Effect of 1–5 Hydroxytryptophan Infusion on Growth Hormone and Prolactin Secretion in Man

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Abstract
The effect of a new soluble ester of 1–5 hydroxytryptophan (1–5 HTP, Ro 3–5940, 200 mginfusion) on prolactin (PRL) and growth hormone (GH) release was tested in 11 young, healthy subjects (6 men, 5 women). To minimize side-effects, peripheral decarboxylase inhibition was achieved with benserazide (Ro 4–4602.) PRL increased significantly (P <0.01)after benserazide alone in all subjects. A further significant increase (P < 0.01) of PRL plasma levels occurred only in women up to 90 min after the infusion of 1–5 HTP wasdiscontinued. Benserazide administration had no effect of basal GH levels, but a significant increase of GH release (P < 0.01) was noticed 30–120 min after the end of 1–5 HTP infusion in both men and women. The mean peak value of GH plasma levels after 1–5 HTP administration was 32.0 ± 8.8 ng/ml. It was postulated that benserazide penetrated at the level of the pituitary, decreasing the synthesis of dopamine and consequently reducing its known inhibitory effect on PRL release. The PRL increase (statistically significant only in women), as well as the release of GH after 1–5 HTP infusion, was considered as further evidence for stimulatory serotoninergic control of both PRL and GH secretion.