The chemistry of both ROS and RNS is influenced by the presence of a transition metal such as iron
Enzyme systems are present that produce and degrade some ROS & RNS
ROS/RNS under the control of enzyme systems are thought to participate in cellular signaling
ROS/RNS participate in controlling such activities as metabolism, proliferation, migration, differentiation,
cytoskeleton dynamics
Some modifications of macromolecules by ROS/RNS e.g. at cysteine residues (creating disulfide bonds and altering
protein structure) are reversible; these are thought to be important in cell signaling
In excess, ROS/RNS react with lipids, proteins and nucleic acids, altering structure and function
Irreversible modifications are thought to participate in cellular damage
ROS & RNS have been implicated in cardiovascular diseases:
Hypertension
CHF
Atherosclerosis
Atrial fibrillation
Cardiovascular complications of diabetes
Measurement of specific ROS/RNS and therefore identification of which ROS/RNS are involved in which processes in
which context are hindered by:
Their short half-life (as little as nanoseconds)
Low concentrations
Subcellular locations
Lack (to date) of specific, sensitive, robust, and reproducible assays
Multiple assays have been developed and increasing information on ROS/RNS and their cellular biology, relevance to
clinical endpoints, and interventions to optimize outcomes are expected in the coming years