메뉴 건너뛰기




Volumn 68, Issue 3, 2014, Pages 561-566

Acylated phenylethanoid glycosides, echinacoside and acteoside from Cistanche tubulosa, improve glucose tolerance in mice

Author keywords

Acteoside; Aldose reductase inhibitor; Cistanche tubulosa; Echinacoside; Glucose tolerance improvement effect

Indexed keywords

ACARBOSE; ACETYLATED PHENYLETHANOID GLYCOSIDE; ACTEOSIDE; ECHINACOSIDE; GLYCOSIDE; UNCLASSIFIED DRUG;

EID: 84904638082     PISSN: 13403443     EISSN: 18610293     Source Type: Journal    
DOI: 10.1007/s11418-014-0837-9     Document Type: Article
Times cited : (63)

References (33)
  • 1
    • 0028312287 scopus 로고
    • Phenylethanoid glycosides in plants: Structure and biological activity
    • Jiménez C, Riguera R (1994) Phenylethanoid glycosides in plants: structure and biological activity. Nat Prod Rep 11:591-606 (Pubitemid 24977280)
    • (1994) Natural Product Reports , vol.11 , Issue.6 , pp. 591-606
    • Jimenez, C.1    Riguera, R.2
  • 2
    • 58149237183 scopus 로고    scopus 로고
    • Naturally occurring phenylethanoid glycosides: Potential leads for new therapeutics
    • Fu G, Pang H, Wong YH (2008) Naturally occurring phenylethanoid glycosides: potential leads for new therapeutics. Curr Med Chem 15:2592-2613
    • (2008) Curr Med Chem , vol.15 , pp. 2592-2613
    • Fu, G.1    Pang, H.2    Wong, Y.H.3
  • 4
    • 84981834309 scopus 로고
    • Isolierung und konstitution des echinacosids, eines glykosids aus den wurzeln von Echinacea angustifolia D. C. 6. mitteilung über antibakterielle stoffe
    • Stoll A, Renz J, Brack A (1950) Isolierung und konstitution des echinacosids, eines glykosids aus den wurzeln von Echinacea angustifolia D. C. 6. mitteilung über antibakterielle stoffe. Helv Chim Acta 33:1877-1893
    • (1950) Helv Chim Acta , vol.33 , pp. 1877-1893
    • Stoll, A.1    Renz, J.2    Brack, A.3
  • 6
    • 0011480604 scopus 로고
    • Isolation from Verbascum sinuatum of two new glucosides, verbascoside and isoverbascoside
    • Scarpati ML, Dell MF (1963) Isolation from Verbascum sinuatum of two new glucosides, verbascoside and isoverbascoside. Ann Chim 53:356-367
    • (1963) Ann Chim , vol.53 , pp. 356-367
    • Scarpati, M.L.1    Dell, M.F.2
  • 7
    • 0014316417 scopus 로고
    • Sugar esters. IV. Acteoside and neoacteoside, sugar esters from Syringa vulgaris
    • Birkofer L, Kaiser C, Thomas U (1968) Sugar esters. IV. acteoside and neoacteoside, sugar esters from Syringa vulgaris. Z Naturforsch, B: Chem Sci 23:1051-1058
    • (1968) Z Naturforsch, B: Chem Sci , vol.23 , pp. 1051-1058
    • Birkofer, L.1    Kaiser, C.2    Thomas, U.3
  • 8
    • 0000225759 scopus 로고
    • Structures of varbascoside and orobanchoside, caffeic acid sugar esters from Orobanche rapum -genistae
    • Andary C, Wylde R, Laffite C, Privat G, Winternitz F (1982) Structures of varbascoside and orobanchoside, caffeic acid sugar esters from Orobanche rapum -genistae. Phytochemistry 21:1123-1127
    • (1982) Phytochemistry , vol.21 , pp. 1123-1127
    • Andary, C.1    Wylde, R.2    Laffite, C.3    Privat, G.4    Winternitz, F.5
  • 9
    • 0141710417 scopus 로고
    • A new glycoside, kusaginin isolated from Clerodendron trichotomum
    • Sakurai A, Kato T (1983) A new glycoside, kusaginin isolated from Clerodendron trichotomum. Bull Chem Soc Jpn 56:1573-1574
    • (1983) Bull Chem Soc Jpn , vol.56 , pp. 1573-1574
    • Sakurai, A.1    Kato, T.2
  • 10
    • 0347481468 scopus 로고    scopus 로고
    • Protective Effect of Acteoside on Carbon Tetrachloride-Induced Hepatotoxicity
    • DOI 10.1016/j.lfs.2003.07.020
    • Lee KJ, Woo E-R, Choi CY, Shin DW, Lee DG, You HJ, Jeong HG (2004) Protective effect of acteoside on carbon tetrachlorideinduced hepatotoxicity. Life Sci 74:1051-1064 (Pubitemid 37522138)
    • (2004) Life Sciences , vol.74 , Issue.8 , pp. 1051-1064
    • Lee, K.J.1    Woo, E.-R.2    Choi, C.Y.3    Shin, D.W.4    Lee, D.G.5    You, H.J.6    Jeong, H.G.7
  • 11
    • 59649109539 scopus 로고    scopus 로고
    • Metabolism of echinacoside, a good antioxidant, in rats: Isolation and identification of its biliary metabolites
    • Jia C, Shi H, Jin W, Zhang K, Jiang Y, Zhao M, Tu P (2009) Metabolism of echinacoside, a good antioxidant, in rats: isolation and identification of its biliary metabolites. Drug Metab Dispos 37:431-438
    • (2009) Drug Metab Dispos , vol.37 , pp. 431-438
    • Jia, C.1    Shi, H.2    Jin, W.3    Zhang, K.4    Jiang, Y.5    Zhao, M.6    Tu, P.7
  • 12
    • 84863055306 scopus 로고    scopus 로고
    • Echinacoside stimulates cell proliferation and prevents cell apoptosis in intestinal epithelial MODE-K cells by up-regulation of transforming growth factor-β1 expression
    • Jia Y, Guan Q, Guo Y, Du C (2012) Echinacoside stimulates cell proliferation and prevents cell apoptosis in intestinal epithelial MODE-K cells by up-regulation of transforming growth factor-β1 expression. J Pharmacol Sci 118:99-108
    • (2012) J Pharmacol Sci , vol.118 , pp. 99-108
    • Jia, Y.1    Guan, Q.2    Guo, Y.3    Du, C.4
  • 13
    • 84870854146 scopus 로고    scopus 로고
    • Echinacoside promotes bone regeneration by increasing OPG/RANKL ratio in MC3T3-E1 cells
    • Li F, Yang Y, Zhu P, Chen W, Qi D, Shi X, Zhang C, Yang Z, Li P (2012) Echinacoside promotes bone regeneration by increasing OPG/RANKL ratio in MC3T3-E1 cells. Fitoterapia 83:1443-1450
    • (2012) Fitoterapia , vol.83 , pp. 1443-1450
    • Li, F.1    Yang, Y.2    Zhu, P.3    Chen, W.4    Qi, D.5    Shi, X.6    Zhang, C.7    Yang, Z.8    Li, P.9
  • 14
    • 84875962439 scopus 로고    scopus 로고
    • Antiosteoporotic activity of echinacoside in ovariectomized rats
    • Li F, Yang X, Yang Y, Guo C, Zhang C, Yang Z, Li P (2013) Antiosteoporotic activity of echinacoside in ovariectomized rats. Phytomedicine 20:549-557
    • (2013) Phytomedicine , vol.20 , pp. 549-557
    • Li, F.1    Yang, X.2    Yang, Y.3    Guo, C.4    Zhang, C.5    Yang, Z.6    Li, P.7
  • 15
    • 33749242780 scopus 로고    scopus 로고
    • Phenylethanoid oligoglycosides and acylated oligosugars with vasorelaxant activity from Cistanche tubulosa
    • DOI 10.1016/j.bmc.2006.07.018, PII S0968089606005736
    • Yoshikawa M, Matsuda H, Morikawa T, Xie H, Nakamura S, Muraoka O (2006) Phenylethanoid oligoglycosides and acylated oligosugars with vasorelaxant activity from Cistanche tubulosa. Bioorg Med Chem 14:7468-7475 (Pubitemid 44486801)
    • (2006) Bioorganic and Medicinal Chemistry , vol.14 , Issue.22 , pp. 7468-7475
    • Yoshikawa, M.1    Matsuda, H.2    Morikawa, T.3    Xie, H.4    Nakamura, S.5    Muraoka, O.6
  • 16
    • 77249140419 scopus 로고    scopus 로고
    • Acylated phenylethanoid oligoglycosides with hepatoprotective activity from the desert plant Cistanche tubulosa
    • Morikawa T, Pan Y, Ninomiya K, Imura K, Matsuda H, Yoshikawa M, Yuan D, Muraoka O (2010) Acylated phenylethanoid oligoglycosides with hepatoprotective activity from the desert plant Cistanche tubulosa. Bioorg Med Chem 18:1882-1890
    • (2010) Bioorg Med Chem , vol.18 , pp. 1882-1890
    • Morikawa, T.1    Pan, Y.2    Ninomiya, K.3    Imura, K.4    Matsuda, H.5    Yoshikawa, M.6    Yuan, D.7    Muraoka, O.8
  • 18
    • 33646416502 scopus 로고    scopus 로고
    • Monoterpene constituents from Cistanche tubulosa: Chemical structures of kankanosides A-E and kankanol
    • Xie H, Morikawa T, Matsuda H, Nakamura S, Muraoka O, Yoshikawa M (2006) Monoterpene constituents from Cistanche tubulosa: chemical structures of kankanosides A-E and kankanol. Chem Pharm Bull 54:669-675
    • (2006) Chem Pharm Bull , vol.54 , pp. 669-675
    • Xie, H.1    Morikawa, T.2    Matsuda, H.3    Nakamura, S.4    Muraoka, O.5    Yoshikawa, M.6
  • 21
    • 76449110648 scopus 로고    scopus 로고
    • The hypocholesterolemic effects of Cistanche tubulosa extract, a Chinese traditional crude medicine, in mice
    • Shimoda H, Tanaka J, Takahara Y, Takemoto K, Shan S-J, Su M-H (2009) The hypocholesterolemic effects of Cistanche tubulosa extract, a Chinese traditional crude medicine, in mice. Am J Chin Med 37:1125-1138
    • (2009) Am J Chin Med , vol.37 , pp. 1125-1138
    • Shimoda, H.1    Tanaka, J.2    Takahara, Y.3    Takemoto, K.4    Shan, S.-J.5    Su, M.-H.6
  • 22
    • 0036185571 scopus 로고    scopus 로고
    • Absolute stereostructure of potent β-glucosidase inhibitor, salacinol, with unique thiosugar sulfonium sulfate inner salt structure from Salacia reticulata
    • DOI 10.1016/S0968-0896(01)00422-9, PII S0968089601004229
    • Yoshikawa M, Morikwa T, Matsuda H, Tanabe G, Muraoka O (2002) Absolute stereostructure of potent α-glucosidase inhibitor, salacinol, with unique thiosugar sulfonium sulfate inner salt structure from salacia reticulata. Bioorg Med Chem 10:1547-1554 (Pubitemid 34214717)
    • (2002) Bioorganic and Medicinal Chemistry , vol.10 , Issue.5 , pp. 1547-1554
    • Yoshikawa, M.1    Morikawa, T.2    Matsuda, H.3    Tanabe, G.4    Muraoka, O.5
  • 23
    • 77950811206 scopus 로고    scopus 로고
    • Quantitative determination of potent aglucosidase inhibitors, salacinol and kotalanol, in Salasia species using liquid chromatography-mass spectrometry
    • Muraoka O, Morikawa T, Miyake S, Akaki J, Ninomiya K, Yoshikawa M (2010) Quantitative determination of potent aglucosidase inhibitors, salacinol and kotalanol, in Salasia species using liquid chromatography-mass spectrometry. J Pharm Biomed Anal 52:770-773
    • (2010) J Pharm Biomed Anal , vol.52 , pp. 770-773
    • Muraoka, O.1    Morikawa, T.2    Miyake, S.3    Akaki, J.4    Ninomiya, K.5    Yoshikawa, M.6
  • 24
    • 78651412197 scopus 로고    scopus 로고
    • Quantitative analysis of neosalacinol and neokotalanol, another two potent a-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography
    • Muraoka O, Morikawa T, Miyake S, Akaki J, Ninomiya K, Pongpiriyadacha Y, Yoshikawa M (2011) Quantitative analysis of neosalacinol and neokotalanol, another two potent a-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography. J Nat Med 65:142-148
    • (2011) J Nat Med , vol.65 , pp. 142-148
    • Muraoka, O.1    Morikawa, T.2    Miyake, S.3    Akaki, J.4    Ninomiya, K.5    Pongpiriyadacha, Y.6    Yoshikawa, M.7
  • 25
    • 0036594601 scopus 로고    scopus 로고
    • Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity
    • DOI 10.1248/cpb.50.788
    • Matsuda H, Morikawa T, Toguchida I, Yoshikawa M (2002) Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity. Chem Pharm Bull 50:788-795 (Pubitemid 41694896)
    • (2002) Chemical and Pharmaceutical Bulletin , vol.50 , Issue.6 , pp. 788-795
    • Matsuda, H.1    Morikawa, T.2    Toguchida, I.3    Yoshikawa, M.4
  • 26
    • 0032919388 scopus 로고    scopus 로고
    • Medicinal flowers. I. Aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L.
    • Yoshikawa M, Morikawa T, Murakami T, Toguchida I, Harima S, Matsuda H (1999) Medicinal flowers. I. aldose reductase inhibitors and three new eudesmane-type sesquiterpenes, kikkanols A, B, and C, from the flowers of Chrysanthemum indicum L. Chem Pharm Bull 47:340-345 (Pubitemid 29166273)
    • (1999) Chemical and Pharmaceutical Bulletin , vol.47 , Issue.3 , pp. 340-345
    • Yoshikawa, M.1    Morikawa, T.2    Murakami, T.3    Toguchida, I.4    Harima, S.5    Matsuda, H.6
  • 27
    • 0036635201 scopus 로고    scopus 로고
    • Medicinal flowers. VI. Absolute stereostructures of two new flavanone glycosides and a phenylbutanoid glycoside from the flowers of Chrysanthemum indicum L.: Their inhibitory activities for rat lens aldose reductase
    • DOI 10.1248/cpb.50.972
    • Matsuda H, Morikawa T, Toguchida I, Harima S, Yoshikawa M (2002) Medicinal flowers. VI. Absolute stereostructures of two new flavanone glycosides and a phenylbutanoid glycoside from the flowers of Chrysanthemum indicum L.: their inhibitory activities for rat lens aldose reductase. Chem Pharm Bull 50:972-975 (Pubitemid 41694875)
    • (2002) Chemical and Pharmaceutical Bulletin , vol.50 , Issue.7 , pp. 972-975
    • Matsuda, H.1    Morikawa, T.2    Toguchida, I.3    Harima, S.4    Yoshikawa, M.5
  • 28
    • 0036691566 scopus 로고    scopus 로고
    • New flavonol oligoglycosides and polyacylated sucroses with inhibitory effects on aldose reductase and platelet aggregation from the flowers of Prunus mume
    • DOI 10.1021/np020058m
    • Yoshikawa M, Murakami T, Ishiwada T, Morikawa T, Kagawa M, Higashi Y, Matsuda H (2002) New flavonol oligoglycosides and polyacylated sucroses with inhibitory effects on aldose reductase and platelet aggregation from the flowers of Prunus mume. J Nat Prod 65:1151-1155 (Pubitemid 34976494)
    • (2002) Journal of Natural Products , vol.65 , Issue.8 , pp. 1151-1155
    • Yoshikawa, M.1    Murakami, T.2    Ishiwada, T.3    Morikawa, T.4    Kagawa, M.5    Higashi, Y.6    Matsuda, H.7
  • 29
    • 0036664538 scopus 로고    scopus 로고
    • Antidiabetogenic constituents from several natural medicines
    • Matsuda H, Morikawa T, Yoshikawa M (2002) Antidiabetogenic constituents from several natural medicines. Pure Appl Chem 74:1301-1308
    • (2002) Pure Appl Chem , vol.74 , pp. 1301-1308
    • Matsuda, H.1    Morikawa, T.2    Yoshikawa, M.3
  • 30
    • 27744479680 scopus 로고    scopus 로고
    • Bioactive constituents from chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of saussureosides A and B from Saussurea medusa
    • DOI 10.1248/cpb.53.1416
    • Xie H, Wang T, Matsuda H, Morikawa T, Yoshikawa M, Tani T (2005) Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of saussureosides A and B from Saussurea medusa. Chem Pharm Bull 53:1416-1422 (Pubitemid 41634209)
    • (2005) Chemical and Pharmaceutical Bulletin , vol.53 , Issue.11 , pp. 1416-1422
    • Xie, H.1    Wang, T.2    Matsuda, H.3    Morikawa, T.4    Yoshikawa, M.5    Tani, T.6
  • 33
    • 0141677814 scopus 로고    scopus 로고
    • Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis
    • Morikawa T, Kishi A, Pongiriyadacha Y, Matusda H, Yoshikawa M (2003) Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis. J Nat Prod 66:1191-1196 (Pubitemid 37204217)
    • (2003) Journal of Natural Products , vol.66 , Issue.9 , pp. 1191-1196
    • Morikawa, T.1    Kishi, A.2    Pongpiriyadacha, Y.3    Matsuda, H.4    Yoshikawa, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.