A NATURALLY-OCCURRING FURAN FATTY-ACID ENHANCES DRUG-INHIBITION OF THYROXINE-BINDING IN SERUM

被引:16
作者
LIM, CF
STOCKIGT, JR
CURTIS, AJ
WYNNE, KN
BARLOW, JW
TOPLISS, DJ
机构
[1] ALFRED HOSP,EWEN DOWNIE METAB UNIT,COMMERCIAL RD,PRAHRAN,VIC 3181,AUSTRALIA
[2] MONASH UNIV,ALFRED HOSP,DEPT MED,MELBOURNE,VIC 3181,AUSTRALIA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 1993年 / 42卷 / 11期
关键词
D O I
10.1016/0026-0495(93)90200-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We studied the thyroxine (T4)-displacing effects of a naturally occurring, highly albumin-bound furanoid acid that accumulates in serum in renal failure to concentrations in excess of 0.2 mmol/L. This substance, 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF), has been shown to displace acidic drugs from albumin binding. The effects of CMPF on ligand binding were assessed in the following systems: (1) T4 binding to T4-binding globulin (TBG) and transthyretin (TTR), (2) T4 binding in undiluted serum, (3) T4-displacing potency of fenclofenac, furosemide, diflunisal, and aspirin in undiluted serum, (4) serum binding of [14C]-drug preparations, and (5) serum binding of [14C]-oleic acid. CMPF had a minor direct effect on T4 binding to TBG comparable in relative affinity to that of aspirin, ie, almost 7 orders of magnitude less than T4 itself. CMPF alone at a concentration of 0.3 mmol/L, which produced only a 10% to 14% increase in free T4 augmented the T4-displacing effects of high therapeutic concentrations of the various drugs in undiluted serum as follows: furosemide by 180%, fenclofenac by 160%, diflunisal by 130%, and aspirin by 40%. In the presence of fenclofenac, increments of CMPF from 0.075 to 0.3 mmol/L progressively augmented the T4-displacing effect of this drug, associated with a progressive increase in its calculated free concentration. CMPF also inhibited the binding of [14C]-oleic acid, suggesting that in some situations CMPF could also indirectly influence thyroid hormone binding by increasing the unbound concentration of nonesterified fatty acids (NEFA), as previously described. CMPF at a concentration of 1 mmol/L did not inhibit charcoal or talc uptake of triiodothyronine (T3) or T4. These findings indicate that CMPF can inhibit specific T4 binding in serum by increasing the free concentrations of direct competitors. Such "cascade effects" on thyroid hormone binding could influence both the circulating concentrations and tissue delivery of thyroid hormones in renal failure and critical illness. © 1993.
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页码:1468 / 1474
页数:7
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