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dc.contributor.authorKULKARNI, SHUBHANKARen_US
dc.contributor.authorSharda, Sakshien_US
dc.contributor.authorWATVE, MILINDen_US
dc.date.accessioned2019-07-01T05:31:30Z
dc.date.available2019-07-01T05:31:30Z
dc.date.issued2017-08en_US
dc.identifier.citationPLOS ONE, 12(8), e0181536.en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3174
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0181536en_US
dc.description.abstractType 2 diabetes mellitus (T2DM) is believed to be irreversible although no component of the pathophysiology is irreversible. We show here with a network model that the apparent irreversibility is contributed by the structure of the network of inter-organ signalling. A network model comprising all known inter-organ signals in T2DM showed bi-stability with one insulin sensitive and one insulin resistant attractor. The bi-stability was made robust by multiple positive feedback loops suggesting an evolved allostatic system rather than a homeostatic system. In the absence of the complete network, impaired insulin signalling alone failed to give a stable insulin resistant or hyperglycemic state. The model made a number of correlational predictions many of which were validated by empirical data. The current treatment practice targeting obesity, insulin resistance, beta cell function and normalization of plasma glucose failed to reverse T2DM in the model. However certain behavioural and neuro-endocrine interventions ensured a reversal. These results suggest novel prevention and treatment approaches which need to be tested empirically.en_US
dc.language.isoenen_US
dc.publisherPublic Library Scienceen_US
dc.subjectBi-stabilityen_US
dc.subject2 diabetes mellitusen_US
dc.subjectMulti-organ signalling networken_US
dc.subjectSignaling networksen_US
dc.subjectInsulin signalingen_US
dc.subject2017en_US
dc.titleBi-stability in type 2 diabetes mellitus multi-organ signalling networken_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitlePLOS ONEen_US
dc.publication.originofpublisherForeignen_US
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