Gachon Pain Center and Department of Physiology, Gachon University College of Medicine, Incheon 21999, Korea.
Gil Medical Center, Department of Anesthesiology and Pain Medicine, Gachon University, Incheon 21565, Korea.
Int J Mol Sci. 2022 May 21;23(10):5772. doi: 10.3390/ijms23105772.
The transient receptor potential vanilloid 1 (TRPV1) ion channel plays an important role in the peripheral nociceptive pathway. TRPV1 is a polymodal receptor that can be activated by multiple types of ligands and painful stimuli, such as noxious heat and protons, and contributes to various acute and chronic pain conditions. Therefore, TRPV1 is emerging as a novel therapeutic target for the treatment of various pain conditions. Notably, various peptides isolated from venomous animals potently and selectively control the activation and inhibition of TRPV1 by binding to its outer pore region. This review will focus on the mechanisms by which venom-derived peptides interact with this portion of TRPV1 to control receptor functions and how these mechanisms can drive the development of new types of analgesics.
瞬时受体电位香草素 1 (TRPV1) 离子通道在外周伤害性通路中起着重要作用。TRPV1 是一种多模态受体,可被多种配体和疼痛刺激激活,如有害热和质子,并导致各种急性和慢性疼痛状况。因此,TRPV1 作为治疗各种疼痛状况的新的治疗靶点而备受关注。值得注意的是,从毒液动物中分离出的各种肽通过与 TRPV1 的外孔区域结合,有力且选择性地控制 TRPV1 的激活和抑制。这篇综述将集中讨论毒液衍生肽与 TRPV1 的这一部分相互作用以控制受体功能的机制,以及这些机制如何推动新型镇痛药的发展。