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Targeting metabolic syndrome with phytochemicals: Focus on the role of molecular chaperones and hormesis in drug discovery.

Publication Type : Journal Article

Publisher : Pharmacol Res

Source : Pharmacol Res, Volume 159, p.104925 (2020)

Url : https://pubmed.ncbi.nlm.nih.gov/32492491/#:~:text=Several%20phytochemicals%20are%20known%20for,inflammation%20associated%20with%20metabolic%20syndrome.

Keywords : Heat shock proteins, Herbal, Hormesis, inflammation, Metabolic syndromes, metformin, Molecular Chaperones, Phytochemicals, Preconditioning, Stress.

Campus : Kochi

School : School of Pharmacy

Department : Pharmacognosy

Year : 2020

Abstract : Adaptive cellular stress response confers stress tolerance against inflammatory and metabolic disorders. In response to metabolic stress, the key mediator of cellular adaptation and tolerance is a class of molecules called the molecular chaperones (MCs). MCs are highly conserved molecules that play critical role in maintaining protein stability and functionality. Hormesis in this context is a unique adaptation mechanism where a low dose of a stressor (which is toxic at high dose) confers a stress-resistant adaptive cellular phenotype. Hormesis can be observed at different level of biological organization at various measurable endpoints. The MCs are believed to play a key role in adaptation during hormesis. Several phytochemicals are known for their hormetic response and are called phytochemical hormetins. The role of phytochemical-mediated hormesis on the adaptive cellular processes is proposed as a potential therapeutic approach to target inflammation associated with metabolic syndrome. However, the screening of phytochemical hormetins would require a paradigm shift in the methods currently used in drug discovery.

Cite this Research Publication : Lakshmi P. K., Shweta Kumar, Sulakshhna Pawar, Beena Briget Kuriakose, Sudheesh M. S., and Rajesh Singh Pawar, “Targeting metabolic syndrome with phytochemicals: Focus on the role of molecular chaperones and hormesis in drug discovery.”, Pharmacol Res, vol. 159, p. 104925, 2020.

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