| Literature DB >> 30986504 |
Satarupa Deb1, Banashree Chetia Phukan1, Muhammed Khairujjaman Mazumder1, Ankumoni Dutta1, Rajib Paul2, Pallab Bhattacharya3, Rajat Sandhir4, Anupom Borah5.
Abstract
Garcinol, the principal phytoconstituent of plants belonging to the genus Garcinia, is known for its anti-oxidant as well as anti-inflammatory properties, which can be extended to its possible neuroprotective role. Recent reports disseminate the capacity of garcinol to influence neuronal growth and survival, alter the neurochemical status in brain, as well as regulate memory and cognition. The concomitant neuro-rescue property of garcinol may render it as an effective compound in Parkinson's disease (PD) therapeutics since it is capable of ameliorating the related pathophysiological changes. Emerging pieces of evidence linking histone acetylation defects to the progression of neurodegenerative diseases provide an effective basis for targeting PD. Hyperacetylation of histones has been reported in Parkinsonian brain, which demands the use of pharmacological inhibitors of histone acetyltransferases (HAT). Garcinol serves as a potent natural HAT inhibitor and has unveiled promising results in molecular interaction studies against Monoamine oxidase B (MAO-B) and Catechol-O-Methyltransferase (COMT), as well as in L-DOPA induced dyskinesia. This review highlights the prospective implications of garcinol as a novel anti-Parkinsonian agent, and establishes a bridge between histone acetylation defects and the pathological aspects of PD.Entities:
Keywords: Dopamine; Histone acetylation; Neurodegeneration; Neuroinflammation; Oxidative stress; Parkinson's disease; α-synuclein
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Year: 2019 PMID: 30986504 DOI: 10.1016/j.neuint.2019.04.004
Source DB: PubMed Journal: Neurochem Int ISSN: 0197-0186 Impact factor: 3.921