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糖尿病前期和糖尿病小鼠的中枢病理学差异与认知障碍。

Differential central pathology and cognitive impairment in pre-diabetic and diabetic mice.

机构信息

Division of Physiology, School of Medicine, University of Cadiz, Cádiz, Spain.

出版信息

Psychoneuroendocrinology. 2013 Nov;38(11):2462-75. doi: 10.1016/j.psyneuen.2013.05.010. Epub 2013 Jun 21.

DOI:10.1016/j.psyneuen.2013.05.010
PMID:23790682
Abstract

Although age remains the main risk factor to suffer Alzheimer's disease (AD) and vascular dementia (VD), type 2 diabetes (T2D) has turned up as a relevant risk factor for dementia. However, the ultimate underlying mechanisms for this association remain unclear. In the present study we analyzed central nervous system (CNS) morphological and functional consequences of long-term insulin resistance and T2D in db/db mice (leptin receptor KO mice). We also included C57Bl6 mice fed with high fat diet (HFD) and a third group of C57Bl6 streptozotocin (STZ) treated mice. Db/db mice exhibited pathological characteristics that mimic both AD and VD, including age dependent cognitive deterioration, brain atrophy, increased spontaneous hemorrhages and tau phosphorylation, affecting the cortex preferentially. A similar profile was observed in STZ-induced diabetic mice. Moreover metabolic parameters, such as body weight, glucose and insulin levels are good predictors of many of these alterations in db/db mice. In addition, in HFD-induced hyperinsulinemia in C57Bl6 mice, we only observed mild CNS alterations, suggesting that central nervous system dysfunction is associated with well established T2D. Altogether our results suggest that T2D may promote many of the pathological and behavioral alterations observed in dementia, supporting that interventions devoted to control glucose homeostasis could improve dementia progress and prognosis.

摘要

虽然年龄仍然是患阿尔茨海默病(AD)和血管性痴呆(VD)的主要危险因素,但 2 型糖尿病(T2D)已成为痴呆的一个相关危险因素。然而,这种关联的最终潜在机制尚不清楚。在本研究中,我们分析了 db/db 小鼠(瘦素受体 KO 小鼠)长期胰岛素抵抗和 T2D 对中枢神经系统(CNS)形态和功能的影响。我们还包括了高脂肪饮食(HFD)喂养的 C57Bl6 小鼠和第三组 C57Bl6 链脲佐菌素(STZ)处理的小鼠。db/db 小鼠表现出类似于 AD 和 VD 的病理特征,包括年龄相关的认知恶化、脑萎缩、自发性出血增加和 tau 磷酸化,优先影响皮质。在 STZ 诱导的糖尿病小鼠中也观察到了类似的表型。此外,体重、血糖和胰岛素水平等代谢参数是许多 db/db 小鼠这些改变的良好预测指标。此外,在 C57Bl6 小鼠的 HFD 诱导的高胰岛素血症中,我们只观察到中枢神经系统的轻度改变,这表明中枢神经系统功能障碍与已确立的 T2D 有关。总之,我们的结果表明,T2D 可能促进了痴呆中观察到的许多病理和行为改变,这支持了控制血糖稳态的干预措施可能改善痴呆的进展和预后。

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