Insulin resistance in the Zucker diabetic fatty rat: a metabolic characterization of obese and lean phenotypes

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dc.contributor.author leonard, BL
dc.contributor.author Watson, RN
dc.contributor.author Loomes, KM
dc.contributor.author Phillips, ARJ
dc.contributor.author Cooper, GJS
dc.coverage.spatial Germany
dc.date.accessioned 2022-06-20T02:51:22Z
dc.date.available 2022-06-20T02:51:22Z
dc.date.issued 2005
dc.identifier.citation (2005). Acta Diabetologica: an international journal devoted to the study of clinical and experimental diabetes and metabolism, 42(4), 162-170.
dc.identifier.issn 0940-5429
dc.identifier.uri https://hdl.handle.net/2292/60016
dc.description.abstract The Zucker diabetic fatty (ZDF) rat is a commonly used animal model of type 2 diabetes yet complete descriptions of insulin resistance in this model are limited. We present a full characterisation of in vivo insulin resistance in obese (fa/fa) animals compared to lean (+/?) littermates. Anaesthetised, ten-week old, obese ZDF rats and their lean littermates underwent a hyperinsulinaemic euglycaemic glucose clamp. Compared with lean littermates, obese ZDF rats required an 89% lower glucose infusion rate to maintain euglycaemia and showed a 35% decrease in peripheral glucose disposal. Insulin-stimulated glucose uptake (Rg') in obese animals was also significantly less in all skeletal muscles studied. Rg' in cardiac and white adipose tissue was not different between the two groups. Total glycogen content in skeletal and cardiac muscle was significantly less in obese animals, while total glycogen content in the liver was significantly greater than in lean littermates. Glycogen synthesis was also decreased in skeletal muscle of obese animals. Compared with lean animals, total triglyceride content was significantly greater in skeletal muscle, heart and liver of obese ZDF rats. Obese animals also showed significantly increased glucose incorporation into lipid in all of these tissues, indicating an increase in lipogenesis. Collectively, these results provide an integrated characterisation of in vivo insulin resistance in obese ZDF rats and a direct comparison with lean littermates.
dc.format.medium Print
dc.language eng
dc.publisher Springer Science and Business Media LLC
dc.relation.ispartofseries Acta Diabetologia
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.subject Muscle, Skeletal
dc.subject Animals
dc.subject Rats
dc.subject Rats, Zucker
dc.subject Insulin Resistance
dc.subject Obesity
dc.subject Thinness
dc.subject Insulin
dc.subject Glucose
dc.subject Blood Glucose
dc.subject Glucose Clamp Technique
dc.subject Kinetics
dc.subject Male
dc.subject Diabetes
dc.subject Cardiovascular
dc.subject Nutrition
dc.subject Heart Disease
dc.subject 5.1 Pharmaceuticals
dc.subject Metabolic and endocrine
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Endocrinology & Metabolism
dc.subject hyperinsulinaemic euglycaemic clamp
dc.subject Zucker diabetic fatty rat
dc.subject BETA(3)-ADRENERGIC AGONIST CL-316243
dc.subject HEPATIC GLUCOSE-PRODUCTION
dc.subject ZDF RATS
dc.subject PERIPHERAL INSULIN
dc.subject ISOFLURANE ANESTHESIA
dc.subject EUGLYCEMIC CLAMP
dc.subject ACID-METABOLISM
dc.subject INVIVO
dc.subject SENSITIVITY
dc.subject TRENDS
dc.subject 1103 Clinical Sciences
dc.subject 1116 Medical Physiology
dc.subject Biomedical
dc.subject Basic Science
dc.subject Digestive Diseases
dc.subject Liver Disease
dc.title Insulin resistance in the Zucker diabetic fatty rat: a metabolic characterization of obese and lean phenotypes
dc.type Journal Article
dc.identifier.doi 10.1007/s00592-005-0197-8
pubs.issue 4
pubs.begin-page 162
pubs.volume 42
dc.date.updated 2022-05-03T04:44:35Z
dc.rights.holder Copyright: The author en
dc.identifier.pmid 16382303 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/16382303
pubs.end-page 170
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article
pubs.elements-id 59747
pubs.org-id Science
pubs.org-id Biological Sciences
pubs.org-id Science Research
pubs.org-id Maurice Wilkins Centre (2010-2014)
dc.identifier.eissn 1432-5233
pubs.record-created-at-source-date 2022-05-03


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