Tacrolimus Protects against Age-Associated Microstructural Changes in the Beagle Brain
Hamsanandini Radhakrishnan, Margo F. Ubele, Stephanie M. Krumholz, Kathy Boaz, Jennifer L. Mefford, Erin D. Jones, Beverly Meacham, Jeffrey Smiley, László G. Puskás, David K. Powell, Christopher M. Norris, Craig E.L. Stark, Elizabeth Head
Abstract
The overexpression of calcineurin leads to astrocyte hyperactivation, neuronal death, and inflammation, which are characteristics often associated with pathologic aging and Alzheimer's disease. In this study, we tested the hypothesis that tacrolimus, a calcineurin inhibitor, prevents age-associated microstructural atrophy, which we measured using higher-order diffusion MRI, in the middle-aged beagle brain (n = 30, male and female). We find that tacrolimus reduces hippocampal (p = 0.001) and parahippocampal (p = 0.002) neurite density index, as well as protects against an age-associated increase in the parahippocampal (p = 0.007) orientation dispersion index. Tacrolimus also protects against an age-related decrease in fractional anisotropy in the prefrontal cortex (p , 0.0001). We also show that these microstructural alterations precede cognitive decline and gross atrophy. These results support the idea that calcineurin inhibitors may have the potential to prevent aging-related pathology if administered at middle age.