The present study was performed to investigate the variation of phytochemical composition, antioxidant activity and High Performance Liquid Chromatography (HPLC) fingerprinting profiles of three Pyrola species. Thirteen samples (eight P. decorata, three P. calliantha and two P. renifolia) were collected from different regions in China. The tannin, hyperoside and quercetin contents of all samples were determined by reverse-phase HPLC and varied within the range 9.77–34.75, 0.34–2.16 and 0.062–0.147 mg/g dry weigh, respectively. Total flavonoid content was evaluated and varied within the range 16.22–37.82 mg/g dry weight. Antioxidant activity was determined by DPPH assay, with IC50 ranging from 7.96 to 50.33 μg/ml, ABTS?+ and FRAP assay, within the range 612.66–1021.05 and 219.64–398.12 μmol equiv. Trolox/g, respectively. These results revealed that there were significant variations in phytochemical profiles and antioxidant activity among all samples. Due to the higher phytochemical content and significant antioxidant activity, P. calliantha was selected as the most valuable species, and the P. calliantha sample from Left banner of Alxa even possessed the strongest antioxidant activity among all the thirteen samples. Futhermore, Emei Mountain was proved to be the most suitable region for producing P. decorata. Moreover, in order to further evaluate the diversities and quality of Pyrola, HPLC fingerprint analysis coupled with hierarchical cluster and discrimination analyses were introduced to establish a simple, rapid and effective method for accurate identification, classification and quality assessment of Pyrola. Thirteen samples were divided into three groups consistent with their morphological classification. Two types of discriminant functions were generated and the ratio of discrimination was 100%. This method can identify different species of Pyrola and the same species from different regions of origin. Also, it can be used to compare and control the quality of Pyrola and other natural products prepared from them.
References
[1]
Zhang DY, Luo M, Wang W, Zhao CJ, Gu CB, et al. (2013) Variation of active constituents and antioxidant activity in pyrola [P. incarnata Fisch.] from different sites in Northeast China. Food Chem 141: 2213–2219. doi: 10.1016/j.foodchem.2013.05.045
[2]
Chinese Pharmacopoeia Committee (2005) Pharmacopoeia of China. Beijing: Chemical Industry Press. (In Chinese).
[3]
Yamashita CI, Saiki M, Vasconcellos MBA, Sertie JAA (2005) Characterization of trace elements in medicinal plant by neutron activation analysis. Appl. Radiat. Isot 63: 841–846. doi: 10.1016/j.apradiso.2005.05.045
[4]
Liu MG, Xiao GGS, Rong PJ, Zhang ZG, Dong J, et al. (2012) Therapeutic effects of radix dipsaci, pyrola herb, and cynomorium songaricum on bone metabolism of ovariectomized rats. BMC Complement Altern Med 12: 67–85. doi: 10.1186/1472-6882-12-67
[5]
Lou DQ, Yang YZ, Song L, Wang JX (2004) Advances in studies on special plants of Pyrola L. in China. Chin. Tradit. Herbal Drugs 35: 463–466 (In Chinese).
[6]
Yao XH, Zhang DY, Zu YG, Fu YJ, Luo M, et al. (2013) Free radical scavenging capability, antioxidant activity and chemical constituents of Pyrola incarnata Fisch. leaves. Ind. Crops Prod 49: 247–255. doi: 10.1016/j.indcrop.2013.04.058
[7]
Bergeron C, Marston A, Antus S, Gauthier R, Hostettmann K (1998) Flavonoids from pyrola elliptica. Phytochem 49: 233–236. doi: 10.1016/s0031-9422(97)00878-9
[8]
Leonid RP, Kenzo N, Ilya VS, Anna BR (2011) The 1, 4-naphthoquinone derivative from Pyrola rotundifolia activates AMPK phosphorylation in C2C12 myotubes. Fitoterapia 82: 1285–1289. doi: 10.1016/j.fitote.2011.09.005
[9]
Lv ZJ, Wang DM, Li DW (2013) Content of four chemical elements and the forms of their existence in Pyrola decorata occurring in different areas. Journal of Northwest Forestry University 28 (1): 126–129 (In Chinese with English abstract.).
[10]
Lv ZJ, Wang DM, Li DW (2012) Correlation between quality of Pyrola decorata and its ecological factors based on hierarchy-vector analysis. Chinese Journal of Plant Ecology 36 (9): 992–1003 (In Chinese with English abstract.). doi: 10.3724/sp.j.1258.2012.00992
[11]
Zhao Y, Xie ZH, Niu YG, Shi HM, Chen P, et al. (2012) Chemical compositions, HPLC/MS fingerprinting profiles and radical scavenging properties of commercial Gynostemma pentaphyllum (Thunb.) Makino samples. Food Chem 134: 180–188. doi: 10.1016/j.foodchem.2012.02.090
[12]
Jia ZS, Tang MC, Wu JM (1999) The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chem 64: 555–559. doi: 10.1016/s0308-8146(98)00102-2
[13]
Williams WB, Cuvelier ME, Berset C (1995) Use of a free radical method to evaluate antioxidant activity. Lebensm.-Wiss. u. -Technol 28: 25–30.
[14]
Wang SS, Wang DM, Pu WJ, Li DW (2013) Phytochemical profiles, antioxidant and antimicrobial activities of three Potentilla species. BMC Complement Altern Med 13: 321–331. doi: 10.1186/1472-6882-13-321
[15]
Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, et al. (1999) Antioxidantactivity applying an improved ABTS radical cation decolorization assay. Free Radical Bio Med 26: 1231–1237. doi: 10.1016/s0891-5849(98)00315-3
[16]
Benzie IF, Strain J (1996) The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem 239: 70–76. doi: 10.1006/abio.1996.0292
[17]
Li BY, Hu Y, Liang YZ, Xie PS, Du YP (2004) Quality evaluation of fingerprints of herbal medicine with chromatographic data. Analytica Chimica Acta 514: 69–77. doi: 10.1016/j.aca.2004.03.041
[18]
Yang DF, Liang ZS, Duan QM, Zhang YJ (2007) Quality assessment of Cardiotonic Pills by HPLC fingerprinting. Chromatographia 66: 509–514. doi: 10.1365/s10337-007-0359-7
[19]
Alonsosalces RM, Guyot S, Herrero C (2005) Chemometric classification of Basque and French ciders based on their total polyphenol contents and CIELab parameters. Food Chem 91: 91–98. doi: 10.1016/j.foodchem.2004.05.049
[20]
Shi XM, Zhang JS, Tang QJ, Yang Y, Hao RX, et al. (2008) Fingerprint analysis of Lingzhi (Ganoderma) strains by high-performance liquid chromatography coupled with chemometric methods. World J. Microbiol. Biotechnol 24: 2443–2450. doi: 10.1007/s11274-008-9766-7
[21]
Zhao KJ, Dong TTX, Tsim KWK (2003) Molecular genetic and chemical assessment of Radix Angelica (Danggui) in China. J Agric Food Chem 51: 2576–2583. doi: 10.1021/jf026178h
[22]
Peng L, Wang YZ, Zhu HB, Chen QM (2011) Fingerprint profile of active components for Artemisia selengensis Turcz by HPLC–PAD combined with chemometrics. Food Chem 125: 1064–1071. doi: 10.1016/j.foodchem.2010.09.079
[23]
Harwood M, Danielewska-Nikiel B, Borzelleca J, Flamm G, Williams G, et al. (2007) A critical review of the data related to the safety of quercetin and lack of evidence of in vivo toxicity, including lack of genotoxic/carcinogenic properties. Food Chem Toxicol 45(11): 2179–2205. doi: 10.1016/j.fct.2007.05.015
[24]
Yang LC, Li R, Tan J, Jiang ZT (2013) Polyphenolics composition of the leaves of Zanthoxylum bungeanum Maxim. grown in Hebei, China, and their radical scavenging activities. J Agri Food Chem 61(8): 1772–1778. doi: 10.1021/jf3042825
[25]
Robards K, Prernzler PD, Tucker G, Swatsitang P, Glover W (1999) Phenolic compounds and their role in oxidative processes in fruits. Food Chem 80: 561–566. doi: 10.1016/s0308-8146(99)00093-x
[26]
Heim KE, Tagliaferro AR, Bobilya DJ (2002) Flavonoid antioxidants: chemistry, metabolism and structure- activity relationships. Nutri Biochem 13: 572–584. doi: 10.1016/s0955-2863(02)00208-5
[27]
Chantal B, Andrew M, Sandor A, Robert G, Kurt H (1997) Flavonoids from Pyrola elliptica. Phytochem 49: 233–236. doi: 10.1016/s0031-9422(97)00878-9
[28]
Yang J, Chen LH, Zhang Q, Lai MX, Wang Q (2007) Quality assessment of Cortex cinnamomi by HPLC chemical fingerprint, principle component analysis and cluster analysis. J. Sep. Sci 30: 1276–1283. doi: 10.1002/jssc.200600389