Abstract
Forty mg TRH [thyrotropin releasing hormone] per day was given orally for 3 wk to 10 euthyroid women and 10 women with primary hypothyroidism on low replacement doses of thyroxine. Once weekly oral TRH was replaced by an i.v. TRH-test (0.4 mg) with measurement of serum concentration of TSH [thyrotropin], prolactin (PRL), thyroxine (T4), triiodothyronine (T3) and cholesterol. In the normal group, mean serum T4 concentration increased after 1 wk and remained elevated. Serum TSH concentration showed a slight tendency to decline. Maximal rise in TSH concentration after i.v. TRH (.DELTA.TSH) fell from a mean of 4.0 ng/ml to 1.4 ng/ml within 1 wk and stayed low. T3, cholesterol, PRL and .DELTA.PRL were normal and unchanged throughout. In the hypothyroid group T4, T3, cholesterol, PRL and .DELTA.PRL were not influenced by the TRH administration. In 2 patients (with the highest serum T4 concentrations) serum TSH concentration was normal and resistent to i.v. TRH. Of the 8 patients with elevated TSH, basal level and .DELTA.TSH did not change in 2 (with subnormal T4 levels and the highest TSH levels). In the other 6 (with intermediate T4 levels) basal TSH fell from a mean of 10.1 ng/ml to 4.2 ng/ml, and .DELTA.TSH from 10.0 ng/ml to 3.3 ng/ml after 3 wk. In addition to feedback effect of thyroid hormones, the pituitary response to long-term administration of TRH is determined by other factors. Among these may be reduced pituitary TRH receptor capacity and the activity of the TSH producing cells.