Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/24492
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dc.contributor.authorGharanei, S-
dc.contributor.authorRamanjaneya, M-
dc.contributor.authorPatel, AH-
dc.contributor.authorPatel, V-
dc.contributor.authorShabir, K-
dc.contributor.authorAuld, C-
dc.contributor.authorKarteris, E-
dc.contributor.authorKyrou, I-
dc.contributor.authorRandeva, HS-
dc.date.accessioned2022-04-25T09:13:44Z-
dc.date.available2022-04-25T09:13:44Z-
dc.date.issued2022-03-28-
dc.identifier1409-
dc.identifier.citationGharanei, S., Ramanjaneya, M., Patel, A.H., Patel. V, Shabir, K., Auld, C., Karteris, E. Kyrou, I. and Randeva, H.S. (2022) 'NUCB2/Nesfatin-1 Reduces Obesogenic Diet Induced Inflammation in Mice Subcutaneous White Adipose Tissue', Nutrients, 2022, 14 (7), 1409, pp. 1-17. doi: 10.3390/nu14071409.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/24492-
dc.descriptionData Availability Statement: Data are available via the corresponding authors upon reasonable request that does not raise any ethical, privacy, or security concerns.en_US
dc.description.abstractCopyright: © 2022 by the authors. Background: Excess adipose tissue accumulation and obesity are characterised by chronic, low-grade, systemic inflammation. Nestfatin-1 is a neuropeptide derived from the precursor protein nucleobindin-2 (NUCB2), which was initially reported to exert anorexigenic effects. The present study aimed to investigate the effects of an obesogenic diet (OD; high-fat, high-sugar) in NUCB2 knockout (KO) mice and of nesfatin-1 treatment in LPS-stimulated 3T3-L1 preadipocytes. Methods: Subcutaneous white adipose tissue (Sc-WAT) samples from wild type (WT) and NUCB2 KO mice that were fed a normal diet (ND), or the OD for 12 weeks were used for RNA and protein extraction, as well as immunohistochemistry. 3T3-L1 cells were treated with 100 nM nesfatin-1 during differentiation and stimulated with 1 µg/mL LPS for measuring the expression and secretion of pro-inflammatory mediators by qPCR, western blotting, immunofluorescence, Bioplex, and ELISA. Results: Following the OD, the mRNA, protein and cellular expression of pro-inflammatory mediators (Tnfα, Il-6, Il-1β, Adgre1, Mcp1, TLR4, Hmbgb1 and NF-kB) significantly increased in the ScWAT of NUCB2 KO mice compared to ND controls. Adiponectin and Nrf2 expression significantly decreased in the ScWAT of OD-fed NUCB2 KO, without changes in the OD-fed WT mice. Furthermore, nesfatin-1 treatment in LPS-stimulated 3T3-L1 cells significantly reduced the expression and secretion of pro-inflammatory cytokines (Tnfα, Il-6, Il-1β, Mcp1) and hmgb1. Conclusion: An obesogenic diet can induce significant inflammation in the ScWAT of NUCB2 KO mice, involving the HMGB1, NRF2 and NF-kB pathways, while nesfatin-1 reduces the pro-inflammatory response in LPS-stimulated 3T3-L1 cells. These findings provide a novel insight into the metabolic regulation of inflammation in WAT.en_US
dc.description.sponsorshipThis research received no external funding.en_US
dc.format.extent1 - 17-
dc.format.mediumElectronic-
dc.language.isoen_USen_US
dc.publisherMDPI AGen_US
dc.rightsCopyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This is an open access article distributed under the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectadipose tissueen_US
dc.subjectinflammationen_US
dc.subjectnesfatin-1/NUCB2en_US
dc.subjecthigh-fat high-sugar dieten_US
dc.subjectobesogenic dieten_US
dc.subjectobesityen_US
dc.subjectNF-κBen_US
dc.subjectHMGB1en_US
dc.titleNUCB2/Nesfatin-1 Reduces Obesogenic Diet Induced Inflammation in Mice Subcutaneous White Adipose Tissueen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.3390/nu14071409-
dc.relation.isPartOfNutrients-
pubs.issue7-
pubs.publication-statusPublished-
pubs.volume14-
dc.identifier.eissn2072-6643-
Appears in Collections:Dept of Life Sciences Research Papers

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