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Kinetics of Thyroxine (T<sub>4</sub>) and Triiodothyronine (T<sub>3</sub>) Transport in the Isolated Rat Heart

Mirko RosicInstitute of Physiology, Faculty of Medicine, University of Kragujevac, KragujevacSuzana PantovićInstitute of Physiology, Faculty of Medicine, University of Kragujevac, KragujevacAleksandra Tomić-LučićInstitute of Physiology, Faculty of Medicine, University of Kragujevac, KragujevacN Ribarac-StepićInstitute of Nuclear Science ‘Vinca’, BelgradeI.Ž. AndjelkovićInstitute of Physiology, Faculty of Medicine, University of Belgrade,Yugoslavia
Experimental Physiologyjournal2001en
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The dynamics and kinetics of thyroid hormone transport in the isolated rat heart were examined using the modified unidirectional paired tracer dilution method. The uptake of 125 I‐thyroxine ( 125 I‐T 4 ) and 125 I‐triiodothyronine ( 125 I‐T 3 ) from the extracellular space into heart cells was measured relative to the extracellular space marker 3 H‐mannitol. The thyroid hormone maximal uptake was 54.4% for 125 I‐T 4 and 52.15% for 125 I‐T 3 . The thyroid hormone net uptake was 25.69% for 125 I‐T 4 and 25.49% for 125 I‐T 3 . Backflux from the intracellular space was 53.17% for 125 I‐T 4 and 61.59% for 125 I‐T 3 . In the presence of unlabelled thyroid hormones, 125 I‐T 4 and 125 I‐T 3 maximal uptakes were reduced from 10.1 to 59.74% and from 34.6 to 65.3%, respectively, depending on the concentration of the unlabelled hormone, suggesting a saturable mechanism of the thyroid hormone uptake by the heart cells, with K m(T4) = 105.46 μM and the maximal rate of 125 I‐thyroid hormone flux from the extracellular space to heart cells ( V max(T4) ) = 177.84 nM min −1 for 125 I‐T 4 uptake, and K m(T3) = 80.0 μM and V max(T3) = 118.5 nM min −1 for 125 I‐T 3 uptake.

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