Skip to main content
Log in

Structure–activity relationships of flavanones, flavanone glycosides, and flavones in anti-degranulation activity in rat basophilic leukemia RBL-2H3 cells

  • Note
  • Published:
Journal of Natural Medicines Aims and scope Submit manuscript

Abstract

The incidence of type I allergies, which are associated with mast cell degranulation and local inflammation, is increasing, and new treatments are needed. To date, structure–activity relationships of flavonoids in their degranulation-inhibiting activity have not been systematically characterized. In the current study, the degranulation-inhibiting activity of a series of flavonoids was evaluated. The following three observations were made: (1) the activity disappears when a sugar moiety is introduced into the A ring of the flavanone; (2) the activity depends on the number of hydroxyl groups on the B ring; (3) the activity is markedly enhanced when a double bond is introduced into the C ring. The information obtained in the current study may guide the development of a therapy for type I allergies.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

References

  1. Ferrer JL, Austin MB, Stewart C Jr, Noel JP (2008) Structure and function of enzymes involved in the biosynthesis of phenylpropanoids. Plant Physiol Biochem 46:356–370

    Article  CAS  PubMed  Google Scholar 

  2. Havsteen BH (2002) The biochemistry and medical significance of the flavonoids. Pharmacol Ther 96:67–202

    Article  CAS  PubMed  Google Scholar 

  3. Bae EA, Han MJ, Lee M, Kim DH (2000) In vitro inhibitory effect of some flavonoids on rotavirus infectivity. Biol Pharm Bull 23:1122–1124

    Article  CAS  PubMed  Google Scholar 

  4. Gorinstein S, Leontowicz H, Leontowicz M, Krzeminski R, Gralak M, Jastrzebski Z, Park YS, Jung ST, Kang SG, Trakhtenberg S (2007) Effect of hesperidin and naringin on the plasma lipid profile and plasma antioxidant activity in rats fed a cholesterol-containing diet. J Sci Food Agric 87:1257–1262

    Article  CAS  Google Scholar 

  5. Yeh CC, Kao SJ, Lin CC, Wang SD, Liu CJ, Kao ST (2007) The immunomodulation of endotoxin-induced acute lung injury by hesperidin in vivo and in vitro. Life Sci 80:1821–1831

    Article  CAS  PubMed  Google Scholar 

  6. Galati EM, Torovato A, Kirjavainen S, Forestieri AM, Rossitto A, Monforte MT (1996) Biological effects of hesperidin, a Citrus flavonoid. (Note III): antihypertensive and diuretic activity in rat. Farmaco 51:219–221

    CAS  PubMed  Google Scholar 

  7. Hsiao YC, Kuo WH, Chen PN, Chang HR, Lin TH, Yang WE, Hsieh YS, Chu SC (2007) Flavanone and 2′-OH flavanone inhibit metastasis of lung cancer cells via down-regulation of proteinases activities and MAPK pathway. Chem Biol Interact 167:193–206

    Article  CAS  PubMed  Google Scholar 

  8. Son HS, Kim HS, Ju JS (1991) Effects of rutin and hesperidin on total cholesterol concentration, transaminases and alkaline phosphatase activity in carbon tetrachloride treated rats. Hanguk Nonghwahak Hoechi (J Korean Agric Chem Soc) 34:318–326 (In Korean, with summaries in English)

    CAS  Google Scholar 

  9. Zeng LJ, Chen D, Huang QD, Huang Q, Lian YF, Cai WW, Zeng HP, Lin YL (2015) Isolation of a new flavanone from Daidai fruit and hypolipidemic activity of total flavonoids extracts. Nat Prod Res 29:1521–1528

    Article  CAS  PubMed  Google Scholar 

  10. Ou T, Hou X, Guan S, Dai J, Han W, Li R, Wang W, Qu X, Zhang M (2016) Targeting AMPK signalling pathway with natural medicines for atherosclerosis therapy: an integration of in silico screening and in vitro assay. Nat Prod Res 30:1240–1247

    Article  CAS  PubMed  Google Scholar 

  11. Shen SC, Ko CH, Tseng SW, Tsai SH, Chen YC (2004) Structurally related antitumor effects of flavanones in vitro and in vivo: involvement of caspase 3 activation, p21 gene expression, and reactive oxygen species production. Toxicol Appl Pharmacol 197:84–95

    Article  CAS  PubMed  Google Scholar 

  12. Nishihata S, Murata T, Inoue S, Okubo K, Sahashi N, Takahashi H, Hirooka J, Hoshiyama Y, Murayama K, Mezawa A, Yokoyama T, Endo T, Saiga T, Saito Y (2010) Prevalence of Japanese cedar pollinosis in Tokyo: a survey conducted by the Tokyo Metropolitan Government. Clin Exp Allergy Rev 10:8–11

    Article  Google Scholar 

  13. Noshita T, Tai A, Matsumoto T, Miura K, Ikeda K, Hamada Y (2017) Structure-activity relationship of flavanone. Anti-degranulation activity of 7-O-substituted hesperetin. Nat Prod Res 31:2137–2142

    Article  CAS  PubMed  Google Scholar 

  14. Murata K, Takano S, Masuda M, Iinuma M, Matsuda H (2013) Anti-degranulating activity in rat basophil leukemia RBL-2H3 cells of flavanone glycosides and their aglycones in citrus fruits. J Nat Med 67:643–646

    Article  CAS  PubMed  Google Scholar 

  15. Lim H, Kim SB, Park H, Chang HW, Kim HP (2009) New anti-inflammatory synthetic biflavonoid with C-C (6–6′′) linkage: differential effects on cyclooxygenase-2 and inducible nitric oxide synthase. Arch Pharm Res 32:1525–1531

    Article  CAS  PubMed  Google Scholar 

  16. Yang HB, Wang YC, Zhang ZT, Chang Y (2008) Synthesis and crystal structure of pilloin. Turk J Chem 32:87–95

    CAS  Google Scholar 

  17. Bernini R, Crisante F, Ginnasi MC (2011) A convenient and safe O-methylation of flavonoids with dimethyl carbonate (DMC). Molecules 16:1418–1425

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Han HK, Choi SS, Kim YR, Kim HJ, Kang GM, Dong MS, Na CS, Chung HS (2006) Diarylheptanoid and flavonoid with antioxidant activity from Alnus japonica Steud on DPPH free radical scavenging assay. J Food Sci Nur 11:171–175

    CAS  Google Scholar 

  19. Watanabe J, Shinmoto H, Tsushida T (2005) Coumarin and flavone derivatives from estragon ant thyme as inhibitors of chemical mediator release from RBL-2H3 cells. Biosci Biotechnol Biochem 69:1–6

    Article  CAS  PubMed  Google Scholar 

  20. Demo SD, Masuda E, Rossi AB, Throndset BT, Gerard AL, Chan EH, Armstrong RJ, Fox BP, Lorens JB, Payan DG, Scheller RH, Fisher JM (1999) Quantitative measurement of mast cell degranulation using a novel flow cytometric annexin-V binding assay. Cytometry 36:340–348

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors would like to thank Editage (http://www.editage.jp) for English language editing.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Toshiro Noshita or Akihiro Tai.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Noshita, T., Miura, K., Ikeda, K. et al. Structure–activity relationships of flavanones, flavanone glycosides, and flavones in anti-degranulation activity in rat basophilic leukemia RBL-2H3 cells. J Nat Med 72, 551–556 (2018). https://doi.org/10.1007/s11418-017-1169-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11418-017-1169-3

Keywords

Navigation