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dc.contributor.authorGOEL, PRANAYen_US
dc.date.accessioned2019-03-15T11:28:31Z
dc.date.available2019-03-15T11:28:31Z
dc.date.issued2015-11en_US
dc.identifier.citationJournal of Theoretical Biology,384, 131-139.en_US
dc.identifier.issn0022-5193en_US
dc.identifier.issn1095-8541en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2361-
dc.identifier.urihttps://doi.org/10.1016/j.jtbi.2015.07.033en_US
dc.description.abstractMathematical models of glucose, insulin and pancreatic beta-cell mass dynamics are essential to our understanding of the physiological basis of the development of type 2 diabetes. The classical view of diabetes is that the disease develops due to insulin insufficiency. An alternate viewpoint that has recently staged a revival is that diabetogenesis is a hypersecretion disorder. A prominent model of diabetes progression is the βIG model due to Topp and coworkers. Here we study two new variants of the Topp model, which we name “Topp-IR” and “Topp-HS”. Topp-IR is a model in which increasing insulin resistance is sufficient to drive a system away from health towards hyperglycemia. Topp-HS describes the hypersecretion model in mathematical terms. We thus show that the hypersecretion hypothesis is theoretically sound, and is therefore a potential route to diabetes. On the basis of insights derived from modeling, we clarify several subtleties of that argument, including postulating a central role for transient insulin peaks in driving insulin resistance.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectInsulin resistanceen_US
dc.subjectPicture revisiteden_US
dc.subjectMathematical models of glucoseen_US
dc.subjectType 2 diabetesen_US
dc.subjectTheories of diabetogenesisen_US
dc.subject2015en_US
dc.titleInsulin resistance or hypersecretion? The βIG picture revisiteden_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Mathematicsen_US
dc.identifier.sourcetitleJournal of Theoretical Biologyen_US
dc.publication.originofpublisherForeignen_US
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