Zhou Yu, Lian Siheng, Zhang Jin, Lin Donghai, Huang Caihua, Liu Libin, Chen Zhou
Department of Endocrinology, Fujian Medical University Union Hospital, Fuzhou, China.
The School of Pharmacy, Fujian Medical University, Fuzhou, China.
Cell Physiol Biochem. 2018;46(4):1668-1682. doi: 10.1159/000489243. Epub 2018 Apr 20.
BACKGROUND/AIMS: Mitochondrial perturbation is a well-established cause of cognitive decline, but as yet it is unclear how mitochondria-associated neuronal abnormalities in type 1 diabetic (T1DM) brain contribute to cognitive decline.
The streptozotocin (STZ)-induced mouse model of T1DM was used. The Morris water maze test was applied to assess the effect of T1DM on learning and memory. We detected changes in mitochondrial morphology, function and dynamics. Furthermore, we employed metabolomic analysis to reveal the underlying mechanisms of mitochondrial perturbation which contribute to cognitive decline.
Our results show that T1DM impairs mitochondrial dynamics, morphology and function in neurons, associated with a decline in cognitive ability. Metabolomic analyses revealed that T1DM mainly affects metabolic pathways involved in mitochondrial energy failure and impairs the antioxidative system.
These results lay the basis for understanding the underlying mitochondria-associated causes of T1DM-associated cognitive decline and may provide a potential treatment strategy for this condition in future.
背景/目的:线粒体功能紊乱是认知功能下降的一个公认原因,但目前尚不清楚1型糖尿病(T1DM)大脑中与线粒体相关的神经元异常如何导致认知功能下降。
使用链脲佐菌素(STZ)诱导的T1DM小鼠模型。采用莫里斯水迷宫试验评估T1DM对学习和记忆的影响。我们检测了线粒体形态、功能和动力学的变化。此外,我们采用代谢组学分析来揭示导致认知功能下降的线粒体功能紊乱的潜在机制。
我们的结果表明,T1DM损害神经元中的线粒体动力学、形态和功能,与认知能力下降有关。代谢组学分析显示,T1DM主要影响与线粒体能量衰竭相关的代谢途径,并损害抗氧化系统。
这些结果为理解T1DM相关认知功能下降的潜在线粒体相关原因奠定了基础,并可能为未来这种疾病提供潜在的治疗策略。