K Kariya, K Nakamura, K Nomoto, Y Kobayashi, M Namiki
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引用次数: 8
摘要
卟啉衍生物,特别是fe - chlorine6 - na (FeCNa),模拟超氧化物歧化酶(SOD)。通过电子自旋共振(ESR)信号的减少和过氧化氢(H2O2)作为O2-的中间体的增加来确定SOD的活性。用4-氨基安替比林着色。用于癌症光动力治疗(PDT)的氯- e6-Na(1)不显示SOD模拟活性。与牛红细胞超氧化物歧化酶相比,经ESR分析FeCNa的比活性为1/7.5。铁元素Fe-chlorin e6-Na被紧密包裹在分子中,没有参与Fenton反应。FeCNa对pH冲击、热和酶消化等理化处理的SOD模拟活性稳定。对于氧化应激(OS)的荷瘤大鼠,单次腹腔注射FeCNa可以立即缓解OS,并且持续24小时。随后给予FeCNa抑制体内肿瘤生长。
Superoxide dismutase (SOD) activity with Fe-chlorin e6-Na and suppression of malignant tumor growth in rats.
Derivatives of porphyrin, specifically Fe-chlorin e6-Na (FeCNa), mimic superoxide dismutase (SOD). This SOD activity was determined by decrease in electron spin resonance (ESR) signals and increase in hydrogen peroxide (H2O2) as the intermediate of O2-. by the coloration using 4-aminoantipyrin. Chlorin e6-Na used for cancer photodynamic therapy (PDT)(1) does not show SOD mimicking activity. The specific activity of FeCNa, comparing with bovine RBC-SOD, was 1/7.5 as determined by ESR analysis. The iron element of Fe-chlorin e6-Na, being tightly encased in the molecule, did not participate in the Fenton reaction. The SOD mimetic activity of FeCNa was stable against physico-chemical treatment such as pH shock, heat and digestion by pronase. For cancer bearing rats with oxidative stress (OS), immediate relief of OS was possible by a single intraperitoneal injection of FeCNa and relief continued for 24 hours. The subsequent administration of FeCNa suppressed cancer growth in vivo.