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肼屈嗪对小鼠FSall肿瘤微循环功能和热反应的剂量依赖性影响。

Dose-dependent effects of hydralazine on microcirculatory function and hyperthermic response of murine FSall tumors.

作者信息

Kalmus J, Okunieff P, Vaupel P

机构信息

Department of Radiation Medicine, Massachusetts General Hospital, Harvard Medical School, Boston 02114.

出版信息

Cancer Res. 1990 Jan 1;50(1):15-9.

PMID:2293549
Abstract

The effects of the vasodilator hydralazine (HYD) on microcirculatory function and hyperthermic response were studied in early generation isotransplants of a spontaneous C3Hf/Sed mouse fibrosarcoma (FSall). Red blood cell flux (RBC flux) in superficial tumor regions was assessed using laser Doppler flowmetry. A differential microcirculatory response was seen between tumor and normal skin after 0.25 micrograms/g i.p. HYD, the tumor showing a transient increase in flow and the skin remaining almost stable. At 1.0 micrograms/g i.p., the differential response continued, this time with a transient fall in tumor blood flow but again no change in skin flow. High dose hydralazine (10.0 micrograms/g i.p.) was associated with a dramatic and prolonged decrease in tumor blood flow but a lesser and only transient decline in skin flow. Identical doses of hydralazine were given 30 min prior to heat treatment (43.5 degrees C for 15, 30, or 60 min). Tumor growth was measured daily and compared to controls (HT without hydralazine). Hydralazine at 0.25 micrograms/g i.p. did not affect heat induced growth delay. At 1.0 micrograms/g i.p., it significantly increased growth delay upon heat exposures of 15 min, but not after 30 or 60 min HT. Hydralazine at 10 micrograms/g i.p. increased growth delay for all heat doses (P less than 0.05). Hydralazine alone had no influence on growth delay of sham-heated tumors. The results obtained clearly indicate that tumor and normal tissues have microcirculatory differences in the time-course, degree and/or direction of response after hydralazine, and that hydralazine has potential for increasing the response of tumor to HT.

摘要

研究了血管扩张剂肼屈嗪(HYD)对自发C3Hf/Sed小鼠纤维肉瘤(FSall)早期同基因移植瘤的微循环功能和热反应的影响。使用激光多普勒血流仪评估浅表肿瘤区域的红细胞通量(RBC通量)。腹腔注射0.25微克/克HYD后,肿瘤和正常皮肤出现不同的微循环反应,肿瘤血流短暂增加,而皮肤血流几乎保持稳定。腹腔注射1.0微克/克时,这种差异反应持续存在,此时肿瘤血流短暂下降,但皮肤血流再次无变化。高剂量肼屈嗪(腹腔注射10.0微克/克)与肿瘤血流显著且持续减少有关,但皮肤血流减少程度较小且仅为短暂性。在热处理(43.5℃,持续15、30或60分钟)前30分钟给予相同剂量的肼屈嗪。每天测量肿瘤生长情况,并与对照组(未用肼屈嗪的热处理组)进行比较。腹腔注射0.25微克/克的肼屈嗪不影响热诱导的生长延迟。腹腔注射1.0微克/克时,在15分钟热暴露后显著增加生长延迟,但在30或60分钟热处理后则无此作用。腹腔注射10微克/克的肼屈嗪对所有热剂量均增加生长延迟(P<0.05)。单独使用肼屈嗪对假加热肿瘤的生长延迟无影响。获得的结果清楚地表明,肿瘤和正常组织在注射肼屈嗪后的时间进程、反应程度和/或方向上存在微循环差异,并且肼屈嗪具有增强肿瘤对热处理反应的潜力。

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