Neuroprotective effects of Salidroside and its analogue tyrosol galactoside against focal cerebral ischemia in vivo and H2O2-induced neurotoxicity in vitro

Neurotox Res. 2012 May;21(4):358-67. doi: 10.1007/s12640-011-9290-7. Epub 2011 Nov 18.

Abstract

Salidroside (Sal) is a natural antioxidant extracted from the root of Rhodiola rosea L. that elicits neuroprotective effects in vivo and in vitro. Tyrosol galactoside (Tyr), an analog of Sal, was recently synthesized in our laboratory. The purpose of the current study was to investigate and compare the neuroprotective effects of Sal and Tyr against focal cerebral ischemia in vivo and H(2)O(2)-induced neurotoxicity in vitro. Sal and Tyr significantly prevented a cerebral ischemic injury induced by a 2 h middle cerebral artery occlusion and a 24 h reperfusion in rats in vivo. Furthermore, the oxidative insult was markedly attenuated by treatments of Sal and Tyr in the cultured rat cortical neurons after a 30 min exposure to 50 μM of H(2)O(2). Western blot analysis revealed that Sal and Tyr decreased the expression of Bax and restored the balance of pro- and anti-apoptotic proteins. The neuroprotective effects of these two analogues show that Tyr has a better antioxidative action compared with Sal both in vivo and in vitro, and suggest that the antioxidant activity of Sal and Tyr may be partly due to their different substituents in their glycosyl groups. This gives a new insight into the development of therapeutic natural antioxidants against oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / metabolism
  • Brain Ischemia / drug therapy*
  • Brain Ischemia / pathology
  • Cell Survival / drug effects
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Disease Models, Animal
  • Drug Administration Schedule
  • Galactosides / administration & dosage
  • Galactosides / pharmacology
  • Galactosides / therapeutic use*
  • Glucosides / administration & dosage
  • Glucosides / pharmacology
  • Glucosides / therapeutic use*
  • Hydrogen Peroxide / antagonists & inhibitors*
  • Hydrogen Peroxide / toxicity
  • Infarction, Middle Cerebral Artery / drug therapy
  • Infarction, Middle Cerebral Artery / pathology
  • Male
  • Neurons / metabolism
  • Neurons / pathology
  • Neuroprotective Agents / pharmacology
  • Neuroprotective Agents / therapeutic use*
  • Oxidants / antagonists & inhibitors
  • Oxidants / toxicity
  • Phenols / administration & dosage
  • Phenols / pharmacology
  • Phenols / therapeutic use*
  • Phenylethyl Alcohol / administration & dosage
  • Phenylethyl Alcohol / analogs & derivatives*
  • Phenylethyl Alcohol / pharmacology
  • Phenylethyl Alcohol / therapeutic use
  • Primary Cell Culture
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Reperfusion Injury / drug therapy
  • Reperfusion Injury / pathology
  • bcl-2-Associated X Protein / biosynthesis

Substances

  • Apoptosis Regulatory Proteins
  • Galactosides
  • Glucosides
  • Neuroprotective Agents
  • Oxidants
  • Phenols
  • Reactive Oxygen Species
  • bcl-2-Associated X Protein
  • tyrosol galactoside
  • Hydrogen Peroxide
  • rhodioloside
  • Phenylethyl Alcohol