Integrated transcriptomics and metabolomics analysis reveals that C3 and C5 are vital targets of DuZhi Wan in protecting against cerebral ischemic injury

Biomed Pharmacother. 2022 Nov:155:113703. doi: 10.1016/j.biopha.2022.113703. Epub 2022 Sep 19.

Abstract

Background/aims: Duzhi Wan (DZW) has been extensively used in the prevention and treatment of ischemic stroke, but the mechanisms underlying its effects remain unclear. In this study, a combination of transcriptomics, metabolomics and network analysis was applied to identify the preventive mechanism of DZW in middle cerebral artery occlusion (MCAO)-induced ischemia/reperfusion (I/R) injury.

Methods: The mice were divided into five groups: the sham group, I/R group, I/R + Ginaton group, I/R+DZW-L group, and I/R+DZW-H group. Neurological deficit scores and regional cerebral blood flow (rCBF), hematoxylin and eosin (H&E) and Nissl staining results were evaluated. Transcriptomics analysis and metabolomics analysis were applied to identify the key genes and metabolites, and qRT-PCR, ELISA, and immunofluorescence were applied to verify the key targets.

Results: DZW significantly decreased the infarction size and neurological deficit scores, increased the rCBF percentage and neuronal number and improved neuronal morphology after MCAO. Transcriptomics and metabolomics analysis revealed that C3 and C5ar1 were core targets of DZW and indirectly regulated downstream purine metabolism, the pentose phosphate pathway, and glycerophospholipid metabolism-associated pathways via inflammatory cells. Moreover, ELISA, qRT-PCR, and immunofluorescence further confirmed that DZW significantly decreased the expression of C3, C5ar1, C5 and downstream inflammatory cytokines, including IL-6, IL-1β and MMP-9, at the gene and protein levels, suggesting that DZW decreased neuroinflammation and inhibited related metabolic pathways.

Conclusion: C3 and C5 play important roles in the neuroprotective and antineuroinflammatory effects of DZW in protecting against cerebral I/R. This study provides novel insights into the neuroprotective effects of DZW and its clinical application.

Keywords: Antineuroinflammation; C3; C5; Cerebral ischemia/reperfusion injury; Duzhi Wan (DZW); Neuroprotection.

MeSH terms

  • Animals
  • Brain Ischemia* / drug therapy
  • Brain Ischemia* / genetics
  • Brain Ischemia* / metabolism
  • Cytokines / metabolism
  • Eosine Yellowish-(YS) / therapeutic use
  • Glycerophospholipids / therapeutic use
  • Hematoxylin / therapeutic use
  • Infarction, Middle Cerebral Artery / drug therapy
  • Interleukin-6
  • Ischemia / drug therapy
  • Matrix Metalloproteinase 9 / metabolism
  • Metabolomics
  • Mice
  • Neuroprotective Agents* / pharmacology
  • Neuroprotective Agents* / therapeutic use
  • Purines / therapeutic use
  • Reperfusion Injury* / drug therapy
  • Reperfusion Injury* / genetics
  • Reperfusion Injury* / metabolism
  • Transcriptome

Substances

  • Neuroprotective Agents
  • Matrix Metalloproteinase 9
  • Hematoxylin
  • Eosine Yellowish-(YS)
  • Interleukin-6
  • Cytokines
  • Glycerophospholipids
  • Purines