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D-普萘洛尔对甲状腺激素动力学影响的三室分析

Three-compartmental analysis of effects of D-propranolol on thyroid hormone kinetics.

作者信息

van der Heijden J T, Krenning E P, van Toor H, Hennemann G, Docter R

机构信息

Department of Internal Medicine III, University Hospital Rotterdam, The Netherlands.

出版信息

Am J Physiol. 1988 Jul;255(1 Pt 1):E80-6. doi: 10.1152/ajpendo.1988.255.1.E80.

Abstract

Tracer thyroxine (T4), 3.3',5-triiodothyronine (T3), and 3,3',5'-triiodothyronine (rT3) kinetic studies were performed in normal T4 substituted subjects before and during oral D-propranolol treatment to determine whether changes in thyroid hormone metabolism in a propranolol-induced low-T3 syndrome result from inhibition of 5'-deiodination or inhibition of transport of iodothyronines into tissues. Data were analyzed according to a three-compartmental model of distribution and metabolism. T4 plasma appearance rate decreased by 16% (P less than 0.01), reflecting a decreased intestinal absorption of orally administered T4 during propranolol. Serum T4 and free T4 levels increased significantly by 14%, whereas T4 metabolic clearance rate (MCR) was lowered by 26% (P less than 0.001). No changes were observed in size of the three T4 compartments or in fractional and mass transfer rates of T4 from plasma to the rapidly (REP) and slowly (SEP) equilibrating pools. Serum T3, free T3, T3 plasma pool, T3 mass transfer rate to REP and SEP, and the T3 pool masses were all significantly decreased during propranolol to a similar extent as the T3 plasma production rate (PR). T3 MCR decreased by 14% (P less than 0.05). Serum total and free rT3 increased, whereas the rT3 MCR was substantially lowered during propranolol (P less than 0.001). The rT3 plasma pool, rT3 REP and SEP, and the mass transfer rates to REP and SEP increased, whereas no alterations were observed in rT3 PR and fractional transfer rates of rT3 to REP and SEP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在正常接受甲状腺素(T4)替代治疗的受试者中,于口服D-普萘洛尔治疗前及治疗期间进行了示踪甲状腺素(T4)、3,3',5-三碘甲状腺原氨酸(T3)和3,3',5'-三碘甲状腺原氨酸(反T3,rT3)动力学研究,以确定普萘洛尔诱导的低T3综合征中甲状腺激素代谢的变化是由于5'-脱碘作用受抑制还是碘甲状腺原氨酸向组织转运受抑制所致。数据根据分布和代谢的三室模型进行分析。普萘洛尔治疗期间,T4血浆出现率下降了16%(P<0.01),反映口服T4的肠道吸收减少。血清T4和游离T4水平显著升高14%,而T4代谢清除率(MCR)降低了26%(P<0.001)。未观察到三个T4室的大小或T4从血浆到快速平衡池(REP)和缓慢平衡池(SEP)的分数转运率及质量转运率有变化。普萘洛尔治疗期间,血清T3、游离T3、T3血浆池、T3向REP和SEP的质量转运率以及T3池质量均显著下降,下降程度与T3血浆产生率(PR)相似。T3 MCR下降了14%(P<0.05)。血清总rT3和游离rT3升高,而普萘洛尔治疗期间rT3 MCR大幅降低(P<0.001)。rT3血浆池、rT3 REP和SEP以及向REP和SEP的质量转运率增加,而rT3 PR以及rT3向REP和SEP的分数转运率未观察到改变。(摘要截断于250字)

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