Tapia Geronimo P, Agostinelli Lindsay J, Chenausky Sarah D, Padilla Jessica V Salcido, Navarro Vanessa I, Alagh Amy, Si Gabriel, Thompson Richard H, Balivada Sivasai, Khan Arshad M
UTEP Systems Neuroscience Laboratory, Department of Biological Sciences, The University of Texas at El Paso, El Paso, TX 79968, USA.
Ph.D. Program in Bioscience, Department of Biological Sciences, The University of Texas at El Paso, El Paso, TX 79968, USA.
J Clin Med. 2023 Mar 24;12(7):2483. doi: 10.3390/jcm12072483.
Rodent studies indicate that impaired glucose utilization or hypoglycemia is associated with the cellular activation of neurons in the (MY), believed to control feeding behavior and glucose counterregulation. However, such activation has been tracked primarily within hours of the challenge, rather than sooner, and has been poorly mapped within standardized brain atlases. Here, we report that, within 15 min of receiving 2-deoxy-d-glucose (2-DG; 250 mg/kg, i.v.), which can trigger glucoprivic feeding behavior, marked elevations were observed in the numbers of (RB) neuronal cell profiles immunoreactive for the cellular activation marker(s), phosphorylated p44/42 MAP kinases (phospho-ERK1/2), and that some of these profiles were also catecholaminergic. We mapped their distributions within an open-access rat brain atlas and found that 2-DG-treated rats (compared to their saline-treated controls) displayed greater numbers of phospho-ERK1/2 neurons in the (LC) and the (NTS). Thus, the 2-DG-activation of certain RB neurons is more rapid than perhaps previously realized, engaging neurons that serve multiple functional systems and which are of varying cellular phenotypes. Mapping these populations within standardized brain atlas maps streamlines their targeting and/or comparable mapping in preclinical rodent models of disease.
啮齿动物研究表明,葡萄糖利用受损或低血糖与中脑导水管周围灰质(MY)中神经元的细胞激活有关,据信该区域控制进食行为和葡萄糖反向调节。然而,这种激活主要是在受到挑战后的数小时内进行追踪的,而非更早,并且在标准化脑图谱中的定位也很差。在此,我们报告,在静脉注射2-脱氧-D-葡萄糖(2-DG;250mg/kg)后15分钟内,2-DG可引发糖缺乏性进食行为,观察到对细胞激活标志物磷酸化p44/42丝裂原活化蛋白激酶(磷酸化ERK1/2)免疫反应的红核(RB)神经元细胞轮廓数量显著增加,并且其中一些轮廓也是儿茶酚胺能的。我们在一个开放获取的大鼠脑图谱中绘制了它们的分布,发现2-DG处理的大鼠(与其生理盐水处理的对照相比)在蓝斑(LC)和孤束核(NTS)中显示出更多的磷酸化ERK1/2神经元。因此,某些RB神经元的2-DG激活比之前可能意识到的更快,涉及服务于多个功能系统且具有不同细胞表型的神经元。在标准化脑图谱中绘制这些群体的图谱简化了在临床前啮齿动物疾病模型中的靶向和/或可比图谱绘制。