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Glucocard x meter

Manufactured by Arkray
Sourced in Japan

The Glucocard X-meter is a portable blood glucose monitoring device manufactured by Arkray. The device is designed to measure blood glucose levels.

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6 protocols using glucocard x meter

1

Telmisartan Attenuates Diabetic Complications

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Rats were randomly assigned to three groups: control (n = 10), untreated diabetic (n = 15), and telmisartan-treated diabetic (n = 15) group. Intraperitoneal injection of streptozotocin (STZ) 65 mg/kg (Sigma-Aldrich, St. Louis, MO, USA), freshly dissolved in 0.9% saline, was used to induce diabetes. After 48 hours, blood glucose was measured in samples taken from the tail vein, using a glucometer (Glucocard X-meter, Arkray Inc., Japan). Rats were considered diabetic if the blood glucose was >15 mmol/L. Treatment with telmisartan (Boehringer Ingelheim International GmbH, Germany) was started immediately after confirmation of diabetes. telmisartan (10 mg/kg per day) was administered by gavage, dissolved in drinking water, for 10 weeks. telmisartan was stopped one day prior to measurement of the haemodynamic parameters. Weekly, body weights were recorded for all groups and glycosuria was assessed with reagent strips (Combur Test, Roche, Germany) to exclude ketosis in rats with diabetes.
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2

Comprehensive Metabolic Assessment in Mice

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The activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in serum were determined with an Express Plus Biochemistry analyzer (Chiron Diagnostics, Emeryville, CA). Hepatic lipids were extracted as described by Folch et al.32 (link) using a chloroform-methanol mixture (2:1 v/v), and the dried lipid residues were dissolved in 2 ml ethanol. The concentrations of cholesterol, triglycerides, and free fatty acids in the hepatic lipid extracts were measured using commercial kits (Bio-Clinical System, Korea). Blood insulin levels were assayed using ELISA kits (American Laboratory Products Company, Salem, NH). Blood glucose levels were determined by a Glucocard X-Meter (Arkray, Kyoto, Japan). To perform an intraperitoneal glucose tolerance test (IPGTT), glucose solutions (2 g/kg) were administered via intraperitoneal injection to mice after 12-hr fasting. Blood glucose levels were measured at 0, 15, 30, 60, 90, and 120 min after the glucose challenge.
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3

Insulin Resistance Assessment in Mice

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Fasting blood glucose level, serum insulin concentration, and HOMA-IR score

Fasting glucose concentration was directly evaluated using the GlucoCard X-Meter (Arkray, Kyoto, Japan). Serum insulin levels were measured using the Insulin Mouse ELISA kit (80-INSMS-E01, ALPCO, Salem, NH). The Homeostatic Model Assessment-Insulin Resistance (HOMA-IR) score, which is called the homeostasis model assessment of insulin resistance, was calculated using fasting blood glucose and insulin concentrations. HOMAIRscore=fasting blood glucosemmol/L×serum insulinpmol/L/22.5

Oral glucose tolerance tests

After 10 weeks of consuming the experimental diet, according to their respective groups, oral glucose tolerance tests (OGTTs) were performed. All mice were fasted overnight and then provided with 2 g/kg d-glucose solution. Whole blood was collected from the caudal vein, and blood sugar level was measured using a glucose monitoring device (Arkray, Kyoto, Japan) immediately after treatment at 0, 30, 60, 90, and 120 min.
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4

Xenogeneic Islet Transplantation in Diabetic Mice

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The Seoul National University (SNU) designated pathogen free (DPF) pigs aged at least 6 months were used as xenogenic islet donors [22 (link)]. Male alpha 1, 3-galactosyltransferase knock-out mice (GalT KO) aged 7 to 12 weeks (kindly provide from Prof. Chung-Gyu Park, SNU) were used as recipients. Type 1 diabetes was confirmed with a portable glucometer (GLUCOCARD X-METER, Arkray, Kyoto, Japan); if random blood glucose levels from the tail vein exceeded 300 mg/dL for three consecutive days after intraperitoneal one-shot injection of 200 mg/kg dose of streptozotocin (STZ, Sigma-Aldrich, St. Louis, MO, USA; freshly dissolved in 0.01 M citric acid buffer, pH 4.5), the diagnosis of type 1 diabetes was made. The GalT KO mice were maintained at a constant temperature in a cycle of 12 hours of light followed by 12 hours of dark and provided with laboratory chow and water. All of surgical interventions and presurgical and postsurgical animal care were provided in accordance with the Laboratory Animals Welfare Act, the Guide for the Care and Use of Laboratory Animals and the Guidelines and Policies for Rodent Survival Surgery provided by the IACUC (Institutional Animal Care and Use Committee) in College of Medicine, The Catholic University of Korea (approval number: CUMS-2014-0105-02).
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5

Body Weight, Food Intake, and Glucose Homeostasis Analyses

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Body weights were monitored using a precision scale. For feeding studies, mice were singly-housed and acclimatized for 1 week prior to study. Daily food intake was manually measured for 5 consecutive days using a precision scale. Blood samples were collected via tail vein using a capillary collection system with EDTA (Sarstedt). Blood glucose concentration was measured using a glucometer (Glucocard X-meter, Arkray). Glucose tolerance tests (2 g/Kg) were performed on overnight (16 hour) fasted mice. Insulin sensitivity tests (0.2 IU/Kg; Humulin, Lilly) were conducted on 6-hour food-deprived mice.
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6

Oral Glucose Tolerance Assay in Rats

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An oral glucose tolerance test (OGTT) was performed after 16 h fasting. Rats received an oral administration of glucose solution (2 g/kg body weight) by stomach gavage. Blood glucose levels were measured at 0, 15, 30, 60, 90, and 120 min after the glucose challenge, using a Glucocard X-Meter (Arkray, Kyoto, Japan). The area under the curve (AUC) was calculated and the difference (ΔAUC) was reported.
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