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F K Bauer

Publications and source records attributed to F K Bauer.

9 recordsLinked to original sources
PubMed2000

Prevention by dexrazoxane of down-regulation of ryanodine receptor gene expression in anthracycline cardiomyopathy in the rat.

Anthracyclines can cause cumulative dose-related cardiotoxicity characterized by changes in Ca(2+) metabolism, including dysfunction of the sacroplasmic reticulum (SR) and decreased expression of Ca(2+)-handling proteins, such as the ryanodine receptor (RyR2). In this study, we examined the effect of dexrazoxane (ICRF-187), an iron chelator which prevents anthracycline cardiotoxicity, on RyR2 gene expression in rats treated chronically with daunorubicin. Daunorubicin (2.5 mg kg(-1) i.v. weekly for 6 weeks) produced cardiotoxicity as demonstrated by histopathologic changes. The ryanodine receptor/glyceraldehyde phosphate dehydrogenase (GAPDH) mRNA ratio was decreased by 38+/-3% (P<0.02) compared to values in control rats. Dexrazoxane pre-treatment (50 mg kg(-1); 1 h prior to each daunorubicin injection) prevented the decrease in RyR2/GAPDH mRNA ratio and histopathologic lesions in daunorubicin-treated rats. This is the first report that a protective agent such as dexrazoxane can ameliorate the decreased expression of a specific gene involved in anthracycline-induced cardiotoxicity.

Animals↗
PubMed1981

Rubidium-86 uptake by red blood cells of breast cancer patients.

The red blood cell (RBC) uptake of rubidium-86 (Rb-86), a sensitive in vitro test of RBC membrane transport, was measured in 22 controls, 8 patients with benign breast lesions, and 30 stage I/II, 13 stage III/IV untreated breast cancers. Total Rb-86 transport was measured. Following ouabain block, passive transport was determined, allowing calculation of active Rb-86 uptake by difference. There was a significant decrease in total and passive uptake by RBCs from patients with breast cancer when compared to controls and those with benign lesions (total uptake 58.6 +/- 6.1% versus 63.6 +/- 3.9%, P less than 0.01; passive uptake 38.7 +/- 6.8% versus 42.7 +/- 4.6%, P less than 0.02). The Rb-86 uptake returned towards normal in successfully treated stages-II-to-IV patients. There were no correlations with the patient's age, hematocrit, or incubation hematocrit with RBC Rb-86 uptakes. Results from incubation in Krebs-Ringer solution were not consistent with a plasma blocking factor. The RBC potassium content was slightly increased in the cancer patients. This, along with decreased passive transport, eliminates the nonspecific malfunction of the Na-K-pump as an explanation, and suggests that the decreased uptake is a cancer-related phenomenon.

Adolescent↗