Hanson W R, Thomas C
Radiat Res. 1983 Nov;96(2):393-8.
A variety of prostaglandins (PG) protect the gastric and intestinal mucosa when given before damaging agents such as absolute ethanol, acidified taurocholate, boiling water, or nonsteroidal anti-inflammatory agents (NSAI). A synthetic prostaglandin, 16, 16-dimethyl PGE2, shown to be cytoprotective at physiologic levels to the above agents was given to mice 1 hr before or 15 min after 137Cs gamma (gamma) whole-body irradiation. The survival of intestinal stem cells measured by their ability to form in situ colonies of regenerating epithelium was increased when 16, 16-dimethyl PGE2 was given before but not after 137Cs gamma irradiation. The maximum degree of 16, 16-dimethyl PGE2-induced radioprotection was seen when the drug was given 1 hr before irradiation. No radioprotection was seen when the interval between drug and irradiation was 3 hr or longer. When the time between 16, 16-dimethyl PGE2 and irradiation was kept at 1 hr, the degree of radioprotection was dependent on the PG drug dose. There was a steep rise in the number of surviving cells at low doses of PG. These results imply that tumors which secrete PGE2 may in part be protected from the lethal effects of ionizing photon radiation.
在给予绝对乙醇、酸化牛磺胆酸盐、沸水或非甾体抗炎药(NSAI)等损伤剂之前给予多种前列腺素(PG)可保护胃和肠黏膜。一种合成前列腺素16,16-二甲基PGE2在生理水平对上述试剂具有细胞保护作用,在137Csγ全身照射前1小时或照射后15分钟给予小鼠。通过其形成原位再生上皮集落的能力来测量的肠干细胞存活率,在137Csγ照射前给予16,16-二甲基PGE2时增加,而在照射后给予则未增加。当在照射前1小时给予药物时,可观察到16,16-二甲基PGE2诱导的最大程度的辐射防护。当药物与照射之间的间隔为3小时或更长时间时,未观察到辐射防护作用。当16,16-二甲基PGE2与照射之间的时间保持在1小时时,辐射防护程度取决于PG药物剂量。在低剂量的PG时,存活细胞数量急剧上升。这些结果表明,分泌PGE2的肿瘤可能部分免受电离光子辐射的致死效应。