Soo Yeon Baek, Jeehee Lee, Taegwan Kim, Hyelim Lee, Hoon-Seong Choi, Hahnbeom Park, Minseob Koh, Eunha Kim, Michael E Jung, Dimitrios Iliopoulos, Jeong-Yeon Lee, Jonghoon Kim, Sanghee Lee
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2023 OctHistone deacetylases (HDACs) are key epigenetic regulators and classified into four subtypes. Despite the various roles of each HDAC isoform, the lack of selective HDAC inhibitors has limited the elucidation of their roles in biological systems. HDAC11, the sole class-IV HDAC, is highly expressed in the brain, however, the role of HDAC11 in microglia is not fully understood. Based on the modification of MC1568, we developed a novel HDAC inhibitor, 5. Interestingly, 5 suppresses lipopolysaccharide-induced microglial activation by the initiation of autophagy and subsequent inhibition of nitric oxide production. Furthermore, we demonstrated that 5 significantly alleviates depression-like behavior by inhibiting microglial activation in mouse brain. Our discovery reveals that specific pharmacological regulation of HDAC11 induces autophagy and reactive nitrogen species balance in microglia for the first time, which makes HDAC11 a new therapeutic target for depressive disorder. Copyright © 2023 The Authors. Published by Elsevier Masson SAS.. All rights reserved.
Soo Yeon Baek, Jeehee Lee, Taegwan Kim, Hyelim Lee, Hoon-Seong Choi, Hahnbeom Park, Minseob Koh, Eunha Kim, Michael E Jung, Dimitrios Iliopoulos, Jeong-Yeon Lee, Jonghoon Kim, Sanghee Lee. Development of a novel histone deacetylase inhibitor unveils the role of HDAC11 in alleviating depression by inhibition of microglial activation. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Oct;166:115312
PMID: 37567072
View Full Text