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Inhibition of T cell cAMP formation by cyclosporin A and FK506.
- Source :
-
Naunyn-Schmiedeberg's archives of pharmacology [Naunyn Schmiedebergs Arch Pharmacol] 1996 Apr; Vol. 353 (5), pp. 513-6. - Publication Year :
- 1996
-
Abstract
- The influence of the immunosuppressants, cyclosporin A (CsA) and FK506, on cAMP formation was studied in T cells from healthy controls and patients with psoriasis. While basal cAMP levels were not affected, CsA (1 microM) and FK506 (2 nM) prevented the isoprenaline (0.1 microM)-induced increase in cAMP formation. Half-maximal inhibition by FK506 and CsA was observed at about 0.2 nM and 20 nM, respectively. In addition, both agents significantly reduced (by about 50%) the forskolin (8 microM)-stimulated cAMP formation. No differences were noted in cAMP responses (basal, stimulation by isoprenaline, inhibition by CsA and FK506) of T cells from healthy controls and psoriatic patients. We conclude that CsA and FK506 potently and efficiently interfere with the stimulatory adenylyl cyclase pathway in T cells and that regulation of T cell cAMP formation is apparently not altered in psoriasis.
- Subjects :
- Adult
Aged
Colforsin pharmacology
Dose-Response Relationship, Drug
Female
Humans
Isoproterenol pharmacology
Male
Middle Aged
Psoriasis metabolism
T-Lymphocytes metabolism
Cyclic AMP biosynthesis
Cyclosporine pharmacology
Immunosuppressive Agents pharmacology
T-Lymphocytes drug effects
Tacrolimus pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0028-1298
- Volume :
- 353
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Naunyn-Schmiedeberg's archives of pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 8740144
- Full Text :
- https://doi.org/10.1007/BF00169170