Lumbricus Extract Prevents LPS-Induced Inflammatory Activation of BV2 Microglia and Glutamate-Induced Hippocampal HT22 Cell Death by Suppressing MAPK/NF-κB/NLRP3 Signaling and Oxidative Stress.
You-Chang OhYun Hee JeongHye Jin YangWei LiJin Yeul MaPublished in: Current issues in molecular biology (2023)
Microglia-induced inflammatory signaling and neuronal oxidative stress are mutually reinforcing processes central to the pathogenesis of neurodegenerative diseases. Recent studies have shown that extracts of dried Pheretima aspergillum (Lumbricus) can inhibit tissue fibrosis, mitochondrial damage, and asthma. However, the effects of Lumbricus extracts on neuroinflammation and neuronal damage have not been previously studied. Therefore, to evaluate the therapeutic potential of Lumbricus extract for neurodegenerative diseases, the current study assessed the extract's anti-inflammatory and antioxidant activities in BV2 microglial cultures stimulated with lipopolysaccharide (LPS) along with its neuroprotective efficacy in mouse hippocampal HT22 cell cultures treated with excess glutamate. Lumbricus extract dose-dependently inhibited the LPS-induced production of multiple proinflammatory cytokines (tumor necrosis factor-α, interleukin (IL)-6, and IL-1β) and reversed the upregulation of proinflammatory enzymes (inducible nitric oxide synthase and cyclooxygenase-2). Lumbricus also activated the antioxidative nuclear factor erythroid 2-relayed factor 2/heme oxygenase-1 pathway and inhibited LPS-induced activation of the nuclear factor-κB/mitogen-activated protein kinases/NOD-like receptor family pyrin domain containing 3 inflammatory pathway. In addition, Lumbricus extract suppressed the glutamate-induced necrotic and apoptotic death of HT22 cells, effects associated with upregulated expression of antiapoptotic proteins, downregulation of pro-apoptotic proteins, and reduced accumulation of reactive oxygen species. Chromatography revealed that the Lumbricus extract contained uracil, hypoxanthine, uridine, xanthine, adenosine, inosine, and guanosine. Its effects against microglial activation and excitotoxic neuronal death reported herein support the therapeutic potential of Lumbricus for neurodegenerative diseases.
Keyphrases
- lps induced
- oxidative stress
- inflammatory response
- diabetic rats
- anti inflammatory
- nuclear factor
- toll like receptor
- induced apoptosis
- cell death
- lipopolysaccharide induced
- cerebral ischemia
- ischemia reperfusion injury
- dna damage
- nitric oxide synthase
- high glucose
- poor prognosis
- cell cycle arrest
- reactive oxygen species
- chronic obstructive pulmonary disease
- signaling pathway
- rheumatoid arthritis
- nitric oxide
- high resolution
- traumatic brain injury
- stem cells
- cell proliferation
- cystic fibrosis
- mass spectrometry
- cell therapy
- immune response
- heat shock
- binding protein
- subarachnoid hemorrhage
- endothelial cells
- lung function
- ms ms
- metabolic syndrome
- neuropathic pain
- endoplasmic reticulum stress
- brain injury
- stress induced
- heat stress
- cognitive impairment