Sun Xiao, Shim Do-Wan, Han Ji-Won, Shin Woo-Young, Sim Eun-Jeong, Kim Myong-Ki, Heo Kang-Hyuck, Kim Young-Kyu, Koppula Sushruta, Kim Tack-Joong, Kang Tae-Bong, Lee Kwang-Ho
Department of Biotechnology, College of Biomedical & Health Science, Konkuk University, Chungju, Republic of Korea.
Department of Food Science and Engineering, Seowon University, Cheongju, Republic of Korea.
J Ethnopharmacol. 2015 Jul 21;170:81-7. doi: 10.1016/j.jep.2015.05.001. Epub 2015 May 11.
Impatiens textori Miq. (I. textori, Balsaminaceae) is a traditional medicinal herb used for centuries to treat several inflammatory related skin infections and allergic disorders in Asian countries.
In this study, we elucidated the effects of whole plant extracts of I. textori on inflammasome activation using in vitro and in vivo models.
LPS-stimulated murine bone marrow macrophages were used to study the regulatory effect of I. textori extract (IT) on inflammasome activation. ATP, nigericin and MSU were used as danger-associated molecules to activate the NLRP3 inflammasome. An LPS-induced acute lung injury (ALI) mouse model was used to study the in vivo effect of IT on inflammasome activation.
IT treated at 25, 50, and 100μg/mL concentrations suppressed interleukin-1β secretion through the attenuation of NLRP3 inflammasome activation (p<0.001 at 100μg/mL) leading to the decreased amount of ASC oligomerization and caspase-1 maturation. For the in vivo model, IT inhibited the NLRP3 expression and cell recruitment at the lung tissue in the ALI mouse model.
IT exhibited potent anti-inflammatory effects via the attenuation of NLRP3 inflammasome activation supporting the traditional claims and may provide a valuable therapeutic strategy in treating various inflammation-related disorders.
长萼凤仙花(凤仙花科)是一种传统草药,在亚洲国家已有数百年用于治疗多种炎症相关皮肤感染和过敏性疾病的历史。
在本研究中,我们使用体外和体内模型阐明了长萼凤仙花全株提取物对炎性小体激活的影响。
使用脂多糖刺激的小鼠骨髓巨噬细胞研究长萼凤仙花提取物(IT)对炎性小体激活的调节作用。使用三磷酸腺苷、尼日利亚菌素和尿酸钠作为危险相关分子来激活NLRP3炎性小体。使用脂多糖诱导的急性肺损伤(ALI)小鼠模型研究IT对炎性小体激活的体内作用。
浓度为25、50和100μg/mL的IT通过减弱NLRP3炎性小体激活抑制白细胞介素-1β分泌(100μg/mL时p<0.001),导致凋亡相关斑点样蛋白寡聚化和半胱天冬酶-1成熟量减少。对于体内模型,IT在ALI小鼠模型中抑制肺组织中的NLRP3表达和细胞募集。
IT通过减弱NLRP3炎性小体激活表现出强大的抗炎作用,支持了传统说法,并可能为治疗各种炎症相关疾病提供有价值的治疗策略。