Depression and exication induced in mice by two geometric isomers of (+)13,14-didehydro-20-methyl-carboprostacyclin, FCE 22177 and FCE 22176. Comparison with effects on blood pressure and platelet aggregation
- 1 March 1987
- journal article
- research article
- Published by Elsevier in Prostaglandins
- Vol. 33 (3) , 351-362
- https://doi.org/10.1016/0090-6980(87)90018-9
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- The putative prostacyclin receptor antagonist (FCE-22176) is a full agonist on human platelets and NCB-20 cellsEuropean Journal of Pharmacology, 1986
- A stable isosterically modified prostacyclin analogue, FCE-22176, acting as a competitive antagonist to prostacyclin in guinea-pig trachea and atriaEuropean Journal of Pharmacology, 1985
- Identification of the prostacyclin receptor by radiation inactivation.Journal of Biological Chemistry, 1984
- Epoprostenol (prostacyclin, PGI2) binding and activation of adenylate cyclase in platelets of diabetic and control subjects.British Journal of Clinical Pharmacology, 1983
- Prostaglandin profiles in nervous tissue and blood vessels of the brain of various animalsProstaglandins, 1980
- SCHIZOPHRENIA AS A PROSTAGLANDIN DEFICIENCY DISEASEThe Lancet, 1977
- Effects of prostacyclin (PGX) on cyclic AMP concentrations in human plateletsProstaglandins, 1977
- Possible association of schizophrenia with a disturbance in prostaglandin metabolism: a physiological hypothesisPsychological Medicine, 1976
- Comprehensive observational assessment: Ia. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mousePsychopharmacology, 1968