Logo Logo
Switch Language to German

Arnhold, Mike; Dening, Yanina; Chopin, Michaël; Arévalo, Esteban; Schwarz, Mathias; Reichmann, Heinz; Gille, Gabriele; Funk, Richard H. W. and Pan-Montojo, Francisco (2016): Changes in the sympathetic innervation of the gut in rotenone treated mice as possible early biomarker for Parkinson's disease. In: Clinical Autonomic Research, Vol. 26, No. 3: pp. 211-222

Full text not available from 'Open Access LMU'.


Introduction Involvement of the peripheral nervous system (PNS) is relatively common in Parkinson's disease (PD) patients. PNS alterations appear early in the course of the disease and are responsible for some of the non-motor symptoms observed in PD patients. In previous studies, we have shown that environmental toxins can trigger the disease by acting on the enteric nervous system. Material and methods Here, we analyzed the effect of mitochondrial Complex I inhibition on sympathetic neuritis in vivo and sympathetic neurons in vitro. Combining in vivo imaging and protein expression profiling. Results we found that rotenone, a widely used mitochondrial Complex I inhibitor decreases the density of sympathetic neurites innervating the gut in vivo, while in vitro, it induces the redistribution of intracellular alpha-synuclein and neurite degeneration. Interestingly, sympathetic neurons are much more resistant to rotenone exposure than mesencephalic dopaminergic neurons. Conclusion Altogether, these results suggest that enteric sympathetic denervation could be an initial pre-motor alteration in PD progression that could be used as an early biomarker of the disease.

Actions (login required)

View Item View Item