Koppelmann L E, Moore T C, Lemmi C A, Porter D D
Surgery. 1975 Aug;78(2):181-9.
Repeated intratumor injections of SV-40 virus-induced and transplaned syngenic fibrosarcomsa in hamsters with bradykinin (BK) has produced markded slowing of tumor growth in comparison with control saline injections. Growth slowing was greatest when the injections were daily, with a decrease in growth slowing as injections became less frequent. The growth slowing also was dose dependent (greater with 250 mug BK injections than with 50 mug BK injections). BK-injected tumors, on histological study, were found to have marked infiltration with mononuclear cells. This was not encountered in noninjected or saline-injected tumors. Significant mononuclear cell infiltration of noninjected tumors was found in two tumor animals which had had one tumor injectecd with BK. Splenic histidine decarboxylase (HDC) activity was higher in BK tumor-injected animals than in saline tumor-injected animals. Splenic HDC activity was higher when studed nearer the period of daily intratumor injections. The findings of this study suggest a potential role of inportance for inter-related vasoactive substances which act as mediators of inflammation in the study and therapy of neoplasia.
在仓鼠体内,对由SV - 40病毒诱导并移植的同基因纤维肉瘤反复进行瘤内注射缓激肽(BK),与注射对照生理盐水相比,已使肿瘤生长明显减缓。当每天注射时,生长减缓最为显著,随着注射频率降低,生长减缓程度减小。生长减缓也呈剂量依赖性(250微克BK注射比50微克BK注射的生长减缓更明显)。经组织学研究发现,注射BK的肿瘤有明显的单核细胞浸润。在未注射或注射生理盐水的肿瘤中未发现这种情况。在两只肿瘤动物中,其中一个肿瘤注射了BK,未注射的肿瘤也出现了显著的单核细胞浸润。注射BK肿瘤的动物脾脏组氨酸脱羧酶(HDC)活性高于注射生理盐水肿瘤的动物。在更接近每天瘤内注射期间进行研究时,脾脏HDC活性更高。本研究结果表明,相互关联的血管活性物质在肿瘤形成的研究和治疗中作为炎症介质可能具有重要作用。