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dc.contributor.authorLamichhane, Gopal
dc.contributor.authorLiu, Jing
dc.contributor.authorLee, Su-Jeong
dc.contributor.authorLee, Da-Yeon
dc.contributor.authorZhang, Guolong
dc.contributor.authorKim, Yoo
dc.date.accessioned2024-01-17T19:46:49Z
dc.date.available2024-01-17T19:46:49Z
dc.date.issued2024-01-12
dc.identifieroksd_lamichhane_curcumin_mitigates_the_high_2024
dc.identifier.citationLamichhane, G., Liu, J., Lee, S.-J., Lee, D.-Y., Zhang, G., Kim, Y. (2024). Curcumin mitigates the high-fat high-sugar diet-induced impairment of spatial memory, hepatic metabolism, and the alteration of the gut microbiome in alzheimer’s disease-induced (3xtg-ad) mice. Nutrients, 16(2), pp. 240-240. https://doi.org/10.3390/nu16020240
dc.identifier.urihttps://hdl.handle.net/11244/340120
dc.description.abstractThe escalating prevalence of metabolic diseases and an aging demographic has been correlated with a concerning rise in Alzheimer’s disease (AD) incidence. This study aimed to access the protective effects of curcumin, a bioactive flavonoid from turmeric, on spatial memory, metabolic functions, and the regulation of the gut microbiome in AD-induced (3xTg-AD) mice fed with either a normal chow diet (NCD) or a high-fat high-sugar diet (HFHSD). Our findings revealed an augmented susceptibility of the HFHSD-fed 3xTg-AD mice for weight gain and memory impairment, while curcumin supplementation demonstrated a protective effect against these changes. This was evidenced by significantly reduced body weight gain and improved behavioral and cognitive function in the curcumin-treated group. These improvements were substantiated by diminished fatty acid synthesis, altered cholesterol metabolism, and suppressed adipogenesis-related pathways in the liver, along with modified synaptic plasticity-related pathways in the brain. Moreover, curcumin enriched beneficial gut microbiota, including Oscillospiraceae and Rikenellaceae at the family level, and Oscillibacter, Alistipes, Pseudoflavonifractor, Duncaniella, and Flintibacter at the genus level. The observed alteration in these gut microbiota profiles suggests a potential crosswalk in the liver and brain for regulating metabolic and cognitive functions, particularly in the context of obesity-associated cognitive disfunction, notably AD.
dc.formatapplication/pdf
dc.languageen_US
dc.publisherMDPI AG
dc.relation.ispartofNutrients, 16 (2)
dc.relation.urihttp://dx.doi.org/10.3390/nu16020240
dc.rightsThis material has been previously published. In the Oklahoma State University Library's institutional repository this version is made available through the open access principles and the terms of agreement/consent between the author(s) and the publisher. The permission policy on the use, reproduction or distribution of the material falls under fair use for educational, scholarship, and research purposes. Contact Digital Resources and Discovery Services at lib-dls@okstate.edu or 405-744-9161 for further information.
dc.titleCurcumin mitigates the high-fat high-sugar diet-induced impairment of spatial memory, hepatic metabolism, and the alteration of the gut microbiome in alzheimer’s disease-induced (3xtg-ad) mice
dc.date.updated2024-01-14T22:33:45Z
osu.filenameoksd_lamichhane_curcumin_mitigates_the_high_2024.pdf
dc.identifier.doi10.3390/nu16020240
dc.description.departmentDept of Animal and Food Sciences
dc.description.departmentNutritional Sciences
dc.type.genreArticle
dc.type.materialText
dc.subject.keywordsfood sciences
dc.subject.keywordsnutrition and dietetics
dc.subject.keywordsclinical sciences
dc.subject.keywordsnutrition and dietetics
dc.subject.keywordspublic health
dc.identifier.authorORCID: 0000-0003-1487-7578 (Lamichhane, Gopal)
dc.identifier.authorORCID: 0000-0003-0819-8982 (Lee, Su-Jeong)
dc.identifier.authorORCID: 0000-0002-4085-0689 (Lee, Da-Yeon)
dc.identifier.authorORCID: 0000-0003-4781-5816 (Zhang, Guolong)
dc.identifier.authorScopusID: 7405270549 (Zhang, Guolong)
dc.identifier.authorORCID: 0000-0002-4525-1319 (Kim, Yoo)
dc.identifier.authorScopusID: 57218459560 | 57687368900 (Kim, Yoo)
dc.identifier.essn2072-6643


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