Planta Med 2014; 80(04): 262-268
DOI: 10.1055/s-0033-1360340
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Protective Effects of Sulphonated Formononetin in a Rat Model of Cerebral Ischemia and Reperfusion Injury

Haibo Zhu
1   Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang, PR China
3   State Key Laboratory of Long-acting and Targeting Drug Delivery Technologies (Luye Pharma Group Ltd.), Yantai, PR China
,
Libo Zou
1   Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang, PR China
,
Jingwei Tian
2   School of Pharmacy, Yantai University, Yantai, PR China
,
Fei Lin
3   State Key Laboratory of Long-acting and Targeting Drug Delivery Technologies (Luye Pharma Group Ltd.), Yantai, PR China
,
Jie He
3   State Key Laboratory of Long-acting and Targeting Drug Delivery Technologies (Luye Pharma Group Ltd.), Yantai, PR China
,
Jian Hou
3   State Key Laboratory of Long-acting and Targeting Drug Delivery Technologies (Luye Pharma Group Ltd.), Yantai, PR China
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Publikationsverlauf

received 22. September 2013
revised 18. Dezember 2013

accepted 08. Januar 2014

Publikationsdatum:
18. Februar 2014 (online)

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Abstract

Sodium formononetin-3′-sulphonate is a derivative of the plant isoflavone formononetin. The present study aimed to investigate the neuroprotective and angiogenesis effects of sodium formononetin-3′-sulphonate in vivo and in vitro. Treatment with sodium formononetin-3′-sulphonate (3, 7.5, 15, and 30 mg/kg, intravenous injection) could protect the brain from ischemia and reperfusion injury by improving neurological function, suppressing cell apoptosis, and increasing expression levels of vascular endothelial growth factor and platelet endothelial cell adhesion molecule 1 by middle cerebral artery occlusion. Treatment with sodium formononetin-3′-sulphonate (10 and 20 µg/mL) significantly increased cell migration, tube formation, and vascular endothelial growth factor and platelet endothelial cell adhesion molecule levels in human umbilical vein endothelial cells. Our results suggest that sodium formononetin-3′-sulphonate provides significant neuroprotective effects against cerebral ischemia and reperfusion injury in rats, and improves cerebrovascular angiogenesis in human umbilical vein endothelial cells. The protective mechanisms of sodium formononetin-3′-sulphonate may be attributed to the suppression of cell apoptosis and improved cerebrovascular angiogenesis by promoting vascular endothelial growth factor and platelet endothelial cell adhesion molecule expression.

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