EVIDENCE THAT D-FENFLURAMINE ANOREXIA IS MEDIATED BY 5-HT1 RECEPTORS

[21] FROM FENFLURAMINE RACEMATE TO D-FENFLURAMINE - SPECIFICITY AND POTENCY OF THE EFFECTS ON THE SEROTONINERGIC SYSTEM AND FOOD-INTAKE [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 499 : 156 - 166

[22] HEURING RE, 1987, J NEUROSCI, V7, P894

[23] KETANSERIN ANTAGONISES THE ANORECTIC EFFECT OF DL-FENFLURAMINE IN THE RAT [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 145 (02) : 227 - 230

[24] MOLECULAR PHARMACOLOGY OF 5-HT1 AND 5-HT2 RECOGNITION SITES IN RAT AND PIG BRAIN MEMBRANES - RADIOLIGAND BINDING-STUDIES WITH [H-3] 5-HT, [H-3] 8-OH-DPAT, (-) [I-125] IODOCYANOPINDOLOL, [H-3] MESULERGINE AND [H-3] KETANSERIN [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 118 (1-2) : 13 - 23

[25] HOYER D, 1988, IN PRESS J RECEPT RE

[26] D-ISOMERS AND L-ISOMERS OF FENFLURAMINE DIFFER MARKEDLY IN THEIR INTERACTION WITH BRAIN-SEROTONIN AND CATECHOLAMINES IN THE RAT [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 120 (01) : 9 - 15

[27] EVIDENCE FOR A DIFFERENCE IN MECHANISM OF ACTION BETWEEN FENFLURAMINE-INDUCED AND AMPHETAMINE-INDUCED ANOREXIA [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 1973, 25 (01) : 49 - 54

[28] RECEPTOR-BINDING PROFILE OF R-41-468, A NOVEL ANTAGONIST AT 5-HT2 RECEPTORS [J]. LIFE SCIENCES, 1981, 28 (09) : 1015 - 1022

[29] LEYSEN JE, 1985, MOL PHARMACOL, V27, P600

[30] EFFECT OF THE 5HT2 ANTAGONIST RITANSERIN ON FOOD-INTAKE AND ON 5HT-INDUCED ANOREXIA IN THE RAT [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1987, 26 (02) : 333 - 340

[21] FROM FENFLURAMINE RACEMATE TO D-FENFLURAMINE - SPECIFICITY AND POTENCY OF THE EFFECTS ON THE SEROTONINERGIC SYSTEM AND FOOD-INTAKE [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 499 : 156 - 166

[22] HEURING RE, 1987, J NEUROSCI, V7, P894

[23] KETANSERIN ANTAGONISES THE ANORECTIC EFFECT OF DL-FENFLURAMINE IN THE RAT [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 145 (02) : 227 - 230

[24] MOLECULAR PHARMACOLOGY OF 5-HT1 AND 5-HT2 RECOGNITION SITES IN RAT AND PIG BRAIN MEMBRANES - RADIOLIGAND BINDING-STUDIES WITH [H-3] 5-HT, [H-3] 8-OH-DPAT, (-) [I-125] IODOCYANOPINDOLOL, [H-3] MESULERGINE AND [H-3] KETANSERIN [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 118 (1-2) : 13 - 23

[25] HOYER D, 1988, IN PRESS J RECEPT RE

[26] D-ISOMERS AND L-ISOMERS OF FENFLURAMINE DIFFER MARKEDLY IN THEIR INTERACTION WITH BRAIN-SEROTONIN AND CATECHOLAMINES IN THE RAT [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 120 (01) : 9 - 15

[27] EVIDENCE FOR A DIFFERENCE IN MECHANISM OF ACTION BETWEEN FENFLURAMINE-INDUCED AND AMPHETAMINE-INDUCED ANOREXIA [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 1973, 25 (01) : 49 - 54

[28] RECEPTOR-BINDING PROFILE OF R-41-468, A NOVEL ANTAGONIST AT 5-HT2 RECEPTORS [J]. LIFE SCIENCES, 1981, 28 (09) : 1015 - 1022

[29] LEYSEN JE, 1985, MOL PHARMACOL, V27, P600

[30] EFFECT OF THE 5HT2 ANTAGONIST RITANSERIN ON FOOD-INTAKE AND ON 5HT-INDUCED ANOREXIA IN THE RAT [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1987, 26 (02) : 333 - 340