Abstract |
We compared the potential beta-receptor blocker, B 24/76 i.e. 1-(2,4-dichlorophenoxy)-3[2-3,4-dimethoxyphenyl)ethanolamino]-prop an-2-ol, which is characterized by beta 1- adrenoceptor blocking and beta 2- adrenoceptor stimulating properties with propranolol. The studies were performed using an experimental model of isoproterenol-induced heart hypertrophy in rats. A correlation of the blood pressure was neither found in the development nor in the attempt to suppress the development of heart hypertrophy with the two beta-receptor blockers. Both beta-blockers influenced the development of hypertrophy to a different, but not reproducible extent. It was possible to suppress the increased ornithine decarboxylase activity with both beta-blockers in hypertrophied hearts, but there was no effect on the heart mass. Neither propranolol nor B 24/76 could stop the changes in the characteristic myosin isoenzyme pattern of the hypertrophied rat heart. Thus, the investigations did not provide any evidence that the beta-receptor blockers propranolol and B 24/76 have the potency to prevent isoproterenol from producing heart hypertrophy.
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Authors | A Grisk, U Hoffmann, K U Möritz |
Journal | Biomedica biochimica acta
(Biomed Biochim Acta)
Vol. 47
Issue 7
Pg. 681-8
( 1988)
ISSN: 0232-766X [Print] Germany |
PMID | 2974281
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Isoenzymes
- Propranolol
- Myosins
- Ornithine Decarboxylase
- Isoproterenol
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Topics |
- Animals
- Blood Pressure
(drug effects)
- Cardiomegaly
(chemically induced, drug therapy)
- Isoenzymes
(metabolism)
- Isoproterenol
(toxicity)
- Myosins
(metabolism)
- Ornithine Decarboxylase
(metabolism)
- Propranolol
(pharmacology)
- Rats
- Rats, Inbred Strains
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