4.1 Article

Anisodamine Hydrobromide Protects Glycocalyx and Against the Lipopolysaccharide-Induced Increases in Microvascular Endothelial Layer Permeability and Nitric Oxide Production

Journal

CARDIOVASCULAR ENGINEERING AND TECHNOLOGY
Volume 12, Issue 1, Pages 91-100

Publisher

SPRINGER
DOI: 10.1007/s13239-020-00486-8

Keywords

Glycocalyx; Endothelial cell; Anisodamine; Lipopolysaccharide

Funding

  1. National Natural Science Foundation of China [11932014, 11402153]
  2. Chengdu No. 1 Pharmaceutical Co., Ltd. Chengdu, China [19H0383]

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Ani HBr significantly increases EC viability under LPS challenge, reduces cell apoptosis, protects glycocalyx integrity, and alleviates cell permeability and NO production.
Purpose-Anisodamine hydrobromide (Ani HBr) has been used to improve the microcirculation during cardiovascular disorders and sepsis. Glycocalyx plays an important role in preserving the endothelial cell (EC) barrier permeability and nitric oxide (NO) production. We aimed to test the hypothesis that Ani HBr could protect the EC against permeability and NO productionviapreventing glycocalyx shedding. Methods-A human cerebral microvascular EC hCMEC/D3 injury model induced by lipopolysaccharide (LPS) was established. Ani HBr was administrated to ECs with the LPS challenge. Cell viability was performed by Cell Counting Kit-8 assay. Cell proliferation and apoptosis were detected by EdU and Hoechst 33342 staining. Apoptosis and cell cycle were also assessed by flow cytometry with annexin V staining and propidium iodide staining, respectively. Then, adherens junction integrity was evaluated basing on the immunofluorescence staining of vascular endothelial cadherin (VE-cadherin). The glycocalyx component heparan sulfate (HS) was stained in ECs. The cell permeability was evaluated by leakage of fluorescein isothiocyanate (FITC)-dextran. Cellular NO production was measured by the method of nitric acid reductase. Results-Ani HBr at 20 mu g/mL significantly increased the viability of ECs with LPS challenge, but significantly inhibited the cell viability at 80 mu g/mL, showing a bidirectional regulation of cell viability by Ani HBr. Ani HBr had not significantly change the LPS-induced EC proliferation. Ani HBr significantly reversed the induction of LPS on EC apoptosis. Ani HBr reinstated the LPS-induced glycocalyx and VE-cadherin shedding and adherens junction disruption. Ani HBr significantly alleviated LPS-induced EC layer permeability and NO production. Conclusion-Ani HBr protects ECs against LPS-induced increase in cell barrier permeability and nitric oxide productionviapreserving the integrity of glycocalyx. Ani HBr is a promising drug to rescue or protect the glycocalyx.

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