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女性大鼠背内侧腹内侧下丘脑生长激素释放激素神经元类固醇生成因子-1 基因靶标。

Dorsomedial Ventromedial Hypothalamic Nucleus Growth Hormone-Releasing Hormone Neuron Steroidogenic Factor-1 Gene Targets in Female Rat.

机构信息

School of Basic Pharmaceutical and Toxicological Sciences, College of Pharmacy, University of Louisiana Monroe, Monroe, LA, USA.

出版信息

ASN Neuro. 2024;16(1):2403345. doi: 10.1080/17590914.2024.2403345. Epub 2024 Oct 14.

Abstract

The prospect that the ventromedial hypothalamic nucleus (VMN) transcription factor steroidogenic factor-1/NR5A1 (SF-1) may exert sex-dimorphic control of glucose counterregulation is unresolved. Recent studies in male rats show that SF-1 regulates transcription of co-expressed hypoglycemia-sensitive neurochemicals in dorsomedial VMN growth hormone-releasing hormone (Ghrh) neurons. Gene knockdown and laser-catapult-microdissection/single-cell multiplex qPCR techniques were used here in a female rat model to determine if SF-1 control of Ghrh neuron transmitter marker, energy sensor, and estrogen receptor (ER) variant mRNAs varies according to sex. Data show that in females, hypoglycemia elicits a gain of SF-1 inhibitory control of VMNdm Ghrh neuron Ghrh and Ghrh-receptor gene profiles and loss of augmentation of glutaminase transcription; SF-1 gene silencing diminished eu- and hypoglycemic patterns of neuronal nitric oxide gene transcription. SF-1 imposes divergent control of baseline and hypoglycemic glutamate decarboxylase (GAD)-1 (stimulatory) versus GAD2 (inhibitory) mRNAs in that sex. SF-1 stimulates baseline VMNdm Ghrh neuron PRKAA1/AMPKα1 and PRKAA2/AMPKα2 gene expression, yet causes opposite changes in these gene profiles during hypoglycemia. SF-1 exerts glucose-dependent control of ER-alpha and G-protein-coupled ER-1 transcription, but blunts ER-beta gene profiles during eu- and hypoglycemia. In females, SF-1 knockdown did not affect hypercorticosteronemia or hyperglucagonemia, but blunted hypoglycemic suppression of growth hormone secretion. Results show that SF-1 expression is critical for female rat VMNdm Ghrh neuron counterregulatory neurochemical, AMPK catalytic subunit, and ER gene transcription responses to hypoglycemia. Sex differences in direction of SF-1 control of distinctive gene profiles may result in observed disparities in SF-1 regulation of counterregulatory hormone secretion between sexes.

摘要

腹内侧下丘脑核 (VMN) 转录因子类固醇生成因子-1/NR5A1 (SF-1) 可能对葡萄糖的抗调节作用具有性别二态性控制作用,这一前景尚未得到解决。最近在雄性大鼠中的研究表明,SF-1 调节背内侧 VMN 生长激素释放激素 (Ghrh) 神经元中共同表达的低血糖敏感神经化学物质的转录。在这里,我们使用雌性大鼠模型中的基因敲低和激光弹射微量解剖/单细胞多重 qPCR 技术,确定 SF-1 是否控制 Ghrh 神经元递质标志物、能量传感器和雌激素受体 (ER) 变体 mRNA 的表达是否因性别而异。数据表明,在雌性中,低血糖会引起 VMNdm Ghrh 神经元 Ghrh 和 Ghrh 受体基因谱中 SF-1 抑制性控制的增加和谷氨酸酶转录的增强丧失;SF-1 基因沉默减弱了神经元一氧化氮基因转录的正常和低血糖模式。SF-1 对基础状态和低血糖谷氨酸脱羧酶 (GAD)-1(刺激)与 GAD2(抑制)mRNA 在性别上施加了不同的控制。SF-1 刺激基础 VMNdm Ghrh 神经元 PRKAA1/AMPKα1 和 PRKAA2/AMPKα2 基因表达,但在低血糖期间导致这些基因谱的相反变化。SF-1 对 ER-α和 G 蛋白偶联 ER-1 转录施加葡萄糖依赖性控制,但在正常和低血糖期间使 ER-β基因谱变平。在雌性中,SF-1 敲低不会影响高皮质酮血症或高胰高血糖素血症,但会减弱低血糖对生长激素分泌的抑制作用。结果表明,SF-1 的表达对于雌性大鼠 VMNdm Ghrh 神经元抗调节神经化学物质、AMPK 催化亚基和 ER 基因对低血糖的转录反应至关重要。SF-1 对不同基因谱的控制方向的性别差异可能导致观察到的 SF-1 对性别之间抗调节激素分泌的调节差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/360e/11792125/f304e040963f/TASN_A_2403345_F0001_C.jpg

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