메뉴 건너뛰기




Volumn 29, Issue 1, 2015, Pages 73-79

Pentacyclic triterpenoids from spikes of Prunella vulgaris L. inhibit glycogen phosphorylase and improve insulin sensitivity in 3T3-L1 adipocytes

Author keywords

Glycogen phosphorylase; Insulin sensitivity; Lamiaceae Labiatae; Pentacyclic triterpenoid; Prunella vulgaris L

Indexed keywords

2ALPHA,3ALPHA DIHYDROXYLURS 12 EN 28 OIC ACID; 2ALPHA,3BETA DIHYDROXYOLEAN 12 EN 28 OIC ACID; 2ALPHA,3BETA,19ALPHA TETRAHYDROXYURS 12 EN 28 OIC ACID 28BETA DEXTRO GLUCOPYRANOSIDE; 2ALPHA,3BETA,19ALPHA TRIHYDROXYURS 12 EN 28 OIC ACID; 2ALPHA,3BETA,19ALPHA TRIHYDROXYURS 12 EN 28 OIC ACID 28BETA DEXTRO GLUCOPYRANOSIDE; 2ALPHA,3BETA,19ALPHA TRIHYDROXYURS 12 EN 28 OIC ACID 28BETA DEXTRO GLUCOPYRANOSYL BETA DEXTRO GLUCOPYRANOSIDE; 2ALPHA,3BETA,24 TRIHYDROXYOLEAN 12 EN 28 OIC ACID; 2ALPHA,3BETA,24 TRIHYDROXYURS 12 EN 28 OIC ACID; 2ALPHA,3BETA,24 TRIHYDROXYURS 12 EN 28 OIC ACID 28BETA DEXTRO GLUCOPYRANOSIDE; 2ALPHA,3BETA,24 TRIHYDROXYURS 12(30) DIEN 28 OIC ACID; GLYCOGEN PHOSPHORYLASE; INSULIN; METHANOL; OLEANOLIC ACID; PENTACYCLIC TRITERPENE; PLANT MEDICINAL PRODUCT; PRUNELLA VULGARIS EXTRACT; ROTUNDIC ACID 28 O ALPHA DEXTRO GLUCOPYRANOSYL BETA DEXTRO GLUCOPYRANOSIDE; UNCLASSIFIED DRUG; URSOLIC ACID; VULGASIDE I; VULGASIDE II; ENZYME INHIBITOR; GLUCOSE; GLYCOSIDE;

EID: 84920982986     PISSN: 0951418X     EISSN: 10991573     Source Type: Journal    
DOI: 10.1002/ptr.5228     Document Type: Article
Times cited : (20)

References (26)
  • 1
    • 0001294661 scopus 로고
    • Triterpens and triterpene glycosides from the leaves of Ilex rotunda
    • Amimoto K, Yoshikawa K, Arihara S. 1993. Triterpens and triterpene glycosides from the leaves of Ilex rotunda. Phytochemistry 33: 1475-1480.
    • (1993) Phytochemistry , vol.33 , pp. 1475-1480
    • Amimoto, K.1    Yoshikawa, K.2    Arihara, S.3
  • 2
    • 33646027276 scopus 로고    scopus 로고
    • Pentacyclic triterpenes. Part 3: Synthesis and biological evaluation of oleanolic acid derivatives as novel inhibitors of glycogen phosphorylase
    • Chen J, Liu J, Zhang LY, et al. 2006. Pentacyclic triterpenes. Part 3: synthesis and biological evaluation of oleanolic acid derivatives as novel inhibitors of glycogen phosphorylase. Bioorg Med Chem Lett 16: 2915-2919.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 2915-2919
    • Chen, J.1    Liu, J.2    Zhang, L.Y.3
  • 3
    • 56249089655 scopus 로고    scopus 로고
    • Enhanced analysis of triterpenes, flavonoids and phenolic compounds in Prunella vulgaris L. by capillary zone electrophoresis with the addition of running buffer modifiers
    • Cheung HY, Zhang QF. 2008. Enhanced analysis of triterpenes, flavonoids and phenolic compounds in Prunella vulgaris L. by capillary zone electrophoresis with the addition of running buffer modifiers. J Chromatogr A 1213: 231-238.
    • (2008) J Chromatogr A , vol.1213 , pp. 231-238
    • Cheung, H.Y.1    Zhang, Q.F.2
  • 4
    • 33744906765 scopus 로고    scopus 로고
    • Pharmacological activities of natural triterpenoids and their therapeutic implications
    • Dzubak P, Hajduch M, Vydra D, et al. 2006. Pharmacological activities of natural triterpenoids and their therapeutic implications. Nat Prod Rep 23: 394-411.
    • (2006) Nat Prod Rep , vol.23 , pp. 394-411
    • Dzubak, P.1    Hajduch, M.2    Vydra, D.3
  • 5
    • 33846595772 scopus 로고    scopus 로고
    • Triterpenoid saponins from the spikes of Prunella vulgaris
    • Gu XJ, Li YB, Li P, Qian SH, Zhang JF. 2007. Triterpenoid saponins from the spikes of Prunella vulgaris. Helv Chim Acta 90: 72-78.
    • (2007) Helv Chim Acta , vol.90 , pp. 72-78
    • Gu, X.J.1    Li, Y.B.2    Li, P.3    Qian, S.H.4    Zhang, J.F.5
  • 6
    • 0001311327 scopus 로고
    • Triterpenoids from Prunella vulgaris L
    • Kojima H, Ogura H. 1986. Triterpenoids from Prunella vulgaris L. Phytochemistry 3:729-733.
    • (1986) Phytochemistry , vol.3 , pp. 729-733
    • Kojima, H.1    Ogura, H.2
  • 7
    • 0000444442 scopus 로고
    • Pentacyclic triterpenoids from Prunella vulgaris
    • Kojima H, Tominga H, Sato S, Ogura H. 1986. Pentacyclic triterpenoids from Prunella vulgaris. Phytochemistry 26:1107-1111.
    • (1986) Phytochemistry , vol.26 , pp. 1107-1111
    • Kojima, H.1    Tominga, H.2    Sato, S.3    Ogura, H.4
  • 8
    • 79960318828 scopus 로고    scopus 로고
    • Modified Si-Miao-San extract inhibits inflammatory response and modulates insulin sensitivity in hepatocytes through an IKKβ/IRS-1/Akt-dependent pathway
    • Liu K, Luo T, Zhang Z, et al. 2011. Modified Si-Miao-San extract inhibits inflammatory response and modulates insulin sensitivity in hepatocytes through an IKKβ/IRS-1/Akt-dependent pathway. J Ethnopharmacol 136: 473-479.
    • (2011) J Ethnopharmacol , vol.136 , pp. 473-479
    • Liu, K.1    Luo, T.2    Zhang, Z.3
  • 9
    • 77953536163 scopus 로고    scopus 로고
    • Resveratrol modulates adipokine expression and improves insulin sensitivity in adipocytes: Relative to inhibition of inflammatory responses
    • Liu K, Wang H, An Y, Liu BL, Huang F. 2010. Resveratrol modulates adipokine expression and improves insulin sensitivity in adipocytes: relative to inhibition of inflammatory responses. Biochimie 92: 789-796.
    • (2010) Biochimie , vol.92 , pp. 789-796
    • Liu, K.1    Wang, H.2    An, Y.3    Liu, B.L.4    Huang, F.5
  • 10
    • 22744458623 scopus 로고    scopus 로고
    • Triterpenoids from Sanguisorba officinalis
    • Liu X, Cui YX, Yu Q, Yu B. 2005. Triterpenoids from Sanguisorba officinalis. Phytochemistry 66: 1671-1679.
    • (2005) Phytochemistry , vol.66 , pp. 1671-1679
    • Liu, X.1    Cui, Y.X.2    Yu, Q.3    Yu, B.4
  • 11
    • 0032539696 scopus 로고    scopus 로고
    • Discovery of a human liver glycogen phosphorylase inhibitor that lowers blood glucose in vivo
    • Martin WH, Hoover DJ, Armento SJ, et al . 1998. Discovery of a human liver glycogen phosphorylase inhibitor that lowers blood glucose in vivo. Proc Natl Acad Sci U S A 95: 1776-1781.
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 1776-1781
    • Martin, W.H.1    Hoover, D.J.2    Armento, S.J.3
  • 12
    • 79952361538 scopus 로고    scopus 로고
    • A new ursane-type triterpenoid glycoside from Centella asiatica leaves modulates the production of nitric oxide and secretion of TNF-α in activated RAW 264.7 cells
    • Nhiem NX, Tai BH, Quang TH, et al. 2011. A new ursane-type triterpenoid glycoside from Centella asiatica leaves modulates the production of nitric oxide and secretion of TNF-α in activated RAW 264.7 cells. Bioorg Med Chem Lett 21: 1777-1781.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 1777-1781
    • Nhiem, N.X.1    Tai, B.H.2    Quang, T.H.3
  • 15
    • 48749141622 scopus 로고
    • β-glucosyl esters of 19α-hydroxyurs-olic acid derivatives in leaves of Rubus species
    • Takashi S, Takashi T, Osamu T, Naohiro N. 1984. β-glucosyl esters of 19α-hydroxyurs-olic acid derivatives in leaves of Rubus species. Phytochemistry 23: 2829-2834.
    • (1984) Phytochemistry , vol.23 , pp. 2829-2834
    • Takashi, S.1    Takashi, T.2    Osamu, T.3    Naohiro, N.4
  • 16
    • 0034119806 scopus 로고    scopus 로고
    • Anti-allergic and antiinflammatory triterpenes from the herb of Prunella vulgaris
    • Ryu SY, Oak MH, Yoon SK, et al. 2000. Anti-allergic and antiinflammatory triterpenes from the herb of Prunella vulgaris. Planta Med 66:358-360.
    • (2000) Planta Med , vol.66 , pp. 358-360
    • Ryu, S.Y.1    Oak, M.H.2    Yoon, S.K.3
  • 18
    • 78650883771 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of arjunolic acid, bayogenin, hederagonic acid and 4-epi-hederagonic acid as glycogen phosphorylase inhibitors
    • Wen XA, Liu J, Zhang LY, Ni PZ, Sun HB. 2010. Synthesis and biological evaluation of arjunolic acid, bayogenin, hederagonic acid and 4-epi-hederagonic acid as glycogen phosphorylase inhibitors. Chin J Nat Med 6: 441-448.
    • (2010) Chin J Nat Med , vol.6 , pp. 441-448
    • Wen, X.A.1    Liu, J.2    Zhang, L.Y.3    Ni, P.Z.4    Sun, H.B.5
  • 19
    • 45749110639 scopus 로고    scopus 로고
    • Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: Synthesis, structure-activity relationships, and X-ray crystallographic studies
    • Wen XA, Sun HB, Liu J, et al. 2008. Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies. J Med Chem Lett 51: 3540-3554.
    • (2008) J Med Chem Lett , vol.51 , pp. 3540-3554
    • Wen, X.A.1    Sun, H.B.2    Liu, J.3
  • 20
    • 25844437477 scopus 로고    scopus 로고
    • Pentacyclic triterpenes. Part 1: The first examples of naturally occurring pentacyclic triterpenes as a new class of inhibitors of glycogen phosphorylases
    • Wen XA, Sun HB, Liu J, et al. 2005. Pentacyclic triterpenes. Part 1: the first examples of naturally occurring pentacyclic triterpenes as a new class of inhibitors of glycogen phosphorylases. Bioorg Med Chem Lett 15: 4944-4948.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 4944-4948
    • Wen, X.A.1    Sun, H.B.2    Liu, J.3
  • 21
    • 34548833897 scopus 로고    scopus 로고
    • Pentacyclic triterpenes. Part 5: Synthesis and SAR study of corosolic acid derivatives as inhibitors of glycogen phosphorylases
    • Wen XA, Xia J, Cheng KG, et al. 2007. Pentacyclic triterpenes. Part 5: synthesis and SAR study of corosolic acid derivatives as inhibitors of glycogen phosphorylases. Bioorg Med Chem Lett 17: 5777-5782.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 5777-5782
    • Wen, X.A.1    Xia, J.2    Cheng, K.G.3
  • 22
    • 29544449934 scopus 로고    scopus 로고
    • Pentacyclic triterpenes. Part 2: Synthesis and biological activity of maslinic acid derivatives as inhibitors of glycogen phosphorylase
    • Wen XA, Zhang P, Liu J, et al. 2006. Pentacyclic triterpenes. Part 2: synthesis and biological activity of maslinic acid derivatives as inhibitors of glycogen phosphorylase. Bioorg Med Chem Lett 16: 722-726.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 722-726
    • Wen, X.A.1    Zhang, P.2    Liu, J.3
  • 23
    • 79952026605 scopus 로고    scopus 로고
    • Synthesis, biology and clinical significance of pentacyclic triterpenes: A multi-target approach to prevention and treatment of metabolic and vascular diseases
    • Sheng HM, Sun HB. 2011. Synthesis, biology and clinical significance of pentacyclic triterpenes: a multi-target approach to prevention and treatment of metabolic and vascular diseases. Nat Prod Rep 28:543-593.
    • (2011) Nat Prod Rep , vol.28 , pp. 543-593
    • Sheng, H.M.1    Sun, H.B.2
  • 24
    • 0035979775 scopus 로고    scopus 로고
    • Reversal of obesity- and diet-induced insulin resistance with salicylates or targeted disruption of Ikkβ
    • Yuan M, Konstantopoulos N, Lee J, et al. 2001. Reversal of obesity- and diet-induced insulin resistance with salicylates or targeted disruption of Ikkβ. Science 293: 1673-1677.
    • (2001) Science , vol.293 , pp. 1673-1677
    • Yuan, M.1    Konstantopoulos, N.2    Lee, J.3
  • 25
    • 0041708276 scopus 로고
    • Two new ursane glycosides from Prunella vulgaris in France
    • Zhang YJ, Yang CR. 1995. Two new ursane glycosides from Prunella vulgaris in France. Acta Botanica Yunanica 17: 468-472.
    • (1995) Acta Botanica Yunanica , vol.17 , pp. 468-472
    • Zhang, Y.J.1    Yang, C.R.2
  • 26
    • 79951515436 scopus 로고    scopus 로고
    • Luteolin inhibits inflammatory response and improves insulin sensitivity in the endothelium
    • Zhu DQ, Liu K, Yi JL, Liu BL, Liu GL. 2011. Luteolin inhibits inflammatory response and improves insulin sensitivity in the endothelium. Biochimie 93: 506-512.
    • (2011) Biochimie , vol.93 , pp. 506-512
    • Zhu, D.Q.1    Liu, K.2    Yi, J.L.3    Liu, B.L.4    Liu, G.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.