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Inhibition of T cell cAMP formation by cyclosporin A and FK506.

作者信息

Ockenfels H M, Wagner S N, Oeljeklaus P, Schneck B, Nussbaum G, Jakobs K H, Goos M

机构信息

Hautklinik, Universitätsklinikum Essen, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1996 Apr;353(5):513-6. doi: 10.1007/BF00169170.

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.

摘要

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