瞬时受体电位通道
医学
舔
谷氨酸的
麻醉
神经科学
TRPV1型
咳嗽反射
反射
药理学
神经传递
抗焦虑药
迷走神经
自主神经系统
结节状神经节
气压感受器
通风(建筑)
心率
麻醉剂
外围设备
感觉神经
类阿片
化学
神经肽
孤菲肽受体
副交感神经系统
外周化学感受器
呼吸中枢
受体
内科学
疑核
呼吸控制
作者
Peiyu Wang,Jinpiao Zhu,Xuteng Lu,Chang Chen,Bomin Gao,Wanjiang Tao,Keyu Xia,Yang Song,Qiong Shi,Hongcun Gai,晓盼 郝,Feng Liu,Peiyuan Pang,Y LI,Xiaoyi Mo,Xiaodong Wang,Chang Xie,Dongdong Li,Zongze Zhang,Jing Yao
标识
DOI:10.1073/pnas.2525757123
摘要
Aromatic essential oils (EOs) exhibit anxiolytic properties, yet their neural and molecular mechanisms remain to be understood. Here, we found that citronellal, an EO derived from lemongrass, alleviates stress-related anxiety by modulating vagal tone. We identified transient receptor potential vanilloid 3 (TRPV3) channel in nodose ganglion (NG) as the molecular target of citronellal. TRPV3 was also observed to mediate the antistress effects of the inhaled anesthetic sevoflurane. Both sedatives attenuated acute restraint stress-induced hyperactivity of heart and breath rates via glutamatergic neurotransmission along NG-to-caudal nucleus tractus solitarius (cNTS) pathway. This effect was abolished by surgical vagotomy, Trpv3 −/− , or NG-specific Trpv3 knockdown. Cryo-EM structural analysis revealed that sevoflurane occupies a pore-proximal fenestration site, while citronellal binds to the vanilloid site. Re-expression of wild-type TRPV3, but not loss-of-function TRPV3 mutants TRPV3(A560L) or TRPV3(V662A), in Trpv3 −/− NG neurons restored the mouse’s response to both sedatives, thereby modulating heart and respiratory rates. Together, these findings establish peripheral TRPV3 as a multisensory ligand-gated node for vagal modulation of stress responses, and help instruct pathway-specific anxiolytics.
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