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在温和温度下,热疗可增加肿瘤氧合作用。1996年。

Tumour oxygenation is increased by hyperthermia at mild temperatures. 1996.

作者信息

Song C W, Shakil A, Osborn J L, Iwata K

机构信息

Department of Therapeutic Radiology, University of Minnesota Medical School, Minneapolis, MN, USA.

出版信息

Int J Hyperthermia. 2009 Mar;25(2):91-5. doi: 10.1080/02656730902744171.

Abstract

The effects of hyperthermia on the oxygenation status in R3230 AC tumours of Fischer rats were measured using a polarographic oxygen electrode system. The median pO(2) in about 10 mm diameter tumours grown s.c. in the leg of rats was 3.7 +/- 0.3 mm Hg and it significantly increased upon heating at modest temperatures. For example, the tumour pO(2) measured within 10-15 min after heating for 30 min at 42.5 degrees C was about three-fold greater than that in the control tumours. About 62% of pO(2) values measured in control tumours were <5 mm Hg. After heating at 42.5 degrees C for 30 min, 37% of pO(2) values were <5 mm Hg. Such an increase in tumour oxygenation or reoxygenation of hypoxic cells appeared to result from an increase in tumour blood flow caused by the mild temperature hyperthermia. The presence of hypoxic cells in tumours is believed to be a major factor in limiting the effectiveness of radiotherapy, certain chemotherapy drugs and phototherapy. Hyperthermia at mild temperatures easily achievable with the use of presently available clinical hyperthermia devices may be an effective means to overcome the hypoxic protection in the treatment of human tumours.

摘要

使用极谱氧电极系统测量了热疗对Fischer大鼠R3230 AC肿瘤氧合状态的影响。在大鼠腿部皮下生长的直径约10 mm的肿瘤中,中位pO₂为3.7±0.3 mmHg,在适度温度加热后显著升高。例如,在42.5℃加热30分钟后10 - 15分钟内测量的肿瘤pO₂比对照肿瘤中的约大三倍。对照肿瘤中测量的pO₂值约62%<5 mmHg。在42.5℃加热30分钟后,37%的pO₂值<5 mmHg。肿瘤氧合或缺氧细胞的再氧合增加似乎是由轻度温度热疗引起的肿瘤血流增加所致。肿瘤中缺氧细胞的存在被认为是限制放射治疗、某些化疗药物和光疗有效性的主要因素。使用目前可用的临床热疗设备容易实现的轻度温度热疗可能是克服人类肿瘤治疗中缺氧保护的有效手段。

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