Matsui H, Setogawa T, Naora H, Tanaka O
Department of Ophthalmology, Shimane Medical University, Japan.
Histol Histopathol. 1995 Jan;10(1):47-54.
The antiteratogenic effects of PSK, a biological response modifier, were examined using histological and developmental analysis. The whole bodies of pregnant mice were irradiated with X-rays and injected with PSK within ten minutes after irradiation on day 7 of gestation (E7). The foetuses on E18 were examined and a high incidence of malformations were observed in X-ray irradiated embryos. Microphthalmia was the most frequent malformation. PSK administration suppressed the X-ray irradiation-induced ocular anomalies in not only the frequency, as deduced by external observation, but also in histopathological changes in the retina, lens, and cornea. In particular, the incidence of lens aplasia was significantly decreased by PSK administration. Developmental analysis using E10 and E13 embryos revealed that the decrease in the incidence of histopathological changes was first observed within 72 hours after PSK administration. In addition, X-ray irradiation-induced early foetal death (E10-13) was also suppressed by PSK administration. The possible mechanisms of the antiteratogenic effects of PSK are discussed.
使用组织学和发育分析方法研究了生物反应调节剂PSK的抗致畸作用。在妊娠第7天(E7),对怀孕小鼠全身进行X射线照射,并在照射后十分钟内注射PSK。检查E18期的胎儿,在接受X射线照射的胚胎中观察到高畸形发生率。小眼畸形是最常见的畸形。给予PSK不仅抑制了X射线照射引起的眼部异常的频率(通过外部观察推断),而且抑制了视网膜、晶状体和角膜的组织病理学变化。特别是,给予PSK后晶状体发育不全的发生率显著降低。使用E10和E13胚胎进行的发育分析表明,组织病理学变化发生率的降低在给予PSK后72小时内首次观察到。此外,给予PSK也抑制了X射线照射引起的早期胎儿死亡(E10 - 13)。讨论了PSK抗致畸作用的可能机制。