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Publication : Serotonergic dysfunction in the A53T alpha-synuclein mouse model of Parkinson's disease.

First Author  Deusser J Year  2015
Journal  J Neurochem Volume  135
Issue  3 Pages  589-97
PubMed ID  26201615 Mgi Jnum  J:226922
Mgi Id  MGI:5699206 Doi  10.1111/jnc.13253
Citation  Deusser J, et al. (2015) Serotonergic dysfunction in the A53T alpha-synuclein mouse model of Parkinson's disease. J Neurochem 135(3):589-97
abstractText  Parkinson's disease, neuropathologically defined by the aggregation of alpha-synuclein, is characterized by neuropsychiatric symptoms such as depression and anxiety preceding the onset of motor symptoms. A loss of serotonergic neurons or their projections into the hippocampus and alterations in serotonin release may be linked to these symptoms. Here, we investigate the effect of human A53T alpha-synuclein on serotonergic neurons using 12-months-old transgenic mice. We detected human alpha-synuclein in the perikarya of brainstem median and dorsal raphe neurons as well as in serotonergic fibers in the hippocampus. Despite intracellular alpha-synuclein accumulation there was no loss of serotonergic neurons in dorsal and median raphe nuclei of A53T alpha-synuclein mice. However, serotonin levels were significantly reduced in the brainstem. In addition, serotonergic fiber density in the dorsal dentate gyrus was significantly less dense in transgenic mice. Interestingly, we detected a significantly compromised increase in doublecortin+ neuroblasts after chronic treatment with fluoxetine at the site of reduced serotonergic innervation, the infrapyramidal blade of the dorsal dentate gyrus in A53T alpha-synuclein mice. This suggests that alpha-synuclein affects serotonergic projections in a spatially distinct pattern within the hippocampus thereby influencing the response to antidepressant treatment. A transgenic mouse model of Parkinson's disease (PD) shows alpha-synuclein expression in serotonergic neurons of raphe nuclei. Besides lower serotonin levels in the raphe nuclei, a topographical restricted reduction in serotonergic fiber density was present in the hippocampus accompanied by an impaired fluoxetine-response of hippocampal neuroblasts. In conclusion, alpha-synuclein in the serotonergic system may account for psychiatric symptoms in PD. DR, dorsal raphe nucleus; MnR, median raphe nucleus.
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