1. Enhanced tolerability of the 5-hydroxytryptophane challenge test combined with granisetron
- Author
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Gabriel E. Jacobs, Imc Kamerling, J. van Pelt, Frans G. Zitman, Jma van Gerven, Roel H. DeRijk, and ML de Kam
- Subjects
Adult ,Male ,Adolescent ,Hydrocortisone ,Vomiting ,Nausea ,Dopamine Agents ,Granisetron ,Placebo ,5-Hydroxytryptophan ,Young Adult ,Double-Blind Method ,medicine ,Humans ,Drug Interactions ,Pharmacology (medical) ,Pharmacology ,Cross-Over Studies ,Dose-Response Relationship, Drug ,business.industry ,Carbidopa ,Crossover study ,Domperidone ,Prolactin ,Psychiatry and Mental health ,Tolerability ,Area Under Curve ,Anesthesia ,5-HTP challenge test granisetron HPA-axis pharmacokinetics pharmacodynamics serotonergic function healthy-volunteers serotonin emesis nausea ,Antidepressive Agents, Second-Generation ,Antiemetics ,medicine.symptom ,business ,medicine.drug - Abstract
A recently developed oral serotonergic challenge test consisting of 5-Hydroxytryptophane (5-HTP, 200 mg) combined with carbidopa (CBD, 100 mg + 50 mg) exhibited dose-related neuroendocrine responsiveness and predictable pharmacokinetics. However, its applicability is limited by nausea and vomiting. A randomized, double-blind, placebo-controlled, four-way crossover trial was performed in 12 healthy male volunteers. The 5-HTP/CBD-challenge was combined with two oral anti-emetics (granisetron, 2 mg or domperidone, 10 mg) to investigate its reliability when side-effects are suppressed. The neuroendocrine response (serum cortisol and prolactin), the side-effect profile [Visual Analogue Scale Nausea (VAS)] and vomiting subjects per treatment were the main outcome measures. Compared to 5-HTP/CBD/placebo, 5-HTP/CBD/ granisetron had no impact on cortisol [% change with 95% confidence interval: −7.1% (18.9; 6.5)] or prolactin levels [−9.6% (−25.1; 9.1)]; 5-HTP/CBD/domperidone increased cortisol [+13.0% (−4.2; 33.4)], and increased prolactin extensively [+336.8% (245.7; 451.9)]. Compared to placebo, VAS Nausea increased non-significantly with granisetron [+7.6 mm (−1.3; 16.5)], as opposed to domperidone [+16.2 mm (7.2; 25.2)] and 5-HTP/CBD/placebo [+14.7 mm (5.5; 23.8)]. No subjects vomited with granisetron, compared to two subjects treated with 5-HTP/CBD/placebo and five subjects with domperidone. Compared with 5-HTP/CBD/placebo, granisetron addition decreased Cmax of 5-HTP statistically significantly different (from 1483 to 1272 ng/ml) without influencing AUC0— ∞. Addition of granisetron to the combined 5-HTP/CBD challenge suppresses nausea and vomiting without influencing the neuroendocrine response or pharmacokinetics, enhancing its clinical applicability in future psychiatric research and drug development.
- Published
- 2008
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