Abstract |
The present study was designed to investigate whether or not reduction of carnitine content could protect isoproterenol (ISP)-induced myocardial injury using 3-(2,2,2-trimethylhydrazinium) propionate (TMHP), gamma-butyrobetaine hydroxylase inhibitor. Rats were divided into 4 groups; the control group: untreated, the TMHP-1 group: TMHP (100 mg/kg) was administered intraperitoneally, and ISP (10 mg/kg) was administered subcutaneously on the following day, the TMHP-7 group: TMHP (100 mg/kg) for 7 successive days, and ISP (10 mg/kg) on the eighth day, the ISP group: ISP (10 mg/kg) was administered. Rats were cervically dislocated 15 hours after ISP administration, and heart mitochondrial electron-transport activity ( NADH-cytochrome c reductase, succinate-cytochrome c reductase, and cytochrome c oxidase) were measured enzymatically. Activity of succinate-cytochrome c reductase was not affected significantly by ISP, however, NADH-cytochrome c reductase and cytochrome c oxidase were significantly reduced in the ISP and TMHP groups. Administration with TMHP for 7 successive days lessened the reduction of the activities. Mitochondrial electron-transport system plays an important role in cellular energy transduction. These results suggested that mitochondrial dysfunction induced by ISP is related to carnitine-dependent fatty acid metabolism and that TMHP reduces the myocardial injury.
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Authors | Y Hanaki, S Sugiyama, T Ozawa |
Journal | Research communications in chemical pathology and pharmacology
(Res Commun Chem Pathol Pharmacol)
Vol. 64
Issue 1
Pg. 157-60
(Apr 1989)
ISSN: 0034-5164 [Print] United States |
PMID | 2546223
(Publication Type: Journal Article)
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Chemical References |
- Methylhydrazines
- 3-(2,2,2-trimethylhydrazine)propionate
- Mixed Function Oxygenases
- gamma-Butyrobetaine Dioxygenase
- NADH Dehydrogenase
- Electron Transport Complex IV
- Isoproterenol
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Topics |
- Animals
- Electron Transport
- Electron Transport Complex IV
(metabolism)
- In Vitro Techniques
- Isoproterenol
(pharmacology)
- Methylhydrazines
(pharmacology)
- Mitochondria, Liver
(drug effects, enzymology)
- Mixed Function Oxygenases
(antagonists & inhibitors)
- NADH Dehydrogenase
(metabolism)
- Rats
- Rats, Inbred Strains
- gamma-Butyrobetaine Dioxygenase
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