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pubmed-article:2924319pubmed:abstractTextIn order to evaluate the potential of a highly selective Ca2+ entry blocker (nisoldipine) and of 5-hydroxytryptamine (5-HT) as adjuvant in hyperthermia treatment, we studied the differential flow response and time-course of tumor and normal tissue temperature following the administration of the two substances and during ultrasound heating. In 12 rats bearing Walker 256 carcinomas i.p. injection of 0.2-0.4 mg/kg nisoldipine caused a reduction in the tumor-to-muscle flow relationship of 4.4 +/- 1.9 (SD) to 1.74 +/- 0.86 as determined by intraarterial 133Xe injection; i.p. injection of 2-8 mg/kg 5-HT (N = 13) caused a respective reduction from 3.9 +/- 2.67 to 1.3 +/- 1.59. During a 20-min period of 41 degrees C normal tissue temperature-controlled ultrasound heating without drugs, tumor temperature attained 40.8 +/- 0.9 degrees C (N = 16). Nisoldipine or 5-HT injection at continuing 41 degrees C normal tissue temperature controlled energy delivery produced an instantaneous further increment of tumor temperature, eventually to 44.0 +/- 1.14 degrees C or 44.2 +/- 1.26 degrees C, respectively, after a period of 20 min. Injection of 0.9% NaCl (N = 4) solution caused only insignificant changes. Blood pressure and muscle perfusion were distinctly influenced by nisoldipine, but not by 5-HT. Since both drugs instantaneously increased the temperature differential between tumor and normal tissue, though by different vasoaction, they should be considered as adjuvants in hyperthermia.lld:pubmed
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pubmed-article:2924319pubmed:pagination1768-72lld:pubmed
pubmed-article:2924319pubmed:dateRevised2003-11-14lld:pubmed
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pubmed-article:2924319pubmed:year1989lld:pubmed
pubmed-article:2924319pubmed:articleTitleIncreased thermal response to ultrasound in the Walker carcinosarcoma treated with vasoactive drugs.lld:pubmed
pubmed-article:2924319pubmed:affiliationInstitute for Nuclear Medicine, German Cancer Research Center, Heidelberg.lld:pubmed
pubmed-article:2924319pubmed:publicationTypeJournal Articlelld:pubmed