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Neuroprotective Activity of Some Marine Fungal Metabolites in the 6-Hydroxydopamin- and Paraquat-Induced Parkinson's Disease Models.


ABSTRACT: A new melatonin analogue 6-hydroxy-N-acetyl-?-oxotryptamine (1) was isolated from the marine-derived fungus Penicillium sp. KMM 4672. It is the second case of melatonin-related compounds isolation from microfilamentous fungi. The neuroprotective activities of this metabolite, as well as 3-methylorsellinic acid (2) and 8-methoxy-3,5-dimethylisochroman-6-ol (3) from Penicillium sp. KMM 4672, candidusin A (4) and 4?-dehydroxycandidusin A (5) from Aspergillus sp. KMM 4676, and diketopiperazine mactanamide (6) from Aspergillus flocculosus, were investigated in the 6-hydroxydopamine (6-OHDA)- and paraquat (PQ)-induced Parkinson's disease (PD) cell models. All of them protected Neuro2a cells against the damaging influence of 6-OHDA to varying degrees. This effect may be realized via a reactive oxygen species (ROS) scavenging pathway. The new melatonin analogue more effectively protected Neuro2A cells against the 6-OHDA-induced neuronal death, in comparison with melatonin, as well as against the PQ-induced neurotoxicity. Dehydroxylation at C-3? and C-4? significantly increased free radical scavenging and neuroprotective activity of candidusin-related p-terphenyl polyketides in both the 6-OHDA- and PQ-induced PD models.

SUBMITTER: Yurchenko EA 

PROVIDER: S-EPMC6265791 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Neuroprotective Activity of Some Marine Fungal Metabolites in the 6-Hydroxydopamin- and Paraquat-Induced Parkinson's Disease Models.

Yurchenko Ekaterina A EA   Menchinskaya Ekaterina S ES   Pislyagin Evgeny A EA   Trinh Phan Thi Hoai PTH   Ivanets Elena V EV   Smetanina Olga F OF   Yurchenko Anton N AN  

Marine drugs 20181121 11


A new melatonin analogue 6-hydroxy-<i>N</i>-acetyl-β-oxotryptamine (<b>1</b>) was isolated from the marine-derived fungus <i>Penicillium</i> sp. KMM 4672. It is the second case of melatonin-related compounds isolation from microfilamentous fungi. The neuroprotective activities of this metabolite, as well as 3-methylorsellinic acid (<b>2)</b> and 8-methoxy-3,5-dimethylisochroman-6-ol (<b>3</b>) from <i>Penicillium</i> sp. KMM 4672, candidusin A (<b>4</b>) and 4″-dehydroxycandidusin A (<b>5</b>) f  ...[more]

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