Activation of transient receptor potential A1 channels by mustard oil, tetrahydrocannabinol and Ca2+ reveals different functional channel states

• Published in: Neuroscience 2008-07, Vol.154 (4), p.1467-1476
• Main Authors: Cavanaugh, E.J, Simkin, D, Kim, D
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; calcium; Calcium - pharmacology; Dronabinol - pharmacology; Fundamental and applied biological sciences. Psychology; Hallucinogens - pharmacology; HeLa Cells; Humans; Membrane Potentials - physiology; Mice; mustard oil; Mustard Plant; Neurology; Neurons - drug effects; Neurons - metabolism; Patch-Clamp Techniques; Plant Oils - pharmacology; polyphosphate; pungent chemicals; Rats; Transient Receptor Potential Channels - metabolism; trigeminal neuron; TRP ion channel; Vertebrates: nervous system and sense organs
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2008.04.048

Abstract Our recent study has shown that activation of transient receptor potential A1 channel (TRPA1) by pungent chemicals such as allyl-isothiocyanate (AITC) requires an unidentified cytosolic factor whose action can be mimicked by inorganic polyphosphates. Thus, AITC and other pungent chemicals fail to activate TRPA1 in excised patches. It is unclear whether TRPA1 switches to a conformation that is insensitive to the pungent chemicals, or whether TRPA1 simply becomes completely non-functional and insensitive to all activators when the cytosolic factor is absent. To help distinguish between these possibilities, the effects of Δ9 -tetrahydrocannabinol (THC) and Ca2+ that are structurally different from pungent chemicals were tested on AITC-sensitive and AITC-insensitive states of TRPA1. In HeLa cells transiently expressing mouse TRPA1, activation of TRPA1 by THC was slow and weak from the extracellular side (cell-attached; K1/2 >20 μM), but was faster and more potent from the intracellular side (inside-out; K1/2 , ∼0.7 μM), and this did not require the presence of a polyphosphate. Similar results were observed in rat trigeminal neurons. Increasing the extracellular [Ca2+ ] from ∼0-1-3 mM activated TRPA1 in cell-attached patches. Elevation of cytosolic [Ca2+ ] using thapsigargin (inhibitor of Ca2+ -ATPAse) and histamine (that elevates IP3 ) also activated TRPA1 in cell-attached patches. Similar to pungent chemicals, Ca2+ (1–5 μM) failed to activate TRPA1 in inside-out patches, unless polyphosphates were present. These results show that TRPA1 can exist in different functional states: a native state (cell-attached patch) and a non-native state (excised patch). THC can activate TRPA1 even in the absence of polyphosphates, whereas pungent chemicals and Ca2+ require it for activation.