Abstract |
Oxysophoridine (OSR) is a bioactive alkaloid extracted from the Sophora alopecuroides Linn. Our aim is to explore the potential anti- inflammation mechanism of OSR in cerebral ischemic injury. Mice were intraperitoneally pretreated with OSR (62.5, 125, and 250 mg/kg) or nimodipine (Nim) (6 mg/kg) for 7 days followed by cerebral ischemia. The inflammatory-related cytokines in cerebral ischemic hemisphere tissue were determined by immunohistochemistry staining, Western blot and enzyme-like immunosorbent assay (ELISA). OSR-treated groups observably suppressed the nuclear factor kappa B (NF-κB), intercellular adhesion molecule-1 (ICAM-1), inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2). OSR-treated group (250 mg/kg) markedly reduced the inflammatory-related protein prostaglandin E2 ( PGE2), tumor necrosis factor alpha (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), and interleukin-8 (IL-8). Meanwhile, it dramatically increased the interleukin-10 (IL-10). Our study revealed that OSR protected neurons from ischemia-induced injury in mice by downregulating the proinflammatory cytokines and blocking the NF-κB pathway.
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Authors | Yong-Sheng Wang, Yu-Xiang Li, Peng Zhao, Hong-Bo Wang, Ru Zhou, Yin-Ju Hao, Jie Wang, Shu-Jing Wang, Juan Du, Lin Ma, Tao Sun, Jian-Qiang Yu |
Journal | Inflammation
(Inflammation)
Vol. 38
Issue 6
Pg. 2259-68
(Dec 2015)
ISSN: 1573-2576 [Electronic] United States |
PMID | 26178478
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Alkaloids
- Anti-Inflammatory Agents
- Cytokines
- Icam1 protein, mouse
- Inflammation Mediators
- Neuroprotective Agents
- Rela protein, mouse
- Transcription Factor RelA
- oxysophoridine
- Intercellular Adhesion Molecule-1
- Nitric Oxide
- Nitric Oxide Synthase Type II
- Nos2 protein, mouse
- Ptgs2 protein, mouse
- Cyclooxygenase 2
- Dinoprostone
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Topics |
- Alkaloids
(pharmacology)
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Brain
(drug effects, metabolism, pathology)
- Brain Ischemia
(drug therapy, metabolism, pathology)
- Cyclooxygenase 2
(metabolism)
- Cytokines
(metabolism)
- Dinoprostone
(metabolism)
- Disease Models, Animal
- Dose-Response Relationship, Drug
- Inflammation Mediators
(metabolism)
- Intercellular Adhesion Molecule-1
(metabolism)
- Male
- Mice, Inbred ICR
- Neuroprotective Agents
(pharmacology)
- Nitric Oxide
(metabolism)
- Nitric Oxide Synthase Type II
(metabolism)
- Reperfusion Injury
(metabolism, pathology, prevention & control)
- Signal Transduction
(drug effects)
- Time Factors
- Transcription Factor RelA
(metabolism)
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