Abstract | AIM: METHODS: Female adult C57BL/6 mice were immunized with MOG35-55 to induce chronic EAE. Fasudil was injected on day 3 p.i. (early Fasudil treatment), or at the onset of EAE (late Fasudil treatment). Normal saline was injected in other mice as EAE controls in a similar manner. Clinical score and body mass were recorded every other day. The expressions of iNOS on microglia and p-NF-κB/p65 on astrocytes were measured by immunohistochemistry and Western blotting. The levels of IL-1β and TNF-α in spinal cord homogenate were determined by ELISA. RESULTS:
Fasudil delayed onset and ameliorated the severity of EAE. Fasudil inhibited the expression of iNOS on microglia and p-NF-κB/p65 on astrocytes in spinal cords, accompanied by the inhibition of inflammatory factors IL-1β and TNF-α. CONCLUSION:
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Authors | Yan-hua Li, Chun-yun Liu, Pei-jun Zhang, Jie-zhong Yu, Ning Ji, Yan-yan Yan, Ling Feng, Hai-fei Zhang, Bao-guo Xiao, Cun-gen Ma |
Journal | Xi bao yu fen zi mian yi xue za zhi = Chinese journal of cellular and molecular immunology
(Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi)
Vol. 28
Issue 12
Pg. 1242-5
(Dec 2012)
ISSN: 1007-8738 [Print] China |
PMID | 23232512
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Interleukin-1beta
- NF-kappa B
- Tumor Necrosis Factor-alpha
- 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
- fasudil
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Topics |
- 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
(administration & dosage, analogs & derivatives)
- Animals
- Astrocytes
(drug effects, immunology)
- Encephalomyelitis, Autoimmune, Experimental
(drug therapy, genetics, immunology)
- Female
- Humans
- Interleukin-1beta
(genetics, immunology)
- Mice
- Mice, Inbred C57BL
- NF-kappa B
(genetics, immunology)
- Neuroglia
(drug effects, immunology)
- Spinal Cord
(drug effects, immunology)
- Tumor Necrosis Factor-alpha
(genetics, immunology)
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