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<mods:namePart>Villa Pérez, Pablo .</mods:namePart>
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<mods:namePart>Merino, Beatriz</mods:namePart>
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<mods:namePart>Fernández Díaz, Cristina M. .</mods:namePart>
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<mods:namePart>Cidad, Pilar</mods:namePart>
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<mods:namePart>Lobatón, Carmen D.</mods:namePart>
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<mods:namePart>Moreno, Alfredo</mods:namePart>
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<mods:namePart>Muturi, Harrison T. .</mods:namePart>
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<mods:namePart>Ghadieh, Hilda E. .</mods:namePart>
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<mods:namePart>Najjar, Sonia M. .</mods:namePart>
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<mods:namePart>Leissring, Malcolm A.</mods:namePart>
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<mods:namePart>Cózar Castellano, Irene</mods:namePart>
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<mods:namePart>Perdomo Hernández, Germán M.</mods:namePart>
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<mods:dateAccessioned encoding="iso8601">2018-10-11T10:26:09Z</mods:dateAccessioned>
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<mods:dateAvailable encoding="iso8601">2018-10-11T10:26:09Z</mods:dateAvailable>
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<mods:dateIssued encoding="iso8601">2018-11</mods:dateIssued>
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<mods:identifier type="issn">0026-0495</mods:identifier>
<mods:identifier type="uri">http://hdl.handle.net/10259/4965</mods:identifier>
<mods:identifier type="doi">10.1016/j.metabol.2018.08.001</mods:identifier>
<mods:abstract>The role of insulin-degrading enzyme (IDE), a metalloprotease with high affinity for insulin, in insulin clearance remains poorly understood. OBJECTIVE: This study aimed to clarify whether IDE is a major mediator of insulin clearance, and to define its role in the etiology of hepatic insulin resistance.&#xd;
&#xd;
Methods&#xd;
We generated mice with liver-specific deletion of Ide (L-IDE-KO) and assessed insulin clearance and action.&#xd;
&#xd;
Results&#xd;
L-IDE-KO mice exhibited higher (~20%) fasting and non-fasting plasma glucose levels, glucose intolerance and insulin resistance. This phenotype was associated with ~30% lower plasma membrane insulin receptor levels in liver, as well as ~55% reduction in insulin-stimulated phosphorylation of the insulin receptor, and its downstream signaling molecules, AKT1 and AKT2 (reduced by ~40%). In addition, FoxO1 was aberrantly distributed in cellular nuclei, in parallel with up-regulation of the gluconeogenic genes Pck1 and G6pc. Surprisingly, L-IDE-KO mice showed similar plasma insulin levels and hepatic insulin clearance as control mice, despite reduced phosphorylation of the carcinoembryonic antigen-related cell adhesion molecule 1, which upon its insulin-stimulated phosphorylation, promotes receptor-mediated insulin uptake to be degraded.&#xd;
&#xd;
Conclusion&#xd;
IDE is not a rate-limiting regulator of plasma insulin levels in vivo</mods:abstract>
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<mods:topic>nsulin-degrading enzyme</mods:topic>
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<mods:topic>Hepatic insulin resistance</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Insulin recepto</mods:topic>
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<mods:subject>
<mods:topic>Carcinoembryonic antigen-related cell adhesion molecule 1</mods:topic>
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<mods:titleInfo>
<mods:title>Liver-specific ablation of insulin-degrading enzyme causes hepatic insulin resistance and glucose intolerance, without affecting insulin clearance in mice</mods:title>
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