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Letter to the EditorFull Access

Thyroid Hormones and Seasonal Mood Change

To the Editor: Several studies of peripheral thyroid economy in seasonal affective disorder have shown inconsistent results (1). However, measurements of the peripheral thyroid state may not provide a reliable index of the central thyroid state (2).

In contrast to the peripheral tissues, where most of the nuclear-bound triiodothyronine (T3) is imported from the plasma pool, in the brain the supply of T3 depends mostly on the cellular uptake and intracellular deiodination of thyroxin by type II 5′-iodothyronine deiodinase (3). The existence of a separate pathway in the brain for thyroxin deiodination suggests that the adult central nervous system has the ability to autoregulate thyroid status (4).

A short photoperiod and low ambient temperature are direct stimuli that could affect type II 5′-iodothyronine deiodinase activity (5). Other effects of temperature and photoperiod (e.g., decreased pituitary and gonadal hormones) could be indirect factors that stimulate type II 5′-iodothyronine deiodinase activity. Thus, seasonal changes in light andtemperature may affect the metabolism of brain thyroid hormones.

T3 may itself be a neurotransmitter, and it may have an antidepressant effect (6). It enhances the effects of norepinephrine (7), serotonin (8), and γ-aminobutyric acid (9). Small alterations of brain thyroid economy, independent of peripheral changes in thyroid status, may produce significant behavioral effects. Therefore, it is reasonable to suggest that brain thyroid hormones might be involved in the mechanisms of seasonal changes in mood and behavior.

References

1. Sher L, Rosenthal NE, Wehr TA: Free thyroxine and thyroid-stimulating hormone levels in patients with seasonal affective disorder and matched controls. J Affect Disord 1999; 56:195–199Crossref, MedlineGoogle Scholar

2. Esposito S, Prange AJ Jr, Golden RN: The thyroid axis and mood disorders: overview and future prospects. Psychopharmacol Bull 1997; 33:205–217MedlineGoogle Scholar

3. Crantz FR, Silva JE, Larsen PR: An analysis of the sources and quantity of 3,5,5′-triiodothyronine specifically bound to nuclear receptors in rat cerebral cortex and cerebellum. Endocrinology 1982; 110:367–375Crossref, MedlineGoogle Scholar

4. Dratman M, Crutchfield F, Gordon J, Jennings A: Iodothyronine homeostasis in rat brain during hypo-hyperthyroidism. Am J Physiol 1983; 245:185–193Google Scholar

5. Puig-Domingo M, Guerrero JM, Vaughan MK, Little JC, Reiter RJ: Activation of cerebrocortical type II 5′-deiodinase activity in Syrian hamsters kept under short photoperiod and reduced ambient temperature. Brain Res Bull 1989; 22:975–979Crossref, MedlineGoogle Scholar

6. Mason GA, Walker CH, Prange AJ Jr: L-Triiodothyronine: is this peripheral hormone a central neurotransmitter? Neuropsychopharmacology 1993; 3:253–258Google Scholar

7. Gordon JT, Martens DA, Tomlinson EE, Greenberg J, Dratman MB: Desmethylimipramine, a potent inhibitor of synaptosomal norepinephrine intake, has diverse effects on thyroid hormone processing in rat brain, II: effect on in vivo 5′-deiodination of [125I]thyroxine. Brain Res 1994; 634:96–104Crossref, MedlineGoogle Scholar

8. Mason GA, Bondy SC, Nemeroff CB, Walker CH, Prange AJ Jr: The effects of thyroid state on beta-adrenergic and serotonergic receptors in rat brain. Psychoneuroendocrinology 1987; 12:261–270Crossref, MedlineGoogle Scholar

9. Mason GA, Walker CH, Prange AJ Jr: Modulation of gamma-aminobutyric acid uptake of rat brain synaptosomes by thyroid hormones. Neuropsychopharmacology 1987; 1:63–70Crossref, MedlineGoogle Scholar