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S., Razavi, B.M., and Hosseinzadeh, H. (2018). A review of the effects of Capsicum annuum L. and its constituent, capsaicin, in metabolic syndrome. Iran. J. Basic Med. Sci. 21: 439–448.

      36 Sharma, A., Kumar, V., Giridhar, P., and Ravishankar, G.A. (2008). Induction of in vitro flowering in Capsicum frutescens under the influence of silver nitrate and cobalt chloride and pollen transformation. Electron. J. Biotechnol. 11: 1–6.

      37 Shotorbani, N.Y., Jamei, R., and Heidari, R. (2013). Antioxidant activities of two sweet pepper Capsicum annuum L. varieties phenolic extracts and the effects of thermal treatment. Avicenna J. Phytomed. 3: 25–34.

      38 Sooch, B.S., Thakur, M.R., and Kaur, G. (1977). Evaluation of some chili (Capsicum annuum L.) genotypes for capsaicin and ascorbic acid contents. Indian Food Packer 31: 9–11.

      39 Stjärne, P., Rinder, J., Hedén-Blomquist, E. et al. (1998). Capsaicin desensitization of the nasal mucosa reduces symptoms upon allergen challenge in patients with allergic rhinitis. Acta Otolaryngol. 118: 235–239.

      40 Sudha, G. and Ravishankar, G.A. (2002). Influence of calcium channel modulators in capsaicin production by cell suspension cultures of Capsicum frutescens Mill. Curr. Sci. 83: 480–484.

      41 Sudha, G. and Ravishankar, G.A. (2003). Influence of methyl jasmonate and salicylic acid in the enhancement of capsaicin production in cell suspension cultures of Capsicum frutescens Mill. Curr. Sci. 85: 1212–1217.

      42 Sun, T., Xu, Z., Wu, C.-T. et al. (2007). Antioxidant activities of different colored sweet bell peppers (Capsicum annuum L.). J. Food Sci. 72: S98–S102.

      43 Swamy, S., Krupakar, A., Chandran, D.S., and Koshy, E.P. (2014). Direct regeneration protocols of five Capsicum annuum L. varieties. Afr. J. Biotechnol. 13: 307–312.

      44 Thomas, B.V., Schreiber, A.A., and Weisskpof, C.P. (1998). Simple method for quantitation of capsaicinoids in peppers using capillary gas chromatography. J. Agric. Food. Chem. 46: 2655–2663.

      45 Varindra, Saikia, S., Sandhu, R., and Gosal, S.S. (2000). Effect of nutrient limitation on capsaicin production in callus cultures derived from pericarp and seedling explants of Capsicum annuum L. varieties. Plant Tissue Cult. Biotech. 10: 9–16.

      46 Yosipovitch, G., Mengesha, Y., Facliaru, D., and David, M. (2005). Topical capsaicin for the treatment of acute lipodermatosclerosis and lobular panniculitis. J. Dermatol. Treat. 16: 178–180.

      2.21.1 Ethnopharmacological Properties and Phytochemistry

      Carthamus tinctorius L. (Fam. – Asteraceae) is a very good purgative, analgesic, antipyretic, and an antidote to poisoning (Asgarpanah and Kazemivash 2013). It is a useful plant for painful menstrual problems, postpartum hemorrhage, whooping cough and chronic bronchitis, rheumatism, and sciatica (Wang and Li 1985). The flowers of C. tinctorius are an important medicinal material in prescriptions used for cardiovascular, cerebrovascular, and gynecological diseases (Yao et al. 2016). In China, the water extract of C. tinctorius has been developed as an intravenous injection, which is extensively applied to treat cardiovascular diseases clinically (Zhou et al. 2009). Its dye is mainly used as a coloring agent (Shirwaikar et al. 2010).

      Several flavonoids were isolated and identified as 6-hydroxyquercetin 3,6,7-tri-O-β-D-glucoside, 6-hydroxykaempferol-3,6-di-O-β-D-glucoside-7-O-β-D-glucuronide, 6-hydroxykaempferol-3,6,7-tri-O-β-D-glucoside, 6-hydroxykaempferol-3-O-β-D-glucoside, 6-hydroxykaempferol-3-O-β-D-rutinoside, 6-hydroxykaempferol-6,7-di-O-β-D-glucoside, 6-hydroxyapigenin-6-O-β-D-glucoside-7-O-β-D-glucuronide, 6-hydroxykaempferol-3,6-di-O-β-D-glucoside, 6-hydroxykaempferol-3-O-β-rutinoside-6-O-β-D-glucoside, and (2S)-4′,5-dihydroxyl-6,7-di-O-β-D-glucopyranosyl flavanone from C. tinctorius (Fan et al. 2011). Two quinochalcone C-glycosides, carthorquinosides A and B, were isolated from the florets of C. tinctorius (Yue et al. 2016).

      Carthamus tinctorius was evaluated for antioxidant activities against several models in vitro. The antioxidant activity was determined on the basis of the capacity to scavenge DPPH radical and 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonate) (ABTS) radical and reduced Fe3+ of different polar fractions. Five major components were isolated and identified from water extract as 6-hydroxykaempferol 3,6,7-tri-O-β-D-glucoside, 6-hydroxykaempferol 3-O-β-rutinoside-6-O-β-D-glucoside, 6-hydroxykaempferol 3-O-β-D-glucoside, hydroxysafflor yellow A, and anhydrosafflor yellow B. By evaluating and comparing the antioxidative effects of different fractions and obtained compounds, the results showed that water extract displayed significantly high antioxidative activities and 6-hydroxykaempferol glycosides and quinochalcone C-glycosides were found as main contribution for their antioxidant property (Yue et al. 2013, 2014).