Plant substances as anti-HIV agents selected according to their putative mechanism of action

被引:68
作者
Cos, P
Maes, L
Vanden Berghe, D
Hermans, N
Pieters, L
Vlietinck, A
机构
[1] Univ Antwerp, Dept Pharmaceut Sci, Lab Pharmacognosy, B-2610 Antwerp, Belgium
[2] Univ Antwerp, Lab Pharmaceut Microbiol, B-2610 Antwerp, Belgium
来源
JOURNAL OF NATURAL PRODUCTS | 2004年 / 67卷 / 02期
关键词
D O I
10.1021/np034016p
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Despite the continuous advances made in antiretroviral combination therapy, AIDS has become the leading cause of death in Africa and the fourth worldwide. Today, many research groups are exploring the biodiversity of the plant kingdom to find new and better anti-HIV drugs with novel mechanisms of action. In this review, plant substances showing a promising anti-HIV activity are discussed according to the viral targets with which they interact. Most of these compounds, however, interfere with early steps in the HIV replication, such as the virus entry steps and the viral enzymes reverse transcriptase and integrase, whereas until now almost no plant compounds have been found to interact with the many other viral targets. Since some plant substances are known to modulate several cellular factors, such as NF-kappa B and TNF-alpha, which are also involved in the replication of HIV, their role as potential anti-HIV products is also discussed. In conclusion, several plant-derived antiviral agents are good candidates to be further studied for their potential in the systemic therapy and/or prophylaxis of HIV infections, most probably in combination with other anti-HIV drugs.
引用
收藏
页码:284 / 293
页数:10
相关论文
共 133 条
[1]   ORAL DEXTRAN SULFATE (UA001) IN THE TREATMENT OF THE ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS) AND AIDS-RELATED COMPLEX [J].
ABRAMS, DI ;
KUNO, S ;
WONG, R ;
JEFFORDS, K ;
NASH, M ;
MOLAGHAN, JB ;
GORTER, R ;
UENO, R .
ANNALS OF INTERNAL MEDICINE, 1989, 110 (03) :183-188
[2]   Oxidative stress and plasma antioxidant micronutrients in humans with HIV infection [J].
Allard, JP ;
Aghdassi, E ;
Chau, J ;
Salit, I ;
Walmsley, S .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1998, 67 (01) :143-147
[3]   Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: Synthesis, biological evaluation, and molecular modeling [J].
Artico, M ;
Di Santo, R ;
Costi, R ;
Novellino, E ;
Greco, G ;
Massa, S ;
Tramontano, E ;
Marongiu, ME ;
De Montis, A ;
La Colla, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (21) :3948-3960
[4]   Homonojirimycin isomers and N-alkylated homonojirimycins: Structural and conformational basis of inhibition of glycosidases [J].
Asano, N ;
Nishida, M ;
Kato, A ;
Kizu, H ;
Matsui, K ;
Shimada, Y ;
Itoh, T ;
Baba, M ;
Watson, AA ;
Nash, RJ ;
Lilley, PMD ;
Watkin, DJ ;
Fleet, GWJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (14) :2565-2571
[5]   The plant ribosome inactivating proteins luffin and saporin are potent inhibitors of HIV-1 integrase [J].
Au, TK ;
Collins, RA ;
Lam, TL ;
Ng, TB ;
Fong, WP ;
Wan, DCC .
FEBS LETTERS, 2000, 471 (2-3) :169-172
[6]   Cellular factors as alternative targets for inhibition of HIV-1 [J].
Baba, M .
ANTIVIRAL RESEARCH, 1997, 33 (03) :141-152
[7]   THE MANNOSE-SPECIFIC PLANT-LECTINS FROM CYMBIDIUM HYBRID AND EPIPACTIS-HELLEBORINE AND THE (N-ACETYLGLUCOSAMINE)N-SPECIFIC PLANT LECTIN FROM URTICA-DIOICA ARE POTENT AND SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS AND CYTOMEGALOVIRUS REPLICATION INVITRO [J].
BALZARINI, J ;
NEYTS, J ;
SCHOLS, D ;
HOSOYA, M ;
VANDAMME, E ;
PEUMANS, W ;
DECLERCQ, E .
ANTIVIRAL RESEARCH, 1992, 18 (02) :191-207
[8]   Activation of latent HIV-1 expression by the potent anti-tumor promoter 12-deoxyphorbol 13-phenylacetate [J].
Bocklandt, S ;
Blumberg, PM ;
Hamer, DH .
ANTIVIRAL RESEARCH, 2003, 59 (02) :89-98
[9]   Antimalarial chemotherapeutic peroxides: artemisinin, yingzhaosu A and related compounds [J].
Borstnik, K ;
Paik, IH ;
Shapiro, TA ;
Posner, GH .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2002, 32 (13) :1661-1667
[10]   Natural products as targeted modulators of the nuclear factor-κB pathway [J].
Bremner, P ;
Heinrich, M .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2002, 54 (04) :453-472