The Urine Metabolome of R6/2 and zQ175DN Huntington's Disease Mouse Models.
Roberto SpezialeCamilla MontesanoGiulia Di PietroDaniel Oscar CiceroVincenzo SummaEdith MonteagudoLaura OrsattiPublished in: Metabolites (2023)
Huntington's disease (HD) is caused by the expansion of a polyglutamine (polyQ)-encoding tract in exon 1 of the huntingtin gene to greater than 35 CAG repeats. It typically has a disease course lasting 15-20 years, and there are currently no disease-modifying therapies available. Thus, there is a need for faithful mouse models of HD to use in preclinical studies of disease mechanisms, target validation, and therapeutic compound testing. A large variety of mouse models of HD were generated, none of which fully recapitulate human disease, complicating the selection of appropriate models for preclinical studies. Here, we present the urinary liquid chromatography-high-resolution mass spectrometry analysis employed to identify metabolic alterations in transgenic R6/2 and zQ175DN knock-in mice. In R6/2 mice, the perturbation of the corticosterone metabolism and the accumulation of pyrraline, indicative of the development of insulin resistance and the impairment of pheromone excretion, were observed. Differently from R6/2, zQ175DN mice showed the accumulation of oxidative stress metabolites. Both genotypes showed alterations in the tryptophan metabolism. This approach aims to improve our understanding of the molecular mechanisms involved in HD neuropathology, facilitating the selection of appropriate mouse models for preclinical studies. It also aims to identify potential biomarkers specific to HD.
Keyphrases
- mouse model
- liquid chromatography
- high resolution mass spectrometry
- oxidative stress
- insulin resistance
- high fat diet induced
- endothelial cells
- mass spectrometry
- metabolic syndrome
- stem cells
- cell therapy
- dna damage
- ms ms
- adipose tissue
- dna methylation
- copy number
- genome wide
- wild type
- simultaneous determination
- ultra high performance liquid chromatography
- solid phase extraction