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dc.contributor.authorPatterson, Steven
dc.contributor.authorScullion, Siobhan M. J.
dc.contributor.authorMcCluskey, Jane T.
dc.contributor.authorFlatt, Peter R.
dc.contributor.authorMcClenaghan, Neville H.
dc.date.accessioned2018-06-29T21:34:04Z
dc.date.available2018-06-29T21:34:04Z
dc.date.issued2007-05
dc.identifierER4490
dc.identifier.citationPatterson, S., Scullion, S., McCluskey, J., Flatt, P. & McClenaghan, N. (2007-05) Prolonged exposure to homocysteine results in diminished but reversible pancreatic _-cell responsiveness to insulinotropic agents, Diabetes/Metabolism Research and Reviews, vol. 23, pp. 324-334.
dc.identifier.issn15207552
dc.identifier.urihttp://doi.org/10.1002/dmrr.699
dc.identifier.urihttps://eresearch.qmu.ac.uk/handle/20.500.12289/4490
dc.description.abstractBACKGROUND: Plasma homocysteine levels may be elevated in poorly controlled diabetes with pre-existing vascular complications and/or nephropathy. Since homocysteine has detrimental effects on a wide diversity of cell types, the present study examined the effects of long-term homocysteine exposure on the secretory function of clonal BRIN-BD11 beta-cells. METHODS: Acute insulin secretory function, cellular insulin content and viability of BRIN-BD11 cells were assessed following long-term (18 h) exposure to homocysteine in culture. RT-PCR and Western blot analysis were used to determine the expression of key beta-cell genes and proteins. Cells were cultured for a further 18 h without homocysteine to determine any long-lasting effects. RESULTS: Homocysteine (250-1000 micromol/L) exposure reduced insulin secretion at both moderate (5.6 mmol/L) and stimulatory (16.7 mmol/L) glucose by 48-63%. Similarly, insulin secretory responsiveness to stimulatory concentrations of alanine, arginine, 2-ketoisocaproate, tolbutamide, KCl, elevated Ca2+, forskolin and PMA, GLP-1, GIP and CCK-8 were reduced by 11-62% following culture with 100-250 micromol/L homocysteine. These inhibitory effects could not simply be attributed to changes in cellular insulin content, cell viability, H2O2 generation or any obvious alterations of gene/protein expression for insulin, glucokinase, GLUT2, VDCC, or Kir6.2 and SUR1. Additional culture for 18 h in standard culture media after homocysteine exposure restored secretory responsiveness to all agents tested. CONCLUSION: These findings suggest that long-term exposure to high homocysteine levels causes a reversible impairment of pancreatic beta-cell insulinotropic pathways. The in vivo actions of hyperhomocysteinaemia on islet cell function merit investigation.
dc.format.extent324-334
dc.publisherWIley
dc.relation.ispartofDiabetes/Metabolism Research and Reviews
dc.titleProlonged exposure to homocysteine results in diminished but reversible pancreatic _-cell responsiveness to insulinotropic agents
dc.typearticle
dcterms.accessRightsnone
dc.description.facultysch_die
dc.description.volume23
dc.identifier.doihttp://doi:10.1002/dmrr.699
dc.description.ispublishedpub
dc.description.eprintid4490
rioxxterms.typearticle
qmu.authorMcCluskey, Jane T.
dc.description.statuspub
dc.description.number4


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