• Login
    View Item 
    •   Home
    • The Christie Research Publications Repository
    • All Christie Publications
    • View Item
    •   Home
    • The Christie Research Publications Repository
    • All Christie Publications
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of ChristieCommunitiesTitleAuthorsIssue DateSubmit DateSubjectsThis CollectionTitleAuthorsIssue DateSubmit DateSubjectsProfilesView

    My Account

    LoginRegister

    Local Links

    The Christie WebsiteChristie Library and Knowledge Service

    Statistics

    Display statistics

    Impact of bariatric surgery on ABC subtilisin/kexin type 9 (PCSK9) gene expression and inflammation in the adipose tissue of obese diabetic rats

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Thumbnail
    Name:
    Impact of....pdf
    Size:
    1.173Mb
    Format:
    PDF
    Description:
    Found with Open Access Button
    Download
    Authors
    Heald, A. H.
    Fachim, H. A.
    Bashir, B.
    Garside, B.
    Adam, Safwaan
    Iqbal, Z.
    Syed, A. A.
    Donn, R.
    Le Roux, C. W.
    Abdelaal, M.
    White, J.
    Soran, H.
    Show allShow less
    Affiliation
    The Christie Hospital NHS Foundation Trust, Wilmslow Road, Manchester M20 4BX, UK.
    Issue Date
    2023
    
    Metadata
    Show full item record
    Abstract
    Bariatric surgery improves dyslipidaemia and reduces body weight, but it remains unclear how bariatric surgery modulates gene expression in fat cells to influence the proprotein convertase subtilisin/kexin type 9 (PCSK-9) and low-density lipoprotein receptor (LDLR) gene expression. The expression of the PCSK9/LDLR/tumor necrosis factor-alpha (TNFα) gene in adipose tissue was measured in two groups of Zucker Diabetic Sprague Dawley (ZDSD) rats after Roux-en-Y gastric bypass (RYGB) surgery or 'SHAM' operation. There was lower PCSK9 (p = 0.02) and higher LDLR gene expression (p = 0.02) in adipose tissue in rats after RYGB. Weight change did not correlate with PCSK9 gene expression (r = -0.5, p = 0.08) or TNFα gene expression (r = -0.4, p = 0.1). TNFα gene expression was positively correlated with PCSK9 gene expression (r = 0.7, p = 0.001) but not correlated with LDLR expression (r = -0.3, p = 0.3). Circulating triglyceride levels were lower in RYGB compared to the SHAM group (1.1 (0.8-1.4) vs. 1.5 (1.0-4.2), p = 0.038) mmol/L with no difference in cholesterol levels. LDLR gene expression was increased post-bariatric surgery with the potential to reduce the number of circulating LDL particles. PCSK9 gene expression and TNFα gene expression were positively correlated after RYGB in ZDSD rats, suggesting that the modulation of pro-inflammatory pathways in adipose tissue after RYGB may partly relate to PCSK9 and LDLR gene expression.
    Citation
    Heald AH, Fachim HA, Bashir B, Garside B, Adam S, Iqbal Z, et al. Impact of Bariatric Surgery on ABC Subtilisin/Kexin Type 9 (PCSK9) Gene Expression and Inflammation in the Adipose Tissue of Obese Diabetic Rats. International journal of molecular sciences. 2023 Nov 30;24(23). PubMed PMID: 38069302. Pubmed Central PMCID: PMC10707086. Epub 2023/12/09. eng.
    Journal
    International Journal of Molecular Sciences
    URI
    http://hdl.handle.net/10541/626810
    DOI
    10.3390/ijms242316978
    PubMed ID
    38069302
    Additional Links
    https://dx.doi.org/10.3390/ijms242316978
    Type
    Article
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.3390/ijms242316978
    Scopus Count
    Collections
    All Christie Publications

    entitlement

    Related articles

    • Proprotein convertase subtilisin/kexin type 9 deficiency reduces melanoma metastasis in liver.
    • Authors: Sun X, Essalmani R, Day R, Khatib AM, Seidah NG, Prat A
    • Issue date: 2012 Dec
    • β-Estradiol results in a proprotein convertase subtilisin/kexin type 9-dependent increase in low-density lipoprotein receptor levels in human hepatic HuH7 cells.
    • Authors: Starr AE, Lemieux V, Noad J, Moore JI, Dewpura T, Raymond A, Chrétien M, Figeys D, Mayne J
    • Issue date: 2015 Jul
    • Proprotein Convertase Subtilisin/Kexin 9 (PCSK9) Promotes Macrophage Activation via LDL Receptor-Independent Mechanisms.
    • Authors: Katsuki S, K Jha P, Lupieri A, Nakano T, Passos LSA, Rogers MA, Becker-Greene D, Le TD, Decano JL, Ho Lee L, Guimaraes GC, Abdelhamid I, Halu A, Muscoloni A, V Cannistraci C, Higashi H, Zhang H, Vromman A, Libby P, Keith Ozaki C, Sharma A, Singh SA, Aikawa E, Aikawa M
    • Issue date: 2022 Nov 11
    • Peroxisome Proliferator-activated receptor γ activation by ligands and dephosphorylation induces proprotein convertase subtilisin kexin type 9 and low density lipoprotein receptor expression.
    • Authors: Duan Y, Chen Y, Hu W, Li X, Yang X, Zhou X, Yin Z, Kong D, Yao Z, Hajjar DP, Liu L, Liu Q, Han J
    • Issue date: 2012 Jul 6
    • Proprotein convertase subtilisin/kexin type 9 (PCSK9) can mediate degradation of the low density lipoprotein receptor-related protein 1 (LRP-1).
    • Authors: Canuel M, Sun X, Asselin MC, Paramithiotis E, Prat A, Seidah NG
    • Issue date: 2013
    DSpace software (copyright © 2002 - 2025)  DuraSpace
    Quick Guide | Contact Us
    Open Repository is a service operated by 
    Atmire NV
     

    Export search results

    The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

    By default, clicking on the export buttons will result in a download of the allowed maximum amount of items.

    To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

    After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.