Department of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
S&K Therapeutics, Ajou University Campus Plaza 418, 199 Worldcup-ro, Yeongtong-gu, Suwon 16502, Korea.
ACS Chem Neurosci. 2022 Mar 16;13(6):818-833. doi: 10.1021/acschemneuro.1c00831. Epub 2022 Feb 23.
Aberrant activation of the Nod-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome plays an essential role in multiple diseases, including Alzheimer's disease (AD) and psoriasis. We report a novel small-molecule inhibitor, NLRP3-inhibitory compound 7 (NIC7), and its derivative, which inhibit NLRP3-mediated activation of caspase 1 along with the secretion of interleukin (IL)-1β, IL-18, and lactate dehydrogenase. We examined the therapeutic potential of NIC7 in a disease model of AD by analyzing its effect on cognitive impairment as well as the expression of dopamine receptors and neuronal markers. NIC7 significantly reversed the associated disease symptoms in the mice model. On the other hand, NIC7 did not reverse the disease symptoms in the imiquimod (IMQ)-induced disease model of psoriasis. This indicates that IMQ-based psoriasis is independent of NLRP3. Overall, NIC7 and its derivative have therapeutic prospects to treat AD or NLRP3-mediated diseases.
Nod 样受体家族 pyrin 域包含 3(NLRP3)炎性小体的异常激活在多种疾病中发挥着重要作用,包括阿尔茨海默病(AD)和银屑病。我们报告了一种新型小分子抑制剂 NLRP3 抑制化合物 7(NIC7)及其衍生物,它们可抑制 NLRP3 介导的半胱天冬酶 1 的激活以及白细胞介素(IL)-1β、IL-18 和乳酸脱氢酶的分泌。我们通过分析 NIC7 对认知障碍以及多巴胺受体和神经元标志物表达的影响,研究了其在 AD 疾病模型中的治疗潜力。NIC7 显著逆转了小鼠模型中的相关疾病症状。另一方面,NIC7 并未逆转咪喹莫特(IMQ)诱导的银屑病疾病模型中的疾病症状。这表明基于 IMQ 的银屑病与 NLRP3 无关。总体而言,NIC7 及其衍生物具有治疗 AD 或 NLRP3 介导的疾病的治疗前景。