COMPARISON OF THE EFFECTS OF PROPYLTHIOURACIL, AMIODARONE, DIPHENYLHYDANTOIN, PHENOBARBITAL, AND 3-METHYLCHOLANTHRENE ON HEPATIC AND RENAL-T4 METABOLISM AND THYROID-GLAND FUNCTION IN RATS

被引:61
作者
DESANDRO, V
CHEVRIER, M
BODDAERT, A
MELCION, C
CORDIER, A
RICHERT, L
机构
[1] Rhône-Poulenc Rorer, Département Sécurité du Médicament, Centre de Recherche de Vitry-Alfortville, 94403 Vitry sur Seine
关键词
D O I
10.1016/0041-008X(91)90030-I
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We studied the effects of propylthiouracil (PTU), amiodarone (AMIO), diphenylhydantoin (DPH), phenobarbital (PB), and 3-methylcholanthrene (MC) on thyroid histomorphology, on the hepatic and renal enzymes involved in endogenous and exogenous metabolism, and on the plasma levels and pharmacokinetics of thyroid hormones after 7 and 14 days of treatment. PTU and PB, by decreasing both serum tetraiodothyronine (T4) and triiodothyronine (T3), induced a massive increase in serum thyrotropin (TSH) and thus induced thyroid hypertrophy. AMIO and MC, by decreasing respectively serum T3 and T4, also induced an increase of TSH, but to a lesser extent, not sufficient to induce thyroid hypertrophy. Hepatic 5′-deiodinase activity was decreased in all treated rats. Inhibition of this enzyme by PTU was demonstrated in vitro: AMIO also decreased the enzyme activity by a still unelucidated mechanism, which probably requires intact cell plasma membranes, whereas in PB- and MC-treated rats the decrease in enzyme activity certainly resulted from decreased serum concentrations of T4. In PTU-treated rats, and probably in MC-treated rats, decreases in circulating thyroid hormones were primarily due to impairment of synthesis and/or of secretion by the thyroid. In contrast, in PB-treated rats, the decrease in serum thyroid hormone levels seems to be due to increased excretion of these hormones, as T4 serum clearance was significantly increased. PB, a microsomal enzyme inducer, increased the cytochrome b5 and P450 content as well as the cytochrome P450-dependent O-depentylation of pentoxyresorufin. The other type of enzyme inducer, MC, did not affect cytochrome b5 and P450 levels, but did increase the cytochrome P450 dependent O-deethylation of ethoxyresorufin. PB increased the glucuronidation of morphine, whereas MC increased the glucuronidation of 1-naphthol. However, serum T4 clearance, mainly determined by its hepatic conjugation rate, was increased only in PB-treated rats. It appears from this study that the close metabolic relationship between the liver/kidney and the thyroid should be taken into consideration when the findings of chronic toxicology and carcinogenicity studies are interpreted. © 1991.
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页码:263 / 278
页数:16
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