Planta Med 2014; 80(08/09): 671-675
DOI: 10.1055/s-0034-1368592
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Structure-Activity Relationship Study of Dibenzocyclooctadiene Lignans Isolated from Schisandra chinensis on Lipopolysaccharide-Induced Microglia Activation

Authors

  • Di Hu

    1   Development and Utilization Key Laboratory of Northeast Plant Materials of Liaoning Province, Department of Pharmacognosy, Shenyang Pharmaceutical University, Shenyang, China
    2   College of Pharmacy, Harbin University of Commerce, Harbin, Heilongjiang Province, China
  • Na Han

    1   Development and Utilization Key Laboratory of Northeast Plant Materials of Liaoning Province, Department of Pharmacognosy, Shenyang Pharmaceutical University, Shenyang, China
  • Xuechun Yao

    3   Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang, China
  • Zhihui Liu

    1   Development and Utilization Key Laboratory of Northeast Plant Materials of Liaoning Province, Department of Pharmacognosy, Shenyang Pharmaceutical University, Shenyang, China
  • Yu Wang

    4   The Chinese Peopleʼs Liberation Army 463 Hospital, Shenyang, China
  • Jingyu Yang

    3   Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang, China
  • Jun Yin

    1   Development and Utilization Key Laboratory of Northeast Plant Materials of Liaoning Province, Department of Pharmacognosy, Shenyang Pharmaceutical University, Shenyang, China
Further Information

Publication History

received 22 January 2014
revised 07 May 2014

accepted 20 May 2014

Publication Date:
25 June 2014 (online)

Abstract

To explore the relationship of the dibenzocyclooctadiene lignans from Schisandra chinensis to their anti-inflammatory activities, series of dibenzocyclooctadiene lignans were isolated and assessed by testing their inhibitory effects on nitric oxide production in lipopolysaccharide-induced BV2 mouse microglia. It was found, for the first time, that dibenzocyclooctadiene lignans which have S-biphenyl and methylenedioxy groups strongly inhibited LPS-induced microglia activation. The methoxy group on the cyclooctadiene introduced more effectiveness, but the presence of an acetyl group on the cyclooctadiene or hydroxyl group on C-7 decreased the inhibitory activity.