Baturay N Z, Roque H
Department of Pharmaceutical Sciences, College of Pharmacy, St. John's University, Jamaica, New York 11439.
Teratog Carcinog Mutagen. 1991;11(4):195-202. doi: 10.1002/tcm.1770110404.
Bowman-Birk protease inhibitor (BBI), extracted from soybean flour, has been shown to protect cells from damage after UVC irradiation. BBI also reduces the number of transformed foci following exposure to the same doses of UVC irradiation. Proteins have been reported to act as antioxidants by their sheer intracellular bulk. In this study we assessed BBI's ability to attenuate UVC-irradiation-induced peroxidation. Balb c/3T3 cells, clone A31, subcloned by this laboratory were used. Treatment groups consisted of cells suspended in Hanks' Balanced Salt Solution with and without 100 micrograms/ml of a crude soybean extract containing the Bowman-Birk protease inhibitor. Cells were exposed to irradiation in suspension by using GE (G8T5) germicidal lamps which deliver predominantly 254 nm light at 0.385 J/m2/s as measured at the cell surface. Aliquots of UVC-exposed cells were homogenized in HBSS in the presence and absence of 100 micrograms/ml BBI with a motor-driven Teflon pestle and assayed for peroxidation. The results showed significant (P less than 0.0001) protection afforded by BBI against peroxidation at 1.16 (65%), 1.93 (60%, and 2.70 (48%) J/m2 of UVC irradiation. Transformation was reduced to 0.33 foci per dish at all levels of radiation exposure.
从大豆粉中提取的鲍曼-伯克蛋白酶抑制剂(BBI)已被证明能保护细胞免受紫外线C(UVC)照射后的损伤。BBI还能减少在相同剂量UVC照射后转化灶的数量。据报道,蛋白质因其在细胞内的大量存在而具有抗氧化作用。在本研究中,我们评估了BBI减轻UVC照射诱导的过氧化作用的能力。使用了本实验室亚克隆的Balb c/3T3细胞系A31克隆。处理组包括悬浮在汉克斯平衡盐溶液中的细胞,其中一组添加了100微克/毫升含有鲍曼-伯克蛋白酶抑制剂的粗大豆提取物,另一组未添加。细胞在悬浮状态下使用GE(G8T5)杀菌灯进行照射,该灯在细胞表面测得的主要发射波长为254纳米,光强为0.385焦耳/平方米/秒。将暴露于UVC的细胞等分试样在有和没有100微克/毫升BBI的情况下,用电动聚四氟乙烯杵在HBSS中匀浆,并检测过氧化情况。结果显示,在UVC照射剂量为1.16(65%)、1.93(60%)和2.70(48%)焦耳/平方米时,BBI对过氧化有显著(P小于0.0001)的保护作用。在所有辐射暴露水平下,转化灶减少到每平皿0.33个。