Kim Eojin, Choi Deok-Hyeong, Yi Young-Su
Department of Life Sciences, Kyonggi University, Suwon 16227, Republic of Korea.
Molecules. 2024 Dec 13;29(24):5900. doi: 10.3390/molecules29245900.
Quercetin is a natural polyphenolic flavonoid widely found in plants, fruits, and vegetables, and has been reported to play pharmacological roles in numerous pathogenic conditions. The anti-inflammatory effects of quercetin in various inflammatory conditions and diseases have been well-documented. However, its regulatory role in noncanonical inflammasome activation has not yet been demonstrated. This study investigated the anti-inflammatory effects of quercetin in caspase-11 noncanonical inflammasome-activated inflammatory responses in macrophages and a mouse model of acute lethal sepsis. Quercetin protected J774A.1 macrophages from lipopolysaccharide (LPS)-induced cell death and caspase-11 noncanonical inflammasome-induced pyroptosis. It significantly decreased the production and mRNA expression of pro-inflammatory cytokines, such as interleukin (IL)-1β, IL-18, and IL-6, but not tumor necrosis factor (TNF)-α, and inflammatory molecules, such as nitric oxide (NO) and inducible NO synthase in caspase-11 noncanonical inflammasome-activated J774A.1 cells. Mechanistically, quercetin strongly suppressed the autoproteolysis and secretion of caspase-11 and the proteolysis of gasdermin D in caspase-11 noncanonical inflammasome-activated J774A.1 cells. However, quercetin did not inhibit the direct binding of caspase-11 to LPS. In vivo, the study revealed that quercetin increased the survival rate of mice with acute lethal sepsis and decreased serum levels of pro-inflammatory cytokines without causing significant toxicity. In conclusion, this study highlights quercetin-mediated anti-inflammatory action in inflammatory responses and acute lethal sepsis through a novel mechanism that targets the caspase-11 noncanonical inflammasome in macrophages, suggesting quercetin as a promising anti-inflammatory agent in natural medicine.
槲皮素是一种天然多酚类黄酮,广泛存在于植物、水果和蔬菜中,据报道在多种致病条件下发挥药理作用。槲皮素在各种炎症条件和疾病中的抗炎作用已有充分记录。然而,其在非经典炎性小体激活中的调节作用尚未得到证实。本研究调查了槲皮素在巨噬细胞和急性致死性脓毒症小鼠模型中对caspase-11非经典炎性小体激活的炎症反应的抗炎作用。槲皮素保护J774A.1巨噬细胞免受脂多糖(LPS)诱导的细胞死亡和caspase-11非经典炎性小体诱导的细胞焦亡。它显著降低了促炎细胞因子如白细胞介素(IL)-1β、IL-18和IL-6的产生和mRNA表达,但不影响肿瘤坏死因子(TNF)-α,以及在caspase-11非经典炎性小体激活的J774A.1细胞中炎性分子如一氧化氮(NO)和诱导型NO合酶的产生。机制上,槲皮素强烈抑制caspase-11非经典炎性小体激活的J774A.1细胞中caspase-11的自蛋白水解和分泌以及gasdermin D的蛋白水解。然而,槲皮素并不抑制caspase-11与LPS的直接结合。在体内,该研究表明槲皮素提高了急性致死性脓毒症小鼠的存活率,并降低了促炎细胞因子的血清水平,且未引起明显毒性。总之,本研究通过一种靶向巨噬细胞中caspase-11非经典炎性小体的新机制,突出了槲皮素在炎症反应和急性致死性脓毒症中介导抗炎作用,表明槲皮素是天然药物中一种有前景的抗炎剂。