The interaction of metergoline, a 5-HT receptor blocker, and dexfenfluramine in human feeding

E Goodall1, T Silverstone

  • 1Academic Unit of Human Psychopharmacology, Medical College of St. Bartholomew's Hospital, London, U.K.

Insights

Dexfenfluramine (d-FF) reduced hunger and food intake in humans, particularly nonsweet foods. Metergoline (MTG) alone did not affect hunger but increased food intake and partially blocked d-FF's appetite-suppressing effects.

Area of Science:

  • Neuroscience
  • Pharmacology
  • Human Physiology

Background:

  • Dexfenfluramine (d-FF) is known to influence food intake via serotoninergic pathways in animals.
  • The 5-HT antagonist metergoline (MTG) has been used to study these mechanisms.

Purpose of the Study:

  • To investigate the interaction between dexfenfluramine (d-FF) and metergoline (MTG) in humans regarding appetite regulation.
  • To assess the effects of d-FF and MTG on hunger, satiety, and food consumption in healthy male volunteers.

Main Methods:

  • Double-blind, placebo-controlled study with healthy male volunteers.
  • Administration of d-FF (30 mg) or placebo, followed by MTG (4 mg) or placebo.
  • Assessment of hunger and satiety using visual analog scales (VAS) and measurement of food intake via an automated food dispenser (AFD).

Main Results:

  • d-FF significantly reduced hunger and total food intake (1306 kJ / 312 kcal).
  • MTG alone increased food intake and attenuated d-FF's effect on total food intake, though not significantly.
  • d-FF primarily reduced nonsweet food intake, an effect partially attenuated by MTG.

Conclusions:

  • Dexfenfluramine effectively reduces appetite and food intake in humans, acting through serotoninergic mechanisms.
  • Metergoline may partially counteract the appetite-suppressing effects of dexfenfluramine.
  • The findings suggest a complex interaction within the serotoninergic system influencing human appetite for different food types.

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