Immunological evaluation of the mycotoxin patulin in female B6C3F(1) mice

Citation
Gc. Llewellyn et al., Immunological evaluation of the mycotoxin patulin in female B6C3F(1) mice, FOOD CHEM T, 36(12), 1998, pp. 1107-1115
Citations number
22
Categorie Soggetti
Food Science/Nutrition","Pharmacology & Toxicology
Journal title
FOOD AND CHEMICAL TOXICOLOGY
ISSN journal
02786915 → ACNP
Volume
36
Issue
12
Year of publication
1998
Pages
1107 - 1115
Database
ISI
SICI code
0278-6915(199812)36:12<1107:IEOTMP>2.0.ZU;2-T
Abstract
Patulin is a mycotoxin produced by many fungal species of the genera Penici llium, Aspergillus and Bryssochamys. Previous literature reports have sugge sted that patulin is toxic to the immune system. The studies presented were conducted to provide a comprehensive assessment of the effects of patulin on the immune system. Unlike previous reports, the doses of patulin used (0 .08, 0.16, 0.32, 0.64, 1.28 and 2.56 mg/kg) were based on predicted human e xposure levels. Female B6C3F(1) mice were exposed orally to patulin for 28 days. Effects were not observed on final body weight or body weight gain. R elative weight of the liver, spleen, thymus, kidneys with adrenals, and lun gs was not affected. Peripheral blood leucocyte and lymphocyte counts were decreased by approximately 30% in the two highest dose groups. The leucocyt e differential was not altered. Total spleen cell, total T-cell (CD3(+)), h elper T-cell (CD4(+)CD8(-)), B-cell (surface immunoglobulin(+)) and monocyt e (MAC-3(+)) counts were not changed. Cytotoxic T-cell (CD8(+) CD4(-)) coun ts were increased 50% only by the highest dose. Natural killer cell (NK1.1( +)CD3(-)) and monocyte (MAC-1(+)) counts were increased 30% and 24%, respec tively, only in the 0.08 mg/kg group. Humoral immune function as assessed b y antibody-farming cell response and serum IgM titre to sheep erythrocytes, and cell-mediated immune function evaluated utilizing natural killer cell activity and the mixed lymphocyte reaction were not altered. Oral exposure to patulin for 28 days did not alter the ability of female B6C3F(1) mice to mount either a cell-mediated or humoral immune response. (C) 1998 Elsevier Science Ltd. All rights reserved.