Moriya N
Nihon Geka Gakkai Zasshi. 1985 Nov;86(11):1470-9.
Using C3H/He mice, the antitumor effect and mechanism of lipopolysaccharide (LPS) were studied. The antitumor effect of rabbit serum containing tumor necrosis factor (TNF) was also studied. LPS and TNF, which were administered into mice with tumors, induced hemorrhagic necrosis. LPS and TNF significantly inhibited the tumor growth, as compared with findings in the controls. In the initial stage after LPS administration, dilatation of tumor vessels and thrombus formation in tumor vessels were observed in the histologic study. Tumor blood flow was measured by the hydrogen clearance technique. Tumor blood flow was very small, and was remarkably decreased at 2 hours after LPS administration. These results suggest that hemorrhagic necrosis after LPS administration was due to the decrease of the tumor blood flow. In the study in vitro, YAC-1 cells were damaged but K562 cells were not damaged by rabbit serum containing TNF. In order to find the effect of LPS or TNF on cellular immunity, the delayed type hypersensitivity (DTH) was studied. LPS and TNF prevented the decrease of DTH in the tumor bearing mice on day 25.
利用C3H/He小鼠,研究了脂多糖(LPS)的抗肿瘤作用及其机制。还研究了含肿瘤坏死因子(TNF)的兔血清的抗肿瘤作用。将LPS和TNF注射到荷瘤小鼠体内后,诱导了出血性坏死。与对照组相比,LPS和TNF显著抑制了肿瘤生长。在给予LPS后的初始阶段,组织学研究观察到肿瘤血管扩张和肿瘤血管内血栓形成。采用氢清除技术测量肿瘤血流量。肿瘤血流量非常小,在给予LPS后2小时显著降低。这些结果表明,给予LPS后出现的出血性坏死是由于肿瘤血流量减少所致。在体外研究中,含TNF的兔血清可损伤YAC-1细胞,但不损伤K562细胞。为了研究LPS或TNF对细胞免疫的影响,对迟发型超敏反应(DTH)进行了研究。LPS和TNF可防止荷瘤小鼠在第25天时DTH的降低。