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Chae S. C. An Up-To-Date Review of Phytochemicals and Biological Activities in Chrysanthemum Spp. Biosci Biotech Res Asia 2016;13(2).
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An Up-To-Date Review of Phytochemicals and Biological Activities in Chrysanthemum Spp.  

Soo Cheon Chae

Department of Horticultural Science, College of Industrial Sciences, Kongju National University, Daehak-ro 54, Yesan-kun, Chungnam, 32439, Korea Correspondiing Authors E- mail: scchae@kongju.ac.kr

DOI : http://dx.doi.org/10.13005/bbra/2077

ABSTRACT: The Chrysanthemum is a well-known traditional Chinese medicinal herb which has been used as a drug for thousands of years. From the detailed literature survey it is determined that the dried flowers of Chrysanthemum contain organic groups such as alkanes, flavonoids, terpinoids, unsaturated fatty acids and polysaccharides which belongs to Secondary constituents in Phytochemicals classification. The knowledge and analysis of bioactive compounds present in the Chrysanthemums can be used for next generation drug development process. The developments of new drugs against diabetes and prostate cancer have become global concern. Hence the present study leads to identify the new strategies which are needed to develop multi-functional drugs against various human diseases using Chrysanthemum plant. Owing to antifungal, antibacterial and anti-inflammation activities, Chrysanthemum have much attention in the field of biomolecules research. In general Phytochemicals can be classified as primary and secondary constituents. One can understand the fascinating properties of biological compounds via phytochemical analysis which are present in the plants. Therefore, the present study gives a better understanding of phytochemical properties of Chrysanthemum and new foundations for the production of non-toxic and eco-friendly drugs of today and the future.

KEYWORDS: Chrysanthemum; Phytochemicals; Biological activities

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Introduction

Chrysanthemums have a wide range of applications such as efficient drugs for various diseases in traditional medicinal field, healthy herbal tea in food processing, hardy blooms in gardening, and indoor air pollution control in environmental monitoring. In addition to the above appearance, aroma and color of the Chrysanthemums are the main attractive features to researchers. Aroma plays a vital role in determination of quality and market price of Chrysanthemums.  Traditional medicines from these plants have promising properties in improving liver function, decreasing inflammation. These perennial flowering plants are commonly available in Asia, northeastern Europe and most species originate from East Asia1,2. According to the literature survey more varieties of Chrysanthemums are mainly cultivated in china such as Shen-nong Sweet Chrysanthemum, Tender Huang-ju, Chamomile Flower, Hangzhou White Chrysanthemum, Florists Chrysanthemum, etc3-5. Chrysanthemum plants belong to Asteraceae family which has low molecular components include flavonoids6, sesquiterpenes7, triterpenes8, and unsaturated fatty acids9. The volatile chemical compounds of Chrysanthemum essential oil are mainly composed of monoterpenes, sesquiterpenes, aldehydes, acids, esters and alcohols 10-12. Recently, some researchers have paid more attention to characterize the aroma compounds of flowers and essential oils. Xia et al.,13 used GC–MS to analyze the volatile chemical composition from Chrysanthemum. C.morifolium is a most widely used hardy variety, available in many colours which are a better choice for gardens.

Phytochemicals of Chrysanthemum spp

Phytochemicals are biologically active chemical compounds which are derived from plants. They have many health benefits for humans further than those attributed to macronutrients and micronutrients. They play a key role to protect plants from pathogenic infections and damage. Plants have different types of phytochemicals such as Phenolic Acids, Flavonoids and Lignans which contribute to the plant’s color, aroma and flavor. Phytochemicals accumulation takes place in different parts of the plants, such as roots, stems, leaves, flowers, fruits and seeds14. More than 4,000 phytochemicals have been cataloged15 and are classified by protective function, physical characteristics and chemical characteristics16. From the survey of more than 80 research papers it is estimated that About 150 phytochemicals have been studied in detail. Chrysanthemum spp. Leaf contains octa-cosyl alcohol, β-sitosterol, lupeol, α-amyrin, daucosterol, ineupatorolide B, syringin, chlorogenic acid, petasiphenol, physcion, acacetin, eupatilin, quercetin, diosmetin, luteolin, apigenin, apigenin- 7-O-β-D-glucopyranoside, quercetin-3-O-β-D-glucopyranoside, luteolin-7-O-β-D-gluco pyranoside, apigenin-7-O-β-D- neospheroside, and acacetin-7-O-β-D-glucoside. Most of the Chrysanthemum spp flowers contain anthocyanins, cyanidin 3-glucoside and cyanidin 3-(3″-malonoyl) glucoside and carotenoids: lutein, zeaxanthin, β-cryptoxanthin, 13-cis-β-carotene, α-carotene, trans-β-carotene, and 9-cis-β-carotene. The major volatile compounds present in the plants are camphor, α-pinene, chrysanthenone, safranal, myrcene, eucalyptol, 2,4,5,6,7,7ab-hexahydro-1H-indene, verbenone, β-phellandrene and camphene. Recent studies reported by several researchers about phytochemicals found in leaves, flower and essential oil from Chrysanthemum spp are showed in table 1.

 Table 1: Recent studies on phytochemicals of Chrysanthemum spp.

Key findings

 

Reference

 

Recently, chrysanthemum flowers are known as a unique class of material which possess nutritional rich contents such as chlorophyll, carotenoids, soluble sugar, amino acid, vitamin C, flavonoid and chlorogenic acid at the time of bud stage and young flower stage. On the other hand, chrysanthemum flowers having great potential to produce active contents. Therefore both bud stage and young flower stage have been chosen as the best time for harvesting17. Ma et al., 2016
A fundamental understanding study has been made for the optimal time of harvesting of chrysanthemum flowers. From the analysis it is concluded that at the early flower opening stage, the contents of flavonoids and volatile oil were higher. On the other hand the content of chlorogenic acid, luteolin, 3,5-O-dicaffeoyl quinic acid were higher in the middle of the flowers. From the overall analysis 50% -80% fowers blossoming stage was attributed as the optimal time for harvest18. Wu et al., 2016
Generally, α-pinene, β-thujene, α-terpinolen, β-cubebene, caryophyllene, (Z)β-farnesene, (-)-spathulenol, linalool, camphor, camphene, 4-terpineol, Z-citral and 4-isopropyltoluene are typical aroma compounds covered with characteristic aroma of Chrysanthemum essential oils19. Xiao et al., 2016
Totally, 21 compounds were isolated and identified from Leaves of “Chuju” Chrysanthemum morifolium named as octa-cosyl alcohol, β-sitosterol, lupeol, α-amyrin, daucosterol, ineupatorolide B, syringin, chlorogenic acid, petasiphenol, physcion, acacetin, eupatilin, quercetin, diosmetin, luteolin, apigenin, apigenin- 7-O-β-D-glucopyranoside, quercetin-3-O-β-D-glucopyranoside, luteolin-7-O-β-D-gluco pyranoside, apigenin-7-O-β-D- neospheroside, and acacetin-7-O-β-D-glucoside20. Wei et al., 2015
Leaves of Chrysanthemum morifolium are the most widely used well known medicinal resource. The present study mainly foccusses to estimate the main bioactive components such as flavonoids, galuteolin, quercitrin, chlorogenic acid and 3 ,5-O-caffeoylquinic acid21. Wang et al., 2015
An overall assessment using biochemical and differential proteomic data revealed that UV-B radiation could affect biochemical reaction and promote secondary metabolism processes in postharvest flowers22. Yao et al., 2015
The flowers of twenty-three cultivars of Chrysanthemum contained the anthocyanins, cyanidin 3-glucoside and cyanidin 3-(3″-malonoyl) glucoside and the following carotenoids: lutein, zeaxanthin, β-cryptoxanthin, 13-cis-β-carotene, α-carotene, trans-β-carotene, and 9-cis-β-carotene23. Park et al., 2015
A microwave-assisted extraction approach which is mainly based on ionic liquids of different chain lengths was successfully applied to the extraction of ten flavonoid glycosides from the flowering heads of Chrysanthemum morifolium Ramat. The main components were identified as flavonoid glycosides, including three luteolin glycosides, three apigenin glycosides, three kaempferide glycosides, and one acacetin glycoside24. Zhou et al., 2015
Currently, chrysanthemum flowers becoming major research interest due to its major volatile compounds. Therefore, identification of  the major volatile compounds and their relative concentrations in chrysanthemum flowers are essential. The major volatile compounds are camphor, α-pinene, chrysanthenone, safranal, myrcene, eucalyptol, 2,4,5,6,7,7ab-hexahydro-1H-indene, verbenone, β-phellandrene and camphene25. Sun et al., 2015
In this study, three-channel liquid chromatography with electrochemical detection method was applied to the quantitative analysis of caffeoylquinic acids and flavonoids in four cultivars of Chrysanthemum morifolium flowers and their sulfur-fumigated products26. Chen et al., 2015
Interestingly, one new octulosonic acid derivative, chrysannol A, along with 17 known compounds, was isolated from Chrysanthemum indicum flowers27. Luyen et al., 2015
The appropriate UV-B radiation intensity did not decrease in flower yield, and could regulate phenylalanine ammonia lyase enzyme activity and increase active ingredients (anthocyanins, proline, ascorbic acid, chlorogenic acid and flavone) 1content in flowers of two chrysanthemum varieties28. Yao et al., 2014
Five flavones were isolated from Chrysanthemum coronarium L., among them four of which were isolated for the first time from the genus Chrysanthemum. Two were the flavonoid aglycones 5,7-dihydroxy-3,6,4′-trimethoxyflavone and scutellarin-6,7-dimethyl ether. A new flavonoid glycoside, apigenin-7-O-[2″(6”’-O-beta-D-acetylglucopyranosyl)]-6″-O-acetylglucopyranoside, along with two known ones, i. e. apigenin-7-O-(2″-O-beta-D-glucopyranosyl)-beta-D-glucopyranoside and 6-methoxy quercetin-7-O-beta-D-glucopyranoside, were identified29. Abd-Alla et al., 2014
On the basis of the aroma-extract dilution analysis, the odour activity value and sensory evaluations, bicyclic monoterpenes (borneol, bornyl acetate and camphor) and β-caryophyllene are considered to be the main aroma-active compounds of both extraction methods30. Usami et al., 2014
A water-soluble polysaccharide (P2) with a molecular weight of 1.7×10(5)Da was isolated from the hot aqueous extract of flowers of the Chrysanthemum morifolium. Monosaccharide analysis revealed that P2 is an arabinogalactan containing arabinose (38.4% w/w), galactose (58.8% w/w), and glucose (2.8% w/w) in a ratio of 1:1.53:0.0731. Liang et al., 2014
The nine phenolic compounds [(Z)-2-β-d-glucopyranosyloxy-4-methoxycinnamic acid (cis-GMCA), chlorogenic acid, (E)-2-β-d-glucopyranosyloxy-4-methoxycinnamic acid (trans-GMCA), quercetagetin-7-O-β-d-glucopyranoside, luteolin-7-O-β-d-glucoside, apigenin-7-O-β-d-glucoside, chamaemeloside, apigenin 7-O-(6″-O-acetyl-β-d-glucopyranoside), apigenin] and one polyacetylene (tonghaosu) from the flower heads of Chamomile/Chrysanthemum samples has been examined simultaneously by the new rapid UHPLC-UV-QTOF/MS method.32. Avula et al., 2014
Identification of chlorogenic acid, caffeic acid, 1,3-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid, luteolin-7-O-beta-D-glucoside, 3,4-dicaffeoylquinic acid, linarin and luteolin in Chrysanthemum indicum was established using a high-performance liquid chromatography (HPLC) 33. Dai et al., 2013
In GC-MS analysis 35 compounds were identified, and HPLC-PAD methods were reconfirmed and quantitatively determined 5 compounds (chlorogenic acid, luteolin-7-glucoside, linarin, luteolin and acacetin) in phytochemical studies. This is the first report to analyze the chemical constituents by integrates GC-MS with HPLC-PAD and investigated possible mechanisms34. Wu et al., 2013
Analysis of essential oil from Flower and leaf were determined 38 and 36 components, representing 96.4 and 91.0% of the total oil composition, respectively. The most important compound in flower oil were camphor (47.64%), bornyl acetate (11.87%), and nojigiku alcohol (6.29%), whereas those in leaf oil were camphor (39.14%), nojigiku alcohol (10.76%) and γ-muurolene (7.02%). 13 Aroma-active compounds from flower oil and 12 in leaf oil were determined by GC-O analysis 35. Usami et al., 2013
The combination of HPLC/UV and PCA in pressurized hot water extraction can be used favorably as a green and productive approach for characterization and quality control of ubiquitous functional food such as chrysanthemum36. Liu et al., 2013

 

Biological activities of Chrysanthemum sppThe phytochemicals play a significant influence to prevent diseases and promoting health has been studied extensively to establish their efficacy. Identification and isolation of the chemical components, establishment of their biological potency carried out by many researchers both in vitro and in vivo studies have been analyzed through literature survey. From this review, the experimental details reported in literatures which are done in animals, through epidemiological and clinical-case control studies in man are clearly described in table 2. Overproduction of free radicals can induce many human diseases such as diabetes, cancer, stroke, rheumatoid arthritis and atherosclerosis37-39. Antioxidants can alleviate the oxidative stress, which is beneficial for human health40. However, some currently used synthetic free radical scavengers have been demonstrated various side effects41,42. Therefore, functional foods become a promising source of natural antioxidants43,44. It is noteworthy to mention here that Chrysanthemum spp. has many health and medicinal properties such as Antioxidant, skin cancer, antimicrobial activities and various bone diseases. Recent studies on biological activities of Chrysanthemum spp reported by various researchers are shown in table 2

Table 2: Recent studies on biological activities of Chrysanthemum spp.

Key findings

 

Reference

 

Owing to non-toxic and abundance snow chrysanthemum antioxidants become a better alternative to Chrysanthemum morifolium. Snow chrysanthemum possesses higher antioxidant activity compared to Chrysanthemum morifolium. Therefore the research interest arises in snow chrysanthemum due to its excellent antioxidant activity45. Chen et al., 2016
Nowadays, Skin diseases induced by UV radiation such as skin cancer and photoaging become a global concern.   The active components in wild chrysanthemum extract are a promising candidate in drug development for above mentioned skin diseses46. Sun et al., 2016
It is important to mention here that, the essential oil of the Jordanian Chrysanthemum coronarium L. (garland) which is isolated from flower heads having excellent antimicrobial activities against both Gram-negative and Gram-positive bacteria. According to the survey globally more than 1 million people get colon cancer every year. Hence, more effort has been made by researchers towards sensitivity of oil treatments to colon cancer.   47. Bardaweel  et al., 2015
It is noteworthy to mention here that, 3,5-diarylpyrazole analogues become one of the best alternatives to bioactive compounds, as it exhibit several advantages like Aβ aggregation, neuroprotective activity which are useful in Alzheimer’s disease treatment 48. Wu et al., 2015
Interestingly, water-soluble polysaccharide scavenges the DPPH radicals which are caused by H2O2. The anti-oxidative analysis showed PC12 cells damage has been prevented by water-soluble polysaccharide. Hence, it is found as potential natural antioxidant49. Zheng et al., 2015
Chrysanthemum indicum ethanol extract could attenuate cisplatin-induced nephrotoxicity and might be a beneficial agent for acute renal failure management50. Kim et al., 2015
Chrysanthemum morifolium flower extract successfully absorbs luteolin and luteolin monoglucoside, luteolin monoglucuronide and leads to better circulation in humans51. Yasuda et al., 2015
The elevated adiponectin levels lead to amelioration of insulin resistance and the corresponding hypoglycemic effects. Therefore, a hot water extract of edible Chrysanthemum morifolium treated as a potential food for type 2 diabetes52. Yamamoto et al., 2015
In the case of Proanthocyanidins extracted from Kunlun Chrysanthemum flowers, antiaging effect on Drosophila has been noted. In the present study PKCF is found as a suitable candidate in health care, medicine, and cosmetics53. Jing et al., 2015
Chrysanthemum indicum extract could have a potential therapeutic role in bone-related disorders due to its dual effects on osteoclast and osteoblast differentiation54. Baek et al., 2014
The supercritical-carbon dioxide fluid extract from Chrysanthemum indicum Linne plays a vital role against lipopolysaccharide-induced acute lung injury (ALI) in mice. Thus, it can be referred as a potential therapeutic drug for ALI. Its mechanisms were at least partially associated with the modulations of TLR4 signaling pathways55. Wu et al., 2014
The oral intake of peptide mixture and the aqueous extract of Chrysanthemum morifolium had synergistic antimelanogenic and antioxidative effects in UV-irradiated mice56. Gui et al., 2014
According to the literature survey, it can be concluded that fifty compounds were identified from essential oils of the leaves, stems and roots of Chrysanthemum trifurcatum (Desf.) Batt. and Trab. var. macrocephalum. The oil and methanolic extact from C. trifurcatum leaves showed a great potential of antibacterial effect against Bacillus subtilis and Staphylococcus epidermidis, with an IC50 range of 31.25-62.5 µg/ml57. Sassi et al., 2014
The water fraction of Chrysanthemum zawadskii extracts stimulated the differentiation and proliferation of pluripotent epidermal matrix cells in the matrix region and epithelial stem cells found in the basal layer of the epidermis. The water fraction of Chrysanthemum zawadskii extracts may be developed as a therapeutic agent for the prevention of hair loss58. Li et al., 2014
Chrysanthemum indicum is widely used to treat immune-related and infectious disorders in East Asia. C. indicum flower oil contains 1,8-cineole, germacrene D, camphor, α-cadinol, camphene, pinocarvone, β-caryophyllene, 3-cyclohexen-1-ol, and γ-curcumene. Intake of C. indicum flower oil produces no acute oral toxicity, bone marrow micronucleus, and bacterial reverse mutation59. Hwang et al., 2014
Chrysanthemum zawadskii Herbich var. latilobum Kitamura ethanol extract negatively regulates osteoclast differentiation. It act as a potential therapeutic candidate for the treatment of various bone diseases, such as postmenopausal osteoporosis, rheumatoid arthritis, and periodontitis60. Gu et al., 2013
Chrysanthemum zawadskii extract attenuates 2-deoxy-D-ribose-induced cell damage in osteoblastic cells and may be useful for the treatment of diabetes-associated bone disease61. Suh et al., 2013
The hot water extract of Chrysanthemum indicum L. flower inhibited bioactivation of CCl4-induced hepatotoxicity and downregulates CYP2E1 expression in vitro and in vivo studies62. Jeong et al., 2013
Linarin and its aglycone, acacetin from flowers or leaves of Chrysanthemum boreale exhibited sedative and anticonvulsant activities in the present in vivo assays. It can be considered that linarin is one of the promising active compounds effective against anxiety, insomnia, and stress, with acacetin as its active moiety63. Nugroho et al., 2013
The Chrysanthemum lavandulifolium extract, which includes chrysoeriol, sudachitin, and acacetin, has challenging antibiotic effects on Escherichia coli O157:H7 (E. coli O157). The multi-target efficacy of the Chrysanthemum lavandulifolium extract may indicate the potential for the development of more effective and safer drugs that will act as substitutes for existing antibiotics64. Kim et al., 2013

Conclusion

The analysis based on this detailed literature survey it is concluded that Chrysanthemum spp is the best choice for researchers to develop multifunctional drugs. Among various medicinal herbs Chrysanthemum spp is one of the non-toxic, biocompatible and eco-friendly herbs. In order to develop more effective drugs in future for various pathogens one should recognizes phytochemicals and their performances. This paper presents an overview of Chrysanthemum spp phytochemicals and their biological activities in recent years reported by various research groups. Many research works have been done on phytochemicals of flowers and leafs of Chrysanthemum spp plant.  But more innovative research work still required find new phytochemical compounds which lead to develop new pharmaceutical compounds.

References

  1. Deng, C., Mao, Y., Yao, N., Zhang, X. Development of microwave-assisted extraction followed by headspace solid-phase micro extraction and gas chromatography–mass spectrometry for quantification of camphor and borneol in Flos Chrysanthemi Indici. Anal. Chim. Acta., 2006; 575: 120.
    CrossRef
  2. Liu, F., Ong, E.S., Li, S.F. A green and effective approach for characterization and quality control of Chrysanthemum by pressurized hot water extraction in combination with HPLC with UV absorbance detection. Food Chem., 2013; 141: 1807.
    CrossRef
  3. Lin, L.Z., Harnly, J.M. Identification of the phenolic components of Chrysanthemum flower (Chrysanthemum morifolium Ramat), Food Chem. 2010; 120: 319.
    CrossRef
  4. Chu, Q., Fu, L., Guan, Y., Ye, J. Determination and differentiation of Flos Chrysanthemum based on characteristic electrochemical profiles by capillary electrophoresis with electrochemical detection. J. Agric. Food Chem., 2004; 52: 7828.
    CrossRef
  5. Lai, J.P., Lim, Y.H., Su, J., Shen, H.M., Ong, C.N. Identification andcharacterization of major flavonoids and caffeoylquinic acids in three Compositae plants by LC/DAD–APCI/MS. J. Chromatogr. B: Biomed. Sci. Appl. 2007; 848: 215.
  6. Miyazawa, M., Hisama, M. Antimutagenic Activity of Flavonoids from Chrysanthemum morifolium. Biosci., Biotechnol., Biochem., 2003; 67: 2091–2099.
    CrossRef
  7. Yoshikawa, M., Morikawa, T., Toguchida, I., Harima, S., Matsuda, H. Medicinal Flowers. II.1) Inhibitors of Nitric Oxide Production and Absolute Stereostructures of Five New Germacrane-Type Sesquiterpenes, Kikkanols D, D Monoacetate, E, F, and F Monoacetate from the Flowers of Chrysanthemum indicum L.Chem. Pharm. Bull., 2000; 48: 651–656.
    CrossRef
  8. Ukiya, M., Akihisa, T., Yasukawa, K., Kasahara, Y., Kimura, Y., Koike, K., Nikaido, T., Takido, M. Constituents of compositae plants. 2. Triterpene diols, triols, and their 3-o-fatty acid esters from edible chrysanthemum flower extract and their anti-inflammatory effects. J. Agric. Food Chem. 2001; 49: 3187–3197.
    CrossRef
  9. Tsao, R., Attygalle, A.B., Schroeder, F.C., Marvin, C.H., McGarvey, B.D. Isobutylamides of Unsaturated Fatty Acids from Chrysanthemum morifolium. Associated with Host-Plant Resistance against the Western Flower Thrips. J. Nat. Prod. 2003; 66: 1229–1231.
    CrossRef
  10. Jian, L., Sun, M., Zhang, Q. Analysis on aroma compositions in flowers, stemsand leaves of Chrysanthemun indicum var. Aromaticum. J. Northwest A & FUniv. (Nat. Sci. Ed.)., 2014; 11: 87.
  11. Zhu, W., Xie, C. Huang, L., Rong, L., Fang, N., Yu, S. GC–MS analysis of SFE extracts from four kind of Chrysanthemun. Amino Acids Biot. Resour., 2009; 31: 69.
  12. He, Z., Zou, D., Xie, J., Bai, B., Liao, X., Peng, S. Chemical analysis of the essentialoil from the flowers of Cremanthodium brummeo-pilosum by GC–MS. J.Instrum. Anal., 2008; 27: 68.
  13. Xia, X., Xiao, J., Xia, T. Analysis of volatile chemical composition from Chrysanthemum indicum in Hubei Wufeng by GC–MS, Chin. J. Exp. Tradit. Med.Formul., 2013; 19: 132
  14. Costa, M.A., Zia, Z.Q., Davin, L.B., Lewis, N.G. Chapter Four: Toward Engineering the Metabolic Pathways of Cancer-Preventing Lignans in Cereal Grains and Other Crops. In Recent Advances in Phytochemistry., 1999; 33: 67-87.
  15. American Cancer Society. Phytochemicals. Available at http://www.cancer.org/eprise/main/docroot/ETO/c ontent/ETO_5_3X_Phytochemicals, June 2000.
  16. Meagher, E., Thomson, C. Vitamin and Mineral Therapy. In Medical Nutrition and Disease, Blackwell Science Inc, 1999; 2: 33- 58.
  17. Ma, C.H., Chu, J.Z., Shi, X.F., Liu, C.Q., Yao, X.Q. Effects of enhanced UV-B radiation on the nutritional and active ingredient contents during the floral development of medicinal chrysanthemum. J Photochem Photobiol 2016;158: 228-234.
    CrossRef
  18. Wu, X.X., Sun, Y.M., Shen, X.X., Wang, Z.A. Study on combined effects of chemical components for different flowers blossoming degree of yellow medicinal Chrysanthemum morifolium from Zhejiang]. Zhongguo Zhong Yao Za Zhi. 2015; 40(16): 3174-3178.
  19. Xiao, Z., Fan, B., Niu, Y., Wu, M., Liu, J., Ma, S. Characterization of odor-active compounds of various Chrysanthemum essential oils by gas chromatography-olfactometry, gas chromatography-mass spectrometry and their correlation with sensory attributes. J Chromatogr B Analyt Technol Biomed Life Sci., 2016;1009-1010: 152-162.
    CrossRef
  20. Wei, Q., Ji, X.Y., Long, X.S., Li, Q.R., Yin, H. Chemical Constituents from Leaves of “Chuju” Chrysanthemum morifolium and Their Antioxidant Activities in vitro. Zhong Yao Cai. 2015; 38(2):305-310.
  21. Wang, T., Shen, X.G., Guo, Q.S., Zhou, J.S., Mao, P.F., Shen, Z.G. Comparison of major bioactive components from leaves of Chrysanthemum morifolium. Zhongguo Zhong YaoZa Zhi. 2015; 40(9):1670-1675.
  22. Yao, X., Chu, J.Z., Ma, C.H., Si, C., Li, J.G., Shi, X.F., Liu, C.N. Biochemical traits and proteomic changes in postharvest flowers of medicinal chrysanthemum exposed to enhanced UV-B radiation. J Photochem Photobiol B., 2015; 149: 272-279.
    CrossRef
  23. Park, C.H., Chae, S.C., Park, S.Y., Kim, J.K., Kim, Y.J., Chung, S.O., Arasu, M.V., Al-Dhabi, N.A., Park, S.U. Anthocyanin and Carotenoid Contents in Different Cultivars of Chrysanthemum (Dendranthema grandiflorum Ramat.) Flower. Molecules., 2015; 20(6):11090-102.
    CrossRef
  24. Zhou, Y., Wu, D., Cai, P., Cheng, G., Huang, C., Pan, Y. Special Effect of Ionic Liquids on the Extraction of Flavonoid Glycosides from Chrysanthemum morifolium Ramat by Microwave Assistance. Molecules., 2015; 20(5): 7683-7699.
    CrossRef
  25. Sun, H., Zhang, T., Fan, Q., Qi, X., Zhang, F., Fang, W., Jiang, J., Chen, F., Chen, S. Identification of floral scent in chrysanthemum cultivars and wild relatives by gas chromatography-mass spectrometry. Molecules., 2015; 20(4): 5346-5359.
    CrossRef
  26. Chen, L., Kotani, A., Kusu, F., Wang, Z., Zhu, J., Hakamata, H. Quantitative comparison of caffeoylquinic acids and flavonoids in Chrysanthemum morifolium flowers and their sulfur-fumigated products by three-channel liquid chromatography with electrochemical detection. Chem Pharm Bull (Tokyo)., 2015; 63(1):25-32.
    CrossRef
  27. Luyen, B.T., Tai, B.H., Thao, N.P, Cha, J.Y., Lee, H.Y., Lee, Y.M., Kim, Y.H. Anti-inflammatory components of Chrysanthemum indicum flowers. Bioorg Med Chem Lett. 2015; 25(2):266-269.
    CrossRef
  28. Yao, X.Q., Chu, J.Z., He, X.L., Si, C. The effects of UV-B radiation intensity on biochemical parameters and active ingredients in flowers of Qi chrysanthemum and  Huai chrysanthemum. Photochem Photobiol., 2014; 90(6): 1308-1313.
    CrossRef
  29. Abd-Alla, H.I., Albalawy, M.A., Aly, H.F., Shalaby, N.M., Shaker, K.H. Flavone composition and antihypercholesterolemic and antihyperglycemic activities of Chrysanthemum coronarium L. Z Naturforsch C., 2014; 69(5-6):199-208.
    CrossRef
  30. Usami, A., Nakahashi, H., Marumoto, S., Miyazawa, M. Aroma evaluation of setonojigiku (Chrysanthemum japonense var. debile) by hydrodistillation and solvent-assisted flavour evaporation. Phytochem Anal., 2014; 25(6): 561-566.
    CrossRef
  31. Liang, F., Hu, C., He, Z., Pan, Y. An arabinogalactan from flowers of Chrysanthemum morifolium: structural and bioactivity studies. Carbohydr Res., 2014; 87: 37-41.
    CrossRef
  32. Avula, B., Wang, Y.H., Wang, M., Avonto, C., Zhao, J., Smillie, T.J., Rua, D., Khan, I.A. Quantitative determination of phenolic compounds by UHPLC-UV-MS and use of partial least-square discriminant analysis to differentiate chemo-types of Chamomile/Chrysanthemum flower heads. J Pharm Biomed Anal., 2014; 88: 278-288.
    CrossRef
  33. Dai, S., Zhang, M., Cheng, W.M., Zhang, X., Zhang, Q.L., Li, J. Simultaneous determination of eight active components in Chrysanthemum indicum by HPLC. Zhongguo Zhong Yao  Za Zhi., 2013; 38(12): 1961-1965.
  34. Wu, X.L., Li, C.W., Chen, H.M., Su, Z.Q., Zhao, X.N., Chen, J.N., Lai, X.P., Zhang, X.J., Su, Z.R. Anti-Inflammatory Effect of Supercritical-Carbon Dioxide Fluid Extract from Flowers and Buds of Chrysanthemum indicum Linnén. Evid Based Complement Alternat  Med., 2013; 2013: 413237.
  35.  Usami, A., Ono, T., Marumoto, S., Miyazawa, M. Comparison of volatile compounds with  characteristic odor in flowers and leaves of nojigiku (Chrysanthemum japonense).  J Oleo Sci., 2013; 62(8): 631-636.
    CrossRef
  36.  Liu, F., Ong, E.S., Li, S.F. A green and effective approach for characterisation and  quality control of chrysanthemum by pressurized hot water extraction in combination with HPLC with UV absorbance detection. Food Chem., 2013; 141(3):1807-1813.
    CrossRef
  37. De Rosa, S., Cirillo, P., Paglia, A., Sasso, L., Di Palma, V., Chiariello, M. Reactive oxy-gen species and antioxidants in the pathophysiology of cardiovascular disease:does the actual knowledge justify a clinical approach? Curr. Vasc. Pharmacol., 2010; 8: 259–275.
    CrossRef
  38. Oyagbemi, A.A., Azeez, O.I., Saba, A.B. Interactions between reactive oxygenspecies and cancer: the roles of natural dietary antioxidants and their molecularmechanisms of action, Asian Pac. J. Cancer Prev., 2009; 10: 535–544.
  39. Yao, X., Gu, C., Tian, L., Wang, X., Tang, H. Comparative study on the antioxidantactivities of extracts of Coreopsis tinctoria flowering tops from Kunlun Moun-tains, Xinjiang, north-western China. Nat. Prod. Res., 2015; http://dx.doi.org/10.1080/14786419.2015.1015019.
    CrossRef
  40. Pandolfo, M. Drug Insight: antioxidant therapy in inherited ataxia. Nat. Clin.Pract. Neuro., 2008; 4: 86–96.
    CrossRef
  41. Blaszczyk, A., Skolimowski, J. Comparative analysis of cytotoxic, genotoxicand antioxidant effects of 2,2,4,7-tetramethyl-1,2,3,4-tetrahydroquinolineand ethoxyquin on human lymphocytes. Chem. Biol. Interact., 2006; 162: 70–80.
    CrossRef
  42. Błaszczyk, A., Skolimowski, J., Materac, A. Genotoxic and antioxidant activities ofethoxyquin salts evaluated by the comet assay. Chem. Biol. Interact., 2006; 162: 268–273.
    CrossRef
  43. Qian, Z.M., Guan, J., Yang, F.Q., Li, S.P. Identification and quantification of freeradical scavengers in Pu-erh tea by HPLC-DAD-MS coupled online with 2,2_-azinobis(3-ethylbenzthiazolinesulfonic acid)diammonium salt assay. J. Agric.Food Chem., 2008; 56: 11187–11191.
    CrossRef
  44. Li, S.Y., Yu, Y., Li, S.P.  Identification of antioxidants in essential oil of radix Angel-icae sinensis using HPLC coupled with DAD-MS and ABTS-based assay. J. Agric.Food Chem., 2007; 55:  3358–3362.
    CrossRef
  45. Chen, L.X., Hu, D.J., Lam, S.C., Ge, L., Wu, D., Zhao, J., Long, Z.R., Yang, W.J., Fan, B., Li, S.P. Comparison of antioxidant activities of different parts from snow chrysanthemum (Coreopsis tinctoria Nutt.) and identification of their natural antioxidants using high performance liquid chromatography coupled with diode array detection and mass spectrometry and 2,2′-azinobis(3-ethylbenzthiazoline-sulfonic acid) diammonium salt-based assay. J Chromatogr A. 2016; 1428: 134-142.
    CrossRef
  46. Sun, S., Jiang, P., Su, W., Xiang, Y., Li, J., Zeng, L., Yang, S. Wild chrysanthemum extract prevents UVB radiation-induced acute cell death and photoaging. Cytotechnology., 2016; 68(2): 229-240.
    CrossRef
  47.  Bardaweel, S.K., Hudaib, M.M., Tawaha, K.A., Bashatwah, R.M. Studies on the In Vitro Antiproliferative, Antimicrobial, Antioxidant, and Acetylcholinesterase Inhibition Activities Associated with Chrysanthemum coronarium Essential Oil. Evid Based Complement Alternat Med., 2015; 2015: 790838.
  48. Wu, T., Jiang, C., Wang, L., Morris-Natschke, S.L, Miao, H., Gu, L., Xu, J., Lee, K.H, Gu, Q. 3,5-Diarylpyrazole Derivatives Obtained by Ammonolysis of the Total Flavonoids from Chrysanthemum indicum Extract Show Potential for the Treatment of Alzheimer’s Disease. J Nat Prod., 2015; 78(7): 1593-1599.
    CrossRef
  49. Zheng, C., Dong, Q., Chen, H., Cong, Q., Ding, K. Structural characterization of a polysaccharide from Chrysanthemum morifolium flowers and its antioxidant activity. Carbohydr Polym., 2015; 130: 113-121.
    CrossRef
  50. Kim, T.W., Kim, Y.J., Park, S.R., Seo, C.S., Ha, H., Shin, H.K., Jung, J.Y. Chrysanthemum indicum attenuates cisplatin-induced nephrotoxicity both in vivo and in vitro. Nat Prod Commun., 2015; 10(3): 397-402.
  51.  Yasuda, M.T., Fujita, K., Hosoya, T., Imai, S., Shimoi, K. Absorption and Metabolism of  Luteolin and Its Glycosides from the Extract of Chrysanthemum morifolium Flowers  in Rats and Caco-2 Cells. J Agric Food Chem., 2015; 63(35): 7693-7699.
    CrossRef
  52.  Yamamoto, J., Tadaishi, M., Yamane, T., Oishi, Y., Shimizu, M., Kobayashi-Hattori, K. Hot water extracts of edible Chrysanthemum morifolium Ramat. exert antidiabetic effects in obese diabetic KK-Ay mice. Biosci Biotechnol Biochem., 2015; 79(7): 1147-1154.
    CrossRef
  53. Jing, S., Zhang, X., Yan, L.J. Antioxidant activity, antitumor effect, and antiaging property of proanthocyanidins extracted from Kunlun Chrysanthemum flowers. Oxid Med Cell Longev., 2015; 2015: 983484.
  54. Baek, J.M., Kim, J.Y., Cheon, Y.H., Park, S.H., Ahn, S.J., Yoon, K.H., Oh, J., Lee, M.S. Dual Effect of Chrysanthemum indicum Extract to Stimulate Osteoblast Differentiation and Inhibit Osteoclast Formation and Resorption In Vitro. Evid Based Complement Alternat Med., 2014; 2014:176049.
  55. Wu, X.L., Feng, X.X., Li, C.W., Zhang, X.J., Chen, Z.W., Chen, J.N., Lai, X.P., Zhang, S.X., Li, Y.C., Su, Z.R. The protective effects of the supercritical-carbon dioxide fluid extract of Chrysanthemum indicum against lipopolysaccharide-induced acute lung injury in mice via modulating Toll-like receptor 4 signaling pathway. Mediators Inflamm., 2014; 2014: 246407.
  56.  Gui, M., Du, J., Guo, J., Xiao, B., Yang, W., Li, M. Aqueous Extract of Chrysanthemum morifolium ( Jú Huā) Enhances the Antimelanogenic and Antioxidative Activities ofthe Mixture of Soy Peptide and Collagen Peptide. J Tradit Complement Med., 2014; 4(3): 171-176.
    CrossRef
  57. Sassi, A.B., Skhiri, F.H., Chraief, I., Bourgougnon, N., Hammami, M., Aouni, M. Essential oils and crude extracts from Chrysanthemum trifurcatum leaves, stems and roots: chemical composition and antibacterial activity. J Oleo Sci., 2014; 63(6): 607-617.
    CrossRef
  58. Li, Z., Li, J., Gu, L., Begum, S., Wang, Y., Sun, B., Lee, M., Sung, C. Chrysanthemum zawadskii extract induces hair growth by stimulating the proliferation and differentiation of hair matrix. Int J Mol Med., 2014; 34(1): 130-136.
    CrossRef
  59. Hwang, E.S., Kim, G.H. Safety Evaluation of Chrysanthemum indicum L. Flower Oil by  Assessing Acute Oral Toxicity, Micronucleus Abnormalities, and Mutagenicity. Prev Nutr Food Sci., 2013; 18(2): 111-116.
    CrossRef
  60. Gu, D.R., Hwang, J.K., Erkhembaatar, M., Kwon, K.B., Kim, M.S., Lee, Y.R., Lee, S.H. Inhibitory Effect of Chrysanthemum zawadskii Herbich var. latilobum Kitamura Extract on RANKL-Induced Osteoclast Differentiation. Evid Based Complement Alternat Med., 2013; 2013: 509482.
  61. Suh, K.S., Rhee, S.Y., Jung, W.W., Kim, N.J, Jang, Y.P., Kim, H.J., Kim, M.K., Choi, Y.K., Kim, Y.S. Chrysanthemum zawadskii extract protects osteoblastic cells from highly reducing sugar-induced oxidative damage. Int J Mol Med., 2013; 32(1): 241-250.
    CrossRef
  62.  Jeong, S.C., Kim, S.M., Jeong, Y.T., Song, C.H. Hepatoprotective effect of water extract  from Chrysanthemum indicum L. flower. Chin Med., 2013; 8(1): 7.
    CrossRef
  63.  Nugroho, A., Lim, S.C., Choi, J., Park, H.J. Identification and quantification of the sedative and anticonvulsant flavone glycoside from Chrysanthemum boreale. Arch Pharm Res., 2013; 36(1): 51-60.
    CrossRef
  64. Kim, K.S., Lim, D.J., Yang, H.J., Choi, E.K., Shin, M.H., Ahn, K.S., Jung, S.H., Um, J.Y., Jung, H.J., Lee, J.H., Lee, S.G., Jung, S.K., Jang, H.J. The multi-targeted effects of Chrysanthemum herb extract against Escherichia coli O157:H7. Phytother Res., 2013; 27(9): 1398-406.
    CrossRef
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