Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.bbrc.2005.06.021
DC FieldValue
dc.titleStreptozotocin-induced diabetes in the rat is associated with enhanced tissue hydrogen sulfide biosynthesis
dc.contributor.authorYusuf, M.
dc.contributor.authorHuat, B.T.K.
dc.contributor.authorHsu, A.
dc.contributor.authorWhiteman, M.
dc.contributor.authorBhatia, M.
dc.contributor.authorMoore, P.K.
dc.date.accessioned2016-11-16T11:05:27Z
dc.date.available2016-11-16T11:05:27Z
dc.date.issued2005-08-12
dc.identifier.citationYusuf, M., Huat, B.T.K., Hsu, A., Whiteman, M., Bhatia, M., Moore, P.K. (2005-08-12). Streptozotocin-induced diabetes in the rat is associated with enhanced tissue hydrogen sulfide biosynthesis. Biochemical and Biophysical Research Communications 333 (4) : 1146-1152. ScholarBank@NUS Repository. https://doi.org/10.1016/j.bbrc.2005.06.021
dc.identifier.issn0006291X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/130393
dc.description.abstractThis investigation is aimed to determine whether the biosynthesis of H 2S, an endogenous vasodilator gas, is altered in the streptozotocin-diabetic rat. Plasma H2S concentration as well as the activity, and expression, of H2S synthesizing enzymes (namely cystathionine-γ-lyase (CSE) and cystathionine-β-synthetase (CBS)) were measured in various tissues of non-diabetic, streptozotocin-diabetic and insulin-treated diabetic rats. H2S formation in pancreas and liver was increased in diabetic rats. Both CSE and CBS mRNAs were increased in liver of diabetic animals. Similarly, CBS mRNA was increased in pancreas. Insulin treatment restored the changes in H2S metabolism seen. The findings of this study suggest that the metabolism of H2S in pancreas and liver is altered in the streptozotocin-diabetic rat. This is the first study in which a derangement in H2S biosynthesis in diabetes has been demonstrated. H2S may play a part in the aetiology or development of diabetes in this animal model. © 2005 Elsevier Inc. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.bbrc.2005.06.021
dc.sourceScopus
dc.subjectCystathionine-β-synthetase
dc.subjectCystathionine-γ-lyase
dc.subjectDiabetes
dc.subjectGlucose
dc.subjectHydrogen sulfide
dc.subjectInsulin
dc.subjectStreptozotocin
dc.typeArticle
dc.contributor.departmentPHARMACOLOGY
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1016/j.bbrc.2005.06.021
dc.description.sourcetitleBiochemical and Biophysical Research Communications
dc.description.volume333
dc.description.issue4
dc.description.page1146-1152
dc.description.codenBBRCA
dc.identifier.isiut000230538900015
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