Suppr超能文献

在反复用缓激肽注射肿瘤后,肿瘤中单核细胞聚集,生长减缓,宿主脾脏组氨酸脱羧酶活性升高。

Accumulation of mononuclear cells in tumors with growth slowing and elevation in host splenic histidine decarboxylase activity following repeated tumor injections with bradykinin.

作者信息

Koppelmann L E, Moore T C, Lemmi C A, Porter D D

出版信息

Surgery. 1975 Aug;78(2):181-9.

PMID:1154262
Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验