Skip to main content
Erschienen in: Journal of Natural Medicines 3/2016

19.02.2016 | Original Paper

Anti-inflammatory and blood stasis activities of essential oil extracted from Artemisia argyi leaf in animals

verfasst von: Yue-bin Ge, Zhi-gang Wang, Ying Xiong, Xian-ju Huang, Zhi-nan Mei, Zong-guo Hong

Erschienen in: Journal of Natural Medicines | Ausgabe 3/2016

Einloggen, um Zugang zu erhalten

Abstract

Artemisia argyi leaf is a well-known species in traditional Chinese medicine. However, the anti-inflammatory and activating blood stasis activities of its essential oil (AAEO) have not been explored in vivo. The present study measured the contents of three chemical components by gas chromatography (GC). The anti-acute inflammatory effects of AAEO were investigated in dimethyl benzene, glacial acetic acid and carrageenan-induced animals through skin administration or by oral gavage, respectively. The effects of AAEO on haemorheology were studied in a rat acute blood stasis model. The contents of eucalyptol, camphor and borneol in AAEO were 254.4, 51.6 and 58.7 mg/g, respectively. All dosages of AAEO by skin administration significantly decreased the swelling in dimethyl benzene-induced ear oedema and carrageenan-induced paw oedema, and reduced the permeability in glacial acetic acid-induced abdominal blood capillary (p < 0.01). Meanwhile, haemorheology indexes such as whole blood viscosity and the erythrocyte aggregation index significantly decreased only in the high dosage group. In addition, the effects of AAEO by oral gavage were weaker than skin administration at the medium dose in the experiments. It suggests that AAEO has better absorption bioavailability and pharmacological effects through skin administration due to the better skin permeability of essential oil than gastrointestinal absorption.
Literatur
1.
Zurück zum Zitat Deng HY, Shen XY (2013) The mechanism of moxibustion: ancient theory and modern research. Evid Based Complement Alternat Med 2013, 379291PubMedPubMedCentral Deng HY, Shen XY (2013) The mechanism of moxibustion: ancient theory and modern research. Evid Based Complement Alternat Med 2013, 379291PubMedPubMedCentral
2.
Zurück zum Zitat Lao AN, Fujimoto Y, Tatsuno T (1984) Studies on the constituents of Artemisia argyi Levl et Vant. Chem Pharm Bull 32:723–727CrossRef Lao AN, Fujimoto Y, Tatsuno T (1984) Studies on the constituents of Artemisia argyi Levl et Vant. Chem Pharm Bull 32:723–727CrossRef
3.
Zurück zum Zitat Tan RX, Jia ZJ (1992) Eudesmanolides and other constituents from Artemisia argyi. Planta Med 58:370–372CrossRefPubMed Tan RX, Jia ZJ (1992) Eudesmanolides and other constituents from Artemisia argyi. Planta Med 58:370–372CrossRefPubMed
4.
Zurück zum Zitat Nakasugi T, Nakashima M, Komai K (2000) Antimutagens in gaiyou (Artemisia argyi levl. et vant.). J Agr Food Chem 48:3256–3266CrossRef Nakasugi T, Nakashima M, Komai K (2000) Antimutagens in gaiyou (Artemisia argyi levl. et vant.). J Agr Food Chem 48:3256–3266CrossRef
5.
Zurück zum Zitat Seo JM, Kang HM, Son KH, Kim JH, Lee CW, Kim HM, Chang SI, Kwon BM (2003) Antitumor activity of flavones isolated from Artemisia argyi. Planta Med 69:218–222CrossRefPubMed Seo JM, Kang HM, Son KH, Kim JH, Lee CW, Kim HM, Chang SI, Kwon BM (2003) Antitumor activity of flavones isolated from Artemisia argyi. Planta Med 69:218–222CrossRefPubMed
6.
Zurück zum Zitat Shoemaker M, Hamilton B, Dairkee SH, Cohen I, Campbell MJ (2005) In vitro anticancer activity of twelve Chinese medicinal herbs. Phytother Res 19:649–651CrossRefPubMed Shoemaker M, Hamilton B, Dairkee SH, Cohen I, Campbell MJ (2005) In vitro anticancer activity of twelve Chinese medicinal herbs. Phytother Res 19:649–651CrossRefPubMed
7.
Zurück zum Zitat Lee HG, Yu KA, Oh WK, Baeg TW, Oh HC, Ahn JS, Jang WC, Kim JW, Lim JS, Choe YK, Yoon DY (2005) Inhibitory effect of jaceosidin isolated from Artemisia argyi on the function of E6 and E7 oncoproteins of HPV 16. J Ethnopharmacol 98:339–343CrossRefPubMed Lee HG, Yu KA, Oh WK, Baeg TW, Oh HC, Ahn JS, Jang WC, Kim JW, Lim JS, Choe YK, Yoon DY (2005) Inhibitory effect of jaceosidin isolated from Artemisia argyi on the function of E6 and E7 oncoproteins of HPV 16. J Ethnopharmacol 98:339–343CrossRefPubMed
8.
Zurück zum Zitat Adams M, Efferth T, Bauer R (2006) Activity-guided isolation of scopoletin and isoscopoletin, the inhibitory active principles towards CCRF-CEM leukaemia cells and multi-drug resistant CEM/ADR5000 cells, from Artemisia argyi. Planta Med 72:862–864CrossRefPubMed Adams M, Efferth T, Bauer R (2006) Activity-guided isolation of scopoletin and isoscopoletin, the inhibitory active principles towards CCRF-CEM leukaemia cells and multi-drug resistant CEM/ADR5000 cells, from Artemisia argyi. Planta Med 72:862–864CrossRefPubMed
9.
Zurück zum Zitat Khan M, Yu B, Rasul A, Al Shawi A, Yi F, Yang H, Ma T (2012) Jaceosidin induces apoptosis in U87 glioblastoma cells through G2/M phase arrest. Evid Based Complement Alternat Med 2012, 703034PubMed Khan M, Yu B, Rasul A, Al Shawi A, Yi F, Yang H, Ma T (2012) Jaceosidin induces apoptosis in U87 glioblastoma cells through G2/M phase arrest. Evid Based Complement Alternat Med 2012, 703034PubMed
10.
Zurück zum Zitat Kim MJ, Kim DH, Lee KW, Yoon DY, Surh YJ (2007) Jaceosidin induces apoptosis in ras-transformed human breast epithelial cells through generation of reactive oxygen species. Ann N Y Acad Sci 1095:483–495CrossRefPubMed Kim MJ, Kim DH, Lee KW, Yoon DY, Surh YJ (2007) Jaceosidin induces apoptosis in ras-transformed human breast epithelial cells through generation of reactive oxygen species. Ann N Y Acad Sci 1095:483–495CrossRefPubMed
11.
Zurück zum Zitat Lim JC, Park SY, Nam Y, Nguyen TT, Sohn UD (2012) The protective effect of eupatilin against hydrogen peroxide-induced injury involving 5-lipoxygenase in feline esophageal epithelial cells. Korean J Physiol Pharmacol 16:313–320CrossRefPubMedPubMedCentral Lim JC, Park SY, Nam Y, Nguyen TT, Sohn UD (2012) The protective effect of eupatilin against hydrogen peroxide-induced injury involving 5-lipoxygenase in feline esophageal epithelial cells. Korean J Physiol Pharmacol 16:313–320CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Zhang YH, Xue MQ, Bai YC, Yuan HH, Zhao HL, Lan MB (2012) 3,5-Dicaffeoylquinic acid isolated from Artemisia argyi and its ester derivatives exert anti-leucyl-tRNA synthetase of Giardia lamblia (GlLeuRS) and potential anti-giardial effects. Fitoterapia 83:1281–1285CrossRefPubMed Zhang YH, Xue MQ, Bai YC, Yuan HH, Zhao HL, Lan MB (2012) 3,5-Dicaffeoylquinic acid isolated from Artemisia argyi and its ester derivatives exert anti-leucyl-tRNA synthetase of Giardia lamblia (GlLeuRS) and potential anti-giardial effects. Fitoterapia 83:1281–1285CrossRefPubMed
13.
Zurück zum Zitat Bao X, Yuan H, Wang C, Liu J, Lan M (2013) Antitumor and immunomodulatory activities of a polysaccharide from Artemisia argyi. Carbohydr Polym 98:1236–1243CrossRefPubMed Bao X, Yuan H, Wang C, Liu J, Lan M (2013) Antitumor and immunomodulatory activities of a polysaccharide from Artemisia argyi. Carbohydr Polym 98:1236–1243CrossRefPubMed
14.
Zurück zum Zitat Edris AE (2007) Pharmaceutical and therapeutic potentials of essential oils and their individual volatile constituents: a review. Phytother Res 21:308–323CrossRefPubMed Edris AE (2007) Pharmaceutical and therapeutic potentials of essential oils and their individual volatile constituents: a review. Phytother Res 21:308–323CrossRefPubMed
15.
Zurück zum Zitat Huang HC, Wang HF, Yih KH, Chang LZ, Chang TM (2012) Dual bioactivities of essential oil extracted from the leaves of Artemisia argyi as an antimelanogenic versus antioxidant agent and chemical composition analysis by GC/MS. Int J Mol Sci 13:14679–14697CrossRefPubMedPubMedCentral Huang HC, Wang HF, Yih KH, Chang LZ, Chang TM (2012) Dual bioactivities of essential oil extracted from the leaves of Artemisia argyi as an antimelanogenic versus antioxidant agent and chemical composition analysis by GC/MS. Int J Mol Sci 13:14679–14697CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Hu Y, Yang Y, Ning Y, Wang C, Tong Z (2013) Facile preparation of Artemisia argyi oil-loaded antibacterial microcapsules by hydroxyapatite-stabilized Pickering emulsion templating. Colloids Surf B Biointerfaces 112:96–102CrossRefPubMed Hu Y, Yang Y, Ning Y, Wang C, Tong Z (2013) Facile preparation of Artemisia argyi oil-loaded antibacterial microcapsules by hydroxyapatite-stabilized Pickering emulsion templating. Colloids Surf B Biointerfaces 112:96–102CrossRefPubMed
17.
Zurück zum Zitat Guan WQ, Li SF, Yan RX, Huang YF (2006) Comparison of composition and antifungal activity of Artemisia argyi Lévl. et Vant inflorescence essential oil extracted by hydrodistillation and supercritical carbon dioxide. Nat Prod Res 20:992–998CrossRef Guan WQ, Li SF, Yan RX, Huang YF (2006) Comparison of composition and antifungal activity of Artemisia argyi Lévl. et Vant inflorescence essential oil extracted by hydrodistillation and supercritical carbon dioxide. Nat Prod Res 20:992–998CrossRef
18.
Zurück zum Zitat He ZY, Zhang YH, Wei D, Yu RH, Yuan HH, Lan MB (2009) Chemical composition of essential oil from fresh and dried Folium Artemisia argyi from Hubei Province. Chinese Tradit Patent Med 31:1079–1082 He ZY, Zhang YH, Wei D, Yu RH, Yuan HH, Lan MB (2009) Chemical composition of essential oil from fresh and dried Folium Artemisia argyi from Hubei Province. Chinese Tradit Patent Med 31:1079–1082
19.
Zurück zum Zitat Li N, Mao Y, Deng C, Zhang X (2008) Separation and identification of volatile constituents in Artemisia argyi flowers by GC-MS with SPME and steam distillation. J Chromatogr Sci 46:401–405CrossRefPubMed Li N, Mao Y, Deng C, Zhang X (2008) Separation and identification of volatile constituents in Artemisia argyi flowers by GC-MS with SPME and steam distillation. J Chromatogr Sci 46:401–405CrossRefPubMed
20.
Zurück zum Zitat Abad MJ, Bedoya LM, Apaza L, Bermejo P (2012) The Artemisia L. genus: a review of bioactive essential oils. Molecules 17:2542–2566CrossRefPubMed Abad MJ, Bedoya LM, Apaza L, Bermejo P (2012) The Artemisia L. genus: a review of bioactive essential oils. Molecules 17:2542–2566CrossRefPubMed
21.
Zurück zum Zitat Yoshikawa M, Shimada H, Matsuda H, Yamahara J, Murakami N (1996) Bioactive constituents of Chinese natural medicines. I. New sesquiterpene ketones with vasorelaxant effect from Chinese moxa, the processed leaves of Artemisia argyi Levl. et Vant.: moxartenone and moxartenolide. Chem Pharm Bull (Tokyo) 44:1656–1662CrossRef Yoshikawa M, Shimada H, Matsuda H, Yamahara J, Murakami N (1996) Bioactive constituents of Chinese natural medicines. I. New sesquiterpene ketones with vasorelaxant effect from Chinese moxa, the processed leaves of Artemisia argyi Levl. et Vant.: moxartenone and moxartenolide. Chem Pharm Bull (Tokyo) 44:1656–1662CrossRef
22.
Zurück zum Zitat Jeong MA, Lee KW, Yoon DY, Lee HJ (2007) Jaceosidin, a pharmacologically active flavone derived from Artemisia argyi, inhibits phorbol-ester-induced upregulation of COX-2 and MMP-9 by blocking phosphorylation of ERK-1 and -2 in cultured human mammary epithelial cells. Ann N Y Acad Sci 1095:458–466CrossRefPubMed Jeong MA, Lee KW, Yoon DY, Lee HJ (2007) Jaceosidin, a pharmacologically active flavone derived from Artemisia argyi, inhibits phorbol-ester-induced upregulation of COX-2 and MMP-9 by blocking phosphorylation of ERK-1 and -2 in cultured human mammary epithelial cells. Ann N Y Acad Sci 1095:458–466CrossRefPubMed
23.
Zurück zum Zitat Wang S, Li J, Sun J, Zeng KW, Cui JR, Jiang Y, Tu PF (2013) NO inhibitory guaianolide-derived terpenoids from Artemisia argyi. Fitoterapia 85:169–175CrossRefPubMed Wang S, Li J, Sun J, Zeng KW, Cui JR, Jiang Y, Tu PF (2013) NO inhibitory guaianolide-derived terpenoids from Artemisia argyi. Fitoterapia 85:169–175CrossRefPubMed
24.
Zurück zum Zitat Zeng KW, Wang S, Dong X, Jiang Y, Tu PF (2014) Sesquiterpene dimer (DSF-52) from Artemisia argyi inhibits microglia-mediated neuroinflammation via suppression of NF-κB, JNK/p38 MAPKs and Jak2/Stat3 signaling pathways. Phytomedicine 21:298–306CrossRefPubMed Zeng KW, Wang S, Dong X, Jiang Y, Tu PF (2014) Sesquiterpene dimer (DSF-52) from Artemisia argyi inhibits microglia-mediated neuroinflammation via suppression of NF-κB, JNK/p38 MAPKs and Jak2/Stat3 signaling pathways. Phytomedicine 21:298–306CrossRefPubMed
25.
Zurück zum Zitat Lee SH, Kim HK, Seo JM, Kang HM, Kim JH, Son KH, Lee H, Kwon BM, Shin J, Seo Y (2002) Arteminolides B, C, and D, new inhibitors of farnesyl protein transferase from Artemisia argyi. J Org Chem 67:7670–7675CrossRefPubMed Lee SH, Kim HK, Seo JM, Kang HM, Kim JH, Son KH, Lee H, Kwon BM, Shin J, Seo Y (2002) Arteminolides B, C, and D, new inhibitors of farnesyl protein transferase from Artemisia argyi. J Org Chem 67:7670–7675CrossRefPubMed
26.
Zurück zum Zitat Romero A, Planas E, Poveda R, Sánchez S, Pol O, Puig MM (2005) Anti-exudative effects of opioid receptor agonists in a rat model of carrageenan-induced acute inflammation of the paw. Eur J Pharmacol 511:207–217CrossRefPubMed Romero A, Planas E, Poveda R, Sánchez S, Pol O, Puig MM (2005) Anti-exudative effects of opioid receptor agonists in a rat model of carrageenan-induced acute inflammation of the paw. Eur J Pharmacol 511:207–217CrossRefPubMed
27.
Zurück zum Zitat Williams AC, Barry BW (1989) Essential oils as novel human skin penetration enhancers. Int J Pharmaceut 57:R7–R9CrossRef Williams AC, Barry BW (1989) Essential oils as novel human skin penetration enhancers. Int J Pharmaceut 57:R7–R9CrossRef
28.
Zurück zum Zitat Williams AC, Barry BW (1991) Terpenes and the lipid-protein-partitioning theory of skin penetration enhancement. Pharm Res 8:17–24CrossRefPubMed Williams AC, Barry BW (1991) Terpenes and the lipid-protein-partitioning theory of skin penetration enhancement. Pharm Res 8:17–24CrossRefPubMed
29.
Zurück zum Zitat Cal K (2006) Skin penetration of terpenes from essential oils and topical vehicles. Planta Med 72:311–316CrossRefPubMed Cal K (2006) Skin penetration of terpenes from essential oils and topical vehicles. Planta Med 72:311–316CrossRefPubMed
Metadaten
Titel
Anti-inflammatory and blood stasis activities of essential oil extracted from Artemisia argyi leaf in animals
verfasst von
Yue-bin Ge
Zhi-gang Wang
Ying Xiong
Xian-ju Huang
Zhi-nan Mei
Zong-guo Hong
Publikationsdatum
19.02.2016
Verlag
Springer Japan
Erschienen in
Journal of Natural Medicines / Ausgabe 3/2016
Print ISSN: 1340-3443
Elektronische ISSN: 1861-0293
DOI
https://doi.org/10.1007/s11418-016-0972-6

Weitere Artikel der Ausgabe 3/2016

Journal of Natural Medicines 3/2016 Zur Ausgabe