Srisook Klaokwan, Srisook Ekaruth, Nachaiyo Wenuka, Chan-In Mingkwan, Thongbai Jitra, Wongyoo Karnjanapa, Chawsuanthong Sasithorn, Wannasri Kanita, Intasuwan Sudarat, Watcharanawee Kingkan
Department of Biochemistry, Faculty of Science, Burapha University, Muang, Chonburi 20131, Thailand; Centre of Excellence for Innovation in Chemistry, Burapha University, Muang, Chonburi 20131, Thailand.
Centre of Excellence for Innovation in Chemistry, Burapha University, Muang, Chonburi 20131, Thailand; Department of Chemistry, Faculty of Science, Burapha University, Muang, Chonburi 20131, Thailand.
J Ethnopharmacol. 2015 May 13;165:94-102. doi: 10.1016/j.jep.2015.02.043. Epub 2015 Feb 26.
The leaves of Clerodendrum inerme (L.) Gaertn. have commonly been used in Thai traditional medicine for treatment of inflammatory diseases. However, the bioactive compounds responsible for the anti-inflammatory effect of leaves have not been yet determined. The objective of the present study was to isolate these bioactive compounds by bioassay-guided isolation technique and to determine the mode of action of isolated compounds in LPS-induced macrophages.
Anti-inflammatory effect of various fractions (hexane, ethyl acetate and water) of ethanol extract of C. inerme leaves was determined from the production of nitric oxide (NO) in RAW 264.7 macrophage stimulated with LPS. The mRNA and protein levels were determined also by real-time reverse transcription-polymerase chain reaction and western blot analysis, respectively. Leaf bioactive compounds were isolated by bioassay-guided fractionation technique using column chromatography.
The ethyl acetate fraction (EA) among solvent extracts provided the most potent inhibitory activity on NO production. Also, EA reduced the mRNA and protein expressions of inducible nitric oxide synthase (iNOS) in LPS-stimulated macrophages. Three known flavones, acacetin (1), hispidulin (2) and diosmetin (3), were isolated based on inhibition of NO production. Furthermore, hispidulin also inhibited PGE2 production as well as iNOS and cyclooxygenase-2 expressions via the blockade of NF-κB DNA-binding activity and JNKway.
Our results found acacetin (1), hispidulin (2) and diosmetin (3), were responsible for the anti-inflammatory properties of C. inerme leaves. We provide scientific evidence to support the usefulness of C. inerme leaves in traditional medicine for the treatment of inflammation-related diseases.
假茉莉(Clerodendrum inerme (L.) Gaertn.)的叶子在泰国传统医学中常用于治疗炎症性疾病。然而,叶子抗炎作用的生物活性化合物尚未确定。本研究的目的是通过生物测定引导的分离技术分离这些生物活性化合物,并确定分离化合物在脂多糖诱导的巨噬细胞中的作用模式。
从脂多糖刺激的RAW 264.7巨噬细胞中一氧化氮(NO)的产生来测定假茉莉叶乙醇提取物的各种馏分(己烷、乙酸乙酯和水)的抗炎作用。mRNA和蛋白质水平也分别通过实时逆转录-聚合酶链反应和蛋白质印迹分析来测定。通过柱色谱法采用生物测定引导的分级分离技术分离叶生物活性化合物。
溶剂提取物中的乙酸乙酯馏分(EA)对NO产生具有最强的抑制活性。此外,EA降低了脂多糖刺激的巨噬细胞中诱导型一氧化氮合酶(iNOS)的mRNA和蛋白质表达。基于对NO产生的抑制作用,分离出三种已知的黄酮,即刺槐素(1)、圣草素(2)和香叶木素(3)。此外,圣草素还通过阻断NF-κB DNA结合活性和JNK途径抑制前列腺素E2的产生以及iNOS和环氧化酶-2的表达。
我们的结果发现刺槐素(1)、圣草素(2)和香叶木素(3)是假茉莉叶抗炎特性的原因。我们提供了科学证据来支持假茉莉叶在传统医学中治疗炎症相关疾病的有效性。