کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5630572 | 1580617 | 2017 | 11 صفحه PDF | دانلود رایگان |
- The number of granular neurons in the dentate gyrus remains constant until 18 months of age in wild type mice
- Aged APPswe/PS1dE9 mice have reduced working memory and neuroblasts numbers, but normal numbers of granular neurons
- Long-term paroxetine treatment reduces hippocampal Aβ load in 18-month-old APPswe/PS1dE9 mice
- The numbers of neuroblasts and granular neurons are unaffected by paroxetine treatment in 18-month-old APPswe/PS1dE9 mice
Altered neurogenesis may influence hippocampal functions such as learning and memory in Alzheimer's disease. Selective serotonin reuptake inhibitors enhance neurogenesis and have been reported to reduce cerebral amyloidosis in both humans and transgenic mice. We have used stereology to assess the longitudinal changes in the number of doublecortin-expressing neuroblasts and number of granular neurons in the dentate gyrus of APPswe/PS1dE9 transgenic mice. Furthermore, we investigated the effect of long-term paroxetine treatment on the number of neuroblasts and granular neurons, hippocampal amyloidosis, and spontaneous alternation behaviour, a measure of spatial working memory, in transgenic mice. We observed no difference in granular neurons between transgenic and wild type mice up till 18Â months of age, and no differences with age in wild type mice. The number of neuroblasts and the performance in the spontaneous alternation task was reduced in aged transgenic mice. Paroxetine treatment from 9 to 18Â months of age reduced hippocampal amyloidosis without affecting the number of neuroblasts or granular neurons. These findings suggest that the amyloidosis affects the differentiation of neuroblasts and spatial working memory, independent of changes in total granular neurons. Furthermore, while long-term paroxetine treatment may be able to reduce hippocampal amyloidosis, it appears to have no effect on total number of granular neurons or spatial working memory.
Journal: Neurobiology of Disease - Volume 104, August 2017, Pages 50-60