Open Access
Intranasal insulin administration may be highly effective in improving cognitive function in mice with cognitive dysfunction by reversing brain insulin resistance
Author(s) -
Hui Lv,
Lingjiao Tang,
Can-Shou Guo,
Yongming Jiang,
Ce Gao,
Yifan Wang,
Chongdong Jian
Publication year - 2020
Publication title -
cognitive neurodynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.83
H-Index - 41
eISSN - 1871-4099
pISSN - 1871-4080
DOI - 10.1007/s11571-020-09571-z
Subject(s) - insulin resistance , insulin , hyperinsulinemia , medicine , insulin receptor , subventricular zone , endocrinology , hippocampus , neuroscience , psychology , biology , progenitor cell , stem cell , genetics
It is well known in clinical practice that Alzheimer's disease (AD) is closely associated with brain insulin resistance, and the cerebral insulin pathway has been proven to play a critical role in the pathogenesis of AD. However, finding the most efficient way to improve brain insulin resistance remains challenging. Peripheral administration of insulin does not have the desired therapeutic effect and may induce adverse reactions, such as hyperinsulinemia, but intranasal administration may be an efficient way. In the present study, we established a brain insulin resistance model through an intraventricular injection of streptozotocin, accompanied by cognitive impairment. Following intranasal insulin treatment, the learning and memory functions of mice were significantly restored, the neurogenesis in the hippocampus was improved, the level of insulin in the brain increased, and the activation of the IRS-1-PI3K-Akt-GSK3β insulin signal pathway, but not the Ras-Raf-MEK-MAPK pathway, was markedly increased. The olfactory bulb-subventricular zone-subgranular zone (OB-SVZ-SGZ) axis might be the mechanism through which intranasal insulin regulates cognition in brain-insulin-resistant mice. Thus, intranasal insulin administration may be a highly efficient way to improve cognitive function by increasing cerebral insulin levels and reversing insulin resistance.