In vitro and in vivo evaluation of antioxidant activity of Petasites japonicus Maxim. flower buds extracts

References

• Takagi K, Kosumi J, Takeuchi T, et al. Breeding of a new fuki (Petasites japonicus (Sieb. et Zucc.) Fr. Schmidt) cultivar for fukinotou, “AWAHARUKA”. Bull Tokushima Agric For Fish Technol Support Cent. 2014;1:1–6. Japanese.
   Google Scholar
• Takagi K, Kosumi J. Breeding of a new fuki (Petasites japonicus (Sieb. et Zucc.) Fr. Schmidt) cultivar for yama-buki, “MISATO”. Bull Tokushima Agric For Fish Technol Support Cent. 2005;2:23–28. Japanese.
   Google Scholar
• Lee DK, Carstairs IJ, Haggart K, et al. Butterbur, a herbal remedy, attenuates adenosine monophosphate induced nasal responsiveness in seasonal allergic rhinitis. Clin Exp Allergy. 2003;33:882–886.
   PubMed Web of Science ®Google Scholar
• Schapowal A. Randomised controlled trial of butterbur and cetirizine for treating seasonal allergic rhinitis. BMJ. 2002;324:144–146.
   PubMed Web of Science ®Google Scholar
• Brattstrom A. A newly developed extract (Ze 339) from butterbur (Petasites hybridus L.) is clinically efficient in allergic rhinitis (hay fever). Phytomedicine. 2003;10:50–52.
   PubMed Web of Science ®Google Scholar
• Shimoda H, Tanaka J, Yamada E, et al. Anti type I allergic property of Japanese butterbur extract and its mast cell degranulation inhibitory ingredients. J Agric Food Chem. 2006;54:2915–2920.
   PubMed Web of Science ®Google Scholar
• Sakamura S, Yoshihara T, Toyoda K. The constituents of Petasites japonicus: structures of fukic acid and fukinolic acid. Agric Biol Chem. 1973;37:1915–1921.
   Web of Science ®Google Scholar
• Matsuura H, Amano M, Kawabata J, et al. Isolation and measurement of quercetin glucosides in flower buds of Japanese butterbur (Petasites japonicus subsp. gigantea Kitam.). Biosci Biotechnol Biochem. 2002;66:1571–1575.
   PubMed Web of Science ®Google Scholar
• Watanabe S, Hashimoto K, Tazaki H, et al. Radical scavenging activity and inhibition of macrophage NO production by fukinolic acid, a main phenolic constituent in Japanese butterbur (Petasites japonicus). Food Sci Technol Res. 2007;13:366–371.
   Web of Science ®Google Scholar
• Kim SM, Kang SW, Jeon JS, et al. Rapid identification and evaluation of antioxidant compounds from extracts of Petasites japonicus by hyphenated-HPLC techniques. Biomed Chromatogr. 2012;26:199–207.
   PubMed Web of Science ®Google Scholar
• Lin CH, Li CY, Wu TS. A novel phenylpropenoyl sulfonic acid and a new chlorophyll from the leaves of Petasites formosanus KITAMURA. Chem Pharm Bull. 2004;52:1151–1152.
   PubMed Web of Science ®Google Scholar
• Cui HS, Kim MR, Sok DE, et al. Protection by petaslignolide A, a major neuroprotective compound in the butanol extract of Petasites japonicus leaves, against oxidative damage in the brains of mice challenged with kainic acid. J Agric Food Chem. 2005;53:8526–8532.
   PubMed Web of Science ®Google Scholar
• Park CH, Kim MY, Sok DE, et al. Butterbur (Petasites japonicus Max.) extract improves lipid profiles and antioxidant activities in monosodium L-glutamate-challenged mice. J Med Food. 2010;13:1216–1223.
   PubMed Web of Science ®Google Scholar
• Watanabe J, Oki T, Takebayashi J, et al. Extraction efficiency of hydrophilic and lipophilic antioxidants from lyophilized foods using pressurized liquid extraction and manual extraction. J Food Sci. 2014;79:C1665–C1671.
   PubMed Web of Science ®Google Scholar
• Watanabe J, Oki T, Takebayashi J, et al. Improvement and interlaboratory validation of the lipophilic oxygen radical absorbance capacity: determination of antioxidant capacities of lipophilic antioxidant solutions and food extracts. Anal Sci. 2016;32:171–175.
   PubMed Web of Science ®Google Scholar
• Watanabe J, Oki T, Takebayashi J, et al. Method validation by interlaboratory studies of improved hydrophilic oxygen radical absorbance capacity methods for the determination of antioxidant capacities of antioxidant solutions and food extracts. Anal Sci. 2012;28:159–165.
   PubMed Web of Science ®Google Scholar
• Shimamura T, Matsuura R, Tokuda T, et al. Comparison of conventional antioxidant assays for evaluating potencies of natural antioxidants as food additives by collaborative study. J Jpn Soc Food Sci. 2007;54:482–487. Japanese.
   Web of Science ®Google Scholar
• Masuda T, Inouchi T, Fujimoto A, et al. Radical scavenging activity of spring mountain herbs in the Shikoku mountain area and identification of antiradical constituents by simple HPLC detection and LC-MS methods. Biosci Biotechnol Biochem. 2012;76:705–711.
   PubMed Web of Science ®Google Scholar
• Human metabolome database (HMDB) version 4 [Internet]. Canada: Reagents of The Metabolomics Innovation Centre (TMIC); 2018 [cited 2019 May 20]. Available from: http://www.hmdb.ca/spectra/ms_ms/164449
   Google Scholar
• Wanga ZY, Wanga Q, Hanb YQ, et al. Bioactivity-based UPLC/Q-TOF/MS strategy for screening of anti-inflammatory components from Cimicifugae Rhizoma. Chin Chem Lett. 2017;28:476–481.
   Web of Science ®Google Scholar
• He K, Pauli GF, Zheng B, et al. Cimicifuga species identification by high performance liquid chromatography-photodiode array/mass spectrometric/evaporative light scattering detection for quality control of lack cohosh products. J Chromatogr A. 2006;1112:241–254.
   PubMed Web of Science ®Google Scholar
• Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–358.
   PubMed Web of Science ®Google Scholar
• Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972;18:499–502.
   PubMed Web of Science ®Google Scholar
• Ma Y, Cong W, Huang H, et al. Identification of fukinolic acid from Cimicifuga heracleifolia and its derivatives as novel antiviral compounds against enterovirus A71 infection. Int J Antimicrob Agents. 2019;53:128–136.
   PubMed Web of Science ®Google Scholar
• Choi JY, Desta KT, Saralamma VVG, et al. LC–MS/MS characterization, anti-inflammatory effects and antioxidant activities of polyphenols from different tissues of Korean Petasites japonicus (Meowi). Biomed Chromatogr. 2017;31:1–9.
   Web of Science ®Google Scholar
• Han KH, Sekikawa M, Shimada K, et al. Japanese butterbur (Petasites japonicus) leaves increase hepatic oxidative stress in male rats. Biosci Biotechnol Biochem. 2012;76:2026–2031.
   PubMed Web of Science ®Google Scholar
• Kawser Hossain M, Abdal Dayem A, Han J, et al. Molecular mechanisms of the anti-obesity and anti-diabetic properties of flavonoids. Int J Mol Sci. 2016;17:569–600.
   PubMed Web of Science ®Google Scholar
• Cho AS, Jeon SM, Kim MJ, et al. Chlorogenic acid exhibits anti-obesity property and improves lipid metabolism in high-fat diet-induced-obese mice. Food Chem Toxicol. 2010;48:937–943.
   PubMed Web of Science ®Google Scholar
• Watanabe T, Hata K, Hiwatashi K, et al. Suppression of murine preadipocyte differentiation and reduction of visceral fat accumulation by a Petasites japonicus ethanol extract in mice fed a high-fat diet. Biosci Biotechnol Biochem. 2010;74:499–503.
   PubMed Web of Science ®Google Scholar
• Hirono I, Mori H, Yamada K, et al. Carcinogenic activity of petasitenine, a new pyrrolizidine alkaloid isolated from Petasites japonicus Maxim. J Natl Cancer Inst. 1977;58:1155–1157.
   PubMed Web of Science ®Google Scholar
• Hirono I, Haga M, Fujii M, et al. Induction of hepatic tumors in rats by senkirkine and symphytine. J Natl Cancer Inst. 1979;63:469–472.
   PubMed Web of Science ®Google Scholar
• Chen T, Mei N, Fu PP. Genotoxicity of pyrrolizidine alkaloids. J Appl Toxicol. 2010;30:183–196.
   PubMed Web of Science ®Google Scholar
• Ministry of Agriculture, Forestry and Fisheries. Survey of the content of pyrrolidine alkaloids in the domestic butterbur (Japanese) [Internet]; 2018 Aug 31 [cited 2019 May 20]. Available from: http://www.maff.go.jp/j/press/syouan/nouan/180831.html.
   Google Scholar