Planta Med 2015; 81(10): 821-829
DOI: 10.1055/s-0035-1546170
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Imperialine and Verticinone from Bulbs of Fritillaria wabuensis Inhibit Pro-inflammatory Mediators in LPS-stimulated RAW 264.7 Macrophages

Ke Wu
1   Department of Medicinal Natural Products, West China School of Pharmacy, Sichuan University, Chengdu, China
,
Chunfen Mo
2   Lab for Aging Research, Center for Medical Stem Cell Biology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China
,
Hengyi Xiao
2   Lab for Aging Research, Center for Medical Stem Cell Biology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China
,
Yun Jiang
3   State Key Laboratory of Quality Research, Chinese Medicine Institute of Chinese Medical Sciences, University of Macao, Macao, China
,
Bengui Ye
1   Department of Medicinal Natural Products, West China School of Pharmacy, Sichuan University, Chengdu, China
,
Shu Wang
1   Department of Medicinal Natural Products, West China School of Pharmacy, Sichuan University, Chengdu, China
› Author Affiliations
Further Information

Publication History

received 11 January 2015
revised 01 May 2015

accepted 05 May 2015

Publication Date:
01 July 2015 (online)

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Abstract

The bulbs of plants belonging to the Fritillaria cirrhosa-group have been used as antitussive and expectorant herbs in traditional Chinese medicine for thousands of years. In this study, we isolated two isomers of verticinone and imperialine, steroidal alkaloids belonging to the cevanine group, from bulbs of Fritillaria wabuensis, which is a part of the Fritillaria cirrhosa group, and investigated their anti-inflammatory effects and relative mechanisms on lipopolysaccharide-stimulated RAW 264.7 macrophages. Our results clearly demonstrate that verticinone or imperialine could dose-dependently inhibit nitric oxide production and also suppress inducible nitric oxide synthase and cyclooxygenase-2 expressions. In addition, verticinone or imperialine suppress the production of pro-inflammatory cytokines in a dose dependent manner, such as tumor necrosis factor-α and interleukin-1β. The effect of verticinone and imperialine on the activation of nuclear factor-kappaB was also evaluated. The phosphorylation of nuclear factor-kappaB stimulated with LPS is also down-regulated by verticinone or imperialine in a concentration dependent manner, which coincided with the inhibition of phosphorylation forms of inhibitory kappaB-α, a crucial inhibitory factor of nuclear factor-kappaB. Generally, the anti-inflammatory effects and mechanisms of verticinone and imperialine are mediated by the inhibition of the nuclear factor-kappaB activation signaling pathway. According to the results of our researches, verticinone and imperialine may present great potentials to be developed as therapeutics for inflammatory diseases.

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