Increased levels of cyclic adenosine monophosphate contribute to the hyporesponsiveness of mast cells in alloxan diabetes-Reference-Cited by-同舟云学术

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Increased levels of cyclic adenosine monophosphate contribute to the hyporesponsiveness of mast cells in alloxan diabetes

Published:2004-06 Issue:6 Volume:4 Page:755-762
ISSN:1567-5769
Container-title:International Immunopharmacology
language:en
Short-container-title:International Immunopharmacology

Author:

Barreto Emiliano O,Carvalho Vinicius F,Lagente Vincent,Lugnier Claire,Cordeiro Renato S.B,Martins Marco A,e Silva Patrı́cia M.R

Publisher

Elsevier BV

Subject

Pharmacology,Immunology,Immunology and Allergy

Reference26 articles.

1. Asthma and diabetes mellitus: a biochemical basis for antithetical features;Lasser;Med. Hypotheses,1987

2. Inhibition of leukocyte chemotaxis by factor in alloxan-induced diabetes rat plasma;Pereira;Diabetes,1987

3. Direct vital microscopic study of defective leukocyte–endothelial interaction in diabetes mellitus;Fortes;Diabetes,1991

4. Alloxan diabetes reduces pleural mast cell numbers and subsequent eosinophil influx induced by allergen in sensitized rats;Diaz;Int. Arch. Allergy Immunol.,1996

5. Enhanced serum glucocorticoid levels mediate the reduction of serosal mast cell numbers in diabetic rats;Diaz;Life Sci.,2001

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2. Antipruritic mechanisms of topical E6005, a phosphodiesterase 4 inhibitor: Inhibition of responses to proteinase-activated receptor 2 stimulation mediated by increase in intracellular cyclic AMP;Journal of Dermatological Science;2014-12

3. Topical E6005, a novel phosphodiesterase 4 inhibitor, attenuates spontaneous itch-related responses in mice with chronic atopy-like dermatitis;Experimental Dermatology;2014-04-28

4. Activation of PPARγ by restores mast cell numbers and reactivity in alloxan-diabetic rats by reducing the systemic glucocorticoid levels;European Journal of Pharmacology;2012-09

5. Disease Progression in MRL/lpr Lupus-Prone Mice Is Reduced by NCS 613, a Specific Cyclic Nucleotide Phosphodiesterase Type 4 (PDE4) Inhibitor;PLoS ONE;2012-01-11

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