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Sulfosuccinimidyl oleate sodium (Sulfo-N-succinimidyl oleate sodium) 是一种长链脂肪酸,抑制脂肪酸向细胞转运。Sulfosuccinimidyl oleate sodium 是一种有效且不可逆的线粒体呼吸链抑制剂。Sulfosuccinimidyl oleate sodium 结合小胶质细胞表面上的 CD36 受体。具有抗炎作用。
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更新时间:2026/10/7 8:40:05关注度:2533
关键词标签:Sulfo-N-succinimidyl,oleate,sodium
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MCE 国际站:Sulfosuccinimidyl oleate sodium
产品活性:Sulfosuccinimidyl oleate sodium (Sulfo-N-succinimidyl oleate sodium) 是一种长链脂肪酸,抑制脂肪酸向细胞转运。Sulfosuccinimidyl oleate sodium 是一种有效且不可逆的线粒体呼吸链抑制剂。Sulfosuccinimidyl oleate sodium 结合小胶质细胞表面上的 CD36 受体。具有抗炎作用。
研究领域:Autophagy
作用靶点:Mitophagy
In Vitro: Sulfosuccinimidyl oleate (20 µM and 50 µM, 24 hours) alone does not alter the cellular viability. Exposure to 100 ng/ml LPS+5 ng/mL IFNγ modestly, yet significantly reduces the viability of the BV2 cells. Co-treatment with Sulfosuccinimidyl oleate prevents the LPS+IFNγ-induced reduction in the cell viability.
Sulfosuccinimidyl oleate (50 µM, 24 hours) co-treatment significantly reduces the LPS+IFNγ-induced expression of NOS2 and COX-2 in BV2 cells. Western blot analysis reveals a significant LPS/IFNγ-induced upregulation in the phosphorylated form of the p38, which is prevented by co-treatment with Sulfosuccinimidyl oleate (50 µM, 24 hours).
In Vivo: Sulfosuccinimidyl oleate (50 mg/kg; administered once by single oral gavage) significantly reduces the cortical ischemic infarct size compared to vehicle-treated controls in male BALB/cABom mice with pMCAo model. In addition, Sulfosuccinimidyl oleate at 50 mg/kg is suitable to see a beneficial effect after stroke.
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