Carnitine is a naturally occurring inhibitor of thyroid hormone nuclear uptake

被引:31
作者
Benvenga, S [1 ]
Lakshmanan, M [1 ]
Trimarchi, F [1 ]
机构
[1] Univ Messina, Sch Med, Cattedra Endocrinol, Messina, Italy
关键词
D O I
10.1089/thy.2000.10.1043
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Carnitine (3-hydroxy-4N-trimethylammoniumbutanoate) is a naturally occurring quaternary amine that is ubiquitous in mammalian tissues (concentrations in the order of mM). Based on limited studies of approximately 40 years ago, carnitine was considered to be a peripheral antagonist of thyroid hormone (TH) action. These interesting observations have not been explored. To study the biologic basis of this effect, we tested the following possibilities in three TH-responsive cell lines: (1) inhibition of TH entry into cells; (2) inhibition of TH entry into the nucleus; (3) inhibition of TH interaction with the isolated nuclei; and (4) facilitated efflux of TH from cells. On a preliminary basis we had verified that these cell Lines (human skin fibroblasts, human hepatoma cells HepG2, and mouse neuroblastoma cells NE 41A3) take up (14C)carnitine; however, there was no (14C)carnitine uptake into the nuclei. Concentrations of unlabeled carnitine as high as 100 mM did not affect (125I)T3 binding to isolated nuclei or exit of TH from cells, thus excluding possibilities numbered 3 and 4. At 10 mM carnitine, (125I)T3 and (125I)T4 whole-cell uptake was inhibited by approximately 20% in fibroblasts and in HepG2, but by approximately 5% in NE 41A3 cells. Inhibition of T3 nuclear uptake was evaluated in HepG2 and NE 41A3 cells. At 10 mM carnitine, inhibition of T3 nuclear uptake was disproportionately higher, namely approximately 25% in neurons and 35% in hepatocytes. At 50 mM carnitine, there was a minimal additional decrease in whole-cell uptake of either hormone but a marked decrease in T3 nuclear uptake. The latter inhibition was approximately 60% in neurons and 70% in hepatocytes. We are aware of no inhibitor of TH uptake that has such a markedly different effect on the nuclear versus whole-cell uptake. Our data are consistent with carnitine being a peripheral antagonist of TH action, and they indicate a site of inhibition at or before the nuclear envelope.
引用
收藏
页码:1043 / 1050
页数:8
相关论文
共 42 条
[11]  
CEDERBLAD G, 1978, ACTA PHARMACOL TOX, V43, P1
[12]  
CHALLONER DR, 1971, J LAB CLIN MED, V77, P616
[13]   RECEPTOR-MEDIATED UPTAKE OF 3,3',5-TRIIODO-L-THYRONINE BY CULTURED FIBROBLASTS [J].
CHENG, SY ;
MAXFIELD, FR ;
ROBBINS, J ;
WILLINGHAM, MC ;
PASTAN, IH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3425-3429
[14]   ACTIVE-TRANSPORT OF BUTYROBETAINE AND CARNITINE INTO ISOLATED LIVER-CELLS [J].
CHRISTIANSEN, RZ ;
BREMER, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 448 (04) :562-577
[15]  
DEFEICE SL, 1996, J NEW DRUGS, V6, P351
[16]   THE 24-HOUR URINARY-EXCRETION OF CARNITINE AND CREATININE IN NORMAL AND HYPOTHYROID CHILDREN [J].
EANES, RZ ;
BINIEK, RL .
BIOCHEMICAL MEDICINE, 1980, 24 (02) :110-117
[17]   HYDROXYLATION OF GAMMA-BUTYROBETAINE TO CARNITINE IN HUMAN AND MONKEY TISSUES [J].
ENGLARD, S .
FEBS LETTERS, 1979, 102 (02) :297-300
[18]  
FAMULARO G, 1992, L CARNITINE ITS ROLE, P119
[19]  
GONCALVES E, 1989, ENDOCRINOLOGY, V124, P293
[20]   INVIVO STUDIES OF INTESTINAL CARNITINE ABSORPTION IN RATS [J].
GUDJONSSON, H ;
LI, BUK ;
SHUG, AL ;
OLSEN, WA .
GASTROENTEROLOGY, 1985, 88 (06) :1880-1887