Table 5.
Protective mechanisms of SPMs against septic brain injury.
| SPMs | Model | concentration/dose and application | Mechanisms of intervention | Effect/outcome | Reference |
|---|---|---|---|---|---|
| AT-LXA4 | LPS intervention on BV2 cells | incubated with different concentrations (1 nM, 10 nM or 100 nM) of AT-LXA4 for 30 min | Inflammatory cytokines | NO, IL-1β and TNF-α↓ | (63) |
| NF-κB/MAPK/AP-1 pathway | Activation↓ | ||||
| RVD1 | LPS intervention on BV2 cells | incubated with 10 nM of RVD1 for 30 min | Pro-inflammatory marker mRNA expression | IL-6, TNF-α, IL-1β and CD86↓ | (66) |
| Gene expression of miRNAs | MiR-155, miR-21 and miR-146 expression↑, miR-219 expression↓ | ||||
| CLP | RvD1 (5 μg/kg) was injected by caudal vein | Brain function | Learning and cognitive ability↑ | (65) | |
| Inflammatory cells/cytokines | Microglia activity↓, IL-6, TNF-α and IL-1β↓ | ||||
| NF-κB/MAPK/STAT pathways | Activation↓ | ||||
| RVE1 | LPS intervention on BV2 cells | incubated with 10 nM of RVE1 for 30 min | Pro-inflammatory marker mRNA expression | IL-6 and IL-1β↓ | (66) |
| NF-κB pathway | Activation↓ |
mitogen-Activated Protein Kinase (MAPK); nuclear Factor-κB (NF-κB); signal transducer and activator of transcription (STAT). ↑ represents an increase in level; ↓ represents a decrease in level.