Influence of sulfation on anti-myocardial ischemic activity of ophiopogon japonicus polysaccharide

Journal of Asian Natural Products Research

Volumn 11, Issue 4, 2009, Pages 306-321

  Zheng, Qin ^a,b   Feng, Yi ^a   Xu, De Sheng ^a   Lin, Xiao ^a   Chen, Yan Zuo ^a  

^a SHANGHAI UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

^b BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

Anti myocardial ischemia; Derivative; Ophiopogon japonicus; Polysaccharide

Indexed keywords

ISOPRENALINE; LACTATE DEHYDROGENASE; OPHIOPOGON ROOT; POLYSACCHARIDE; SULFATE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHEMICAL MODIFICATION; CONTROLLED STUDY; CORONARY ARTERY BLOOD FLOW; DRUG MECHANISM; DRUG STRUCTURE; ELECTROCARDIOGRAM; GEL PERMEATION CHROMATOGRAPHY; HEART CONTRACTION; HEART MUSCLE ISCHEMIA; INFRARED SPECTROSCOPY; ISOLATED HEART; LACTATE DEHYDROGENASE BLOOD LEVEL; MALE; NONHUMAN; PLANT ROOT; RAT; REPERFUSION; ST SEGMENT; SULFATION; ANIMAL; BLOOD; CHEMISTRY; DISEASE MODEL; DRUG EFFECT; ISCHEMIA; ISOLATION AND PURIFICATION; SPRAGUE DAWLEY RAT; STRUCTURE ACTIVITY RELATION;

OPHIOPOGON JAPONICUS; RATTUS;

ANIMALS; DISEASE MODELS, ANIMAL; ISCHEMIA; MALE; MYOCARDIAL CONTRACTION; OPHIOPOGON; POLYSACCHARIDES; RATS; RATS, SPRAGUE-DAWLEY; STRUCTURE-ACTIVITY RELATIONSHIP; SULFATES;

EID: 66349117714     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020902727363     Document Type: Article

References (14)

1. K.R. Laderoute and K.A. Webster, Circ. Res. 80, 336 (1997).
2. X.P. Yang, D.Y. Guo, J.M. Zhang, and M.C. Wu, Int. Immunopharmacol. 7, 401 (2007).
3. L.J. Wang and Y. Wang, J. Chin. Med. Res. 5, 885 (2005).
4. Q. Zheng, Y. Feng, and D.S. Xu, Asia-Pac. Tradit. Med. 4, 74 (2005).
5. D.S. Xu, Y. Feng, Y.H. Zhou, X.C. Zhang, X. Lin, and H.L. Deng, Chin. Tradit. Pat. Med. 26, 832 (2004).
6. D.S. Xu, Y. Feng, X. Lin, H.L. Deng, J.N. Fang, and Q. Dong, Acta Pharm. Sin. 40, 636 (2005).
7. Q. Zheng, Y. Feng, D.S. Xu, and Y.Z. Cheng, CJITWM 27, 1116 (2007).
8. X.Y. Huang, X.F. Kong, D.Y. Wang, and Y.L. Hu, Nat. Prod. Res. Dev. 19, 328 (2007).
9. G.H. Huo, L.S. Li, and Y.Y. Gao, Chem. Life 22, 194 (2002).
10. M.M. Tomczak, D.K. Hincha, S.D. Estrada, R.E. Feeney, and J.H. Crowe, Biochim. Biophys. Acta 1511, 255 (2001).
11. R.Takano, S. Yoshikawa, T. Ueda,K.Hayashi, S. Hirase, and S. Hara, J. Carbohydr. Chem. 15, 449 (1996).
12. M.J. Melnicoff, J.J. Godleski, and J.P. Bercz, Res. Commun. Chem. Pathol. Pharmacol. 14, 377 (1976).
13. S.N. Stehr, J.C. Ziegeler, A. Pexa, R. Oertel, A. Deussen, T. Koch, and M. Hübler, Anesth. Analog. 104, 186 (2007).
14. A.G. Ciplea, R. Kretzschmar, W. Heimann, M. Kirchengast, and A. Safer, Drug Res. 38, 215 (1988).