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Freestyle blood glucose monitoring system

Manufactured by Abbott

The FreeStyle blood glucose monitoring system is a compact, portable device designed to measure and display the user's blood glucose levels. It utilizes test strips and a small sample of blood to provide accurate readings. The core function of this product is to enable individuals to conveniently monitor their blood glucose levels.

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2 protocols using freestyle blood glucose monitoring system

1

Assessing Diabetes Onset and Insulitis

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The clinical onset of diabetes was determined by the presence of glucose in the urine and elevated capillary blood glucose concentrations. Urine test strips were used to monitor glycosuria, and capillary tail blood glucose levels were measured with a FreeStyle blood glucose monitoring system (Abbott Laboratories, Chicago). Ad-lib fed mice were considered diabetic after 2 consecutive blood glucose values greater than 250 mg/dL obtained in the morning around 10am. For glucose tolerance testing, mice were fasted for 6 hours, and glucose was administered intraperitoneally (1 mg/g body weight); capillary glucose from tail vein was measured before injection, and at 10, 20, 30, 60, 90, and 120 mins post administration.
To score insulitis, pancreata were fixed in 4% formaldehyde solution, dehydrated, and embedded into paraffin; 5 μm sections were stained with H&E and scored for severity of insulitis.
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2

Inducing Diabetic Embryopathy in Mice

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All procedures for animal use were approved by the Institutional Animal Care and Use Committee of University of Maryland School of Medicine. Eight-week old wild-type (WT) female mice were intravenously injected daily with 75 mg/kg STZ over two days to induce diabetes. Blood glucose levels were monitored daily by tail vein puncture and using FreeStyle Blood Glucose Monitoring System (TheraSense, Abbot, Alameda, CA). Mice were considered as having diabetes when their blood glucose levels were greater than or equal to 14 mM. Insulin pellets were then subcutaneously implanted in diabetic mice to restore euglycemia prior to mating to protect early embryonic formation and implantation. Mice were then mated with SOD1-Tg male mice at 3:00 PM to generate WT and SOD1-overexpressing embryos.
Embryonic day 0.5 (E0.5) was designated once the vaginal plug was present on the next morning. On E5.5, insulin pellets were removed to permit frank hyperglycemia (>14mM glucose levels), and exposure of the developing embryos to a hyperglycemic conditions from E7 to E12, which is critical period for early heart development. WT, non-diabetic female mice injected with vehicle and sham operated on for insulin pellet implantation served as non-diabetic controls. On E12.5, mice were euthanized, and embryonic hearts were dissected out of the embryos for analysis.
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