Institute of Biomedical Sciences, Academia Sinica, 128 Academia Road, Section 2, Taipei 115, Taiwan.
Pharmacol Ther. 2012 May;134(2):127-38. doi: 10.1016/j.pharmthera.2011.12.009. Epub 2011 Dec 30.
The acid-sensing ion channel 3 (ASIC3) is a pH sensor that responds to mild extracellular acidification and is predominantly expressed in nociceptors. There is much interest in targeting ASIC3 to relieve pain associated with tissue acidosis, and selective drugs targeting ASIC3 have been used to relieve acid-evoked pain in animal models and human studies. There is accumulating evidence that ASIC3 is widely expressed in many neuronal and non-neuronal cells, such as neurons in the brain and adipose cells, albeit to a lesser extent than in nociceptors. Asic3-knockout mice have reduced anxiety levels and enhanced insulin sensitivity, suggesting that antagonizing ASIC3 has additional benefits. This view is tempered by recent studies suggesting that Asic3-knockout mice may experience cardiovascular disturbances. Due to the development of ASIC3 antagonists as analgesics, we review here the additional benefits, safety, risks, and strategy associated with antagonizing ASIC3 function.
酸敏离子通道 3(ASIC3)是一种 pH 感受器,可对外界环境轻微酸化作出反应,主要表达于伤害感受器中。靶向 ASIC3 以缓解与组织酸中毒相关的疼痛受到了广泛关注,且已有选择性 ASIC3 靶向药物被用于缓解动物模型和人类研究中的酸诱发疼痛。越来越多的证据表明,ASIC3 在许多神经元和非神经元细胞中广泛表达,如大脑中的神经元和脂肪细胞,但表达程度低于伤害感受器。ASIC3 基因敲除小鼠的焦虑水平降低,胰岛素敏感性增强,这表明拮抗 ASIC3 具有额外的益处。然而,最近的研究表明,ASIC3 基因敲除小鼠可能会出现心血管紊乱,这对上述观点有所限制。鉴于 ASIC3 拮抗剂作为镇痛药的发展,我们在此综述了拮抗 ASIC3 功能的额外益处、安全性、风险和策略。