Transient receptor potential A1 is a sensory receptor for multiple products of oxidative stress

TY - JOUR

T1 - Transient receptor potential A1 is a sensory receptor for multiple products of oxidative stress

AU - Andersson, D A

AU - Gentry, Clive

AU - Moss, Sian

AU - Bevan, Stuart

PY - 2008/3/5

Y1 - 2008/3/5

N2 - Transient receptor potential A1 (TRPA1) is expressed in a subset of nociceptive sensory neurons where it acts as a sensor for environmental irritants, including acrolein, and some pungent plant ingredients such as allyl isothiocyanate and cinnamaldehyde. These exogenous compounds activate TRPA1 by covalent modification of cysteine residues. We have used electrophysiological methods and measurements of intracellular calcium concentration ([Ca2+](i)) to show that TRPA1 is activated by several classes of endogenous thiol-reactive molecules. TRPA1 was activated by hydrogen peroxide (H2O2; EC50, 230 mu M), by endogenously occurring alkenyl aldehydes (EC50 : 4-hydroxynonenal 19.9 mu M, 4-oxo-nonenal 1.9 mu M, 4-hydroxyhexenal 38.9 mu M) and by the cyclopentenone prostaglandin, 15-deoxy- Delta(12,14)- prostaglandin J(2) (15d-PGJ(2), EC50: 5.6 mu M). The effect of H2O2 was reversed by treatment with dithiothreitol indicating that H2O2 acts by promoting the formation of disulfide bonds whereas the actions of the alkenyl aldehydes and 15d-PGJ(2) were not reversed, suggesting that these agents form Michael adducts. H2O2 and the naturally occurring alkenyl aldehydes and 15d-PGJ(2) acted on a subset of isolated rat and mouse sensory neurons [similar to 25% of rat dorsal root ganglion (DRG) and similar to 50% of nodose ganglion neurons] to evoke a depolarizing inward current and an increase in [Ca2+](i) in TRPA1 expressing neurons. The abilities of H2O2, alkenyl aldehydes and 15d-PGJ(2) to raise [Ca2+](i) in mouse DRG neurons were greatly reduced in neurons from trpa1(-/-) mice. Furthermore, intraplantar injection of either H2O2 or 15d-PGJ(2) evoked a nocifensive/pain response in wild-type mice, but not in trpa1(-/-) mice. These data demonstrate that multiple agents produced during episodes of oxidative stress can activate TRPA1 expressed in sensory neurons

AB - Transient receptor potential A1 (TRPA1) is expressed in a subset of nociceptive sensory neurons where it acts as a sensor for environmental irritants, including acrolein, and some pungent plant ingredients such as allyl isothiocyanate and cinnamaldehyde. These exogenous compounds activate TRPA1 by covalent modification of cysteine residues. We have used electrophysiological methods and measurements of intracellular calcium concentration ([Ca2+](i)) to show that TRPA1 is activated by several classes of endogenous thiol-reactive molecules. TRPA1 was activated by hydrogen peroxide (H2O2; EC50, 230 mu M), by endogenously occurring alkenyl aldehydes (EC50 : 4-hydroxynonenal 19.9 mu M, 4-oxo-nonenal 1.9 mu M, 4-hydroxyhexenal 38.9 mu M) and by the cyclopentenone prostaglandin, 15-deoxy- Delta(12,14)- prostaglandin J(2) (15d-PGJ(2), EC50: 5.6 mu M). The effect of H2O2 was reversed by treatment with dithiothreitol indicating that H2O2 acts by promoting the formation of disulfide bonds whereas the actions of the alkenyl aldehydes and 15d-PGJ(2) were not reversed, suggesting that these agents form Michael adducts. H2O2 and the naturally occurring alkenyl aldehydes and 15d-PGJ(2) acted on a subset of isolated rat and mouse sensory neurons [similar to 25% of rat dorsal root ganglion (DRG) and similar to 50% of nodose ganglion neurons] to evoke a depolarizing inward current and an increase in [Ca2+](i) in TRPA1 expressing neurons. The abilities of H2O2, alkenyl aldehydes and 15d-PGJ(2) to raise [Ca2+](i) in mouse DRG neurons were greatly reduced in neurons from trpa1(-/-) mice. Furthermore, intraplantar injection of either H2O2 or 15d-PGJ(2) evoked a nocifensive/pain response in wild-type mice, but not in trpa1(-/-) mice. These data demonstrate that multiple agents produced during episodes of oxidative stress can activate TRPA1 expressed in sensory neurons

U2 - 10.1523/JNEUROSCI.5369-07.2008

DO - 10.1523/JNEUROSCI.5369-07.2008

M3 - Article

SN - 1529-2401

VL - 28

SP - 2485

EP - 2494

JO - Journal of Neuroscience

JF - Journal of Neuroscience

IS - 10

ER -