Bockstahler L E, Elespuru R K, Hitchins V M, Carney P G, Olvey K M, Lytle C D
Office of Science and Technology, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20857.
Photochem Photobiol. 1990 Apr;51(4):477-9. doi: 10.1111/j.1751-1097.1990.tb01740.x.
The capacity of human fibroblasts to support plaque formation by Herpes simplex virus following treatment of the cells with gilvocarcin V, a polyaromatic C-glycoside, plus near ultraviolet radiation (UVA, 320-400 nm) was examined. Gilvocarcin V, plus UVA radiation, effectively inhibited host cell capacity at concentrations five orders of magnitude lower than that of 8-methyoxypsoralen required for capacity inhibition at similar levels of UVA radiation. This result extends the observation of unusual biological potency of UVA-activated gilvocarcins from bacterial cells to human cells.
研究了用多环C-糖苷吉尔vocarcin V处理人成纤维细胞并结合近紫外辐射(UVA,320 - 400nm)后,人成纤维细胞支持单纯疱疹病毒形成斑块的能力。在与UVA辐射水平相似的情况下,吉尔vocarcin V加UVA辐射在比抑制能力所需的8-甲氧基补骨脂素浓度低五个数量级的浓度下,有效抑制宿主细胞能力。这一结果将UVA激活的吉尔vocarcin对细菌细胞的异常生物活性的观察扩展到了人类细胞。