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Pharmacological reactivity of neoplastic and non-neoplastic associated neovasculature to vasoconstrictors

机译:肿瘤和非肿瘤相关新脉管系统对血管收缩剂的药理反应

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摘要

Angiogenesis and the pharmacological responses of the tumour and non-tumour associated neovasculature have been investigated. Cannulated sponge discs in mice were used to host the angiogenic stimulators, while 133Xe washout was employed to assess local blood flow. Enhancement of blood flow was detected in implants bearing B16 cells, 3T3 cells and angiotensin II (AII)-treated at day 7. The responses of non-neoplastic associated neovasculature at day 14 post sponge implantation to the vasoconstrictors used endothelin-1 (Et-1), AII, platelet activating factor (PAF) and 5-hydroxytryptamine (5-HT) were dose-dependent. By contrast, the newly formed blood vessels induced by tumour cells were markedly insensitive to the vasoconstrictors agonists Et-1 and AII, while fully responsive to PAF and 5-HT. The vessels resulting from neoplastic stimulus exhibited altered pharmacological reactivity, suggesting that the characteristics of the neovasculature are dependent on the nature of the angiogenic stimuli.
机译:已经研究了肿瘤和与非肿瘤相关的新脉管系统的血管生成和药理反应。小鼠中的空心海绵盘用于容纳血管生成刺激剂,而 133 Xe洗脱用于评估局部血流。在第7天,检测到带有B16细胞,3T3细胞和血管紧张素II(AII)处理的植入物的血流增强。海绵植入后第14天,非肿瘤相关新脉管系统对使用内皮素-1(Et- 1),AII,血小板活化因子(PAF)和5-羟色胺(5-HT)是剂量依赖性的。相比之下,由肿瘤细胞诱导的新形成的血管对血管收缩激动剂Et-1和AII明显不敏感,而对PAF和5-HT完全敏感。由肿瘤刺激产生的血管表现出改变的药理反应性,表明新脉管系统的特征取决于血管生成刺激的性质。

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