Carbonic anhydrase activation profile of indole-based derivatives

J Enzyme Inhib Med Chem. 2021 Dec;36(1):1783-1797. doi: 10.1080/14756366.2021.1959573.

Abstract

Carbonic Anhydrase Activators (CAAs) could represent a novel approach for the treatment of Alzheimer's disease, ageing, and other conditions that require remedial achievement of spatial learning and memory therapy. Within a research project aimed at developing novel CAAs selective for certain isoforms, three series of indole-based derivatives were investigated. Enzyme activation assay on human CA I, II, VA, and VII isoforms revealed several effective micromolar activators, with promising selectivity profiles towards the brain-associated cytosolic isoform hCA VII. Molecular modelling studies suggested a theoretical model of the complex between hCA VII and the new activators and provide a possible explanation for their modulating as well as selectivity properties. Preliminary biological evaluations demonstrated that one of the most potent CAA 7 is not cytotoxic and is able to increase the release of the brain-derived neurotrophic factor (BDNF) from human microglial cells, highlighting its possible application in the treatment of CNS-related disorders.

Keywords: Carbonic anhydrase activators; brain associated human CA VII isoform; indole; microglia.

MeSH terms

  • Brain-Derived Neurotrophic Factor / metabolism
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Carbonic Anhydrases / drug effects*
  • Carbonic Anhydrases / metabolism
  • Cell Survival / drug effects
  • Enzyme Activation
  • Enzyme Activators / chemistry
  • Enzyme Activators / pharmacology*
  • Enzyme-Linked Immunosorbent Assay / methods
  • Humans
  • Indoles / chemistry
  • Indoles / pharmacology*
  • Isoenzymes / drug effects*
  • Isoenzymes / metabolism
  • Microglia / cytology
  • Microglia / drug effects
  • Models, Molecular
  • Proton Magnetic Resonance Spectroscopy
  • Substrate Specificity

Substances

  • Brain-Derived Neurotrophic Factor
  • Enzyme Activators
  • Indoles
  • Isoenzymes
  • BDNF protein, human
  • Carbonic Anhydrases

Grants and funding

This work was supported by University of Campania Luigi Vanvitelli under grant VALERE: Vanvitelli per la Ricerca, ANIMA and VALEREPlus projects, Campania and Regional Government Technology Platform Lotta alle Patologie Oncologiche under grant iCURE, University of Pisa under grant PRA_2020_58 and Italian MIUR under [grant PRIN 2017, 2017XYBP2R].