ISSN:
1573-4919
Keywords:
intramitochondrial Ca2+ intramitochondrial metabolism
;
int
;
mitochondrial Ca2+-transport
;
oxidative phosphorylation
;
pyruvate dehydrogenase
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
Notes:
Abstract In the heart and other mammalian tissues, there are three exclusively intramitochondrial dehydrogenases that occupy key regulatory sites in oxidative metabolism which can be activated by increases in Ca2+ in the approximate range 0.05–5 μM; they are the pyruvate, NAD+-isocitrate and 2-oxoglutarate dehydrogenases. Activation of these enzymes can be demonstrated within intact mitochondria, incubated under expected physiological conditions, when the extramitochondrial concentration of Ca+ is raised within the expected physiological range. Recent studies with fura-2-loaded mitochondria have established that matrix Ca2+ is indeed in the 0.02–2 μM range as the enzymes are activated. There is now good evidence that in the rat heart, increases in cytoplasmic [Ca2+] caused by various inotropic agents result in increases in intramitochondrial Ca2+ and activation of these dehydrogenases. It is argued therefore that matrix Ca2+ may thus be a key regulator of oxidative phosphorylation under such circumstances. The major advantage of such a mechanism of dehydrogenase-based control of this process would be to the energy homeostasis of the cell by allowing stimulated ATP production without the need to decrease the ATP/ADP ratio. Therefore it is also proposed that the major function of the mitochondrial Ca2+-transport system is to regulate matrix Ca2+, and that the ability of mitochondria to buffer the extramitochondrial concentration of Ca2+ may thus only be reserved for pathophysiological conditions of abnormal sarcolemmal Ca2+ influx as perhaps may occur in ischaemia reperfusion.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00220763
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