Mf. Sauvage et al., RELATIONSHIP BETWEEN PSYCHOTROPIC-DRUGS AND THYROID-FUNCTION - A REVIEW, Toxicology and applied pharmacology, 149(2), 1998, pp. 127-135
Some widely used psychoactive drugs, such as tricyclic antidepressants
and antipsychotic phenothiazines exhibit iatrogenic effects on the th
yroid. These side effects may arise from interactions at different ste
ps of thyroid hormone biosynthesis. These drugs can induce a change in
iodine capture by thyroid cells or can complex iodine, making it unav
ailable for thyroid hormone synthesis and thus decreasing thyroid horm
one blood levels; they can also inhibit thyroid peroxidase activity an
d thus T-3 and T-4 synthesis or enhance deiodination of T-4 to T-3 or
to Rt(3) by stimulation of deiodinase activity. Moreover, tricyclic an
tidepressants interfere with the hypothalamic-pituitary-thyroid axis v
ia the noradrenergic or serotonergic systems and might therefore decre
ase T-4 or T-3 blood levels, respectively. Phenothiazines can induce a
utoimmune hypothyroidism, as shown by an increase in the expression of
the major histocompatibility complex antigen and by a production of a
ntithyroglobulin or antithyroperoxidase antibodies. However, all these
mechanisms are only speculative in humans, as they have only been dem
onstrated in vitro or in animal experiments. Clinically, thyroid funct
ion and affective disorders are closely linked. On one hand, the thera
peutic response to antidepressants could be influenced by the thyroid
status; on the other hand, the larger the thyroxin decrease induced by
antidepressants, the better the therapeutic effect might be. Moreover
, cotreatment with thyroid hormones and antidepressant drugs could all
ow either a decrease in the rate of treatment failure or a faster reco
very from depression. As antipsychotic or antidepressant treatments ar
e administered over long periods in humans, their thyroid toxic effect
s must be taken seriously. (C) 1998 Academic Press.