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  • 1
    ISSN: 1573-4919
    Keywords: CoQ10 ; lactate dehydrogenase ; citrate synthase ; creatine kinase ; free radicals ; antioxidant activity ; metabolic adaptation ; papillary muscle ; mitral valve disease ; left ventricle overload
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Coenzyme Q10 (CoQ10) was studied in papillary muscle from 18 patients (52–67 years, 2 females) subjected to open heart surgery due to mitral valve disease. In addition the enzyme activities of lactate dehydrogenase (LD) with its five isozymes, citrate synthase (CS) and mitochondrial CK (CK-MIT) were determined. Myocardial function was assessed by means of left ventricle (LV) angiography. CoQ10 averaged 0.39 (range 0.26–0.59) μg × mg−1 dw. On an individual basis CoQ10 was related to CS activity although not as closely as CK-MIT (r = 0.45, p〈0.05 versus r = 0.86, p〈0.001). The ratio (CoQ10) × (CS activity)−1 was calculated to represent mitochondrial quality. The level of LD3 fraction increase was used to mark for the degree of metabolic stress in the heart. LD3 fraction was negatively related to the quality index (r = −0.71, p〈0.001). Thus, those with a low CoQ10 per unit of CS activity had also a high LD3 isozyme fraction. In a subset of 12 patients with isolated mitral regurgitation due to myxomatous valve degeneration, CoQ10 and the ratio CoQ10 over CS decreased with the degree of LV function impairment (r = −0.58, p〈0.05 and r = −0.68, p〈0.05, respectively). The quality index takes into account not only enzyme activity but also the potential for control of free oxygen radicals.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 13 (1974), S. 559-569 
    ISSN: 0570-0833
    Keywords: Antimetabolites ; Coenzyme Q ; Antimalarial agents ; Malaria ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Malaria is transmitted to man by the bite of the female Anopheles mosquito, man acting as the intermediate host, and the mosquito as the definitive host for the plasmodia. Plasmodia are found to have become resistant to certain chemotherapeutic agents. A new fundamental approach to malaria chemotherapy is based on the biochemical rationale of inhibition of the electron transfer mechanism in the metabolism of plasmodia by antimetabolites of coenzyme Q, which is essential for electron transfer. Coenzyme Q refers to 2,3-dimethoxy-5-methyl-1,4-benzoquinones with isoprenoid chains of varying length on C-6. In this progress report a series of synthetic antimetabolites are presented together with a discussion of their action in current pharmacological tests.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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