AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (1.7 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

Multi-protective effects of wheat embryo globulin on D-gal-induced aging mice

Aimei Liaoa,b,1Xing Lyua,c,1Jiarui MaaYinchen HoubMing HuiaNa LiuaYi ZhaoaYixiang CuiaJihong Huanga,b,d( )
College of Biological Engineering, Henan University of Technology, Luoyang 471000, China
Henan Provincial Key Laboratory of Biological Processing and Nutritional Function of Wheat, Luoyang 471000, China
Zhengzhou Synear Food Co., Ltd., Zhengzhou 450000, China
School of Food and Pharmacy, Xuchang University, Xuchang 461000, China

1 These authors equally contributed to this work.

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

Show Author Information

Abstract

Wheat embryo globulin (WEG) has been proven to possess multiple biological activities, including antioxidative properties, immunomodulatory, and so on. Aged mouse model were established by subcutaneous injection of D-galactose (D-gal), and the effects of WEG on learning, memory, and antioxidant capacity in aging mice were explored through behavioural tests and antioxidant enzyme activities determination. Compared with the Model group, WEG improved the percentage of the platform quadrant, increased the number of crossing platforms, and enhanced the identification indexs. WEG also increased total antioxidant capacity (T-AOC), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) activities in the liver and brains of aging mice, and reduced malondialdehyde (MDA) content. Pathological observations indicated that WEG protected against damage to brain in D-gal-induced aging mice. These results effectively revealed that WEG not only improved the abilities of learning and memory, and the cognitive impairment, but also delayed the aging process of the D-gal-induced mice.

References

[1]

Q. Ding, D. Yang, W. Zhang, et al., Antioxidant and anti-aging activities of the polysaccharide TLH-3 from Tricholoma lobayense, Int. J. Biol. Macromol. 85 (2016) 133-140. https://doi.org/10.1016/j.ijbiomac.2015.12.058.

[2]

F. Galkin, B. Zhang, S.E. Dmitriev, et al., Reversibility of irreversible aging, Ageing Res. Rev. 49 (2019) 104-114. https://doi.org/10.1016/j.arr.2018.11.008.

[3]

M.M. Abdel-Daim, I. Nadia, N.I. Zakhary, et al., Aging, metabolic, and degenerative disorders: biomedical value of antioxidants, Oxid. Med. Cell. Longev. 2018 (2018) 2098123. https://doi.org/10.1155/2018/2098123.

[4]

A. Argyropoulou, N. Aligiannis, I.P. Trougakos, et al., Natural compounds with anti-ageing activity, Nat. Prod. Rep. 30 (2013) 1412-1437. https://doi.org/10.1039/c3np70031c.

[5]

M.M. Abdel-Daim, O.S. El-Tawil, S.G. Bungau, et al., Applications of antioxidants in metabolic disorders and degenerative diseases: mechanistic approach, Oxid. Med. Cell. Longev. 2019 (2019) 4179676. https://doi.org/10.1155/2019/4179676.

[6]

W.R. Bell, Y. An, Y. Kageyama, et al., Neuropathologic, genetic, and longitudinal cognitive profiles in primary age-related tauopathy(PART) and Alzheimer's disease, Alzheimers Dement 15 (2019) 8-16. https://doi.org/10.1016/j.jalz.2018.07.215.

[7]

T. Wyss-Coray, Ageing, neurodegeneration and brain rejuvenation, Nature 539 (2016) 180-186. https://doi.org/10.1038/nature20411.

[8]

F. Zhao, Y. Zhou, L. Gao, et al., Advances in the study of the rat model of aging induced by D-galactose, Acta Pharm. Sin. 52 (2017) 347-354. https://doi.org/10.16438/j.0513-4870.2016-0696.

[9]

K.F. Azman, R. Zakaria, D-galactose-induced accelerated aging model: an overview, Biogerontology 20 (2019) 763-782. https://doi.org/10.1007/s10522-019-09837-y.

[10]

R. Tabassum, N.Y. Jeong, J. Jung, Protective effect of hydrogen sulfide on oxidative stress-induced neurodegenerative diseases, Neural. Regen. Res. 15(2020) 232-241. https://doi.org/10.4103/1673-5374.265543.

[11]

J.Y. Sha, Y.D. Zhou, J.Y. Yang, et al., Maltol (3-hydroxy-2-methyl-4-pyrone)slows D-galactose-induced brain aging process by damping the Nrf2/HO-1-mediated oxidative stress in mice, J. Agric. Food Chem. 67 (2019) 10342-10351. https://doi.org/10.1021/acs.jafc.9b04614.

[12]

A.W.K. Yeung, N.T. Tzvetkov, O.S. El-Tawil, et al., Antioxidants: scientific literature landscape analysis, Oxid. Med. Cell Longev. 2019 (2019) 8278454. https://doi.org/10.1155/2019/8278454.

[13]

J. Zhang, X. Liu, J. Pan, et al., Anti-aging effect of brown black wolfberry on Drosophila melanogaster and D-galactose-induced aging mice, J. Funct. Foods 65 (2020) 103724. https://doi.org/10.1016/j.jff.2019.103724.

[14]

A. Brandolini, A. Hidalgo, Wheat germ: not only a by-product, Int. J. Food Sci. Nutr. 63 (2012) 71-74. https://doi.org/10.3109/09637486.2011.633898.

[15]

Y.Z. Zhang, X. Guan, J.X. Guo, et al., Lowing effect of wheat germ protein(WGP) on cholesterol level in hypercholesterolemic HepG2 cell, J. Biobased. Mater. Bio. 13 (2019) 269-273. https://doi.org/10.1166/jbmb.2019.1845.

[16]

R. He, H. Xing, Z. Wang, et al., Establishment of an enzymatic membrane reactor for angiotensin-converting enzyme inhibitory peptides preparation from wheat germ protein isolates, J. Food Eng. 39 (2016) 296-305. https://doi.org/10.1111/jfpe.12224.

[17]

C.R. Yang, A.M. Liao, Y.X. Cui, et al., Wheat embryo globulin protects against acute alcohol-induced liver injury in mice, Food Chem. Toxicol. 153(2021) 112240. https://doi.org/10.1016/j.fct.2021.112240.

[18]

W. Wu, M. Zhang, C. Sun, et al., Enzymatic preparation of immunomodulatory hydrolysates from defatted wheat germ (Triticum Vulgare) globulin, Int. J. Food Sci. Tech. 51 (2016) 2556-2566. https://doi.org/10.1111/ijfs.13238.

[19]

X.G. Ji, J.H. Huang, M. Hui, et al., Proteomic analysis and immunoregulation mechanism of wheat germ globulin, Protein Peptide Lett. 24 (2017) 1148-1165. https://doi.org/10.2174/0929866524666171026123054.

[20]

M. Atallahi, S.A.A. Akbari, F. Mojab, et al. Effects of wheat germ extract on the severity and systemic symptoms of primary dysmenorrhea: a randomized controlled clinical trial, Iran Red Crescent Med. 16 (2014) 19503. https://doi.org/10.5812/ircmj.19503.

[21]

J. Budni, R. Pacheco, S. da Silva, et al., Oral administration of D-galactose induces cognitive impairments and oxidative damage in rats, Behav. Brain Res. 302 (2016) 35-43. https://doi.org/10.1016/j.bbr.2015.12.041.

[22]

S. Haider, L. Liaquat, S. Shahzad, et al., A high dose of short term exogenous D-galactose administration in young male rats produces symptoms simulating the natural aging process, Life Sci. 124 (2015) 110-119. https://doi.org/10.1016/j.lfs.2015.01.016.

[23]

L. Lei, L. Ou, X. Yu, The antioxidant effect of Asparagus cochinchinensis(Lour. ) Merr. shoot in D-galactose induced mice aging model and in vitro, J. Chin. Med. Assoc. 79 (2016) 205-211. https://doi.org/10.1016/j.jcma.2015.06.023.

[24]

S.U. Rehman, S.A. Shah, T. Ali, et al. Anthocyanins reversed D-galactose-induced oxidative stress and neuroinflammation mediated cognitive impairment in adult rats, Mol. Neurobiol. 54 (2016) 255-271. https://doi.org/10.1007/s12035-015-9604-5.

[25]

P. Wang, H. Sun, D. Liu, et al., Protective effect of a phenolic extract containing indoline amides from Portulaca oleracea against cognitive impairment in senescent mice induced by large dose of D-galactose/NaNO2, J. Ethnopharmacol. 203 (2017) 252-259. https://doi.org/10.1016/j.jep.2017.03.050.

[26]

D.D. Li, W.J. Li, S.Z. Kong, et al., Protective effects of collagen polypeptide from tilapia skin against injuries to the liver and kidneys of mice induced by D-galactose, Biomed. Pharmacother. 117 (2019) 109204. https://doi.org/10.1016/j.biopha.2019.109204.

[27]

C. Wang, Z.X. Cai, W. Wang, et al., Piperine regulates glycogen synthase kinase-3beta-related signaling and attenuates cognitive decline in D-galactose-induced aging mouse model, J. Nutr. Biochem. 75 (2019)108261. https://doi.org/10.1016/j.jnutbio.2019.108261.

[28]

R. d'Hooge, P.P. de Deyn, Applications of the Morris water maze in the study of learning and memory, Brain Res. Rev. 36 (2001) 60-90. https://doi.org/10.1016/s0165-0173(01)00067-4.

[29]

W. Lian, H. Jia, L. Xu, et al., Multi-protection of DL0410 in ameliorating cognitive defects in D-galactose induced aging mice, Front. Aging Neurosci. 9 (2017) 409. https://doi.org/10.3389/fnagi.2017.00409.

[30]

C.V. Vorhees, M.T. Williams, Morris water maze: procedures for assessing spatial and related forms of learning and memory, Nat. Protoc. 1 (2006) 848-858. https://doi.org/10.1038/nprot.2006.116.

[31]

R.Y. Yang, G. Zhao, D.M. Wang, et al., DL0410 can reverse cognitive impairment, synaptic loss and reduce plaque load in APP/PS1 transgenic mice, Pharmacol. Biochem. Behav. 139 (2015) 15-26. https://doi.org/10.1016/j.pbb.2015.10.009.

[32]

Z.H. Ji, C. Liu, H. Zhao, et al., Neuroprotective effect of biatractylenolide against memory impairment in D-galactose-induced aging mice, J. Mol. Neurosci. 55 (2015) 678-683. https://doi.org/10.1007/s12031-014-0407-3.

[33]

P. Adler, C.K. Chiang, J. Mayne, et al., Aging disrupts the circadian patterns of protein expression in the murine hippocampus, Front. Aging Neurosci. 11(2019) 368. https://doi.org/10.3389/fnagi.2019.00368.

[34]

L.S. Mure, H.D. Le, G. Benegiamo, et al., Diurnal transcriptome atlas of a primate across major neural and peripheral tissues, Science 359 (2018)eaao0318. https://doi.org/10.1126/science.aao0318.

[35]

M. Dolatshahi, Y. Farbood, A. Sarkaki, et al., Ellagic acid improves hyperalgesia and cognitive deficiency in 6-hydroxidopamine induced rat model of Parkinson's disease, Iran J. Basic Med. Sci. 18 (2015) 38-46.

[36]

D. Patel, M. Thompson, S. Manna, et al., Urinary metabolomics analyses identify novel markers of malignant adrenocortical neoplasms, J. Am. Coll. Surgeons 221 (2015) S61-S62. https://doi.org/10.1016/j.jamcollsurg.2015.07.135.

[37]

J.S. Miners, R. Jones, S.T. Love. Differential changes in Aβ42 and Aβ40 with age, J. Alzheimers Dis. 40 (2014) 727-735. https://doi.org/10.3233/JAD-132339.

[38]

F. Morroni, G. Sita, A. Graziosi, et al., Neuroprotective effect of caffeic acid phenethyl ester in a mouse model of Alzheimer's disease involves Nrf2/HO-1 pathway, Aging Dis. 9 (2018) 605-622. https://doi.org/10.14336/AD.2017.0903.

[39]

Y. Feng, Y.H. Yu, S.T. Wang, et al., Chlorogenic acid protects D-galactoseinduced liver and kidney injury via antioxidation and anti-inflammation effects in mice, Pharm. Biol. 54 (2016) 1027-1034. https://doi.org/10.3109/13880209.2015.1093510.

[40]

H. Chen, Y. Long, L. Guo, Antiaging effect of Inula britannica on aging mouse model induced by D-galactose, Evid. Based Complement Alternat.Med. 2016 (2016) 6049083. https://doi.org/10.1155/2016/6049083.

[41]

S.C. Ho, J.H. Liu, R.Y. Wu, Establishment of the mimetic aging effect in mice caused by D-galactose, Biogerontology 4 (2003) 15-18. https://doi.org/10.1023/a:1022417102206.

[42]

H. Wei, L. Li, Q. Song, et al., Behavioural study of the D-galactose induced aging model in C57BL/6J mice, Behav. Brain Res. 157 (2005) 245-251.https://doi.org/10.1016/j.bbr.2004.07.003.

[43]

A. Bougatef, M. Hajji, R. Balti, et al., Antioxidant and free radicalscavenging activities of smooth hound (Mustelus mustelus) muscle protein hydrolysates obtained by gastrointestinal proteases, Food Chem. 114 (2009)1198-1205. https://doi.org/10.1016/j.foodchem.2008.10.075.

[44]

Q. Sun, H. Shen, Y. Luo, Antioxidant activity of hydrolysates and peptide fractions derived from porcine hemoglobin, J. Food Sci. Technol. 48 (2011)53-60. https://doi.org/10.1007/s13197-010-0115-0.

[45]

Z. Xie, J. Huang, X. Xu, et al., Antioxidant activity of peptides isolated from alfalfa leaf protein hydrolysate, Food Chem. 111 (2008) 370-376.https://doi.org/10.1016/j.foodchem.2008.03.078.

[46]

Y. Ge, A. Sun, Y. Ni, et al., Some nutritional and functional properties of defatted wheat germ protein, J. Agr. Food Chem. 48 (2000) 6215-6218.https://doi.org/10.1021/jf000478m.

[47]

W.J. Chen, A.M. Liao, Y.C. Hou, et al., Digestive characteristics and peptide release from wheat embryo proteins in vitro, Food Funct. 12 (2021) 2257-2269. https://doi.org/10.1039/d0fo03193c.

[48]

H.A. Elfawy, B. Das, Crosstalk between mitochondrial dysfunction, oxidative stress, and age related neurodegenerative disease: etiologies and therapeutic strategies, Life Sci. 218 (2019) 165-184. https://doi.org/10.1016/j.lfs.2018.12.029.

[49]

Y.H. Pang, S. Ahmed, Y.J. Xu, et al., Bound phenolic compounds and antioxidant properties of whole grain and bran of white, red and black rice, Food Chem. 240 (2018) 212-221. https://doi.org/10.1016/j.foodchem.2017.07.095.

[50]

S. Chikara, L.D. Nagaprashantha, J. Singhal, et al., Oxidative stress and dietary phytochemicals: role in cancer chemoprevention and treatment, Cancer Lett. 413 (2018) 122-134. https://doi.org/10.1016/j.canlet.2017.11.002.

[51]

M. Battino, F. Giampieri, F. Pistollato, et al., Nrf2 as regulator of innate immunity: a molecular Swiss army knife!, Biotechnol. Adv. 36 (2018) 358-370. https://doi.org/10.1016/j.biotechadv.2017.12.012.

[52]

Y. Zhao, A.M. Liao, N. Liu, et al., Potential anti-ageing effects of fermented wheat germ in association with gut microbiota in ageing mice, Food Biosci.42 (2021) 101182. https://doi.org/org/10.1016/j.fbio.2021.101182.

[53]

M. Mackei, J. Vörösházi, C. Sebők, et al., Fermented wheat germ extract as a redox Mmodulator: alleviating endotoxin-triggered oxidative stress in primary cultured rat hepatocytes, Oxid. Med. Cell Longev. 2020 (2020)3181202. https://doi.org/10.1155/2020/3181202.

Food Science and Human Wellness
Pages 1300-1308
Cite this article:
Liao A, Lyu X, Ma J, et al. Multi-protective effects of wheat embryo globulin on D-gal-induced aging mice. Food Science and Human Wellness, 2023, 12(4): 1300-1308. https://doi.org/10.1016/j.fshw.2022.10.012

594

Views

58

Downloads

4

Crossref

4

Web of Science

5

Scopus

0

CSCD

Altmetrics

Received: 07 May 2021
Revised: 04 September 2021
Accepted: 26 October 2021
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/).

Return