Liu Xu, Zhang Jiang-Tao, Hu Yue, Shan Wen-Qi, Wang Zhi-Hong, Fu Qing-Yue, Fu Dan-Ni, Ji Jiang, Liu Tong
Department of Dermatology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Jiangsu Key Laboratory of Neuropsychiatric Diseases and Institute of Neuroscience, Soochow University, Suzhou, China.
Front Med (Lausanne). 2021 Feb 15;8:627725. doi: 10.3389/fmed.2021.627725. eCollection 2021.
Chronic itch is a common distressing symptom of many diseases, which reduced patient's quality of life. The mechanistic study on itch and screening for new anti-itch drugs require the development of new pre-clinical itch animal models. Herein, we established an acute itch model by intradermal (i.d.) injection of low-dose formalin into the neck or cheek in mice. In mice, i.d. injection of formalin (0.1-5%) in the nape of the neck evoked robust scratching behavior in a dose-dependent manner and the dose-response curves showed an inverted "U" shape. I.d. injection of formalin (0.3-0.6%) into the cheek evoked scratching in mice but wiping in rats, while formalin (1.25-5%) induced mixed wiping and scratching behavior in both mice and rats. Further, we found that 0.3% formalin-induced scratching was histamine-independent and significantly attenuated by transient receptor potential ion channel A1 (TRPA1) inhibitor (HC030031) or in TRPA1 knockout (KO) mice, but not affected by transient receptor potential ion channel V1 (TRPV1) inhibitor (capsazepine) or in TRPV1 KO mice. Additionally, 0.3% formalin-induced up-regulation of phosphorylation of extracellular regulated protein kinases (p-ERK) in the dorsal root ganglion (DRG) and scratching were suppressed by intrathecal injection of MEK inhibitor U0126 in mice. Incubation of 0.03% formalin induced the accumulation of intracellular reactive oxygen species (ROS) in the cultured DRG-derived cell line ND7-23, and formalin-induced itch was suppressed by antioxidants in mice. Finally, perfusion of 0.03% formalin induced elevation of intracellular calcium in a subset of primary cultured DRG neurons of mice. Thus, these results indicate that low-dose formalin induced non-histaminergic itch by activation of TRPA1 in mice, which may be employed as a useful acute itch model for screening potential anti-itch drugs.
慢性瘙痒是许多疾病常见的令人苦恼的症状,会降低患者的生活质量。对瘙痒的机制研究以及新型抗瘙痒药物的筛选需要开发新的临床前瘙痒动物模型。在此,我们通过向小鼠颈部或脸颊皮内注射低剂量福尔马林建立了急性瘙痒模型。在小鼠中,在颈部皮内注射福尔马林(0.1 - 5%)以剂量依赖的方式诱发强烈的搔抓行为,剂量 - 反应曲线呈倒“U”形。向小鼠脸颊皮内注射福尔马林(0.3 - 0.6%)会诱发搔抓行为,而向大鼠脸颊注射则诱发擦抹行为,福尔马林(1.25 - 5%)在小鼠和大鼠中均诱发擦抹和搔抓混合行为。此外,我们发现0.3%福尔马林诱发的搔抓行为不依赖组胺,并且在瞬时受体电位离子通道A1(TRPA1)抑制剂(HC030031)作用下或在TRPA1基因敲除(KO)小鼠中显著减弱,但不受瞬时受体电位离子通道V1(TRPV1)抑制剂(辣椒素)作用影响,也不受TRPV1 KO小鼠影响。另外,鞘内注射MEK抑制剂U0126可抑制小鼠中0.3%福尔马林诱发的背根神经节(DRG)中细胞外调节蛋白激酶(p - ERK)磷酸化上调及搔抓行为。0.03%福尔马林孵育可诱导培养的DRG衍生细胞系ND7 - 23中细胞内活性氧(ROS)积累,且小鼠中抗氧化剂可抑制福尔马林诱发的瘙痒。最后,灌注0.03%福尔马林可诱导小鼠原代培养DRG神经元亚群中细胞内钙升高。因此,这些结果表明低剂量福尔马林通过激活小鼠中的TRPA1诱导非组胺能瘙痒,这可作为筛选潜在抗瘙痒药物的有用急性瘙痒模型。