Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jan 29;11(2):336.
doi: 10.3390/ani11020336.

Effects of Chronic Exposure to Low Levels of Dietary Aflatoxin B1 on Growth Performance, Apparent Total Tract Digestibility and Intestinal Health in Pigs

Affiliations

Effects of Chronic Exposure to Low Levels of Dietary Aflatoxin B1 on Growth Performance, Apparent Total Tract Digestibility and Intestinal Health in Pigs

Junning Pu et al. Animals (Basel). .

Abstract

This study aimed to investigate the effects of chronic exposure to low levels of dietary aflatoxin B1 (AFB1) on growth performance, apparent total tract digestibility and intestinal health in pigs. In a 102-day experiment, fourteen barrows (Duroc×Landrace×Yorkshire, initial BW = 38.21 ± 0.45 kg) were randomly divided into control (CON, basal diet) and AFB1 groups (the basal diet supplemented with 280 μg/kg AFB1). Results revealed that the AFB1 exposure decreased the final BW, ADFI and ADG in pigs (p < 0.10). AFB1 exposure also decreased the apparent total tract digestibility of dry mater and gross energy at 50 to 75 kg and 105 to 135 kg stages, and decreased the apparent total tract digestibility of ether extract at 75 to 105 kg stage (p < 0.05). Meanwhile, AFB1 exposure increased serum diamine oxidase activity and reduced the mRNA abundance of sodium-glucose cotransporter 1, solute carrier family 7 member 1 and zonula occluden-1 in the jejunal mucosa (p < 0.05). Furthermore, AFB1 exposure decreased superoxide dismutase activity (p < 0.05) and increased 8-hydroxy-2'-deoxyguanosine content (p < 0.10) in jejunal mucosa. AFB1 exposure also increased tumor necrosis factor-α, interleukin-1β and transforming growth factor-β mRNA abundance in jejunal mucosa and upregulated Escherichia coli population in colon (p < 0.05). The data indicated that chronic exposure to low levels of dietary AFB1 suppressed growth performance, reduced the apparent total tract digestibility and damaged intestinal barrier integrity in pigs, which could be associated with the decreased intestinal antioxidant capacity and the increased pro-inflammatory cytokine production.

Keywords: aflatoxin B1; apparent total tract digestibility; growth performance; intestinal health; pigs.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Méndez-Albores A., Del Río-García J.C., Moreno-Martínez E. Decontamination of aflatoxin duckling feed with aqueous citric acid treatment. Anim. Feed Sci. Technol. 2007;135:249–262. doi: 10.1016/j.anifeedsci.2006.07.009. - DOI
    1. Hernandez-Mendoza A., González-Córdova A.F., Vallejo-Cordoba B., Garcia H.S. Effect of oral supplementation of Lactobacillus reuteri in reduction of intestinal absorption of aflatoxin B1 in rats. J. Basic Microb. 2011;51:263–268. doi: 10.1002/jobm.201000119. - DOI - PubMed
    1. IARC . Working Group on the Evaluation of Carcinogenic Risks to Humans. Chemical Agents and Related Occupations: Iarc Monographs on the Evaluation of Carcinogenic Risks to Humans. Volume 100. International Agency for Research on Cancer; Lyon, France: 2012. pp. 9–562. - PMC - PubMed
    1. Eaton D.L., Gallagher E.P. Mechanisms of Aflatoxin Carcinogenesis. Annu. Rev. Pharmacol. Toxicol. 1994;34:135–172. doi: 10.1146/annurev.pa.34.040194.001031. - DOI - PubMed
    1. Liu T., Ma Q., Zhao L., Jia R., Zhang J., Ji C., Wang X. Protective Effects of Sporoderm-Broken Spores of Ganderma lucidum on Growth Performance, Antioxidant Capacity and Immune Function of Broiler Chickens Exposed to Low Level of Aflatoxin B₁. Toxins. 2016;8:278. doi: 10.3390/toxins8100278. - DOI - PMC - PubMed

LinkOut - more resources