Table 1. Do NO, CO and H2S qualify as gasotransmitters?
Criterion | NO | CO | H2S |
---|---|---|---|
(i) Small gas | ✓ | ✓ | ✓ |
(ii) Membrane-permeable | ✓ | ✓ | ✓ |
(iii) Endogenously synthesised | ✓ | ✓ | ✓ |
(iv) Specific functions; manipulating endogenous levels evokes changes | ✓ antibiotic resistance, virulence, quorum sensing, biofilms, etc. | unclear, except in CO metabolism1 | ✓ antibiotic resistance, oxidative stress resistance |
(v) Effects mimicked by exogenous counterparts | ✓ | Only toxicity can be mimicked by CO or CORMs? | ✓ |
(vi) Specific cellular/molecular targets2 | ✓ | unclear | Only via persulfide chemistry |
We do not regard use of CO as a metabolic substrate as signal transduction or gasotransmitter functions; endogenous CO is not used in this way.
We exclude targets such as metal centres that may lead to toxicity.