Crafting Carbazole-Based Vorinostat and Tubastatin-A-like Histone Deacetylase (HDAC) Inhibitors with Potent in Vitro and in Vivo Neuroactive Functions

被引:16
作者
Reddy, R. Gajendra [1 ,5 ]
Surineni, Goverdhan [2 ]
Bhattacharya, Dwaipayan [1 ]
Marvadi, Sandeep Kumar [2 ]
Sagar, Arpita [4 ]
Kalle, Arunasree M. [4 ]
Kumar, Arvind [3 ,5 ]
Kantevari, Srinivas [2 ,5 ]
Chakravarty, Sumana [1 ,5 ]
机构
[1] Indian Inst Chem Technol, CSIR, Appl Biol Div, Uppal Rd, Hyderabad 500007, Telangana, India
[2] Indian Inst Chem Technol, CSIR, Fluoro & Agrochem Div, Uppal Rd, Hyderabad 500007, Telangana, India
[3] CSIR Ctr Cellular & Mol Biol, Uppal Rd, Hyderabad 500007, Telangana, India
[4] Univ Hyderabad, Sch Life Sci, Dept Anim Biol, Hyderabad 500046, Telangana, India
[5] Acad Sci & Innovat Res AcSIR, Chennai 600113, Tamil Nadu, India
关键词
PROTECTS DOPAMINERGIC-NEURONS; NEURITE OUTGROWTH; NEUROPROTECTION; ACID; DIFFERENTIATION; EXTINCTION; MECHANISM; CULTURES; PATHWAY; GROWTH;
D O I
10.1021/acsomega.9b01950
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Small-molecule inhibitors of HDACs (HDACi) induce hyperacetylation of histone and nonhistone proteins and have emerged as potential therapeutic agents in most animal models tested. The established HDACi vorinostat and tubastatin-A alleviate neurodegenerative and behavioral conditions in animal models of neuropsychiatric disorders restoring the neurotrophic milieu. In spite of the neuroactive pharmacological role of HDACi (vorinostat and tubastatin-A), they are limited by efficacy and toxicity. Considering these limitations and concern, we have designed novel compounds 3-11 as potential HDACi based on the strategic crafting of the key pharmacophoric elements of vorinostat and tubastatin-A into architecting a single molecule. The molecules 3-11 were synthesized through a multistep reaction sequence starting from carbazole and were fully characterized by NMR and mass spectral analysis. The novel molecules 3-11 showed remarkable pan HDAC inhibition and the potential to increase the levels of acetyl H3 and acetyl tubulin. In addition, few novel HDAC inhibitors 4-8, 10, and 11 exhibited significant neurite outgrowth-promoting activity with no observable cytotoxic effects, and interestingly, compound 5 has shown comparably more neurite growth than the parent compounds vorinostat and tubastatin-A. Also, compound 5 was evaluated for possible mood-elevating effects in a chronic unpredictable stress model of Zebrafish. It showed potent anxiolytic and antidepressant-like effects in the novel tank test and social interaction test, respectively. Furthermore, the potent in vitro and in vivo neuroactive compound 5 has shown selectivity for class II over class I HDACs. Our results suggest that the novel carbazole-based HDAC inhibitors, crafted with vorinostat and tubastatin-A pharmacophoric moieties, have potent neurite outgrowth activity and potential to be developed as therapeutics to treat depression and related psychiatric disorders.
引用
收藏
页码:17279 / 17294
页数:16
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