| Literature DB >> 34435330 |
Yoo Jin Shin1,2, Sun Woo Lim1,2, Sheng Cui1,2, Eun Jeong Ko1,2,3, Byung Ha Chung1,2,3, Hong Lim Kim4, Tae Ryong Riew5, Mun Yong Lee5, Chul Woo Yang6,7,8.
Abstract
The influence of long-term tacrolimus treatment on cognitive function remains to be elucidated. Using a murine model of chronic tacrolimus neurotoxicity, we evaluated the effects of tacrolimus on cognitive function, synaptic balance, its regulating protein (Klotho), and oxidative stress in the hippocampus. Compared to vehicle-treated mice, tacrolimus-treated mice showed significantly decreased hippocampal-dependent spatial learning and memory function. Furthermore, tacrolimus caused synaptic imbalance, as demonstrated by decreased excitatory synapses and increased inhibitory synapses, and downregulated Klotho in a dose-dependent manner; the downregulation of Klotho was localized to excitatory hippocampal synapses. Moreover, tacrolimus increased oxidative stress and was associated with activation of the PI3K/AKT pathway in the hippocampus. These results indicate that tacrolimus impairs cognitive function via synaptic imbalance, and that these processes are associated with Klotho downregulation at synapses through tacrolimus-induced oxidative stress in the hippocampus.Entities:
Keywords: Cognitive dysfunction; Hippocampus; Klotho; Oxidative stress; Synaptic imbalance; Tacrolimus
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Year: 2021 PMID: 34435330 DOI: 10.1007/s12035-021-02499-3
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590