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Natural Products and Bioprospecting· 2026Q1

Methyl eugenol increases neural microcirculation to promote nerve repair by regulating endothelial cell and Schwann cell communication via Ptn/Sdc4

Zifeng Zhuang, Shaozi Lin, 李怡萱, Xiaokang Xie et al.

Short summary

Methyl eugenol enhances neural microcirculation to promote nerve repair in rats with chronic constriction injury (CCI) by upregulating Ptn/Sdc4 signaling between endothelial and Schwann cells.

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Key points

  • Methyl eugenol treatment improved neural microcirculation and promoted nerve repair in rats subjected to chronic constriction injury (CCI).
  • Nerve injury (CCI) was found to reduce communication between endothelial cells and Schwann cells, specifically via the Ptn/Sdc4 signaling pathway.
  • Methyl eugenol increased endothelial cell tube formation and the release of pleiotrophin (Ptn).
  • Ptn, released by endothelial cells, acted on syndecan-4 (Sdc4) in Schwann cells, promoting their migration and enhancing overall neural microcirculation.

AI-generated from the title and abstract; the full text is not read.

Abstract

Neuromicrocirculatory disorders often accompany nerve injury. Improving neural microcirculation can promote the repair of injured nerves. Methyl eugenol is a major bioactive component of Asarum heterotropoides and has been reported to exert analgesic effects in chronic pain. This study aimed to demonstrate that methyl eugenol can enhance neural microcirculation and thereby promote nerve repair. A combination of single-cell sequencing and mRNA sequencing revealed that pleiotrophin (Ptn)/syndecan-4 (Sdc4) is vital for coupling between endothelial cells and Schwann cells. A total of 32 rats were randomly assigned to four groups, namely, the Sham, chronic constriction injury (CCI) 7d, CCI 14d, and CCI 21d groups, to assess whether endothelial Schwann cell communication is diminished following CCI. After an endothelial cell-Schwann cell coculture system was established, methyl eugenol, Ptn siRNA, and Sdc4 siRNA were administered. In a separate experiment, 32 SD rats were randomly divided into four experimental groups: the Sham, CCI, ibuprofen, and methyl eugenol groups. CellChat analysis revealed that nerve injury reduced the degree of communication between endothelial cells and Schwann cells, especially communication via Ptn/Sdc4. CCI disrupted neural microcirculation, lowered Ptn levels, and increased Sdc4 expression. In cell experiments, methyl eugenol promoted rat aortic endothelial cells tube formation and increased the release of Ptn, which acted on Sdc4 in rat Schwann cells (RSC96) to promote migration, but did not directly promote RSC96 cell migration in the absence of endothelial cell-derived factors. Treatment with methyl eugenol increased neural microcirculation to promote nerve repair in rats subjected to CCI. In addition, methyl eugenol further increased Ptn levels. CCI led to neural microcirculatory dysfunction and nerve injury. Methyl eugenol promote nerve repair by enhancing neural microcirculation through regulation of endothelial cell and Schwann cell communication via Ptn/Sdc4.

The authors' abstract, as published at the source. Natural Products and Bioprospecting, 2026 · DOI ↗

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Field: Cellular and Molecular Neuroscience

Cellular and Molecular NeuroscienceNeuroscience