Qin Yan, Liu Qingqing, Wang Saiying, Wang Qinhui, Du Yaya, Yao Jingyue, Chen Yue, Yang Qi, Wu Yumei, Liu Shuibing, Zhao Minggao, Wei Gaofei, Yang Le
Precision Pharmacy and Drug Development Center, Department of Pharmacy, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Department of Pharmacology, School of Pharmacy, Air Force Medical University, Xi'an 710072, China.
ACS Pharmacol Transl Sci. 2024 Feb 16;7(4):1002-1012. doi: 10.1021/acsptsci.3c00282. eCollection 2024 Apr 12.
Chronic pain is a complex disease. It seriously affects patients' quality of life and imposes a significant economic burden on society. Santacruzamate A (SCA) is a natural product isolated from marine cyanobacteria in Panama. In this study, we first demonstrated that SCA could alleviate chronic inflammatory pain, pain-related anxiety, and depression emotions induced by complete Freund's adjuvant in mice while inhibiting microglial activation in the anterior cingulate cortex. Moreover, SCA treatment attenuated lipopolysaccharide (LPS)-induced inflammatory response by downregulating interleukin 1β and 6 (IL-1β and IL-6) and tumor necrosis factor-α (TNF-α) levels in BV2 cells. Furthermore, we found that SCA could bind to soluble epoxide hydrolase (sEH) through molecular docking technology, and the thermal stability of sEH was enhanced after binding of SCA to the sEH protein. Meanwhile, we identified that SCA could reduce the sEH enzyme activity and inhibit sEH protein overexpression in the LPS stimulation model. The results indicated that SCA could alleviate the development of inflammation by inhibiting the enzyme activity and expression of sEH to further reduce chronic inflammatory pain. Our study suggested that SCA could be a potential drug for treating chronic inflammatory pain.
慢性疼痛是一种复杂的疾病。它严重影响患者的生活质量,并给社会带来巨大的经济负担。圣克鲁扎酯A(SCA)是一种从巴拿马海洋蓝藻中分离出的天然产物。在本研究中,我们首先证明SCA可以减轻小鼠由完全弗氏佐剂诱导的慢性炎性疼痛、疼痛相关的焦虑和抑郁情绪,同时抑制前扣带回皮质中的小胶质细胞激活。此外,SCA处理通过下调BV2细胞中白细胞介素1β和6(IL-1β和IL-6)以及肿瘤坏死因子-α(TNF-α)的水平来减轻脂多糖(LPS)诱导的炎症反应。此外,我们发现SCA可以通过分子对接技术与可溶性环氧化物水解酶(sEH)结合,并且SCA与sEH蛋白结合后sEH的热稳定性增强。同时,我们确定SCA可以降低LPS刺激模型中的sEH酶活性并抑制sEH蛋白的过表达。结果表明,SCA可以通过抑制sEH的酶活性和表达来减轻炎症的发展,从而进一步减轻慢性炎性疼痛。我们的研究表明,SCA可能是一种治疗慢性炎性疼痛的潜在药物。