| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6284187 | Neuroscience Letters | 2012 | 5 Pages |
Insulin-like growth factor-1 (IGF-1) has been demonstrated to have neuroprotective effects, but little is known concerning its role in vascular dementia (VaD). This study aimed to evaluate expression of IGF-1 signaling in hippocampus in rat model of VaD, and probe the underlying mechanisms. Permanent occlusion of bilateral common carotid arteries (2-VO) was used as VaD model. Learning and memory functions were declined significantly in 2-VO rats, and these impairments were further deteriorated with the prolongation of 2-VO treatment. IGF-1, IGF-1 receptor (IGF-1R), total Akt and phosphorylated Akt (p-Akt) were all measured at 1, 2 and 4 months following 2-VO injury. Compared with controls, IGF-1, IGF-1 mRNA and p-Akt expression were significantly decreased in hippocampus of 2-VO rats. However, changes of IGF-1R and total Akt levels were not significant. These results suggest that down-regulation of IGF-1 and p-Akt may contribute to the impairments of learning and memory functions after 2-VO. IGF-1/IGF-1R signaling system may involved in the onset and development of VaD.
► We used 2-VO as a VaD model and observed over 4 months. ► We examined expression of IGF-1/IGF-1R signaling in hippocampus of the VaD model. ► Down-regulation of IGF-1/IGF-1R signaling may be one of the mechanisms of VaD. ► Supplementation with exogenous IGF-1 may be a compensatory mechanism for VaD.
