Pridopidine subtly ameliorates motor skills in a mouse model for vanishing white matter.
Ellen OudejansDiede WitkampGino V Hu-A-NgLeoni HoogterpGemma van Rooijen-van LeeuwenIris KruijffPleun SchonewilleZeinab Lalaoui El MouttalibiImke H BartelinkMarjo S van der KnaapTruus E M AbbinkPublished in: Life science alliance (2024)
The leukodystrophy vanishing white matter (VWM) is characterized by chronic and episodic acute neurological deterioration. Curative treatment is presently unavailable. Pathogenic variants in the genes encoding eukaryotic initiation factor 2B (eIF2B) cause VWM and deregulate the integrated stress response (ISR). Previous studies in VWM mouse models showed that several ISR-targeting compounds ameliorate clinical and neuropathological disease hallmarks. It is unclear which ISR components are suitable therapeutic targets. In this study, effects of 4-phenylbutyric acid, tauroursodeoxycholic acid, or pridopidine (PDPD), with ISR targets upstream or downstream of eIF2B, were assessed in VWM mice. In addition, it was found that the composite ataxia score represented motor decline of VWM mice more accurately than the previously used neuroscore. 4-phenylbutyric acid and tauroursodeoxycholic acid did not improve VWM disease hallmarks, whereas PDPD had subtle beneficial effects on motor skills. PDPD alone does not suffice as treatment in VWM mice but may be considered for combination therapy. Also, treatments aimed at ISR components upstream of eIF2B do not improve chronic neurological deterioration; effects on acute episodic decline remain to be investigated.
Keyphrases
- combination therapy
- mouse model
- white matter
- liver failure
- multiple sclerosis
- type diabetes
- medical students
- skeletal muscle
- transcription factor
- genome wide
- dna methylation
- brain injury
- mass spectrometry
- blood brain barrier
- wild type
- smoking cessation
- acute respiratory distress syndrome
- cerebral ischemia
- replacement therapy