
ACS Chemical Neuroscience BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
9.20
自引率
4.00%
发文量
323
审稿时长
1 months
期刊介绍: ACS Chemical Neuroscience publishes high-quality research articles and reviews that showcase chemical, quantitative biological, biophysical and bioengineering approaches to the understanding of the nervous system and to the development of new treatments for neurological disorders. Research in the journal focuses on aspects of chemical neurobiology and bio-neurochemistry such as the following: Neurotransmitters and receptors Neuropharmaceuticals and therapeutics Neural development—Plasticity, and degeneration Chemical, physical, and computational methods in neuroscience Neuronal diseases—basis, detection, and treatment Mechanism of aging, learning, memory and behavior Pain and sensory processing Neurotoxins Neuroscience-inspired bioengineering Development of methods in chemical neurobiology Neuroimaging agents and technologies Animal models for central nervous system diseases Behavioral research
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