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Promethion cages

Manufactured by Sable Systems
Sourced in United States

Promethion cages are a series of laboratory animal enclosures designed for housing small rodents, such as mice and rats, in a controlled environment. The cages provide a secure and regulated space for housing and monitoring these animals during scientific research and experiments.

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5 protocols using promethion cages

1

Comprehensive Locomotion Monitoring of Mice

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Total activity measurements of freely moving mice were made every 30 days after PLX dosing in Promethion cages (Sable Systems International). At each time point, mice were first randomized and placed individually in Promethion cages for 4 to 6 days. Real-time cage activity recording was continuous during the entire session using a combination of a running wheel with sensors to measure speed and distance traveled, three balances to measure body weight, food and water consumption, and a matrix of infrared light beams to measure XYZ movements with 0.25 cm resolution. Analysis of these metrics was used to detect behaviors such as sleep, rearing and general locomotion. For each mouse, data used for analyses were average readings per light or dark cycle. Data from the first circadian cycle were excluded due to variable behavior during habituation. To calculate the activity scores, wheel use, locomotion and rearing were first normalized to a 0–1 scale by the maximum value in the whole dataset, and then the geometric mean of the normalized values for each session was calculated.
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2

Metabolic Effects of NanoSOD in Mice

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A separate set of mice were used for energy expenditure and, intraperitoneal insulin (ITT) and glucose tolerance tests (GTT). Because of the short duration of the treatment, we measured energy expenditure after 2 or 4 injections, ITT after 5 injections, and GTT after 7 injections of NanoSOD. For energy expenditure studies, mice were acclimatized for 2 days and housed individually in Promethion cages (Sable Systems Int). We recorded VO2, VCO2, and food intake for 36 h. Measurements for 12 h light and 12 h dark cycles are reported separately. For ITT and GTT, mice were fasted for 5 h and injected (i.p.) with insulin (0.75 units/kg body weight) and glucose (1g/kg body weight), respectively. Changes in blood glucose levels were recorded at various time points.
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3

Urinary Albumin-Creatinine Ratio in Rats

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The rats in each group were fed in the promethion cages (Sable Systems International, USA), and 24 h urine was collected 4 weeks later. After the total amount of urine was determined, 3 mL of urine was centrifuged at 3,000 rpm for 10 min at 4°C, and the supernatant was taken. The 24 h microalbumin (mALB) in urine was detected using an automatic biochemical analyzer (Olympus, Japan) to calculate the urinary albumin/creatinine ratio (ACR).
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4

Body Composition Analysis of Transgenic Mice

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Posterior subcutaneous fat pads and epididymal fat pads were excised, weighed and expressed as % body weight. Body composition analyses and indirect calorimetry were performed using Promethion cages (Sable Systems International) at the Vanderbilt Mouse Metabolic Phenotyping Center by monitoring 30-week-old K14-VEGF-C and WT controls for 2 weeks in single housed cages.
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5

Automated Monitoring of Mouse Behaviors

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Total activity measurements of freely moving mice were made every 30 days after PLX dosing in Promethion cages (Sable Systems International). At each time point, mice were first randomized and placed individually in Promethion cages for 4 to 6 days. Real-time cage activity recording was continuous during the entire session using a combination of a running wheel with sensors to measure speed and distance traveled, three balances to measure body weight, food and water consumption, and a matrix of infrared light beams to measure XYZ movements with 0.25 cm resolution. Analysis of these metrics was used to detect behaviors such as sleep, rearing and general locomotion. For each mouse, data used for analyses were average readings per light or dark cycle. Data from the first circadian cycle were excluded due to variable behavior during habituation. To calculate the activity scores, wheel use, locomotion and rearing were first normalized to a 0-1 scale by the maximum value in the whole dataset, and then the geometric mean of the normalized values for each session was calculated.
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