Mixture of peanut skin extract and fish oil improves memory in mice via modulation of anti-oxidative stress and regulation of BDNF/ERK/CREB signaling pathways

Nutrients

Volumn 8, Issue 5, 2016, Pages

  Xiang, Lan ^a   Cao, Xue Li ^a   Xing, Tian Yan ^b   Mori, Daisuke ^c   Tang, Rui Qi ^a   Li, Jing ^a   Gao, Li Juan ^a   Qi, Jian Hua ^a  

^a ZHEJIANG UNIVERSITY   (China)

^b Hangzhou Simo Pharmaceutics Co Ltd   (China)

^c Gifu Shellac Mfg Co Ltd   (Japan)

Author keywords

Brain derived neurotrophic factor; ERK; Fish oil; Oxidative stress; Peanut skin extract

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR; CYCLIC AMP RESPONSIVE ELEMENT BINDING PROTEIN; FISH OIL; MALONALDEHYDE; MITOGEN ACTIVATED PROTEIN KINASE; NERVE GROWTH FACTOR; PEANUT EXTRACT; PEANUT SKIN EXTRACT; PROTEIN KINASE B; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG; ANTIOXIDANT; CREB1 PROTEIN, MOUSE; PLANT EXTRACT;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BEHAVIORAL SCIENCE; BIOASSAY; BRAIN CORTEX; COGNITION; CONTROLLED STUDY; ENZYME ACTIVITY; GENE EXPRESSION; HIPPOCAMPUS; LEARNING; MALE; MEMORY ASSESSMENT; MORRIS WATER MAZE TEST; MOUSE; NEURITE; NONHUMAN; OXIDATIVE STRESS; PC12 CELL LINE; PHASE CONTRAST MICROSCOPY; PROTEIN PHOSPHORYLATION; REAL TIME POLYMERASE CHAIN REACTION; REGULATORY MECHANISM; SPATIAL MEMORY TEST; WESTERN BLOTTING; Y-MAZE TEST; ANIMAL; ARACHIS; CHEMISTRY; DRUG EFFECTS; GENE EXPRESSION REGULATION; GENETICS; METABOLISM;

ANIMALS; ANTIOXIDANTS; ARACHIS; BRAIN-DERIVED NEUROTROPHIC FACTOR; CYCLIC AMP RESPONSE ELEMENT-BINDING PROTEIN; EXTRACELLULAR SIGNAL-REGULATED MAP KINASES; FISH OILS; GENE EXPRESSION REGULATION; MICE; OXIDATIVE STRESS; PLANT EXTRACTS;

EID: 84964839627     PISSN: None     EISSN: 20726643     Source Type: Journal    
DOI: 10.3390/nu8050256     Document Type: Article

References (35)

1. Schirmer, S.H.; Werner, C.M.; Binder, S.B.; Faas, M.E.; Custodis, F.; Böhm, M.; Laufs, U. Effects of omega-3 fatty acids on postprandial triglycerides and monocyte activation. Atherosclerosis 2012, 225, 166-172. [CrossRef] [PubMed]
2. Cole, G.M.; Lim, G.P.; Yang, F.; Teter, B.; Begum, A.; Ma, Q.; Harris-White, M.E.; Frautschy, S.A. Prevention of Alzheimer's disease: Omega-3 fatty acid and phenolic anti-oxidant interventions. Neurobiol. Aging 2005, 26, 133S-136S. [CrossRef] [PubMed]
3. Im, D.S. Omega-3 fatty acids in anti-inflammation (pro-resolution) and GPCRs. Prog. Lipid Res. 2012, 51, 232-237. [CrossRef] [PubMed]
4. Iagher, F.; de Brito Belo, S.R.; Souza, W.M.; Nunes, J.R.; Naliwaiko, K.; Sassaki, G.L.; Bonatto, S.J.; de Oliveira, H.H.; Brito, G.A.; de Lima, C.; et al. Anti-tumor and anti-cachectic effects of shark liver oil and fish oil: Comparison between independent or associative chronic supplementation in walker 256 tumor-bearing rats. Lipids Health Dis. 2013, 12, 146. [CrossRef] [PubMed]
5. Ishida, S. Lifestyle-related diseases and anti-aging ophthalmology: Suppression of retinal and choroidal pathologies by inhibiting renin-angiotensin system and inflammation. Nihon Ganka Gakkai Zasshi 2009, 113, 403-422. [PubMed]
6. Albert, B.B.; Cameron-Smith, D.; Hofman, P.L.; Cutfield, W.S. Oxidation of marine omega-3 supplements and human health. Biomed. Res. Int. 2013, 2013, 464921. [CrossRef] [PubMed]
7. Liu, X.; Shibata, T.; Hisaka, S.; Kawai, Y.; Osawa, T. DHA hydroperoxides as a potential inducer of neuronal cell death: A mitochondrial dysfunction-mediated pathway. J. Clin. Biochem. Nutr. 2008, 43, 26-33. [CrossRef] [PubMed]
8. Enns, J.E.; Yeganeh, A.; Zarychanski, R.; Abou-Setta, A.M.; Friesen, C.; Zahraska, P.; Taylor, C.G. The impact of omega-3 polyunsaturated fatty acid supplementation on the incidence of cardiovascular events and complications in peripheral arterial disease: A systematic review and meta-analysis. BMC Cardiovasc. Disord. 2014, 14, 70. [CrossRef] [PubMed]
9. Morrison, C.D.; Pistell, P.J.; Ingram, D.K.; Johnson, W.D.; Liu, Y.; Fernandez-Kim, S.O.; White, C.L.; Purpera, M.N.; Uranga, R.M.; Bruce-Keller, A.J.; et al. High fat diet increases hippocampal oxidative stress and cognitive impairment in aged mice: Implications for decreased Nrf2 signaling. J. Neurochem. 2010, 114, 1581-1589. [CrossRef] [PubMed]
10. Greenwood, C.E.; Winocur, G. High-fat diets, insulin resistance and declining cognitive function. Neurobiol. Aging 2005, 26, S42-S45. [CrossRef] [PubMed]
11. Pistell, P.J.; Morrison, C.D.; Gupta, S.; Knight, A.G.; Keller, J.N.; Ingram, D.K.; Bruce-Keller, A.J. Cognitive impairment following high fat diet consumption is associated with brain inflammation. J. Neuroimmunol. 2010, 219, 25-32. [CrossRef] [PubMed]
12. Sanders, T.H.; McMichael, R.W.; Hendrix, K.W., Jr. Occurrence of resveratrol in edible peanuts. J. Agric. Food Chem. 2000, 48, 1243-1246. [CrossRef] [PubMed]
13. Georgiev, V.; Ananga, A.; Tsolova, V. Recent advances and uses of grape flavonoids as nutraceuticals. Nutrients 2014, 6, 391-415. [CrossRef] [PubMed]
14. Khan, N.; Khymenets, O.; Urpí-Sardà, M.; Tulipani, S.; Garcia-Aloy, M.; Monagas, M.; Mora-Cubillos, X.; Llorach, R.; Andres-Lacueva, C. Cocoa polyphenols and inflammatory markers of cardiovascular disease. Nutrients 2014, 6, 844-880. [CrossRef] [PubMed]
15. Ravishankar, D.; Rajora, A.K.; Greco, F.; Osborn, H.M. Flavonoids as prospective compounds for anti-cancer therapy. Int. J. Biochem. Cell Biol. 2013, 45, 2821-2831. [CrossRef] [PubMed]
16. Oršolić, N.; Sirovina, D.; Gajski, G.; Garaj-Vrhovac, V.; JazvinšćakJembrek, M.; Kosalec, I. Assessment of DNA damage and lipid peroxidation in diabetic mice: Effects of propolis and epigallocatechingallate (EGCG). Mutat. Res. 2013, 757, 36-44. [CrossRef] [PubMed]
17. Cordero-Herrera, I.; Martín, M.Á.; Goya, L.; Ramos, S. Cocoa flavonoids attenuate high glucose-induced insulin signalling blockade and modulate glucose uptake and production in human HepG2 cells. Food Chem. Toxicol. 2014, 64, 10-19. [CrossRef] [PubMed]
18. Sarnoski, P.J.; Johnson, J.V.; Reed, K.A.; Tanko, J.M.; O'Keefe, S.F. Separation and characterization of proanthocyanidins in Virginia type peanut skins by LC-MS. Food Chem. 2012, 131, 927-939. [CrossRef]
19. Bansode, R.R.; Randolph, P.; Hurley, S.; Ahmedna, M. Evaluation of hypolipidemic effects of peanut skin-derived polyphenols in rats on a western-diet. Food Chem. 2012, 135, 1659-1666. [CrossRef] [PubMed]
20. Catalan, U.; Fernandez-Castillejo, S.; Angles, N.; Morello, J.R.; Yebras, M.; Solà, R. Inhibition of the transcription factor c-Jun by the MAPK family, and not the NF-κB pathway, suggests that peanut extract has anti-inflammatory properties. Mol. Immunol. 2012, 52, 125-132. [CrossRef] [PubMed]
21. Gao, L.J.; Xiang, L.; Luo, Y.; Wang, G.F.; Li, J.Y.; Qi, J.H. Gentisides, C.-K: Nine new neuritogenic compounds from the traditional Chinese medicine Gentiana rigescens Franch. Bioorg. Med. Chem. 2010, 18, 6995-7000. [CrossRef] [PubMed]
22. Beppe, G.J.; Dongmo, A.B.; Foyet, H.S.; Tsabang, N.; Olteanu, Z.; Cioanca, O.; Hancianu, M.; Dimo, T.; Hritcu, L. Memory-enhancing activities of the aqueous extract of Albiziaadianthifolia leaves in the 6-hydroxydopamine-lesion rodent model of Parkinson's disease. BMC Complement. Altern. Med. 2014, 14, 142. [CrossRef] [PubMed]
23. Sun, K.Y.; Yang, W.; Huang, Y.N.; Wang, Y.F.; Xiang, L.; Qi, J.H. Leu452His mutation in lipoprotein lipase gene transfer associated with hypertriglyceridemia in mice in vivo. PLoS ONE 2013, 8, e75462. [CrossRef] [PubMed]
24. Hashimoto, M.; Katakura, M.; Tanabe, Y. n -3 fatty acids effectively improve the reference memory-related learning ability associated with increased brain docosahexaenoic acid-derived docosanoids in aged rats. Biochim. Biophys. Acta 2015, 1851, 203-209. [CrossRef] [PubMed]
25. Jeong, E.J.; Lee, K.Y.; Kim, S.H.; Sung, S.H.; Kim, Y.C. Cognitive-enhancing and antioxidant activities of iridoid glycosides from Scrophularia buergeriana in scopolamine-treated mice. Eur. J. Pharmacol. 2008, 588, 78-84. [CrossRef] [PubMed]
26. Sano, M.; Ernesto, C.; Thomas, R.G.; Klauber, M.R.; Schafer, K.; Grundman, M. A controlled trial of selegiline, alpha-to copherol, or both as treatment for Alzheimer's disease. The Alzheimer's Disease Cooperative Study. N. Engl. J. Med. 1997, 336, 1216-1222. [CrossRef] [PubMed]
27. Nade, V.S.; Kanhere, S.V.; Kawale, L.A.; Yadav, A.V. Cognitive enhancing and antioxidant activity of ethyl acetate soluble fraction of the methanol extract of Hibiscus rosa sinensis in scopolamine-induced amnesia. Indian J. Pharmacol. 2011, 43, 137-142. [CrossRef] [PubMed]
28. Piche, L.A.; Draper, H.H.; Cole, P.D. Malondialdehyde excretion by subjects consuming cod liver oil vs. a concentrate of n -3 fatty acids. Lipids 1988, 23, 370-371. [CrossRef] [PubMed]
29. Bekinschtein, P.; Cammarota, M.; Katche, C.; Slipczuk, L.; Rossato, J.I.; Goldin, A.; Izquierdo, I.; Medina, J.H. BDNF is essential to promote persistence of long-term memory storage. Proc. Natl. Acad. Sci. USA 2008, 105, 2711-2716. [CrossRef] [PubMed]
30. Restivo, L.; Vetere, G.; Bontempi, B.; Ammassari-Teule, M. The formation of recent and remote memory is associated with time-dependent formation of dendritic spines in the hippocampus and anterior cingulate cortex. J. Neurosci. 2009, 29, 8206-8214. [CrossRef] [PubMed]
31. Bramham, C.R.; Alme, M.N.; Bittins, M.; Kuipers, S.D.; Nair, R.R.; Pai, B.; Panja, D.; Schubert, M.; Soule, J.; Tiron, A.; et al. The Arc of synaptic memory. Exp. Brain Res. 2010, 200, 125-140. [CrossRef] [PubMed]
32. Kong, L.B.; Yang, Z.Y.; An, R.; Ding, S.H. Effects of special brain area cerebral blood flow abnormal perfusion on learning and memory function and its molecular mechanism in rats. Front. Biol. China 2008, 3, 147-153. [CrossRef]
33. Alonso, M.; Medina, J.H.; Pozzo-Miller, L. ERK1/2 activation is necessary for BDNF to increase dendritic spine density in hippocampal CA1 pyramidal neurons. Learn. Mem. 2004, 11, 172-178. [CrossRef] [PubMed]
34. Mizuno, M.; Yamada, K.; Olariu, A.; Nawa, H.; Nabeshima, T. Involvement of brain-derived neuotrophic factor in spatial memory formation and maintenance in a radial arm maze test in rats. J. Neurosci. 2000, 20, 7116-7121. [PubMed]
35. Ou, L.C.; Gean, P.W. Regulation of amygdata-dependent learning by brain-derived neurotrophic factor is mediated by extracellular signal-regulated kinase and phosphatidyliostiol-3-kinase. Neuopsychopharmacology 2006, 31, 287-296. [CrossRef] [PubMed]