Marker–free imaging of α–Synuclein aggregates in a rat model of Parkinson′ disease using Raman microspectroscopy

A hallmark of Parkinson9 disease (PD) is the formation of Lewy bodies in the brain. Lewy bodies are rich in the aggregated form of misfolded α–Synuclein (α–Syn). The brain from PD patients can only be analysed after post–mortem, limiting the diagnosis of PD to the manifestation of motor symptoms. In PD patients and animal models phosphorylated α–Syn was detected in the gut, thus, raising the hypothesizes that early–stage PD could be diagnosed based on colon tissues biopsies. Non–invasive marker–free technologies represent an ideal method to potentially detect aggregated α–Syn in vivo. Raman microspectroscopy has been established for the detection of molecular changes such as alterations of protein structures. Here, the olfactory bulb in the brain and the muscularis mucosae of colon tissue sections of a human BAC–SNCA transgenic (TG) rat model was analysed using Raman imaging and microspectroscopy. Raman images from TG and WT rats were investigated using spectral, principal component and true component analysis. Spectral components indicated protein aggregates (spheroidal oligomers) in TG rat brain and colon tissues even at a young age but not in WT. In summary, we have demonstrated that Raman imaging is capable to detect α–Syn aggregates in colon tissues of a PD rat model and making it a promising tool for future use in PD pathology.