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    <subfield code="a">ART-2021-125001</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Bellés, A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-6546-6149</subfield>
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    <subfield code="a">Native and saturated bovine lactoferrin modulate the expression of toll-like receptors (TLRS) in mice treated with antibiotics. P0203. 29th United European Gastroenterology Week Virtual 2021</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Introduction: The gut microbiota plays a fundamental role in protection against pathogen infections but also in the regulation of the immune sys-tem. The antibiotic administration can result in gut microbiota alterations and changes in the eectiveness of innate immune responses. As micro-biota composition changes, the altered community will present dierent microbial-associated molecular patterns to Toll-like receptors (TLRs), which can cascade down through various immune responses, including changes in the expression of TLR receptors [1]. In this context, finding ingredients that can modulate the immune system is becoming a major focus of interest to produce functional foods. Bovine lactoferrin is a milk protein with many biological properties, including an-tibacterial and immunomodulatory activity [2].Aims &amp; Methods: The objective was to determine the eects of native (nLf) and saturated (sLf) bovine lactoferrin on TLR receptor expression of colon from mice treated or untreated with the antibiotic clindamycin, to evalu-ate its potential to be added in functional foods.Male C57BL/6 mice of 8 weeks old were randomly divided into six groups (n=5 per group): vehicle, clindamycin (Clin), native bovine lactoferrin (nLf), nLf + clindamycin (nLf_Clin), iron-saturated bovine lactoferrin (sLf) and sLf + clindamycin (sLf_Clin). Vehicle received saline orally for 10 days. Clin was gavaged for 10 days with saline and on day 4 received a single IP injection of 200 µg of clindamycin. nLf and sLf  were gavaged for 10 days with 35 mg of nLf or sLf. The groups nLf_Clin and sLf_Clin were gavaged with nLf or sLf and on day 4 received an injection of clindamycin.The gene expression (mRNA) of TLR1-9 receptors was determined in the colon from mice by RT-PCR and relative expression levels of genes were calculated using the 2 -∆∆CT method.Results: The expression of TLR2, TLR4, TLR5 and TLR6 was not modified in any of the treated groups. The expression of TLR1 was increased in sLf, nLf_Clin and sLf_Clin treated groups, indicating that the eect of sLf on TLR1 expression was maintained despite the treatment with Clin. The expression of TLR8 and TLR9 decreased in Clin, nLf and nLf_Clin groups. However, the levels of these receptors in sLf_Clin were similar to Vehicle, demonstrating the immunomodulatory capacity of sLf  to restore these receptor levels, in a situation of intestinal dysbiosis.  Finally, respect to TLR3 and TLR7, only the group of mice treated with sLf_Clin showed an increase in the expression of this receptor. Conclusion: Saturated bovine lactoferrin can restore the expression levels of TLR8 and TLR9 in conditions of intestinal dysbiosis induced by antibiot-ics. These results confirm the immunomodulatory properties of lactoferrin, which have great interest for the design of functional foods.</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">by</subfield>
    <subfield code="u">http://creativecommons.org/licenses/by/3.0/es/</subfield>
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    <subfield code="a">GASTROENTEROLOGY &amp; HEPATOLOGY</subfield>
    <subfield code="b">23 / 92 = 0.25</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">Oncology</subfield>
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    <subfield code="a">Gastroenterology</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Aguirre-Ramírez, D.</subfield>
    <subfield code="0">(orcid)0000-0002-1829-6319</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Abad, I.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sánchez, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5964-823X</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Grasa, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-5306-9365</subfield>
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    <subfield code="1">1012</subfield>
    <subfield code="2">410</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmac.Fisiol.y Med.L.F.</subfield>
    <subfield code="c">Área Fisiología</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">2008</subfield>
    <subfield code="2">780</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Produc.Animal Cienc.Ali.</subfield>
    <subfield code="c">Área Tecnología de Alimentos</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">9, 58 (2021), 376</subfield>
    <subfield code="p">United European Gastroenterol. j.</subfield>
    <subfield code="t">United European Gastroenterology Journal</subfield>
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    <subfield code="s">202809</subfield>
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    <subfield code="u">https://onlinelibrary.wiley.com/doi/epdf/10.1002/ueg2.12144</subfield>
    <subfield code="z">Texto completo de la revista</subfield>
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    <subfield code="a">2023-06-02-11:02:43</subfield>
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