In vitro antiviral activity from Acanthospermum australe on herpesvirus and poliovirus

被引:17
作者
Rocha Martins, Lucia Regina [1 ]
Brenzan, Mislaine Adriana [1 ]
Nakamura, Celso Vataru [2 ]
Dias Filho, Benedito Prado [2 ]
Nakamura, Tania Ueda [2 ]
Ranieri Cortez, Lucia Elaine [3 ]
Garcia Cortez, Diogenes Aparicio [1 ]
机构
[1] Univ Estadual Maringa, Dept Farm & Farmacol, BR-87020900 Maringa, Parana, Brazil
[2] Univ Estadual Maringa, Dept Anal Clin, BR-87020900 Maringa, Parana, Brazil
[3] Cesumar, Dept Farm, Maringa, Parana, Brazil
关键词
Acanthospermum australe; antiviral activity; herpesvirus; poliovirus; cytotoxicity; OCCURRING TERPENE DERIVATIVES; MEDICINAL-PLANTS; MELAMPOLIDES; EXTRACT; VIRUS; FLAVONOIDS; HISPIDUM; LEAVES; AGENTS; DRUGS;
D O I
10.3109/13880209.2010.493177
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: The Asteraceae family has been of interest to researchers due to the presence of polyphenolic compounds, mainly flavonoids, which demonstrated antiviral activity. Objective: The hydroethanol extract of the aerial parts of Acanthospermum australe (Loefl.) Kuntze (Asteraceae) and its fractions, were evaluated in vitro for their potential cytotoxic and antiviral activity against bovine herpesvirus and human poliovirus. Materials and methods: The sulforhodamine B colorimetric assay were used to evaluate the capacity of the hydroethanol extract and fractions to inhibit the lytic activity of herpes and poliovirus in infected cell cultures and their influence on the viability of uninfected cell cultures. Results and discussion: A progressive increase in the antiviral effect against herpesvirus was observed in the course of the purification process of the extract. The hydroethanol extract had a 50% antiviral effective concentration (EC50) at 70 mu g/mL and 36 mu g/mL for herpes and poliovirus, respectively, and it exhibited no cytotoxicity. The fractions F3 (dichloromethane) and F4 (dichloromethane: ethyl acetate (1: 1 v/v)) both showed EC50 at 6.25 mu g/mL against herpesvirus, and these fractions showed cytotoxic concentrations (CC50) at 12.7 and 11.7 mu g/mL, respectively. These fractions had no effect against poliovirus in the concentrations tested. From the bioactive F3, a diterpene lactone (acanthoaustralide-1-O-acetate) was isolated at a concentration of 0.5% and from F4 two flavonoids (quercetin and chrysosplenol D) were isolated at concentrations of 0.14 and 0.24%, respectively. Conclusion: The present study reports for the first time the antiviral activity of extracts and fractions from A. australe aerial parts.
引用
收藏
页码:26 / 31
页数:6
相关论文
共 27 条
[1]   Evaluation of selected Sudanese medicinal plants for their in vitro activity against hemoflagellates, selected bacteria, HIV-1-RT and tyrosine kinase inhibitory, and for cytotoxicity [J].
Ali, H ;
König, GM ;
Khalid, SA ;
Wright, AD ;
Kaminsky, R .
JOURNAL OF ETHNOPHARMACOLOGY, 2002, 83 (03) :219-228
[2]   Evaluation of the antiherpetic activity of standardized extracts of Achyrocline satureioides [J].
Bettega, JMR ;
Teixeira, H ;
Bassani, VL ;
Barardi, CRM ;
Simoes, CMO .
PHYTOTHERAPY RESEARCH, 2004, 18 (10) :819-823
[3]   NATURALLY OCCURRING TERPENE DERIVATIVES .179. NEW MELAMPOLIDES AND CIS, CIS-GERMACRANOLIDES FROM SPECIES OF THE SUBTRIBE MELAMPODIINAE [J].
BOHLMANN, F ;
JAKUPOVIC, J ;
ZDERO, C ;
KING, RM ;
ROBINSON, H .
PHYTOCHEMISTRY, 1979, 18 (04) :625-630
[4]   NATURALLY-OCCURRING TERPENE DERIVATIVES .331. 2 SESQUITERPENE AND 3 DITERPENE LACTONES FROM ACANTHOSPERMUM-AUSTRALE [J].
BOHLMANN, F ;
JAKUPOVIC, J ;
DHAR, AK ;
KING, RM ;
ROBINSON, H .
PHYTOCHEMISTRY, 1981, 20 (05) :1081-1083
[5]   NEW MELAMPOLIDES FROM ACANTHOSPERMUM-AUSTRALE [J].
BOHLMANN, F ;
SCHMEDAHIRSCHMANN, G ;
JAKUPOVIC, J .
PLANTA MEDICA, 1984, 50 (01) :37-39
[6]   Plant products as antimicrobial agents [J].
Cowan, MM .
CLINICAL MICROBIOLOGY REVIEWS, 1999, 12 (04) :564-+
[7]   6-METHOXY FLAVONOIDS FROM ACANTHOSPERMUM-AUSTRALE [J].
DEBENEDETTI, S ;
MARTINO, V ;
PALACIOS, P ;
COUSSIO, JD .
JOURNAL OF NATURAL PRODUCTS, 1987, 50 (02) :325-325
[8]   Antimicrobial activity of the leaves and flowering tops of Acanthospermum hispidum [J].
Fleischer, TC ;
Ameade, EPK ;
Sawer, IK .
FITOTERAPIA, 2003, 74 (1-2) :130-132
[9]   ACANTHOSPERMAL-A AND ACANTHOSPERMAL-B, 2 NEW MELAMPOLIDES FROM ACANTHOSPERMUM SPECIES [J].
HERZ, W ;
KALYANARAMAN, PS .
JOURNAL OF ORGANIC CHEMISTRY, 1975, 40 (24) :3486-3491
[10]   Novel antiviral agents: a medicinal plant perspective [J].
Jassim, SAA ;
Naji, MA .
JOURNAL OF APPLIED MICROBIOLOGY, 2003, 95 (03) :412-427