Oral lactoferrin treatment resolves amoebic intracecal infection in C3H/HeJ mice

被引:1
|
作者
Leon-Sicairos, Nidia [4 ,5 ]
Martinez-Pardo, Leonardo [1 ]
Sanchez-Hernandez, Beatriz [2 ]
de la Garza, Mireya [3 ]
Carrero, Julio Cesar [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Invest Biomed, Dept Inmunol, Mexico City 70228, DF, Mexico
[2] Inst Nacl Nutr Salvador Zubiran, Dept Genet, Mexico City 14000, DF, Mexico
[3] IPN, Ctr Invest & Estudios Avanzados, Dept Biol Celular, Mexico City 7350, DF, Mexico
[4] Univ Autonoma Sinaloa, Fac Med, Unidad Invest, Culiacan 80246, Sinaloa, Mexico
[5] Hosp Pediatr Sinaloa, Dept Invest, Culiacan 80200, Sinaloa, Mexico
关键词
lactoferrin; amoebiasis; protection; in vivo; mice; ENTAMOEBA-HISTOLYTICA; METRONIDAZOLE RESISTANCE; MUCOSAL IMMUNITY; HUMAN-MILK; IRON; ACTIVATION; ANTIBODIES; REVERSAL; PARASITE; GROWTH;
D O I
10.1139/O2012-008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Entamoeba histolytica is a protozoan parasite that causes amoebiasis, an illness that affects many people around the world. We have previously reported that lactoferrin is able to kill E. histolytica in in vitro cultures. The aim of the present study was to evaluate the therapeutic effect of orally administered bovine lactoferrin in the control of intestinal amoebiasis of susceptible C3H/HeJ mice. The results showed that 20 mg lactoferrin/kg orally administered each day for 1 week was able to eliminate the infection in 63% of the mice, since neither trophozoites nor evidence of epithelial damage and (or) swelling were found in tissue sections of the cecum. The rest of the treated animals (37%) showed a decrease in trophozoite numbers and mucus secreted to the lumen, as compared with untreated and infected mice (p < 0.05). By immunohistochemistry, the profile of secreted cytokines in the cecum revealed that infected but untreated animals showed a mixed Th1/regulatory cytokines profile, whereas the cecum of mice treated (cured) showed a Th2 cytokine profile (IL-4) and expression of the multifunctional IL-6. In addition, cytokines and increasing cecal production of total IgA antibodies were found associated with little inflammation and disease control observed in the cecum of lactoferrin-treated animals. These results suggest that oral administration of lactoferrin can control intestinal amoebic infection probably by killing amoebas or favoring their removal and reestablish the antiinflammatory intestinal environment.
引用
收藏
页码:435 / 441
页数:7
相关论文
共 50 条
  • [41] SUPPRESSION OF POLYCLONAL B-CELL MITOGENESIS DURING SCRAPIE INFECTION OF C3H/HEJ AND BALB/C MICE
    PRUSINER, SB
    GARFIN, DE
    PANITCH, H
    STITES, DP
    ZITNIK, L
    JOURNAL OF CELL BIOLOGY, 1977, 75 (02): : A402 - A402
  • [42] Treatment of alopecia areata in C3H/Hej mice with the topical immunosuppressant FK506 (Tacrolimus)
    Freyschmidt-Paul, P
    Ziegler, A
    McElwee, KJ
    Happle, R
    Kissling, S
    Sundberg, JP
    Hoffmann, R
    EUROPEAN JOURNAL OF DERMATOLOGY, 2001, 11 (05) : 405 - 409
  • [43] A NEW MUTATION, GLD, THAT PRODUCES LYMPHOPROLIFERATION AND AUTOIMMUNITY IN C3H HEJ MICE
    ROTHS, JB
    MURPHY, ED
    EICHER, EM
    JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 159 (01): : 1 - 20
  • [44] MITOTIC RATE OF SPONTANEOUS MAMMARY GLAND ADENOCARCINOMA IN C3H/HEJ MICE
    BERTALANFFY, FD
    NATURE, 1963, 198 (487) : 496 - &
  • [45] Dietary vitamin A altered the progression of alopecia areata in C3H/HeJ mice
    Everts, H. B.
    Sundberg, J. P.
    Johnson, C. J.
    EXPERIMENTAL DERMATOLOGY, 2010, 19 (06) : 597 - 597
  • [46] AN ALOPECIA AREATA-LIKE DISEASE IN AGING C3H/HEJ MICE
    SUNDBERG, JP
    CORDY, W
    HOGAN, M
    KING, LE
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 100 (04) : 512 - 512
  • [47] Activin A Increases the Bone Mass of Grafted Bone in C3H/HeJ Mice
    H. Hirotani
    M. Ohtsuka-Isoya
    S. Mori
    R. Sakai
    Y. Eto
    S. Echigo
    H. Shinoda
    Calcified Tissue International, 2002, 70 : 330 - 338
  • [48] LACK OF ORAL TOLERANCE IN C3H-HEJ MICE
    KIYONO, H
    MCGHEE, JR
    WANNEMUEHLER, MJ
    MICHALEK, SM
    JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (02): : 605 - 610
  • [49] LACK OF ORAL TOLERANCE IN C3H-HEJ MICE
    KIYONO, H
    WANNEMUEHLER, MJ
    MICHALEK, SM
    MCGHEE, JR
    FEDERATION PROCEEDINGS, 1981, 40 (03) : 1026 - 1026
  • [50] AN ALOPECIA AREATA-LIKE DISEASE IN AGING C3H/HEJ MICE
    SUNDBERG, JP
    KING, LE
    CLINICAL RESEARCH, 1992, 40 (04): : A781 - A781