Metallomics · 2014 · 10 citations · 22 references
MedicineBiochemistryPathologyDiabetologyHepatologyHistopathologyDiabetes MellitusDiabetes Mellitus BiochemistryInsulin ResistancePancreatic DiseasesPancreatic PathologyZinc MetabolismDiabetes Mellitus PathophysiologyType 2 Diabetes PathophysiologyZinc Biochemistry
The relationship between biometals, such as zinc (Zn(2+)), vanadium, copper, cobalt, and magnesium ions, and diabetes therapy has been recognized for several years. In particular, the antidiabetic activities of Zn(2+) and oxovanadium (VO(2+)) complexes have been measured using biochemical approaches. In the present study, diabetic KK-A(y) mice were treated with bis(1-oxy-2-pyridine-thiolato)Zn(2+) (Zn(opt)2) and bis(1-oxy-2-pyridine-thiolato)VO(2+) (VO(opt)2) for 4 weeks, and the antidiabetic activities of these metal complexes were evaluated using biochemical and morphological methods. Additionally, zinc gluconate (Zn(glc)2) and bis(ethylmaltolato)VO(2+) (VO(emal)2) were used as reference compounds. Pancreatic islet cells were smaller, and there was a tendency towards a lower islet cell area ratio in Zn(opt)2-treated mice compared with nontreated KK-A(y) mice. Furthermore, plasma insulin concentrations were significantly reduced to 27.2% of insulin concentrations in nontreated KK-A(y) mice. These results suggest that Zn(opt)2 administration provides morphological and biochemical improvements in hyperinsulinaemia. In contrast, in mice that received Zn(glc)2 and VO(2+) complexes, the islet cell size and islet cell area ratio did not differ from those in nontreated controls. Zn(opt)2- and VO(opt)2-treated mice exhibited significantly lower fat deposition and fat deposition area ratio in the liver (63.6% and 65.8% of nontreated KK-A(y) mice, respectively) compared to those observed in nontreated KK-A(y) mice. The differences in morphological improvements of the pancreas and liver owing to Zn(opt)2 or VO(opt)2 treatment may be explained by differences in the sites of actions of Zn(2+) and VO(2+) complexes in different organs in KK-A(y) mice. In conclusion, Zn(opt)2 exhibited superior antidiabetic effects over those of VO(opt)2, and this was owing to greater amelioration of the morphological parameters of the liver and pancreas.
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Impaired Glucose Tolerance as a Disorder of Insulin Action
Stephen Lillioja, David M. Mott, Barbara V. Howard et al. · New England Journal of Medicine · 1988 · 582 citations
Medicine, Endocrinology, Physiology +15
General Survey of Diabetic Features of Yellow KK Mice
Hisashi Iwatsuka, Akio Shino, Ziro Suzuoki · Endocrinologia Japonica · 1970 · 271 citations · Full text
Medicine, Endocrinology, Physiology +17