Neural Regeneration Research ›› 2017, Vol. 12 ›› Issue (2): 235-241.doi: 10.4103/1673-5374.200807

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3′-Daidzein sulfonate sodium improves mitochondrial functions after cerebral ischemia/reperfusion injury

Wa Yuan, Qin Chen, Jing Zeng, Hai Xiao, Zhi-hua Huang, Xiao Li, Qiong Lei   

  1. Gannan Medical University, Ganzhou, Jiangxi Province, China
  • Received:2017-01-19 Online:2017-02-15 Published:2017-02-15
  • Contact: Jing Zeng,zengjing6168@163.com.
  • Supported by:

    This study was supported by the National Natural Science Foundation of China, No. 81160399, 81560583; the Science and Technology Landing Project of China, No. KJLD13085; the Science and Technology Project of the Education Department of Jiangxi Province of China, No. GJJ12560.

Abstract:

3′-Daidzein sulfonate sodium is a new synthetic water-soluble compound derived from daidzein (an active ingredient of the kudzu vine root). It has been shown to have a protective effect on cerebral ischemia/reperfusion injury in rats. We plan to study the mechanism of its protective effect. 3′-Daidzein sulfonate sodium was injected in rats after cerebral ischemia/reperfusion injury. Results showed that 3′-daidzein sulfonate sodium significantly reduced mitochondrial swelling, significantly elevated the mitochondrial membrane potential, increased mitochondrial superoxide dismutase and glutathione peroxidase activities, and decreased mitochondrial malondialdehyde levels. 3′-Daidzein sulfonate sodium improved the structural integrity of the blood-brain barrier and reduced blood-brain barrier permeability. These findings confirmed that 3′-daidzein sulfonate sodium has a protective effect on mitochondrial functions after cerebral ischemia/reperfusion injury, improves brain energy metabolism, and provides protection against blood-brain barrier damage.

Key words: nerve regeneration, 3′-daidzein sulfonate sodium, cerebral ischemia/reperfusion injury, infarct volume, anti-oxidation, mitochondria, mitochondrial membrane swelling, mitochondrial membrane potential, superoxide dismutase, malondialdehyde, glutathione peroxidase, blood-brain barrier, neural regeneration