Sadeghi Akram, Hami Javad, Razavi Shahnaz, Esfandiary Ebrahim, Hejazi Zahra
Department of Anatomical Sciences and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Anatomical Sciences, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Int J Prev Med. 2016 Mar 10;7:57. doi: 10.4103/2008-7802.178531. eCollection 2016.
Diabetes mellitus is associated with cognitive deficits in humans and animals. These deficits are paralleled by neurophysiological and structural changes in brain. In diabetic animals, impairments of spatial learning, memory, and cognition occur in association with distinct changes in hippocampus, a key brain area for many forms of learning and memory and are particularly sensitive to changes in glucose homeostasis. However, the multifactorial pathogenesis of diabetic encephalopathy is not yet completely understood. Apoptosis plays a crucial role in diabetes-induce neuronal loss in hippocampus.
The effects of diabetes on hippocampus and cognitive/behavioral dysfunctions in experimental models of diabetes are reviewed, with a focus on the negative impact on increased neuronal apoptosis and related cellular and molecular mechanisms.
Of all articles that were assessed, most of the experimental studies clearly showed that diabetes causes neuronal apoptosis in hippocampus through multiple mechanisms, including oxidative stress, inhibition of caspases, disturbance in expression of apoptosis regulator genes, as well as deficits in mitochondrial function. The balance between pro-apoptotic and anti-apoptotic signaling may determine the neuronal apoptotic outcome in vitro and in vivo models of experimental diabetes.
Dissecting out the mechanisms responsible for diabetes-related changes in the hippocampal cell apoptosis helps improve treatment of impaired cognitive and memory functions in diabetic individuals.
糖尿病与人类和动物的认知缺陷有关。这些缺陷与大脑的神经生理和结构变化同时出现。在糖尿病动物中,空间学习、记忆和认知障碍与海马体的明显变化相关,海马体是许多形式学习和记忆的关键脑区,对葡萄糖稳态变化特别敏感。然而,糖尿病性脑病的多因素发病机制尚未完全阐明。细胞凋亡在糖尿病诱导的海马神经元丢失中起关键作用。
综述糖尿病实验模型中糖尿病对海马体及认知/行为功能障碍的影响,重点关注对神经元凋亡增加及相关细胞和分子机制的负面影响。
在所有评估的文章中,大多数实验研究清楚地表明,糖尿病通过多种机制导致海马神经元凋亡,包括氧化应激、半胱天冬酶抑制、凋亡调节基因表达紊乱以及线粒体功能缺陷。促凋亡信号和抗凋亡信号之间的平衡可能决定实验性糖尿病体外和体内模型中的神经元凋亡结果。
剖析导致糖尿病相关海马细胞凋亡变化的机制有助于改善糖尿病患者认知和记忆功能受损的治疗。