Creatine transport and pathological changes in creatine transporter deficient mice

The severe impact on brain function and lack of effective therapy for patients with creatine (Cr) transporter deficiency motivated the generation of three ubiquitous Slc6a8 deficient mice (-/y). While each mouse knock-out line has similar behavioral effects at 2 to 3 months of age, other features critical to the efficient use of these mice in drug discovery are unclear or lacking: the concentration of Cr in brain and heart differ widely between mouse lines, there are limited data on histopathologic changes, and no data on Cr uptake. Here, we determined survival, measured endogenous Cr and uptake of its deuterium-labeled analogue Cr-d3 using a liquid chromatography coupled with tandem mass spectrometry assay, and performed comprehensive histopathologic examination on the Slc6a8(-/y) mouse developed by Skelton et al. Our results show that Slc6a8(-/y) mice have widely varying organ-specific uptake of Cr-d3, significantly diminished growth with the exception of brain, progressive vacuolar myopathy, and markedly shortened lifespan.

Automated summary

This study conducted a comprehensive investigation on creatine (Cr) transporter deficiency in three ubiquitous Slc6a8 deficient mice, revealing significant differences in organ-specific uptake of Cr-d3, restricted growth except for the brain, progressive vacuolar myopathy, and markedly shortened lifespan in these mice.