Abstract |
Myasthenia gravis (MG) is frequently treated by corticosteroids such as methylprednisolone. However, continuous treatment with steroids often results in adverse effects. In the present study we evaluated the therapeutic potential of a combination of suboptimal doses of methylprednisolone ( Solumedrol) and Pentoxifylline (PTX), a general phosphodiesterase (PDE) inhibitor, in rat experimental autoimmune MG (EAMG). This combined treatment resulted in a pronounced suppressive effect on EAMG and was by far more effective than each of the drugs administered separately at these low doses. The suppressive effect on EAMG was accompanied by decreased humoral and cellular responses to AChR as well as down-regulated mRNA expression levels of Th1 cytokines and IL-10 in lymph node cells and of PDE-4 and cathepsin-l in the muscle. This study demonstrates the potential of PTX as a steroid-sparing agent in the management of myasthenia gravis.
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Authors | Renuka T R Menon, Tali Feferman, Revital Aricha, Miriam C Souroujon, Sara Fuchs |
Journal | Journal of neuroimmunology
(J Neuroimmunol)
Vol. 201-202
Pg. 128-35
(Sep 15 2008)
ISSN: 0165-5728 [Print] Netherlands |
PMID | 18632163
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies
- Cytokines
- Glucocorticoids
- Phosphodiesterase Inhibitors
- Receptors, Cholinergic
- Pentoxifylline
- Methylprednisolone
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Topics |
- Animals
- Antibodies
(blood)
- Body Weight
(drug effects)
- Cytokines
(genetics, metabolism)
- Disease Models, Animal
- Dose-Response Relationship, Drug
- Drug Therapy, Combination
- Female
- Gene Expression Regulation
(drug effects)
- Glucocorticoids
(therapeutic use)
- Methylprednisolone
(therapeutic use)
- Muscle, Skeletal
(drug effects, metabolism)
- Myasthenia Gravis, Autoimmune, Experimental
(blood, drug therapy, pathology)
- Pentoxifylline
(therapeutic use)
- Phosphodiesterase Inhibitors
(therapeutic use)
- Rats
- Rats, Inbred Lew
- Receptors, Cholinergic
(immunology)
- Severity of Illness Index
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