Literature DB >> 3733373

Investigation of the interaction of cardiotoxic anticancer agents using the fetal mouse heart organ culture system.

B F Kimler, R D Rethorst, G G Cox.   

Abstract

The fetal mouse heart organ culture system was utilized in an effort to document and predict the potential cardiotoxic effects of ionizing radiation, Adriamycin (ADR), and Dihydroxyanthraquinone (DHAQ); alone and in combination. These antineoplastic agents have been shown to produce clinical cardiomyopathy which is often dose-limiting. Fetal mouse hearts (gestational day 17) were removed and placed in a culture system of 6-well microtiter plates. A single heart was placed in each well on a piece of aluminium mesh, above the culture medium but bathed by capillary action. The plates were then placed in a 100% oxygen environment and incubated at 37 degrees C. Treatments performed on day 1 after culture were Cs-137 irradiation (10, 20, or 40 Gy); ADR (10, 30, or 100 micrograms/ml); DHAQ (5, 20, or 50 micrograms/ml); or various combinations of drugs and radiation. Hearts were checked every day for functional activity as evidenced by continuous heart best. Untreated hearts beat rhythmically for up to 9 days (average = 6.8 days); treated hearts stopped beating between 2 and 7 days after treatment. Using this endpoint of functional retention time (FRT), dose response curves were obtained for all individual agents. Combinations of ADR and DHAQ (at concentrations that resulted in FRTs of 3.5 days) produced no greater effect than either agent alone. However, the combination of radiation (FRT = 5.3 days) with ADR, DHAQ or both drugs was more effective than was drug alone. This system may help to predict the cardiotoxic effects that result from the use of these drugs and radiation.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3733373     DOI: 10.1007/bf00194591

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  16 in total

1.  Letter: Gamma-irradiation of mammalian beating heart cells in vitro. Effects on cellular function.

Authors:  T J Lampidis; R R Weichselbaum; J B Little
Journal:  Int J Radiat Biol Relat Stud Phys Chem Med       Date:  1975-07

2.  A clinicopathologic analysis of adriamycin cardiotoxicity.

Authors:  E A Lefrak; J Pitha; S Rosenheim; J A Gottlieb
Journal:  Cancer       Date:  1973-08       Impact factor: 6.860

Review 3.  The design, synthesis and development of a new class of potent antineoplastic anthraquinones.

Authors:  C C Cheng; R K Zee-Cheng
Journal:  Prog Med Chem       Date:  1983

4.  Comparison of antineoplastic activity of aminoethylaminoanthraquinones and anthracycline antibiotics.

Authors:  C C Cheng; G Zbinden; R K Zee-Cheng
Journal:  J Pharm Sci       Date:  1979-03       Impact factor: 3.534

5.  Ultrastructural evidence of cardiac damage resulting from thoracic irradiation and anthracyclines in the rat.

Authors:  B F Kimler; C M Mansfield; D J Svoboda; G G Cox
Journal:  Int J Radiat Oncol Biol Phys       Date:  1984-08       Impact factor: 7.038

6.  Cardiac evaluation of mitoxantrone.

Authors:  D V Unverferth; B J Unverferth; S P Balcerzak; T A Bashore; J A Neidhart
Journal:  Cancer Treat Rep       Date:  1983-04

7.  Effect of dihydroxyanthraquinone (NSC 279836) and thoracic irradiation on long-term survival of rats.

Authors:  B F Kimler; S D Henderson; C M Mansfield; D J Svoboda; C C Cheng
Journal:  Cancer Res       Date:  1982-07       Impact factor: 12.701

8.  Activity of a novel anthracenedione, 1,4-dihydroxy-5,8-bis(((2-[(2-hydroxyethyl)amino]ethyl)amino])-9,10-anthracenedione dihydrochloride, against experimental tumors in mice.

Authors:  R E Wallace; K C Murdock; R B Angier; F E Durr
Journal:  Cancer Res       Date:  1979-05       Impact factor: 12.701

9.  Experimental antitumor activity of aminoanthraquinones.

Authors:  R K Johnson; R K Zee-Cheng; W W Lee; E M Acton; D W Henry; C C Cheng
Journal:  Cancer Treat Rep       Date:  1979-03

10.  Comparison of cardiotoxicity of two anthracenediones and doxorubicin in rats.

Authors:  G Zbinden; A K Beilstein
Journal:  Toxicol Lett       Date:  1982-05       Impact factor: 4.372

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