TRPA1 Is a Component of the Nociceptive Response to CO2

被引:105
作者
Wang, Yuanyuan Y. [1 ]
Chang, Rui B. [1 ]
Liman, Emily R. [1 ]
机构
[1] Univ So Calif, Dept Biol Sci, Neurobiol Sect, Los Angeles, CA 90089 USA
基金
美国国家卫生研究院;
关键词
ION-CHANNEL; CAPSAICIN RECEPTOR; CARBON-DIOXIDE; PAIN PATHWAY; K+ CHANNELS; DROSOPHILA; TRANSDUCTION; ACTIVATION; NEURONS; TASTE;
D O I
10.1523/JNEUROSCI.2715-10.2010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In humans, high concentrations of CO2, as found in carbonated beverages, evoke a mixture of sensations that include a stinging or pungent quality. The stinging sensation is thought to originate with the activation of nociceptors, which innervate the respiratory, nasal, and oral epithelia. The molecular basis for this sensation is unknown. Here we show that CO2 specifically activates a subpopulation of trigeminal neurons that express TRPA1, a mustard oil- and cinnamaldehyde-sensitive channel, and that these responses are dependent on a functional TRPA1 gene. TRPA1 is sufficient to mediate responses to CO2 as TRPA1 channels expressed in HEK-293 cells, but not TRPV1 channels, were activated by bath-applied CO2. CO2 can diffuse into cells and produce intracellular acidification, which could gate TRPA1 channels. Consistent with this mechanism, TRPA1 channels in excised patches were activated in a dose-dependent manner by intracellular protons. We conclude that TRPA1, by sensing intracellular acidification, constitutes an important component of the nociceptive response to CO2.
引用
收藏
页码:12958 / 12963
页数:6
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