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Research Article | Open Access

Immunomodulatory effect of ethanol-soluble oligopeptides from Atlantic cod (Gadus morhua)

Zhen YuanaMeilian YangaDongyang ZhuaDi WuaShuzhen Chenga,bChao WuaHesham R. El-SeedicMing Dua ( )
School of Food Science and Technology, National Engineering Research Center of Seafood, Dalian Polytechnic University, Dalian 116034, China
Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China
Pharmacognosy Group, Department of Medicinal Chemistry, Uppsala University, Biomedical Centre, Uppsala 75123, Sweden

Peer review under responsibility of KeAi Communications Co., Ltd.

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Abstract

There are many active substances in Atlantic cod (Gadus morhua) explaining the variety of biological activities. In order to study the immunomodulatory activity and the mechanism of Atlantic cod peptides at the cellular level. In this study, cod peptides were isolated by 80 % ethanol extraction method, the isolated ethanol-soluble cod peptides (CP-ES) were investigated and their immunomodulatory activity was verified. Additionally, CP-ES showed lower molecular weight and more hydrophobic amino acids. CP-ES could promote the proliferation of spleen lymphocytes and T lymphocytes in mice, suggesting that CP-ES may regulate adaptive immunity. It promoted the release of NO and the expression of iNOS, TNF-α, IL-6 and IL-1β genes in macrophages, suggesting that CP-ES may regulate innate immunity. CP-ES could promote the expression of TLR2 gene, and the peptides identified in CP-ES were docked with TLR2 to predict the peptides playing a major role in CP-ES. These results suggested that CP-ES may regulate the immune activity of both innate and adaptive lines.

References

[1]

Y. Wu, C. Zhu, Y. Zhang, et al., Immunomodulatory and antioxidant effects of pomegranate peel polysaccharides on immunosuppressed mice, J. Biol. Macromol. 137 (2019) 504-511. https://dx.doi.org/10.1016/j.ijbiomac.2019.06.139.

[2]

Y. Chen, W. Xie, C. Qu, et al., Immunoenhancement of dried cod skin collagen Oligo-peptides on cyclophosphamide-induced immunosuppression in mice, Int. J. Clin. Exp. Med. 12 (2019) 7047-7055.

[3]

Q. Yang, X. Cai, M. Huang, et al., A specific peptide with immunomodulatory activity from Pseudostellaria heterophylla and the action mechanism, J. Funct. Foods 68 (2020) 1-9. https://dx.doi.org/10.1016/j.jff.2020.103887.

[4]

L. Su, Y. Wang, J. Wang, et al., Structural basis of TLR2/TLR1 activation by the synthetic agonist diprovocim, J. Med. Chem. 62 (2019) 2938-2949. https://dx.doi.org/10.1021/acs.jmedchem.8b01583.

[5]

M. Jin, S.E. Kim, J.Y. Heo, et al., Crystal structure of the TLR1-TLR2 heterodimer induced by binding of a tri-acylated lipopeptide, Cell 130 (2007) 1071-1082. https://dx.doi.org/10.1016/j.cell.2007.09.008.

[6]

C. Ji, Z. Zhang, J. Chen, et al., Immune-enhancing effects of a novel glucan from purple sweet potato Ipomoea batatas (L.) lam on RAW264.7 macrophage cells via TLR2- and TLR4-mediated pathways, J. Agr. Food Chem 69 (2021) 9313-9325. https://dx.doi.org/10.1021/acs.jafc.1c03850.

[7]

S. Bakke, A.E. Jordal, P. Gomez-Requeni, et al., Dietary protein hydrolysates and free amino acids affect the spatial expression of peptide transporter PepT1 in the digestive tract of Atlantic cod (Gadus morhua), Comp. Biochem. Physiol. B, Biochem. Mol. Biol. 156 (2010) 48-55. https://dx.doi.org/10.1016/j.cbpb.2010.02.002.

[8]

A. Doyle, M.E. Cowan, H. Migaud, et al., Neuroendocrine regulation of reproduction in Atlantic cod (Gadus morhua): evidence of Eya3 as an integrator of photoperiodic cues and nutritional regulation to initiate sexual maturation, Comp. Biochem. Physiol. Part A Mol. Integr. Physiol 260 (2021) 1-11. https://dx.doi.org/10.1016/j.cbpa.2021.111000.

[9]

A.D. Hawkins, A.N. Popper, Sound detection by Atlantic cod: an overview, J. Acoust. Soc. Am. 148 (2020) 3027-3041. https://dx.doi.org/10.1121/10.0002363.

[10]

P.J.B. Hart, Alaska codfish chronicle. a history of the Pacific cod fishery in Alaska, Fish Fishs (Oxf) 21 (2020) 1. https://dx.doi.org/10.1111/faf.12444.

[11]

A.T. Girgih, R. He, F.M. Hasan, et al., Evaluation of the in vitro antioxidant properties of a cod (Gadus morhua) protein hydrolysate and peptide fractions, Food Chem 173 (2015) 652-659. https://dx.doi.org/10.1016/j.foodchem.2014.10.079.

[12]

N. Li, S. Lv, Y. Ma, et al., In vitro antioxidant and anti-aging properties of swim bladder peptides from Atlantic cod (Gadus morhua), Int. J. Food Prop 23 (2020) 1416-1429. https://dx.doi.org/10.1080/10942912.2020.1807565.

[13]

K.H. Sabeena Farvin, L.L. Andersen, J. Otte, et al., Antioxidant activity of cod (Gadus morhua) protein hydrolysates: fractionation and characterisation of peptide fractions, Food Chem 204 (2016) 409-419. https://dx.doi.org/10.1016/j.foodchem.2016.02.145.

[14]

H. Niu, Z. Wang, H. Hou, et al., Protective effect of cod (Gadus macrocephalus) skin collagen peptides on acetic acid-induced gastric ulcer in rats, J. Food Sci 81 (2016) H1807-H1815. https://dx.doi.org/10.1111/1750-3841.13332.

[15]

W. He, G. Su, D. Sun-Waterhouse, et al., In vivo anti-hyperuricemic and xanthine oxidase inhibitory properties of tuna protein hydrolysates and its isolated fractions, Food Chem 272 (2019) 453-461. https://dx.doi.org/10.1016/j.foodchem.2018.08.057.

[16]

Z. Xu, F. Zhao, H. Chen, et al., Nutritional properties and osteogenic activity of enzymatic hydrolysates of proteins from the blue mussel (Mytilus edulis), Food Funct 10 (2019) 7745-7754. https://dx.doi.org/10.1039/c9fo01656b.

[17]

M. Tu, S. Xu, Z. Xu, et al., Identification of dual-function bovine lactoferrin peptides released using simulated gastrointestinal digestion, Food Biosci. 39 (2021) 1-6. https://dx.doi.org/10.1016/j.fbio.2020.100806.

[18]

Z. Xu, H. Chen, F. Fan, et al., Bone formation activity of an osteogenic dodecapeptide from blue mussels (Mytilus edulis), Food Funct 10 (2019) 5616-5625. https://dx.doi.org/10.1039/C9FO01201J.

[19]

Z. Dai, D. Su, Y. Zhang, et al., Immunomodulatory activity in vitro and in vivo of verbascose from mung beans (Phaseolus aureus), J. Agr. Food Chem 62 (2014) 10727-10735. https://dx.doi.org/10.1021/jf503510h.

[20]

L. Wen, Y. Jiang, X. Zhou, et al., Structure identification of soybean peptides and their immunomodulatory activity, Food Chem 359 (2021) 1-8. https://dx.doi.org/10.1016/j.foodchem.2021.129970.

[21]

Z. Khiari, M. Ndagijimana, M. Betti, Low molecular weight bioactive peptides derived from the enzymatic hydrolysis of collagen after isoelectric solubilization/precipitation process of turkey by-products, Poult. Sci. 93 (2014) 2347-2362. https://dx.doi.org/10.3382/ps.2014-03953.

[22]

M. Chalamaiah, W. Yu, J. Wu, Immunomodulatory and anticancer protein hydrolysates (peptides) from food proteins: a review, Food Chem 245 (2018) 205-222. https://dx.doi.org/10.1016/j.foodchem.2017.10.087.

[23]

S.M. Lewis, A. Williams, S.C. Eisenbarth, Structure-function of the immune system in the spleen, Sci. Immunol. 4 (2019) 1-25. https://dx.doi.org/10.1126/sciimmunol.aau6085.

[24]

R. Golub, J. Tan, T. Watanabe, et al., Origin and immunological functions of spleen stromal cells, Trends Immunol 39 (2018) 503-514. https://dx.doi.org/10.1016/j.it.2018.02.007.

[25]

J. Goral, Ethanol and inflammation, Curr. Med. Chem 6 (2007) 264-270. https://dx.doi.org/10.2174/187152307783219970.

[26]

L. Wen, D. Shi, T. Zhou, et al., Immunomodulatory mechanism of α-D-(1→6)-glucan isolated from banana, RSC Adv 9 (2019) 6995-7003. https://dx.doi.org/10.1039/c9ra00113a.

[27]

K. He, Y. Zeng, H. Tian, et al., Macrophage immunomodulatory effects of low molecular weight peptides from Mytilus coruscus via NF-κB/MAPK signaling pathways, J. Funct. Foods 83 (2021) 1-12. https://dx.doi.org/10.1016/j.jff.2021.104562.

[28]

D. Lozano-Ojalvo, E. Molina, R. Lopez-Fandino, Hydrolysates of egg white proteins modulate T- and B-cell responses in mitogen-stimulated murine cells, Food Funct 7 (2016) 1048-1056. https://dx.doi.org/10.1039/c5fo00614g.

[29]

Q. Yang, X. Cai, M. Huang, et al., Isolation, identification, and immunomodulatory effect of a peptide from Pseudostellaria heterophylla protein hydrolysate, J. Agr. Food Chem 68 (2020) 12259-12270. https://dx.doi.org/10.1021/acs.jafc.0c04353.

[30]

K. Bisht, W.H. Choi, S.Y. Park, et al., Curcumin enhances non-inflammatory phagocytic activity of RAW264.7 cells, Biochem. Biophys. Res. Commun. 379 (2009) 632-636. https://dx.doi.org/10.1016/j.bbrc.2008.12.135.

[31]

J. Jubrail, N. Kurian, F. Niedergang, Macrophage phagocytosis cracking the defect code in COPD, Biomed. J. 40 (2017) 305-312. https://dx.doi.org/10.1016/j.bj.2017.09.004.

[32]

Y. Chang, A. Guo, Y. Jing, et al., Immunomodulatory activity of puerarin in RAW264.7 macrophages and cyclophosphamide-induced immunosuppression mice, Immunopharmacol. Immunotoxicol. 43 (2021) 223-229. https://dx.doi.org/10.1080/08923973.2021.1885043.

[33]

W. Sosroseno, M. Musa, M. Ravichandran, et al., Effect of inhibition of inducible nitric oxide synthase (iNOS) on the murine splenic immune response induced by Aggregatibacter (Actinobacillus) actinomycetemcomitans lipopolysaccharide, Eur. J. Oral Sci 116 (2008) 31-36. https://dx.doi.org/10.1111/j.1600-0722.2007.00501.x.

[34]

Q. Xue, Y. Yan, R. Zhang, et al., Regulation of iNOS on immune cells and its role in diseases, Int. J. Mol. Sci. 19 (2018) 1-13. https://dx.doi.org/10.3390/ijms19123805.

[35]

P. Pratheeshkumar, G. Kuttan, Modulation of immune response by Vernonia cinerea L. inhibits the proinflammatory cytokine profile, iNOS, and COX-2 expression in LPS-stimulated macrophages, Immunopharmacol. Immunotoxicol. 33 (2011) 73-83. https://dx.doi.org/10.3109/08923971003745977.

[36]

P. Mahdavi Sharif, P. Jabbari, S. Razi, et al., Importance of TNF-alpha and its alterations in the development of cancers, Cytokine 130 (2020) 1-13. https://dx.doi.org/10.1016/j.cyto.2020.155066.

[37]

Y. Kawahito, "IL-6 is a treatment target for a variety of immune diseases"-the benefit and prospect of IL-6 inhibitor, Mod. Rheumatol. 29 (2019) 1-3. https://dx.doi.org/10.1080/14397595.2018.1559783.

[38]

N.L. Christopher, T. Jordan, L.L. Doris, et al., IL-1β is an innate immune sensor of microbial proteolysis, Sci. Immunol. 1 (2016) 1-8. https://dx.doi.org/10.1126/sciimmunol.aah3539.

[39]

J.P. Mandala, S. Ahmad, A. Pullagurla, et al., Toll-like receptor 2 polymorphisms and their effect on the immune response to ESAT-6, Pam3CSK4 TLR2 agonist in pulmonary tuberculosis patients and household contacts, Cytokine 126 (2020) 1-12. https://dx.doi.org/10.1016/j.cyto.2019.154897.

[40]

A. Karimollah, A. Hemmatpur, N. Hosseini, et al., Tropisetron balances immune responses via TLR2, TLR4 and JAK2/STAT3 signalling pathway in LPS-stimulated PBMCs, Basic Clin. Pharmacol. Toxicol. 128 (2021) 669-676. https://dx.doi.org/10.1111/bcpt.13565.

[41]

S. Jiang, H. Yin, R. Li, et al., The activation effects of fucoidan from sea cucumber Stichopus chloronotus on RAW264.7 cells via TLR2/4-NF-κB pathway and its structure-activity relationship, Carbohydr. Polym. 270 (2021) 1-8. https://dx.doi.org/10.1016/j.carbpol.2021.118353.

[42]

W.N. Baba, B. Baby, P. Mudgil, et al., Pepsin generated camel whey protein hydrolysates with potential antihypertensive properties: identification and molecular docking of antihypertensive peptides, LWT-Food Sci. Technol 143 (2021) 1-10. https://dx.doi.org/10.1016/j.lwt.2021.111135.

Food Science and Human Wellness
Pages 1192-1203
Cite this article:
Yuan Z, Yang M, Zhu D, et al. Immunomodulatory effect of ethanol-soluble oligopeptides from Atlantic cod (Gadus morhua). Food Science and Human Wellness, 2023, 12(4): 1192-1203. https://doi.org/10.1016/j.fshw.2022.10.002

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Received: 30 January 2022
Revised: 17 February 2022
Accepted: 04 March 2022
Published: 18 November 2022
© 2023 Beijing Academy of Food Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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