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

dc.contributor.author Reddy, R. Gajendra
dc.contributor.author Surineni, Goverdhan
dc.contributor.author Bhattacharya, Dwaipayan
dc.contributor.author Marvadi, Sandeep Kumar
dc.contributor.author Sagar, Arpita
dc.contributor.author Kalle, Arunasree M.
dc.contributor.author Kumar, Arvind
dc.contributor.author Kantevari, Srinivas
dc.contributor.author Chakravarty, Sumana
dc.date.accessioned 2022-03-27T01:01:42Z
dc.date.available 2022-03-27T01:01:42Z
dc.date.issued 2019-10-22
dc.description.abstract 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.
dc.identifier.citation ACS Omega. v.4(17)
dc.identifier.uri 10.1021/acsomega.9b01950
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acsomega.9b01950
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/3904
dc.title Crafting Carbazole-Based Vorinostat and Tubastatin-A-like Histone Deacetylase (HDAC) Inhibitors with Potent in Vitro and in Vivo Neuroactive Functions
dc.type Journal. Article
dspace.entity.type
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