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1.
Acta Pharmacol Sin ; 45(7): 1366-1380, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38538717

ABSTRACT

Parkinson's disease (PD) is the second most common neurodegenerative disease, and its prevalence is increasing. Currently, no effective therapies for PD exist. Marine-derived natural compounds are considered important resources for the discovery of new drugs due to their distinctive structures and diverse activities. In this study, tetrahydroauroglaucin (TAG), a polyketide isolated from a marine sponge, was found to have notable neuroprotective effects on MPTP/MPP+-induced neurotoxicity. RNA sequencing analysis and metabolomics revealed that TAG significantly improved lipid metabolism disorder in PD models. Further investigation indicated that TAG markedly decreased the accumulation of lipid droplets (LDs), downregulated the expression of RUBCN, and promoted autophagic flux. Moreover, conditional knockdown of Rubcn notably attenuated PD-like symptoms and the accumulation of LDs, accompanied by blockade of the neuroprotective effect of TAG. Collectively, our results first indicated that TAG, a promising PD therapeutic candidate, could suppress the accumulation of LDs through the RUBCN-autophagy pathway, which highlighted a novel and effective strategy for PD treatment.


Subject(s)
Lipid Metabolism , Neuroprotective Agents , Animals , Lipid Metabolism/drug effects , Neuroprotective Agents/pharmacology , Neuroprotective Agents/therapeutic use , Homeostasis/drug effects , Porifera/chemistry , Mice , Mice, Inbred C57BL , Autophagy/drug effects , Male , Parkinson Disease/drug therapy , Parkinson Disease/metabolism , Polyketides/pharmacology , Humans
2.
Org Lett ; 23(14): 5587-5591, 2021 07 16.
Article in English | MEDLINE | ID: mdl-34190564

ABSTRACT

The solid-state cultivation of Acaulium sp. H-JQSF isolated from Armadillidium vulgare produces acautalides A-C (1-3) as skeletally unprecedented Diels-Alder adducts of a 14-membered macrodiolide to an octadeca-9,11,13-trienoic acid. The acautalide structures, along with the intramolecular transesterifications of 1-acylglycerols, were elucidated by mass spectrometry, nuclear magnetic resonance, chemical transformation, and single-crystal X-ray diffraction. Compounds 1-3 were found to be neuroprotective with antiparkinsonic potential in the 1-methyl-4-phenylpyridinium-challenged nematode model, with the magnitude impacted by the glycerol esterification.


Subject(s)
Ascomycota/chemistry , Macrolides/pharmacology , Animals , Crystallography, X-Ray , Macrolides/chemistry , Macrolides/isolation & purification , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Structure
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