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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004171naa a2200505 4500
001oai:lup.lub.lu.se:467f9920-2b9b-4f1e-95f9-42ea7bf9ba3c
003SwePub
008160401s2010 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/16739082 URI
024a https://doi.org/10.1007/s00125-010-1795-82 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Friedrichsen, M.4 aut
2451 0a Differential aetiology and impact of phosphoinositide 3-kinase (PI3K) and Akt signalling in skeletal muscle on in vivo insulin action
264 c 2010-05-29
264 1b Springer Science and Business Media LLC,c 2010
520 a Aims/hypothesis Insulin resistance in skeletal muscle is a key factor in the development of type 2 diabetes and although some studies indicate that this could be partly attributed to reduced content and activity of various proximal and distal insulin signalling molecules, consensus is lacking. We therefore aimed to investigate the regulation of proximal insulin signalling in skeletal muscle and its effect on glucose metabolism in a large non-diabetic population. Methods We examined 184 non-diabetic twins with gold-standard techniques including the euglycaemic-hyperinsulinaemic clamp. Insulin signalling was evaluated at three key levels, i.e. the insulin receptor, IRS-1 and V-akt murine thymoma viral oncogene (Akt) levels, employing kinase assays and phospho-specific western blotting. Results Proximal insulin signalling was not associated with obesity, age or sex. However, birthweight was positively associated with IRS-1-associated phosphoinositide 3-kinase (PI3K; IRS-1-PI3K) activity (p=0.04); maximal aerobic capacity ((V) over dotO(2max)), paradoxically, was negatively associated with IRS-1-PI3K (p=0.02) and Akt2 activity (p=0.01). Additionally, we found low heritability estimates for most measures of insulin signalling activity. Glucose disposal was positively associated with Akt-308 phosphorylation (p<0.001) and Akt2 activity (p=0.05), but not with insulin receptor tyrosine kinase or IRS-1-PI3K activity. Conclusions/interpretation With the exception of birthweight, 'classical' modifiers of insulin action, including genetics, age, sex, obesity and (V) over dotO(2max), do not seem to mediate their most central effects on whole-body insulin sensitivity through modulation of proximal insulin signalling in skeletal muscle. We also demonstrated an association between Akt activity and in vivo insulin sensitivity, suggesting a role of Akt in control of in vivo insulin resistance and potentially in type 2 diabetes.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Endokrinologi och diabetes0 (SwePub)302052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Endocrinology and Diabetes0 (SwePub)302052 hsv//eng
653 a Insulin
653 a Insulin action
653 a Human
653 a Assay methods
653 a Hormone receptors
653 a Insulin sensitivity
653 a resistance
700a Poulsen, P.4 aut
700a Richter, E. A.4 aut
700a Hansen, B. F.4 aut
700a Birk, J. B.4 aut
700a Ribel-Madsen, R.4 aut
700a Stender-Petersen, K.4 aut
700a Nilsson, E.4 aut
700a Beck-Nielsen, H.4 aut
700a Vaag, Allanu Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups4 aut0 (Swepub:lu)med-ava
700a Wojtaszewski, J. F. P.4 aut
710a Genomik, diabetes och endokrinologib Forskargrupper vid Lunds universitet4 org
773t Diabetologiad : Springer Science and Business Media LLCg 53:9, s. 1998-2007q 53:9<1998-2007x 1432-0428x 0012-186X
856u http://dx.doi.org/10.1007/s00125-010-1795-8y FULLTEXT
856u https://link.springer.com/content/pdf/10.1007%2Fs00125-010-1795-8.pdf
8564 8u https://lup.lub.lu.se/record/1673908
8564 8u https://doi.org/10.1007/s00125-010-1795-8

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