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10.1186/s12929-017-0394-0

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suck abstract from ncbi


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pmid29157234
      J+Biomed+Sci 2017 ; 24 (1 ): 87
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  • Zinc transporters and insulin resistance: therapeutic implications for type 2 diabetes and metabolic disease #MMPMID29157234
  • Norouzi S ; Adulcikas J ; Sohal SS ; Myers S
  • J Biomed Sci 2017[Nov]; 24 (1 ): 87 PMID29157234 show ga
  • 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.
  • |Animals [MESH]
  • |Biological Transport [MESH]
  • |Blood Glucose/*metabolism [MESH]
  • |Carrier Proteins/*genetics/metabolism [MESH]
  • |Diabetes Mellitus, Type 2/genetics/*therapy [MESH]
  • |Homeostasis [MESH]
  • |Humans [MESH]
  • |Insulin Resistance/*genetics [MESH]
  • |Metabolic Diseases/genetics/therapy [MESH]
  • |Mice [MESH]
  • |Rats [MESH]


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