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Salidroside suppressed OGD/re-oxygenation-induced reactive oxygen species (ROS) production, p53 mitochondrial translocation and cyclophilin D (Cyp-D) association as well as mitochondrial membrane potential (MMP) decrease in H9c2 cells. Salidroside activated Akt and promoted transcription of NF-E2-related factor 2 (Nrf2)-regulated genes (heme oxygenase-1 (HO-1) and quinone oxidoreductase 1 (NQO-1)). Salidroside alleviated the pulmonary symptoms of PQ-induced ALI, at least partially, by repressing inflammatory cell infiltration and the expression of TGF-β1 resulting in delayed lung fibrosis. Salidroside exerts a protective effect in CLP-induced sepsis by attenuating the proinflammatory responses, enhancing bacterial clearance, and preserving adaptive immunity. Salidroside may be a promising therapeutic strategy for the treatment of sepsis. Salidroside decreased the ST elevation induced by ISO, decreased serum levels of CK-MB, LDH, TNF-α, IL-6, SOD, and MDA. In addition, Salidroside increased SOD activity and decreased MDA content in myocardial tissue.Salidroside also decreased Nox2 and 4, NF-κBP65, P-NF-κBP65, and AP1 protein levels in the heart.
| Molecular Weight | 300.3 |
| Formula | C14H20O7 |
| CAS Number | 10338-51-9 |
| Form | Solid |
| Solubility (25°C) | DMSO 60mg/mL Water 60mg/mL Ethanol 4mg/mL |
| Storage | 2-8°C, protect from light |
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