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Abstract 213: Differential Effects of Nanoformulated Copper/zinc Superoxide Dismutase in Regulating Fasting Blood Glucose Levels in Mice Fed a Low versus High Fat Diet

Authors :
Devika S. Manickam
Cyrus Desouza
Alexander V. Kabanov
Curtis Perriotte-Olson
Gopalakrishnan Natarajan
Saraswathi Viswanathan
Source :
Arteriosclerosis, Thrombosis, and Vascular Biology. 36
Publication Year :
2016
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2016.

Abstract

We previously reported that nanoformulated copper/zinc superoxide dismutase (nanoSOD) ameliorates adipose tissue inflammation without altering systemic glucose homeostasis in a mouse model of diet-induced obesity. A recent report showed that mice lacking SOD1 exhibit insulin resistance only upon low fat (chow) but not high fat (HF)-diet feeding suggesting that the effect of nanoSOD in modulating systemic glucose levels may depend on the diet type. The objective of this study is to determine the effectiveness of nanoSOD in altering muscle gene expression and/or systemic glucose handling in mice fed a low versus high fat (HF) diet. Six-eight wk old wild type C57BL/6 mice were fed a low fat chow diet (CD) or a HF fat (45%) for 10 wk. The mice were injected with nanoSOD (1000 units/kg body wt.) once in two days for fifteen days. The fasting blood glucose level was significantly reduced in CD+NanoSOD-treated mice compared to CD control ( P . Insulin tolerance test revealed that nanoSOD-treated mice showed improved glucose handling in response to insulin in CD but not in HF diet-fed mice. The muscle mRNA expression of LPL , a gene involved in fatty acid uptake, was significantly increased ( P ACOX-1 , a fatty acid oxidation gene, showed a trend towards an increase ( P ACOX1, CPT1a , and CPT2 were significantly down-regulated in CD+nanoSOD treated mice. Moreover, the expression of FASN ( P SREBP1 ( P PCX which promotes both gluconeogenesis and lipogenesis was significantly reduced ( P

Details

ISSN :
15244636 and 10795642
Volume :
36
Database :
OpenAIRE
Journal :
Arteriosclerosis, Thrombosis, and Vascular Biology
Accession number :
edsair.doi...........fa00d43661eea3f9d809bf1e7e383ada
Full Text :
https://doi.org/10.1161/atvb.36.suppl_1.213