Kariya K, Nakamura K, Nomoto K, Kobayashi Y, Namiki M
Department of Biochemistry, Kitasato University School of Medicine, Kanagawa, Japan.
Cancer Biother. 1995 Summer;10(2):139-45. doi: 10.1089/cbr.1995.10.139.
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.
卟啉衍生物,特别是二氢卟吩e6钠(FeCNa),可模拟超氧化物歧化酶(SOD)的作用。这种SOD活性是通过电子自旋共振(ESR)信号的降低以及作为O2-中间体的过氧化氢(H2O2)的增加来确定的。通过使用4-氨基安替比林进行显色反应来测定。用于癌症光动力疗法(PDT)的二氢卟吩e6钠(1)不显示SOD模拟活性。通过ESR分析确定,与牛红细胞SOD相比,FeCNa的比活性为1/7.5。二氢卟吩e6钠中的铁元素紧密包裹在分子中,不参与芬顿反应。FeCNa的SOD模拟活性对诸如pH冲击、加热和链霉蛋白酶消化等物理化学处理具有稳定性。对于患有氧化应激(OS)的荷癌大鼠,单次腹腔注射FeCNa可立即缓解OS,并且缓解持续24小时。随后给予FeCNa可在体内抑制癌症生长。