Laboratório de Bioenergética e Estresse Oxidativo (LABOX), Departamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina (UFSC), Campus Universitário - Córrego Grande, Bloco C 201/214, Florianópolis, SC, 88040-900, Brazil.
Programa de Pós-Graduação em Biociências e Saúde, Área de Ciências da Vida, Universidade do Oeste de Santa Catarina, Joaçaba, 89600-000, Brazil.
Mol Neurobiol. 2019 Mar;56(3):1539-1557. doi: 10.1007/s12035-018-1175-9. Epub 2018 Jun 14.
Chronic metabolic alterations may represent a risk factor for the development of cognitive impairment, dementia, or neurodegenerative diseases. Hyperglycemia and obesity are known to imprint epigenetic markers that compromise the proper expression of cell survival genes. Here, we showed that chronic hyperglycemia (60 days) induced by a single intraperitoneal injection of streptozotocin compromised cognition by reducing hippocampal ERK signaling and by inducing neurotoxicity in rats. The mechanisms appear to be linked to reduced active DNA demethylation and diminished expression of the neuroprotective transcription factor REST. The impact of the relationship between adiposity and DNA hypermethylation on REST expression was also demonstrated in peripheral blood mononuclear cells in obese children with reduced levels of blood ascorbate. The reversible nature of epigenetic modifications and the cognitive impairment reported in obese children, adolescents, and adults suggest that the correction of the anthropometry and the peripheral metabolic alterations would protect brain homeostasis and reduce the risk of developing neurodegenerative diseases.
慢性代谢改变可能是认知障碍、痴呆或神经退行性疾病发展的一个风险因素。高血糖和肥胖已知会留下表观遗传标记,从而损害细胞存活基因的正常表达。在这里,我们表明,通过单次腹腔注射链脲佐菌素诱导的慢性高血糖(60 天)通过降低海马 ERK 信号传导并在大鼠中诱导神经毒性来损害认知。这些机制似乎与活性 DNA 去甲基化减少和神经保护转录因子 REST 的表达减少有关。在肥胖儿童外周血单核细胞中,也证明了肥胖与 DNA 高甲基化之间的关系对 REST 表达的影响,这些肥胖儿童血液抗坏血酸水平降低。表观遗传修饰的可逆性和肥胖儿童、青少年和成年人报告的认知障碍表明,纠正人体测量和外周代谢改变将保护大脑的内稳态并降低发生神经退行性疾病的风险。