Abstract
The 70 % EtOH extract of Polygonum cuspidatum showed inhibitory action against HIV-1-induced syncytium formation at non-cytotoxic
concentrations in vitro with a 50 % effective concentration (EC50 ) of 13.94 ± 3.41 µg/mL. Through bioactivity-guided fractionation, 20 phenolic compounds,
including eight stilbenoids, were isolated from the roots of Polygonum cuspidatum , and their anti-HIV‐1 activities were evaluated. Results showed that compounds 1, 13, 14 , and 16 demonstrated fairly strong antiviral activity against HIV-1-induced cytopathic effects
in C8166 lymphocytes at non-cytotoxic concentrations, with EC50 values of 4.37 ± 1.96 µg/mL, 19.97 ± 5.09, 14.4 ± 1.34 µg/mL, and 11.29 ± 6.26 µg/mL
and therapeutic index (TI) values of 8.12, > 10.02, > 13.89, and > 17.71, respectively.
Other compounds showed either weak or no effects. Compound 6 also showed weak inhibition (153.42 ± 19.25 µg/mL); however, it possesses very good
water solubility and showed almost no cytotoxicity (> 2000 µg/mL), therefore achieving
a fairly good TI (13.04). The activities of the two compounds (3 and 18 ) from Polygonum multiflorum were also assayed. The relationship between molecular structures and their bioactivities
was also discussed.
Key words
Polygonum cuspidatum
-
Polygonum multiflorum
- Polygonaceae - chemical components - anti‐HIV‐1 activity
References
1
Fauci A S.
Twenty-five years of HIV/AIDS.
Science.
2006;
313
409
2 UNAIDS .The 2008 Report on the global AIDS epidemic. http://www.unaids.org/en/KnowledgeCentre/HIVData/GlobalReport/2008/2008_Global_report.asp Accessed September 1, 2009
3
Singh I P, Bharate S B, Bhutani K K.
Anti-HIV natural products.
Curr Sci.
2005;
89
269-290
4
Asres K, Seyoum A, Veeresham C, Bucar F, Gibbons S.
Naturally derived anti-HIV agents.
Phytother Res.
2005;
19
557-581
5
Kimura Y, Kozawa M, Baba K, Hata K.
New constitutents of roots of Polygonum cuspidatum .
Planta Med.
1983;
48
164-168
6
Kubo M, Kimura Y, Shin H, Haneda T, Tani T, Namba K.
Studies on the antifungal substances of crude drugs (II). On the roots of Polygonum cuspidatum Sieb. et Zucc. (Polygonaceae).
Shoyakugaku Zasshi.
1981;
35
58-61
7
Jayatilake G S, Jayasuriya H, Lee E S, Koonchanok N M, Geahlen R L, Ashendel C L,
McLaughlin J L, Chang C J.
Kinase inhibitors from Polygonum cuspidatum .
J Nat Prod.
1993;
56
1805-1810
8
Hegde V R, Pu H, Patel M, Black T, Soriano A, Zhao W, Gullo V P, Chan T M.
Two new bacterial DNA primase inhibitors from the plant Polygonum cuspidatum .
Bioorg Med Chem Lett.
2004;
14
2275-2277
9
Xiao K, Xuan L, Xu Y, Bai D.
Stilbene glycoside sulfates from Polygonum cuspidatum .
J Nat Prod.
2000;
63
1373-1376
10
Xiao K, Xuan L, Xu Y, Bai D, Zhong D.
Constituents from Polygonum cuspidatum .
Chem Pharm Bull (Tokyo).
2002;
50
605-608
11
Xiao K, Xuan L, Xu Y, Zhong D, Wang Z, Zhang N.
Dimeric stilbene glycosides from Polygonum cuspidatum .
Eur J Org Chem.
2002;
564-568
12 Xiao K, Zhang H J, Xuan L J, Zhang J, Xu Y M, Bai D L.
Stilbenoids: chemistry and bioactivities. Atta-ur-Rahman Studies in natural products chemistry. Amsterdam; Elsevier B.V. 2008:
453-646
13
Chang J S, Liu H W, Wang K C, Chen M C, Chiang L C, Hua Y C, Lin C C.
Ethanol extract of Polygonum cuspidatum inhibits hepatitis B virus in a stable HBV-producing cell line.
Antiviral Res.
2005;
66
29-34
14
Wang Z J, Wang X Y, Chen Z M.
Research about antiviral effect of ethyl acetate component of Rhizoma Polygoni cuspidati
on herpes virus hominis.
Zhongguo Xiandai Yongyong Yaoxue Zazhi.
1999;
16
27-31
15
Jiang Y, Wan H, Bao Z, Zhu G.
Evaluation of antiviral effect of Polygonum cuspidatum water extract with a model of murine acquired immunodeficiency syndrome.
Virol Sin (Zhongguo Bingduxue).
1998;
13
306-311
16
Ngoc T M, Minh P T H, Hung T M, Thuong P T, Lee I S, Min B S, Bae K.
Lipoxygenase inhibitory constituents from rhubarb.
Arch Pharm Res.
2008;
31
598-605
17
Cui C B, Tezuka Y, Kikuch T, Nakano H, Tamaoki T, Park J H.
Constituents of a fern, Davallia mariesii Moore. Isolation and identification of a novel norcarotane sequiterpene glycoside,
a chromone glucuronide, and two epicatechin glycosides.
Chem Pharm Bull (Tokyo).
1992;
40
2035-2040
18
Sun M X, Li X, Liu W Y, Xiao K.
5,7-Dimethoxyisobenzofuran-1 (3H)-one.
Acta Crystallogr E.
2009;
65
o2146
19
Thompson R S, Jacques D, Haslam E, Tanner R J N.
Plant proanthocyanidins. Part I. Introduction; the isolation, structure, and distribution
in nature of plant procyanidins.
J Chem Soc [Perkin I].
1972;
1387-1399
20
Takani M, Nakano M, Takahashi K.
Studies on constituents of medicinal plants. XIX. Constituents of Schizandra nigra MAX. (3).
Chem Pharm Bull (Tokyo).
1977;
25
3388-3390
21
Xiao K, Xuan L J, Xu Y M, Bai D L.
Studies on the chemical constituents of Polygonum cuspidatum .
Chin Pharm J.
2003;
38
12-14
22
Sano K, Sanada S, Ida Y, Shoji J.
Studies on the constituents of the bark of Kalopanax pictus Nakai.
Chem Pharm Bull (Tokyo).
1991;
39
865-870
23
Zhang G H, Wang Q, Chen J J, Zhang X M, Tam S C, Zheng Y T.
The anti-HIV-1 effect of scutellarin.
Biochem Biophys Res Commun.
2005;
334
812-816
24
Xiao K, Xuan L J, Xu Y M, Bai D L.
Novel stilbene glycosides from Polygonum multiflorum .
Acta Bot Sin.
2002;
44
1491-1494
25
Heredia A, Davis C, Redfield R.
Synergistic inhibition of HIV-1 in activated and resting peripheral blood mononuclear
cells, monocyte-derived macrophages, and selected drug-resistant isolates with nucleoside
analogues combined with a natural product, resveratrol.
J Acquir Immune Defic Syndr.
2000;
25
246-255
26
Zheng Y T, Zhang W F, Ben K L, Wang J H.
In vitro immunotoxicity and cytotoxicity of trichosanthin against human normal immunocytes
and leukemia-lymphoma cells.
Immunopharmacol Immunotoxicol.
1995;
17
69-79
27
Zheng Y T, Ben K L, Jin S W.
Anti-HIV-1 activity of trichobitacin, a novel ribosome-inactivating protein.
Acta Pharmacol Sin.
2000;
21
179-182
1 These authors contributed equally to this work.
Prof. Dr. Yongtang Zheng
Key Laboratory of Animal Models and Human Diseases Mechanisms and Laboratory of Molecular
Immunopharmacology Kunming Institute of Zoology Chinese Academy of Sciences
Kunming
Yunnan 650223
People's Republic of China
Telefon: + 86 87 15 19 56 84
Fax: + 86 87 15 19 56 84
eMail: zhengyt@mail.kiz.ac.cn
Associate Prof. Dr. Kai Xiao
Lab of Toxicology & Pharmacology Faculty of Naval Medicine The Second Military Medical University
800 Xinangyin Road
Shanghai 200433
People's Rapublic of China
Telefon: + 86 21 81 87 11 29
Fax: + 86 21 81 87 11 28
eMail: kaixiaocn@gmail.com