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中风前诱导及正常化胰岛素抵抗分别加重和改善功能恢复。

The Pre-Stroke Induction and Normalization of Insulin Resistance Respectively Worsens and Improves Functional Recovery.

机构信息

NeuroCardioMetabol Group, Department of Clinical Science and Education, Södersjukhuset, Internal Medicine, Karolinska Institutet, 118 83 Stockholm, Sweden.

Neurology Department, Internal Medicine, Södersjukhuset, 118 83 Stockholm, Sweden.

出版信息

Int J Mol Sci. 2023 Feb 16;24(4):3989. doi: 10.3390/ijms24043989.

Abstract

Type 2 diabetes (T2D) impairs post-stroke recovery, and the underlying mechanisms are unknown. Insulin resistance (IR), a T2D hallmark that is also closely linked to aging, has been associated with impaired post-stroke recovery. However, whether IR worsens stroke recovery is unknown. We addressed this question in mouse models where early IR, with or without hyperglycemia, was induced by chronic high-fat diet feeding or sucrose supplementation in the drinking water, respectively. Furthermore, we used 10-month-old mice, spontaneously developing IR but not hyperglycemia, where IR was normalized pharmacologically pre-stroke with Rosiglitazone. Stroke was induced by transient middle cerebral artery occlusion and recovery was assessed by sensorimotor tests. Neuronal survival, neuroinflammation and the density of striatal cholinergic interneurons were also assessed by immunohistochemistry/quantitative microscopy. Pre-stroke induction and normalization of IR, respectively, worsened and improved post-stroke neurological recovery. Moreover, our data indicate a potential association of this impaired recovery with exacerbated neuroinflammation and a decreased density of striatal cholinergic interneurons. The global diabetes epidemic and population aging are dramatically increasing the percentage of people in need of post-stroke treatment/care. Our results suggest that future clinical studies should target pre-stroke IR to reduce stroke sequelae in both diabetics and elderly people with prediabetes.

摘要

2 型糖尿病(T2D)会损害中风后的恢复,其潜在机制尚不清楚。胰岛素抵抗(IR)是 T2D 的一个标志,也与衰老密切相关,与中风后恢复受损有关。然而,IR 是否会使中风恢复恶化尚不清楚。我们在小鼠模型中研究了这个问题,通过慢性高脂肪饮食喂养或在饮用水中添加蔗糖,分别诱导早期 IR 伴或不伴高血糖。此外,我们使用了 10 个月大的小鼠,它们自发地发展出 IR 但没有高血糖,在中风前用罗格列酮进行药物治疗使 IR 正常化。通过短暂性大脑中动脉闭塞诱导中风,并通过感觉运动测试评估恢复情况。通过免疫组织化学/定量显微镜评估神经元存活、神经炎症和纹状体胆碱能中间神经元的密度。中风前 IR 的诱导和正常化分别使中风后的神经恢复恶化和改善。此外,我们的数据表明,这种恢复受损可能与神经炎症加剧和纹状体胆碱能中间神经元密度降低有关。全球糖尿病流行和人口老龄化正在极大地增加需要中风后治疗/护理的人群比例。我们的研究结果表明,未来的临床研究应针对中风前的 IR,以减少糖尿病患者和有前驱糖尿病的老年人的中风后遗症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6def/9964646/6ac490313724/ijms-24-03989-g001.jpg

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