SELECTIVE ANTIVIRAL ACTIVITY OF SYNTHETIC SOLUBLE L-TYROSINE AND L-DOPA MELANINS AGAINST HUMAN-IMMUNODEFICIENCY-VIRUS INVITRO

被引:90
|
作者
MONTEFIORI, DC
ZHOU, JY
机构
[1] Department of Pathology, Vanderbilt University Medical School, Nashville, TN
关键词
MELANIN; ANTIVIRAL THERAPY; ACQUIRED IMMUNE DEFICIENCY SYNDROME;
D O I
10.1016/0166-3542(91)90037-R
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Melanins are pigments found in hair, skin, irides of the eye, and brain. Their functions in mammals include protection from exposure to sunlight, camouflage from predators, sexual recognition within species, and possible electron transfer reactants. Most natural melanins exist in an insoluble form, which is one reason there is little information on the biological properties of soluble melanins. Here, synthetic soluble melanins were obtained by chemical oxidation of L-tyrosine or spontaneous oxidation of L-beta-3,4-dihydroxyphenylalanine (L-dopa). Replication of human immunodeficiency virus types 1 and 2 (HIV-1 and HIV-2) was inhibited by soluble melanin in two human lymphoblastoid cell lines (MT-2 and H9) and in phytohemagglutinin-stimulated human T cells. Effective concentrations of 0.15-10 mu-g/ml had no cell toxicity. Melanin blocked infection by cell-free virus and interfered with HIV-induced syncytium formation and cytopathic effects when fusion-susceptible, uninfected cells, were mixed with chronically infected cells. Melanin also impeded the HIV-1 envelope surface glycoprotein, and T cell specific monoclonal antibody leu-3a (CD4), but not leu-5b (CD2), from binding to the surface of MT-2 cells. No effect on HIV-1 reverse transcriptase activity in viral lysates was observed. These results identify a unique biological property of melanin, and suggest that soluble melanins may represent a new class of pharmacologically active substances which should be further investigated for potential therapeutic utility in the treatment of Acquired Immune Deficiency Syndrome (AIDS).
引用
收藏
页码:11 / 26
页数:16
相关论文
共 44 条
  • [41] SYNTHETIC NUCLEOSIDES AND NUCLEOTIDES .30. SYNTHESIS AND ANTIVIRAL ACTIVITY OF 3'-AZIDO, 2',3'-UNSATURATED AND 2',3'-DIDEOXY DERIVATIVES OF E-5-STYRYL-2'-DEOXYURIDINE ON HUMAN-IMMUNODEFICIENCY-VIRUS
    YAMAGUCHI, T
    SANEYOSHI, M
    NUCLEOSIDES & NUCLEOTIDES, 1992, 11 (2-4): : 373 - 382
  • [42] Green Synthesized Zinc Oxide Nanoparticles Based on Cestrum diurnum L. of Potential Antiviral Activity against Human Corona 229-E Virus
    Alrabayah, Ibrahim N.
    Elhawary, Seham S.
    Kandil, Zeinab A.
    El-Kadder, Essam M. Abd
    Moemen, Yasmine S.
    Saleh, Abdulrahman M.
    El Raey, Mohamed A.
    MOLECULES, 2023, 28 (01):
  • [43] Antifungal activity of Arctotis arctotoides (L.f.) O. Hoffm. and Gasteria bicolor Haw. against opportunistic fungi associated with human immunodeficiency virus/acquired immunodeficiency syndrome
    Otang, Wilfred M.
    Grierson, Donald S.
    Ndip, Roland N.
    PHARMACOGNOSY MAGAZINE, 2012, 8 (30) : 135 - 140
  • [44] INVITRO ANTIVIRAL ACTIVITY OF POLYOXOMOLYBDATES - MECHANISM OF INHIBITORY EFFECT OF PM-104 (NH4)12H2(EU4(MOO4)(H2O)16(MO7O24)4) . 13H2O ON HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1
    INOUYE, Y
    TOKUTAKE, Y
    YOSHIDA, T
    SETO, Y
    HUJITA, H
    DAN, K
    YAMAMOTO, A
    NISHIYA, S
    YAMASE, T
    NAKAMURA, S
    ANTIVIRAL RESEARCH, 1993, 20 (04) : 317 - 331