Research Institute of Pharmaceutical Sciences, Musashino University, 1-1-20 Shinmachi, Nishitokyo, Tokyo 202-8585, Japan.
Center for Medical Education, Sapporo Medical University, South-1 West-17, Chuo-ku, Sapporo, Hokkaido 060-8556, Japan.
J Clin Biochem Nutr. 2014 Sep;55(2):90-6. doi: 10.3164/jcbn.13-107. Epub 2014 Aug 5.
With the aim of developing effective anti-inflammatory drugs, we have been investigating the biochemical effects of shikonin of "Shikon" roots, which is a naphthoquinone with anti-inflammatory and antioxidative properties. Shikonin scavenged reactive oxygen species like hydroxyl radical, superoxide anion (O2 (•-)) and singlet oxygen in previous studies, but its reactivity with reactive oxygen species is not completely understood, and comparison with standard antioxidants is lacking. This study aimed elucidation of the reactivity of shikonin with nitric oxide radical and reactive oxygen species such as alkyl-oxy radical and O2 (•-). By using electron paramagnetic resonance spectrometry, shikonin was found unable of reacting with nitric oxide radical in a competition assay with oxyhemoglobin. However, shikonin scavenged alkyl-oxy radical from 2,2'-azobis(2-aminopropane) dihydrochloride with oxygen radical absorbance capacity, ORAC of 0.25 relative to Trolox, and showed a strong O2 (•-)-scavenging ability (42-fold of Trolox; estimated reaction rate constant: 1.7 × 10(5) M(-1)s(-1)) in electron paramagnetic resonance assays with CYPMPO as spin trap. Concerning another source of O2 (•-), the phagocyte NADPH oxidase (Nox2), shikonin inhibited the Nox2 activity by impairing catalysis when added before enzyme activation (IC50: 1.1 µM; NADPH oxidation assay). However, shikonin did not affect the preactivated Nox2 activity, although having potential to scavenge produced O2 (•-). In conclusion, shikonin scavenged O2 (•-) and alkyl-oxy radical, but not nitric oxide radical.
为了开发有效的抗炎药物,我们一直在研究“紫草”根中的萘醌类化合物紫草素的生化作用,它具有抗炎和抗氧化作用。在以前的研究中,紫草素清除了羟自由基、超氧阴离子 (O2 (•-)) 和单线态氧等活性氧,但对其与活性氧的反应性还不完全了解,也缺乏与标准抗氧化剂的比较。本研究旨在阐明紫草素与一氧化氮自由基和活性氧如烷氧基自由基和 O2 (•-) 的反应性。通过使用电子顺磁共振波谱法,发现紫草素在与氧合血红蛋白的竞争测定中不能与一氧化氮自由基反应。然而,紫草素从 2,2'-偶氮双(2-氨基丙烷)二盐酸盐中清除烷氧基自由基,其氧自由基吸收能力(ORAC)为 Trolox 的 0.25,在以 CYPMPO 为自旋捕获剂的电子顺磁共振测定中表现出很强的 O2 (•-)-清除能力(Trolox 的 42 倍;估计反应速率常数:1.7×10(5) M(-1)s(-1))。关于另一种 O2 (•-)来源,吞噬细胞 NADPH 氧化酶 (Nox2),紫草素在酶激活前加入时通过损害催化作用抑制 Nox2 活性(IC50:1.1 µM;NADPH 氧化测定)。然而,尽管紫草素有潜力清除产生的 O2 (•-),但它不影响预激活的 Nox2 活性。总之,紫草素清除了 O2 (•-)和烷氧基自由基,但不能清除一氧化氮自由基。