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Stroma-Free Human Hemoglobin A Decreases R3230Ac Rat Mammary Adenocarcinoma Blood Flow and Oxygen Partial Pressure
We examined the effect of a nitric oxide (NO) quencher, stroma-free human hemoglobin A (${\rm HbA}_{0}$; 0.01, 0.05, 0.1, 0.2 g/kg), on the blood flow measured using the Doppler flow technique, tumor oxygen pressure ($p{\rm O}_{2}$) and the diameter of the arterioles using R3230Ac mammary adenocarci...
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Published in: | Radiation research 1997-02, Vol.147 (2), p.185-194 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | We examined the effect of a nitric oxide (NO) quencher, stroma-free human hemoglobin A (${\rm HbA}_{0}$; 0.01, 0.05, 0.1, 0.2 g/kg), on the blood flow measured using the Doppler flow technique, tumor oxygen pressure ($p{\rm O}_{2}$) 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 ${\rm HbA}_{0}$ decreased both central tumor and peripheral tumor blood flow by 20-30% (P < 0.05). Tumor $p{\rm O}_{2}$ decreased 28% with 0.2 g/kg ${\rm HbA}_{0}$, from 15 mm Hg (baseline) to 11 mm Hg at 10 min (P = 0.02). Although 0.2 g/kg ${\rm HbA}_{0}$ increased blood flow 55% in the left quadriceps muscle proximal to the implanted tumor (P < 0.05), ${\rm HbA}_{0}$ had little effect on blood flow in right quadriceps muscle with no tumor implanted, and increased right quadriceps $p{\rm O}_{2}$, from 21 mm Hg (baseline) to 23 mm Hg at 10 min (P = 0.03). ${\rm HbA}_{0}$ 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 ${\rm HbA}_{0}$ (P = 0.037) and remained stable through 60 min of observation (P = 0.005). ${\rm HbA}_{0}$ selectively reduces tumor blood flow and tumor $p{\rm O}_{2}$ 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. |
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ISSN: | 0033-7587 1938-5404 |
DOI: | 10.2307/3579420 |