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三碘-L-甲状腺原氨酸在体内对甲状腺功能减退大鼠肝线粒体中ADP/O比值和表观H⁺/O比值的快速改变。

The rapid alteration by tri-iodo-L-thyronine in vivo of both the ADP/O ratio and the apparent H+/O ratio in hypothyroid-rat liver mitochondria.

作者信息

Crespo-Armas A, Mowbray J

出版信息

Biochem J. 1987 Feb 1;241(3):657-61. doi: 10.1042/bj2410657.

Abstract

Mitochondria from the livers of thyroidectomized rats have a lowered ADP/O ratio, which can be restored to normal within 15 min after intravenous injection of a near-physiological dose of tri-iodothyronine. Thyroidectomy lowered the measured delta pH, which appears to be compensated by a rise (not statistically significant) in the membrane potential, so that the protonmotive force is unaltered. A simple simulation technique is described for use in estimating H+/O ratios by the oxygen-pulse technique, which circumvents the problem that this ratio can be seriously underestimated because of re-uptake of protons from the bulk phase by the mitochondria before their expulsion is complete. By this procedure the H+/O ratio of hypothyroid mitochondria is shown to be lowered by the same factor as the ADP/O ratio, and both these ratios are very rapidly restored in parallel by hormone administration. Although these findings could be consistent with a proposal that tri-iodothyronine rapidly modulates by some mechanism the efficiency of the respiratory-chain-linked proton pumps, the kinetic properties of the proton exchange suggest that the bulk-phase protons measured may not reflect faithfully those that drive the ATP synthetase.

摘要

甲状腺切除大鼠肝脏中的线粒体,其ADP/O比值降低,在静脉注射接近生理剂量的三碘甲状腺原氨酸后15分钟内,该比值可恢复正常。甲状腺切除降低了测得的ΔpH,这似乎由膜电位的升高(无统计学意义)所补偿,从而使质子动力势保持不变。描述了一种简单的模拟技术,用于通过氧脉冲技术估算H⁺/O比值,该技术规避了由于线粒体在质子排出完全之前从本体相中重新摄取质子而可能严重低估该比值的问题。通过该程序表明,甲状腺功能减退的线粒体的H⁺/O比值与ADP/O比值以相同的系数降低,并且通过给予激素,这两个比值都能非常迅速地同时恢复。尽管这些发现可能与三碘甲状腺原氨酸通过某种机制快速调节呼吸链相关质子泵效率的提议一致,但质子交换的动力学特性表明,测得的本体相质子可能无法如实反映驱动ATP合酶的质子。

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Short-term control of mitochondrial adenine nucleotide translocator by thyroid hormone.
Eur J Biochem. 1984 Feb 15;139(1):95-9. doi: 10.1111/j.1432-1033.1984.tb07981.x.
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