Salidroside orchestrates metabolic reprogramming by regulating the Hif-1α signalling pathway in acute mountain sickness

Pharm Biol. 2021 Dec;59(1):1540-1550. doi: 10.1080/13880209.2021.1992449.

Abstract

Context: Rhodiola crenulata (Hook. f. et Thoms.) H. Ohba (Crassulaceae) is used to prevent and treat acute mountain sickness. However, the mechanisms underlying its effects on the central nervous system remain unclear.

Objective: To investigate the effect of Rhodiola crenulata on cellular metabolism in the central nervous system.

Materials and methods: The viability and Hif-1α levels of microglia and neurons at 5% O2 for 1, 3, 5 and 24 h were examined. We performed the binding of salidroside (Sal), rhodiosin, tyrosol and p-hydroxybenzyl alcohol to Hif-1α, Hif-1α, lactate, oxidative phosphorylation and glycolysis assays. Forty male C57BL/6J mice were divided into control and Sal (25, 50 and 100 mg/kg) groups to measure the levels of Hif-1α and lactate.

Results: Microglia sensed low oxygen levels earlier than neurons, accompanied by elevated expression of Hif-1α protein. Salidroside, rhodiosin, tyrosol, and p-hydroxybenzyl alcohol decreased BV-2 (IC50=1.93 ± 0.34 mM, 959.74 ± 10.24 μM, 7.47 ± 1.03 and 8.42 ± 1.63 mM) and PC-12 (IC50=6.89 ± 0.57 mM, 159.28 ± 8.89 μM, 8.65 ± 1.20 and 8.64 ± 1.42 mM) viability. They (10 μM) reduced Hif-1α degradation in BV-2 (3.7-, 2.5-, 2.9- and 2.5-fold) and PC-12 cells (2.8-, 2.8-, 2.3- and 2.0-fold) under normoxia. Salidroside increased glycolytic capacity but attenuated oxidative phosphorylation. Salidroside (50 and 100 mg/kg) treatment increased the protein expression of Hif-1α and the release of lactate in the brain tissue of mice.

Conclusions: These results suggest that Sal induces metabolic reprogramming by regulating the Hif-1α signalling pathway to activate compensatory responses, which may be the core mechanism underlying the effect of Rhodiola crenulata on the central nervous system.

Keywords: Rhodiola crenulata; glycolysis; lactate; oxidative phosphorylation.

MeSH terms

  • Acute Disease
  • Altitude Sickness / drug therapy*
  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Cell Survival / drug effects
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Glucosides / administration & dosage
  • Glucosides / isolation & purification
  • Glucosides / pharmacology*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • PC12 Cells
  • Phenols / administration & dosage
  • Phenols / isolation & purification
  • Phenols / pharmacology*
  • Rats
  • Rhodiola / chemistry*
  • Signal Transduction / drug effects

Substances

  • Glucosides
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Phenols
  • rhodioloside

Grants and funding

This work was supported by the National Science and Technology Major Project under Grant number 2019ZX09201004-001-022 and the National Natural Science Foundation of China under Grant number 81774155.