Kim Juhye Lena, La Gamma Edmund F, Estabrook Todd, Kudrick Necla, Nankova Bistra B
The Regional Neonatal Center, Maria Fareri Children's Hospital at Westchester Medical Center, Valhalla, New York, United States of America.
Departments of Pediatrics, Biochemistry and Molecular Biology, Division of Newborn Medicine, New York Medical College, Valhalla, New York, United States of America.
PLoS One. 2017 Feb 24;12(2):e0172789. doi: 10.1371/journal.pone.0172789. eCollection 2017.
Recurrent hypoglycemia can occur as a major complication of insulin replacement therapy, limiting the long-term health benefits of intense glycemic control in type 1 and advanced type 2 diabetic patients. It impairs the normal counter-regulatory hormonal and behavioral responses to glucose deprivation, a phenomenon known as hypoglycemia associated autonomic failure (HAAF). The molecular mechanisms leading to defective counter-regulation are not completely understood. We hypothesized that both neuronal (excessive cholinergic signaling between the splanchnic nerve fibers and the adrenal medulla) and humoral factors contribute to the impaired epinephrine production and release in HAAF. To gain further insight into the molecular mechanism(s) mediating the blunted epinephrine responses following recurrent hypoglycemia, we utilized a global gene expression profiling approach. We characterized the transcriptomes during recurrent (defective counter-regulation model) and acute hypoglycemia (normal counter-regulation group) in the adrenal medulla of normal Sprague-Dawley rats. Based on comparison analysis of differentially expressed genes, a set of unique genes that are activated only at specific time points after recurrent hypoglycemia were revealed. A complementary bioinformatics analysis of the functional category, pathway, and integrated network indicated activation of the unfolded protein response. Furthermore, at least three additional pathways/interaction networks altered in the adrenal medulla following recurrent hypoglycemia were identified, which may contribute to the impaired epinephrine secretion in HAAF: greatly increased neuropeptide signaling (proenkephalin, neuropeptide Y, galanin); altered ion homeostasis (Na+, K+, Ca2+) and downregulation of genes involved in Ca2+-dependent exocytosis of secretory vesicles. Given the pleiotropic effects of the unfolded protein response in different organs, involved in maintaining glucose homeostasis, these findings uncover broader general mechanisms that arise following recurrent hypoglycemia which may afford clinicians an opportunity to modulate the magnitude of HAAF syndrome.
反复低血糖可能作为胰岛素替代治疗的主要并发症出现,限制了强化血糖控制对1型和晚期2型糖尿病患者的长期健康益处。它损害了对葡萄糖剥夺的正常反调节激素和行为反应,这一现象被称为低血糖相关自主神经功能衰竭(HAAF)。导致反调节缺陷的分子机制尚未完全明确。我们推测,神经元因素(内脏神经纤维与肾上腺髓质之间胆碱能信号过度)和体液因素均导致了HAAF中肾上腺素生成和释放受损。为了进一步深入了解反复低血糖后介导肾上腺素反应减弱的分子机制,我们采用了全基因组表达谱分析方法。我们对正常斯普拉格-道利大鼠肾上腺髓质在反复低血糖(反调节缺陷模型)和急性低血糖(正常反调节组)期间的转录组进行了表征。基于对差异表达基因的比较分析,揭示了一组仅在反复低血糖后特定时间点被激活的独特基因。对功能类别、途径和整合网络的补充生物信息学分析表明未折叠蛋白反应被激活。此外,还确定了反复低血糖后肾上腺髓质中至少另外三个改变的途径/相互作用网络,它们可能导致HAAF中肾上腺素分泌受损:神经肽信号大幅增加(前脑啡肽、神经肽Y、甘丙肽);离子稳态改变(Na +、K +、Ca2 +)以及参与分泌囊泡钙依赖性胞吐作用的基因下调。鉴于未折叠蛋白反应在不同器官中具有维持葡萄糖稳态的多效性作用,这些发现揭示了反复低血糖后出现的更广泛的一般机制,这可能为临床医生提供一个调节HAAF综合征严重程度的机会。