2. Academic Validation
  3. The role of salvianolic acid B and benzoylpaeoniflorin in enhancing angiogenesis through Nrf2/HO-1/VEGFA signaling axis in ischemic stroke recovery

The role of salvianolic acid B and benzoylpaeoniflorin in enhancing angiogenesis through Nrf2/HO-1/VEGFA signaling axis in ischemic stroke recovery

  • Pharm Biol. 2026 Dec;64(1):67-86. doi: 10.1080/13880209.2025.2605571.
Chao Zhao 1 2,  Xiaodan Bai 3,  Yi Ding 1,  Aiguo Zeng 2,  Aidong Wen 1,  Qiang Fu 2 4,  Jingwen Wang 1
Affiliations

Affiliations

  • 1 Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
  • 2 Department of Pharmaceutical Analysis, School of Pharmacy, Xi'an Jiaotong University, Xi'an, China.
  • 3 Department of Pharmacy, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
  • 4 Department of Pharmaceutical Analysis, College of Pharmacy, Shenzhen Technology University, Shenzhen, China.
PMID: 41433220 DOI: 10.1080/13880209.2025.2605571
Abstract

Context: Angiogenesis is one of the essential protective mechanisms that promote neural repair and regeneration after ischemic stroke (IS). Salvianolic Acid B (SAB) and Benzoyl paeoniflorin (BP) are compounds extracted from the Chinese medicines Salvia miltiorrhiza Bunge and Paeonia suffruticosa Andrews, respectively.

Objective: We investigated whether SAB combined with BP alleviated IS by promoting micrangium angiogenesis and determined the potential molecular mechanisms.

Materials and methods: The impact of SAB-BP on angiogenesis after IS was investigated in middle cerebral artery occlusion (MCAO) rat model, ponatinib-induced ischemic stroke in zebrafish, and human umbilical vein endothelial cells (HUVECs). The neuroprotective effect of SAB-BP in rats was assessed using behavior tests and histopathological staining. The cerebral thrombosis assessment and angiogenesis assay were performed in the zebrafish model. Cell proliferation and angiogenesis in oxygen-glucose deprivation and reperfusion (OGD/R) HUVECs were assessed through cell viability, tube formation, migration, and invasion assays. Western blot analysis and immunofluorescence staining were used to determine the protein expression levels of Nrf2, HO-1, and VEGFA.

Results: The findings indicated that SAB-BP significantly reduced neurological impairment following IS and promoted the formation of functional vessels in the cerebral ischemic penumbra. Furthermore, SAB-BP up-regulated the protein expression of Nrf2, HO-1, HIF-1α, and VEGFA. Intriguingly, the pro-angiogenic effect of SAB-BP markedly restrained by adding the inhibitor of Nrf2 (ML385).

Discussion and conclusion: Our study demonstrates that SAB-BP enhances angiogenesis following IS by modulating the Nrf2/HO-1/VEGFA signaling axis both in vivo and in vitro. SAB-BP could serve as a promising therapeutic agent for IS recovery.

Keywords

Nrf2/HO-1/VEGFA signaling axis; Salvianolic acid B; angiogenesis; benzoylpaeoniflorin; ischemic stroke.

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