Individual and combined mycotoxins deoxynivalenol, nivalenol, and fusarenon-X induced apoptosis in lymphoid tissues of mice after oral exposure

被引:15
作者
Aupanun, Sawinee [1 ,2 ]
Poapolathep, Saranya [1 ,2 ]
Phuektes, Patchara [3 ]
Giorgi, Mario [4 ]
Zhang, Zhaowei [5 ]
Oswald, Isabelle P. [6 ]
Poapolathep, Amnart [1 ,2 ]
机构
[1] Kasetsart Univ, Fac Vet Med, Dept Pharmacol, Bangkok 10900, Thailand
[2] KU, NRU, CASAF, KU Inst Adv Studies, Bangkok 10900, Thailand
[3] Khonkaen Univ, Fac Vet Med, Dept Pathobiol, Khon Kaen 40002, Thailand
[4] Univ Pisa, Dept Vet Sci, Via Livornese, I-56122 Pisa, Italy
[5] Chinese Acad Agr Sci, Oil Crops Res Inst, Wuhan 430062, Hubei, Peoples R China
[6] Univ Toulouse, Toxalim Res Ctr Food Toxicol, INRA, ENVT,INP Purpan,UPS, Toulouse, France
关键词
Deoxynivalenol; Nivalenol; Fusarenon-X; Mycotoxin combination; Lymphoid tissues; TRICHOTHECENE VOMITOXIN DEOXYNIVALENOL; HUMAN T-CELLS; GENE-EXPRESSION; IN-SITU; MITOCHONDRIA; INDUCTION; TRANSPORT; GLYCOPROTEIN; INVOLVEMENT; HISTOLOGY;
D O I
10.1016/j.toxicon.2019.04.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lymphocytes are involved in the adaptive immune response and are highly sensitive to type B trichothecenes. In grains and their products, deoxynivalenol (DON) is the most widely distributed trichothecene. It usually co-occurs with other type B members, such as nivalenol (NIV) and fusarenon-X (FX), because they are all produced by the same Fusarium fungi. However, the combined effects of mycotoxins are complex and cannot be predicted based on individual toxicity. Thus, the adverse effects of combined toxins are of increasing concern. The aim of this study was to compare the toxicity to lymphoid tissues of mice of DON alone or mixed with NIV or FX. Forty, 3-week-old male ICR mice were given a single oral administration of a vehicle control, one toxin, binary, or ternary mixtures and then sacrificed at 12 h after exposure. Mice treated with FX alone showed marked nuclear condensation and fragmentation of lymphocytes in the cortical thymus and germinal center of Peyer's patches and spleen. Similarly, these animals clearly displayed TUNEL- and Caspase-3-positive cells in the regions. In contrast, minimal changes were noticed in the lymphoid tissues of mice receiving combined toxins when compared to this toxin alone. In addition, oral exposure to FX alone significantly up-regulated the relative expression of Bax, Caspase-3, Caspase-9, and Trp53. These data increase our understanding of the toxic actions of DON, NIV, and FX alone or in combination to lymphocytes and can be used to assess the possible risk associated with their co-occurrences in foodstuffs to human and animal health.
引用
收藏
页码:83 / 94
页数:12
相关论文
共 54 条
  • [1] Toxicological interactions between the mycotoxins deoxynivalenol, nivalenol and their acetylated derivatives in intestinal epithelial cells
    Alassane-Kpembi, Imourana
    Puel, Olivier
    Oswald, Isabelle P.
    [J]. ARCHIVES OF TOXICOLOGY, 2015, 89 (08) : 1337 - 1346
  • [2] New insights into mycotoxin mixtures: The toxicity of low doses of Type B trichothecenes on intestinal epithelial cells is synergistic
    Alassane-Kpembi, Imourana
    Kolf-Clauw, Martine
    Gauthier, Thierry
    Abrami, Roberta
    Abiola, Francois A.
    Oswald, Isabelle P.
    Puel, Olivier
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2013, 272 (01) : 191 - 198
  • [3] [Anonymous], 1993, IARC Monogr Eval Carcinog Risks Hum, V56, P445
  • [4] INSITU END-LABELING DETECTS DNA STRAND BREAKS IN APOPTOSIS AND OTHER PHYSIOLOGICAL AND PATHOLOGICAL STATES
    ANSARI, B
    COATES, PJ
    GREENSTEIN, BD
    HALL, PA
    [J]. JOURNAL OF PATHOLOGY, 1993, 170 (01) : 1 - 8
  • [5] Individual and combined cytotoxicity of major trichothecenes type B, deoxynivalenol, nivalenol, and fusarenon-X on Jurkat human T cells
    Aupanun, Sawinee
    Phuektes, Patchara
    Poapolathep, Saranya
    Alassane-Kpembi, Imourana
    Oswald, Isabelle P.
    Poapolathep, Amnart
    [J]. TOXICON, 2019, 160 : 29 - 37
  • [6] Apoptosis and gene expression in Jurkat human T cells and lymphoid tissues of fusarenon-X-treated mice
    Aupanun, Sawinee
    Phuektes, Patchara
    Poapolathep, Saranya
    Sutjarit, Samak
    Giorgi, Mario
    Poapolathep, Amnart
    [J]. TOXICON, 2016, 123 : 15 - 24
  • [7] Oral exposure of fusarenon-X induced apoptosis in Peyer's patches, thymus, and spleen of mice
    Aupanun, Sawinee
    Poapolathep, Saranya
    Imsilp, Kanjana
    Prapong, Teerasak
    Poapolathep, Amnart
    [J]. RESEARCH IN VETERINARY SCIENCE, 2015, 102 : 217 - 222
  • [8] Evaluation of the intestinal absorption of deoxynivalenol and nivalenol by an in vitro gastrointestinal model, and the binding efficacy of activated carbon and other adsorbent materials
    Avantaggiato, G
    Havenaar, R
    Visconti, A
    [J]. FOOD AND CHEMICAL TOXICOLOGY, 2004, 42 (05) : 817 - 824
  • [9] INDUCTION OF CYTOKINE MESSENGER-RNAS IN MICE AFTER ORAL-EXPOSURE TO THE TRICHOTHECENE VOMITOXIN (DEOXYNIVALENOL) - RELATIONSHIP TO TOXIN DISTRIBUTION AND PROTEIN-SYNTHESIS INHIBITION
    AZCONAOLIVERA, JI
    OUYANG, Y
    MURTHA, J
    CHU, FS
    PESTKA, JJ
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 133 (01) : 109 - 120
  • [10] Involvement of mitochondria-mediated apoptosis in deoxynivalenol cytotoxicity
    Bensassi, Fatma
    Gallerne, Cindy
    El Dein, Ossama Sharaf
    Lemaire, Christophe
    Hajlaoui, Mohamed Rabeh
    Bacha, Hassen
    [J]. FOOD AND CHEMICAL TOXICOLOGY, 2012, 50 (05) : 1680 - 1689