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Zinc transporters and insulin resistance: therapeutic implications for type 2 diabetes and metabolic disease.


ABSTRACT: BACKGROUND:Zinc is a metal ion that is essential for growth and development, immunity, and metabolism, and therefore vital for life. Recent studies have highlighted zinc's dynamic role as an insulin mimetic and a cellular second messenger that controls many processes associated with insulin signaling and other downstream pathways that are amendable to glycemic control. MAIN BODY:Mechanisms that contribute to the decompartmentalization of zinc and dysfunctional zinc transporter mechanisms, including zinc signaling are associated with metabolic disease, including type 2 diabetes. The actions of the proteins involved in the uptake, storage, compartmentalization and distribution of zinc in cells is under intense investigation. Of these, emerging research has highlighted a role for several zinc transporters in the initiation of zinc signaling events in cells that lead to metabolic processes associated with maintaining insulin sensitivity and thus glycemic homeostasis. CONCLUSION:This raises the possibility that zinc transporters could provide novel utility to be targeted experimentally and in a clinical setting to treat patients with insulin resistance and thus introduce a new class of drug target with utility for diabetes pharmacotherapy.

SUBMITTER: Norouzi S 

PROVIDER: S-EPMC5694903 | biostudies-other | 2017 Nov

REPOSITORIES: biostudies-other

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Zinc transporters and insulin resistance: therapeutic implications for type 2 diabetes and metabolic disease.

Norouzi Shaghayegh S   Adulcikas John J   Sohal Sukhwinder Singh SS   Myers Stephen S  

Journal of biomedical science 20171120 1


<h4>Background</h4>Zinc is a metal ion that is essential for growth and development, immunity, and metabolism, and therefore vital for life. Recent studies have highlighted zinc's dynamic role as an insulin mimetic and a cellular second messenger that controls many processes associated with insulin signaling and other downstream pathways that are amendable to glycemic control.<h4>Main body</h4>Mechanisms that contribute to the decompartmentalization of zinc and dysfunctional zinc transporter mec  ...[more]

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