首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >STROMA-FREE HUMAN HEMOGLOBIN A DECREASES R3230AC RAT MAMMARY ADENOCARCINOMA BLOOD FLOW AND OXYGEN PARTIAL PRESSURE
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STROMA-FREE HUMAN HEMOGLOBIN A DECREASES R3230AC RAT MAMMARY ADENOCARCINOMA BLOOD FLOW AND OXYGEN PARTIAL PRESSURE

机译:无Strroma的人类血红蛋白A降低R3230AC大鼠乳腺腺癌的血流和氧分压

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We examined the effect of a nitric oxide (NO) quencher, stroma-free human hemoglobin A (HbA(0); 0.01, 0.05, 0.1, 0.2 g/kg), on the blood flow measured using the Doppler flow technique, tumor oxygen pressure (pO(2)) and the diameter of the arterioles using R3230Ac mammary adenocarcinoma as the tumor model. In female Fischer 344 rats with 1-cm-diameter tumors implanted in the lateral aspect of the left quadriceps, intravenous infusion of 0.1 and 0.2 g/kg HbA(0) decreased both central tumor and peripheral tumor blood flow by 20-30% (P < 0.05). Tumor pO(2) decreased 28% with 0.2 g/kg HbA(0), from 15 mm Hg (baseline) to 11 mm Hg at 10 min (P = 0.02). Although 0.2 g/kg HbA(0) increased blood flow 55% in the left quadriceps muscle proximal to the implanted tumor (P < 0.05), HbA(0) had little effect on blood flow in right quadriceps muscle with no tumor implanted, and increased right quadriceps pO(2), from 21 mm Hg (baseline) to 23 mm Hg at 10 min (P = 0.03). HbA(0) increased mean arterial pressure 5-10% in a manner that was dependent on dose while heart rate concurrently decreased 9-19%. The diameter of the arterioles supplying the tumor was rapidly reduced 10% by 0.2 g/kg HbA(0) (P = 0.037) and remained stable through 60 min of observation (P = 0.005). HbA(0) selectively reduces tumor blood flow and tumor pO(2) through vasoconstriction of the arterioles supplying the tumor. Vascular NO quenching provides an alternative to NO synthase inhibition as a means to achieve the goal of selective tumor hypoxia. (C) 1997 by Radiation Research Society. [References: 35]
机译:我们检查了一氧化氮(NO)淬灭剂,无基质人血红蛋白A(HbA(0); 0.01、0.05、0.1、0.2 g / kg)对使用多普勒血流技术测量的血流,肿瘤氧的影响压力(pO(2))和使用R3230Ac乳腺腺癌作为肿瘤模型的小动脉直径。在雌性Fischer 344大鼠中,其在左股四头肌外侧植入直径为1厘米的肿瘤,静脉输注0.1和0.2 g / kg HbA(0)可使中心肿瘤和周围肿瘤的血流减少20-30%( P <0.05)。肿瘤pO(2)在0.2 g / kg HbA(0)时在15分钟时从15 mm Hg(基线)降至11 mm Hg(P = 0.02)降低了28%。尽管0.2 g / kg HbA(0)使靠近植入肿瘤的左股四头肌的血流量增加了55%(P <0.05),但HbA(0)对未植入肿瘤的右股四头肌的血流影响很小,并且右股四头肌pO(2)在10分钟时从21毫米汞柱(基线)增加到23毫米汞柱(P = 0.03)。 HbA(0)以取决于剂量的方式使平均动脉压增加5-10%,而心率同时下降9-19%。供应肿瘤的小动脉直径迅速降低了10%,为0.2 g / kg HbA(0)(P = 0.037),并且在60分钟的观察过程中保持稳定(P = 0.005)。 HbA(0)通过供应肿瘤的小动脉的血管收缩选择性减少肿瘤血流量和肿瘤pO(2)。血管NO猝灭提供了NO合酶抑制的替代方法,以实现选择性肿瘤缺氧的目的。 (C)1997年,辐射研究学会。 [参考:35]

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