Synthesis of a natural quinoline alkaloid isolated from the deep-sea-derived fungus and its potential as a therapeutic for Parkinson's disease

J Asian Nat Prod Res. 2023 May;25(5):446-455. doi: 10.1080/10286020.2022.2104259. Epub 2022 Aug 18.

Abstract

2-(Quinoline-8-carboxamido)benzoic acid (2-QBA; 1) is a natural quinoline alkaloid isolated from the deep-sea-derived fungus Aspergillus sp. SCSIO06786. Alkaloid 1 was synthesized by an amidation reaction of 8-quinolinecaroxylic acid with methyl anthranilate, followed by hydrolysis. The neuroprotective properties of 1 were evaluated using a Caenorhabditis elegans Parkinson's disease model, which revealed that 1 significantly ameliorated 1-methyl-4-phenylpyridinium (MPP+)-induced dopaminergic neurodegeneration in a dose-dependent manner. MPP+-induced behavioral defects in worms, including impaired locomotion and basal slowing ability, were restored by treatment with 1. We further demonstrated that treatment with 1 modulates the formation of neurotoxic α-synuclein oligomers by suppressing α-synuclein expressions and enhancing proteasome activity. These results suggest that 1 is a promising therapeutic candidate for the treatment of Parkinson's disease.

Keywords: 2-(Quinoline-8-carboxamido)benzoic acid; Caenorhabditis elegans; Parkinson’s disease; anthranilic acid; dopaminergic neurodegeneration.

MeSH terms

  • 1-Methyl-4-phenylpyridinium
  • Alkaloids* / pharmacology
  • Animals
  • Caenorhabditis elegans / metabolism
  • Disease Models, Animal
  • Fungi / metabolism
  • Neuroprotective Agents* / pharmacology
  • Parkinson Disease* / drug therapy
  • Parkinson Disease* / metabolism
  • Quinolines* / metabolism
  • Quinolines* / pharmacology
  • alpha-Synuclein / metabolism

Substances

  • alpha-Synuclein
  • Alkaloids
  • 1-Methyl-4-phenylpyridinium
  • Quinolines
  • Neuroprotective Agents