Prolactin and Growth Hormone Synthesis: Effects of Perphenazine,α-Methyltyrosine and Estrogen in Different Thyroid States 1

Abstract

Summary

The effects of thyroid hormones on prolactin (PRL) and growth hormone (GH) synthesis by the rat anterior pituitary gland were assessed in vitro. A marked reduction (84–87%) in the rate of H³-leucine incorporation into GH was evident 2–4 weeks after thyroidectomy, while incorporation into PRL was 52–71% less than that measured in glands from intact rats. A single injection of T₄ (200 μg/kg) administered to thyroidectomized (THX) rats 48 hr before sacrifice significantly increased incorporation into both pituitary hormones, although the stimulation of GH synthesis was much more dramatic.

Perphenazine, α-methyltyrosine and estrogen enhanced the rate of PRL synthesis in intact rats. Thyroid ablation did not affect the response to perphenazine, but significantly increased the response to α-methyltyrosine and estrogen. On the other hand, administration of T₄ to THX rats receiving perphenazine, α-methyltyrosine or estrogen diminished the stimulatory influence of these treatments on PRL synthesis.

Perphenazine, α-methyltyrosine and estrogen had no effect on the rate of GH synthesis in THX rats, nor did they alter the ability of T₄ to restore GH synthesis in these animals.

These results indicate that GH synthesis in the rat is dependent upon thyroid hormones and support the concept that these hormones exert their stimulatory effect directly on pituitary somatotrophs. Pituitary lactotrophs, however, appear to retain much of their capacity to synthesize PRL under conditions of thyroid deficiency. The changes in pituitary PRL levels and synthesis rate induced by thyroid ablation might reflect differences in the number rather than the activity of these cells.

We gratefully acknowledge the technical assistance of Mr. Ronald C. Pace.