Prodrugs of Persulfides, Sulfur Dioxide, and Carbon Disulfide: Important Tools for Studying Sulfur Signaling at Various Oxidation States

Antioxid Redox Signal. 2020 Nov 10;33(14):1046-1059. doi: 10.1089/ars.2019.7880. Epub 2020 Mar 6.

Abstract

Significance: Bioactive sulfur species such as hydrogen sulfide (H2S), persulfide species (R-SnSH, n ≥ 1), hydrogen polysulfide (H2Sn, n ≥ 2), sulfur dioxide (SO2), and carbon disulfide (CS2) participate in various physiological and/or pathological pathways such as vasodilation, apoptosis, inflammation, and energy metabolism regulation. The oxidation state of the individual sulfur species endows them unique biological activities. Recent Advances: There have been great strides made in achieving molecular understanding of the sulfur-signaling processes. Critical Issues: The development of various chemical tools that deliver reactive sulfur species in a controllable manner has played an important role in understanding the different roles of various sulfur species. In this review, we focus on three types of sulfur species, including persulfide, SO2, and CS2. Starting with a brief introduction of their physiological functions, we will then assess the various drug delivery strategies to generate persulfide species, SO2, and CS2 as research tools and potentially as therapeutic agents. Future Directions: Development of donors of various sulfur species that respond to distinct stimulus is critical for this field. Another key to the long-term success of this field is the identification of an area of unmet medical need that can be addressed with these sulfur species.

Keywords: carbon disulfide; gasotransmitter; hydrogen polysulfide; hydrogen sulfide; persulfide species; sulfur dioxide.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Carbon Disulfide / administration & dosage
  • Carbon Disulfide / metabolism*
  • Carbon Disulfide / pharmacology
  • Drug Delivery Systems
  • Drug Development
  • Humans
  • Metabolic Networks and Pathways
  • Oxidation-Reduction
  • Oxidative Stress
  • Prodrugs / administration & dosage
  • Prodrugs / metabolism*
  • Prodrugs / pharmacology
  • Signal Transduction
  • Sulfides / administration & dosage
  • Sulfides / metabolism*
  • Sulfides / pharmacology
  • Sulfur / metabolism
  • Sulfur Dioxide / administration & dosage
  • Sulfur Dioxide / metabolism*
  • Sulfur Dioxide / pharmacology

Substances

  • Prodrugs
  • Sulfides
  • persulfides
  • Sulfur Dioxide
  • Sulfur
  • Carbon Disulfide