Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.6.3.14 (ATP synthase)
7,042 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The effects of amiodarone on the respiration of isolated mouse liver mitochondria have been determined. Amiodarone (200 microM) had a biphasic effect on state 4 respiration supported by either glutamate plus malate or succinate. Initially, the respiratory rate was increased. This stimulatory effect was not prevented by oligomycin (an inhibitor of ATP synthase). It was associated with marked accumulation of amiodarone in the mitochondria, and with collapse of the mitochondrial membrane potential. This initial uncoupling effect was followed by a progressive decrease in the state 4 respiration rate, leading eventually to marked inhibition. Preincubation for 5 min with amiodarone (200 microM) also decreased markedly ADP-stimulated (state 3) respiration, ATP production and dinitrophenol-stimulated (uncoupled) respiration supported by glutamate plus malate (which donate electrons to complex I), and respiration supported by succinate (which donate electrons to complex II), but did not affect respiration supported by duroquinol (donating electrons to complex III) or by ascorbate plus N,N,N',N'-tetramethyl-p-phenylenediamine (donating electrons to cytochrome c). Preincubation with amiodarone (150-200 microM) decreased markedly respiration mediated by fatty acids of various chain length and respiration mediated by citrate, a tricarboxylic acid cycle substrate. We conclude that amiodarone has a dual effect on mitochondrial respiration. The initial uncoupling effect is probably due to the entry of protonated amiodarone, releasing a proton in the matrix. Accumulation of amiodarone soon leads to inhibition of the respiratory chain at the levels of complex I and complex II and to decreased ATP formation.
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PMID:Dual effect of amiodarone on mitochondrial respiration. Initial protonophoric uncoupling effect followed by inhibition of the respiratory chain at the levels of complex I and complex II. 197 17

The effects of amiodarone on mitochondrial ATPase (EC 3.6.1.3) and lactate dehydrogenase (LDH: EC 1.1.1.27) activities were studied in guinea pig mitochondrial preparations in order to test the hypothesis that amiodarone exerts some of its effects as a result of multiple actions on membrane-bound enzymes and receptors. Amiodarone inhibited the ATPase activity in the range of 10 pM to 10 mM (n = 10) with IC50 values of 56.4 +/- 7.2 microM. However, although the inhibitory action was very significant (P < 0.0001, compared to the control) in the concentration range of 100 pM to 10 microM, the differences in individual enzyme responses showed very weak correlation with drug concentration. In this region, the inhibitory effects were almost constant at approximately 37%. Below 100 pM and above this range however, the concentration-response relationships were steep, reaching total inhibition at approximately 2.5 mM. Amiodarone also exerted concentration-dependent inhibitory effects on lactate dehydrogenase activity. However, over the effective inhibitory concentration range (5-95%) of 7.5 microM to 2.5 mM (n = 8) and IC50 value of 108 +/- 6 microM, its inhibitory potency was twofold weaker than that of its ATPase inhibition. We propose that these actions contribute, at least in part, to the mechanism(s) of some of the pharmacological actions of amiodarone.
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PMID:Actions of amiodarone on mitochondrial ATPase and lactate dehydrogenase activities in guinea pig heart preparations. 825 7