Dhaka Ajay, Murray Amber N, Mathur Jayanti, Earley Taryn J, Petrus Matt J, Patapoutian Ardem
Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Neuron. 2007 May 3;54(3):371-8. doi: 10.1016/j.neuron.2007.02.024.
ThermoTRPs, a subset of the Transient Receptor Potential (TRP) family of cation channels, have been implicated in sensing temperature. TRPM8 and TRPA1 are both activated by cooling; however, it is unclear whether either ion channel is required for thermosensation in vivo. We show that mice lacking TRPM8 have severe behavioral deficits in response to cold stimuli. In thermotaxis assays of temperature gradient and two-temperature choice assays, TRPM8-deficient mice exhibit strikingly reduced avoidance of cold temperatures. TRPM8-deficient mice also lack behavioral response to cold-inducing icilin application and display an attenuated response to acetone, an unpleasant cold stimulus. However, TRPM8-deficient mice have normal nociceptive-like responses to subzero centigrade temperatures, suggesting the presence of at least one additional noxious cold receptor. Finally, we show that TRPM8 mediates the analgesic effect of moderate cooling after administration of formalin, a painful stimulus. Therefore, depending on context, TRPM8 contributes to sensing unpleasant cold stimuli or mediating the effects of cold analgesia.
瞬时受体电位(TRP)阳离子通道家族的一个亚群——热TRP通道,与温度感知有关。TRPM8和TRPA1都可被冷却激活;然而,尚不清楚这两种离子通道在体内的温度感觉中是否是必需的。我们发现,缺乏TRPM8的小鼠对冷刺激有严重的行为缺陷。在温度梯度趋温性试验和双温度选择试验中,缺乏TRPM8的小鼠对低温的回避明显减少。缺乏TRPM8的小鼠对诱导寒冷的艾西利定应用也没有行为反应,并且对丙酮(一种令人不适的冷刺激)的反应减弱。然而,缺乏TRPM8的小鼠对零下摄氏度温度具有正常的伤害性样反应,这表明至少存在一种额外的有害冷感受器。最后,我们表明,TRPM8在给予福尔马林(一种疼痛刺激)后介导适度冷却的镇痛作用。因此,根据具体情况,TRPM8有助于感知令人不适的冷刺激或介导冷镇痛的作用。