Page 44 - Pharma News Letter Vol1 Issue2 - Converted By Dr. Ahmed Rashed
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Chapter VI

                       Journal of Biochemical and Molecular Toxicology

                                                 2023 Mar;37(3):e23266


                       Fingolimod attenuates ovalbumin-induced airway
                 inflammation via inhibiting MAPK/ERK signaling in mice












             Mirhan N. Makled , Ahmed R. El-Sheakh ,
                                                       1 2
                               1
             1  Department of Pharmacology and Toxicology,
             Faculty  of  Pharmacy,  Mansoura  University,
             Mansoura,  Egypt.

             2   Future  Studies  and  Risks  Management  &
             National  Committee  of  Drugs,  Academy
             of  Scientific  Research,  Ministry  of  Higher
             Education,  ElSayeda  Zeinab,  Egypt.
             Abstract

             The current study was designed to investigate
             the potential anti-inflammatory and antioxidant
             effects of fingolimod against Ovalbumin (Ova)-
             induced allergic airway inflammation compared
             to dexamethasone. Fingolimod was given (0.5
             mg/kg/day, p.o.) for sensitized mice 1 h before
             Ova challenge from Days 19 to 24. Fingolimod     challenged  mice.  In  conclusion,  the  current
             significantly  inhibited  Ova-induced  elevation   study  demonstrated  the  anti-inflammatory and
             of inflammatory cells and eosinophils numbers    antioxidant  effects  of  fingolimod  in  allergic
             in  bronchoalveolar  lavage  fluid  (BALF)  and   airway  inflammation  that  might  be  associated
             reduced  concentrations  of  immunoglobulin      with  the  downregulation  of  mitogen  activated
             E  in  serum  and  of  sphingosine-1-phosphate,   kinases  signaling  to  decrease  T  helper  2
             interleukin  (IL)-4,  and  IL-13  in  BALF.      cytokine secretion (IL-4 and IL-13) and MCP-
             Fingolimod  inhibited  microvascular  leakage    1  expression,  along  with  the  inhibition  of
             and edema as reflected by the decreased lung/    oxidative  stress.
             body  weight  index.  These  findings  were
             supported  by  histopathological  examination    https://doi.org/10.1002/jbt.23266
             results  showing  that  fingolimod  substantially
             decreased perivascular edema and inflammatory
             cell  infiltration.  Fingolimod  also  attenuated
             Ova-induced  oxidative  stress  as  evidenced
             by  decreased  malondialdehyde  concentration
             along with increasing concentrations of reduced
             glutathione  and  superoxide  dismutase  in  lung
             tissues. Fingolimod also significantly decreased
             monocyte  chemoattractant  protein-1  (MCP-
             1), p-ERK, and p-P38 in lung tissues of Ova-

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