Cao H, Zhang W, Li M, Yang Y, Li Y
Anhui Provincial Key Laboratory of Cancer Research and Clinical Laboratory Diagnosis, school of laboratory Medicine, Bengbu Medical College, Bengbu 233030, China.
Clinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2023 Sep 20;43(9):1476-1484. doi: 10.12122/j.issn.1673-4254.2023.09.04.
To investigate the effect of Isodopharicin C (Iso C), a traditional Chinese herbal medicine extract, on NLRP3 inflammasome activation and lipopolysaccharide (LPS)-induced septic shock in mice.
Murine bone marrow-derived macrophages (BMDM) and human monocytic THP-1 cells were stimulated with LPS before treatment with different NLRP3 inflammasome agonists to activate canonical NLRP3 inflammasomes. The non-canonical NLRP3 inflammasomes were activated by intracellular LPS transfection, and AIM2 inflammasomes were activated with poly A: T. The cleavage of caspase-1 induced by NLRP3 activation was measured using Western blotting. The levels of NLRP3-dependent and -independent pro-inflammatory cytokines in the cell culture supernatant were detected using ELISA, and the intracellular potassium ion concentration was measured using ICP-OES. In the animal experiment, C57BL/6J mouse models of septic shock (induced by intraperitoneal LPS injection) were treated with Iso C, and the levels of IL-1β, TNF-α and IL-6 in the serum and peritoneal lavage fluid were detected using ELISA. The survival time of the mice was observed within 48 h after LPS injection and a survival curve was plotted.
In BMDM cells, Iso C dose-dependently inhibited the activation of canonical NLRP3 inflammasomes and non-canonical NLRP3 inflammasomes (<0.05) without obviously affecting the secretion levels of TNF-α and IL-6 (>0.05), the activation of AIM2 inflammasomes (>0.05), or K + efflux, the upstream signaling of NLRP3 activation (>0.05). Iso C inhibited the activation of canonical NLRP3 inflammasomes in human THP-1 cells. In septic C57BL/6J mice, Iso C treatment significantly reduced IL-1β levels in the serum and peritoneal lavage fluid, and prolonged the survival time of the mice (<0.05).
Iso C specifically inhibits NLRP3 inflammasome activation and alleviates septic shock in mice, and can serve as a potential small molecule compound for treatment of inflammatory diseases.
研究中药提取物异佛手柑内酯C(Iso C)对小鼠NLRP3炎性小体激活及脂多糖(LPS)诱导的脓毒症休克的影响。
在用不同的NLRP3炎性小体激动剂处理之前,用LPS刺激小鼠骨髓来源的巨噬细胞(BMDM)和人单核细胞THP-1细胞,以激活经典NLRP3炎性小体。通过细胞内LPS转染激活非经典NLRP3炎性小体,并用聚A:T激活AIM2炎性小体。使用蛋白质印迹法检测NLRP3激活诱导的caspase-1裂解。使用酶联免疫吸附测定法(ELISA)检测细胞培养上清液中NLRP3依赖性和非依赖性促炎细胞因子的水平,并使用电感耦合等离子体质谱法(ICP-OES)测量细胞内钾离子浓度。在动物实验中,用Iso C处理脓毒症休克的C57BL/6J小鼠模型(通过腹腔注射LPS诱导),并使用ELISA检测血清和腹腔灌洗液中IL-1β、TNF-α和IL-6的水平。观察LPS注射后48小时内小鼠的存活时间,并绘制生存曲线。
在BMDM细胞中,Iso C剂量依赖性地抑制经典NLRP3炎性小体和非经典NLRP3炎性小体的激活(P<0.05),而不明显影响TNF-α和IL-6的分泌水平(P>0.05)、AIM2炎性小体的激活(P>0.05)或K+外流,即NLRP3激活的上游信号(P>0.05)。Iso C抑制人THP-1细胞中经典NLRP3炎性小体的激活。在脓毒症C57BL/6J小鼠中,Iso C治疗显著降低血清和腹腔灌洗液中IL-1β水平,并延长小鼠存活时间(P <0.05)。
Iso C特异性抑制NLRP3炎性小体激活并减轻小鼠脓毒症休克,可作为治疗炎症性疾病的潜在小分子化合物。