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Bat 10

Manufactured by Physitemp
Sourced in United States

The BAT-10 is a digital thermometer designed for precise temperature measurement. It features a range of -20°C to 50°C with an accuracy of ±0.1°C. The device is powered by a 9V battery and is suitable for a variety of laboratory and industrial applications.

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7 protocols using bat 10

1

Anesthesia and Hemodynamic Monitoring in Rats

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Rats were anesthetized by intraperitoneal injection of medetomidine, midazolam, and butorphanol (0.15 mg/kg, 2.0 mg/kg, and 2.5 mg/kg, respectively). An additional third of the initial dose was injected upon limb extraction response to pain stimulation. Temperature was measured using a rectal probe (BAT-10, Physitemp Instruments Inc, Clifton, NJ) and maintained at 37°C with a heating pad. Polyethylene catheters (PE50, Natsume, Tokyo, Japan) were placed into the left femoral artery and vein for blood withdrawal/sampling and fluid administration, respectively. A Millar transducer catheter (SPR-320; AD Instruments, Bella Vista, NSW, Australia) was placed into the abdominal aorta from the right femoral artery for blood pressure monitoring. Electrocardiograms, heart rate, arterial blood pressure, and body temperature were continuously recorded using a polygraph (Powerlab System, LabChart; AD Instruments, Bella Vista, NSW, Australia).
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2

Core Body Temperature Measurement in Mice

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Core body temperature in conscious mice was recorded on a Physitemp BAT-10 digital thermometer after gentle insertion of a flexible rectal probe (Physitemp, Clifton, NJ).
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3

Measuring Core Body Temperature in Mice

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Core body temperature of WT and Il10−/− mice was measured at room temperature using rectal probe (BAT-10) purchased from Physitemp.
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4

Anesthesia and Instrumentation for Rat Hemodynamics

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Male Sprague–Dawley rats, weighing 280 to 320 g, 7–8 weeks old, were provided by the Animal Center of Jinling Hospital, Nanjing, China. All rats were housed in controlled room on a 12-h light–dark cycle and fed a standard laboratory diet. This study was approved by the Ethics Committee of Jinling Hospital and was performed in accordance with the guidelines for the use of experimental animals by the National Institutes of Health. For experiments, animals were fasted overnight except for free access to water. Animals were anesthetized with intraperitoneal injection of 2% sodium pentobarbital (50 mg/kg) and intubated tracheally with a 14-gauge cannula. Polyethylene catheters were inserted into the left femoral artery and vein and flushed intermittently with saline solution which containing 2.5 IU/ml bovine heparin. The arterial catheter line was connected to a pressure transducer (PT-100, Chengdu Taimeng Software Co.LTD, China) to measure mean aortic pressure (MAP) and the venous catheter was used for medical administration, and the electrocardiogram was recorded by subcutaneous needle electrodes. Core temperature was monitored by a rectal temperature probe (BAT-10, Physitemp Instruments Inc) throughout the experiment to ensure appropriate temperature management.
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5

Intraperitoneal Hyperthermia Protocol

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Intraperitoneal hyperthermia was induced by i.p. administration of 2 + 2 mL saline solution preheated in water bath to 43 °C and separated by 5 min [9 (link)]. Hyperthermia treatment (HT) was performed immediately before the i.p. application of CP. CP was administered intraperitoneally at dose of 5 or 10 mg kg−1. Systemic body temperature was determined before and during hyperthermia procedure using an electronic thermometer (BAT-10, Physitemp Instruments, Clifton, NJ, USA) with a rectal probe (RET-3, Physitemp Instruments, Clifton, NJ, USA). Intraperitoneal temperature was measured by the needle probe that was introduced to a depth of 1 cm into peritoneal cavity of mice treated with hyperthermia. Hyperthermia with applied procedure was well tolerated by the animals.
It is important to emphasize that during the heating phase, the intra-abdominal temperature was stable, ranging from 42.5–43 °C, whereas rectal temperature was not significantly affected. During the cooling phase, the temperature in the peritoneal cavity of treated mice decreased to normal values approximately 15 min after applying the hyperthermal procedure [11 (link),19 (link)].
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6

Metabolic Profiling Across Lifespan

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Metabolic parameters were evaluated across the lifespan as detailed here and in Figure 1A and 1B. Body weight and food intake per cage were recorded weekly in rats from the obesity and diabetes studies, from P21. Every 2 weeks body temperature was assessed in rats from the obesity and diabetes studies by inserting a thermocouple probe into the rectum (BAT-10, Physitemp, Clifton, NJ). Cumulative energy intake (kcal) was calculated as the difference in food weight divided by the number of rats that had access to it and the number of days they had access, and transformed to kcal [31 (link)].
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7

Optimized Langendorff Cardiac Cell Isolation

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Using the Langendorff apparatus (Fig. 2B), perfusate was maintained at 37°C by adjusting the water bath temperature and checking the outflow temperature at valve 2 using a thermometer probe (cat. #: BAT-10, Physitemp). Once the heart was mounted onto the apparatus, it was flushed of blood using a modified Krebs-Ringer solution (without Ca 2+ ) referred to as "perfusion" buffer and then perfused with "digestion" buffer that incorporates proteolytic enzymes (collagenase B, D, and protease XIV; buffer composition and recipe in Supplementary Table S2, S3). The conditions for efficient tissue digestion were optimised for neonatal through to adult hearts (<14 min), including flow rate, concentrations of proteolytic enzymes, and volumes of buffers (details in Table 1). After digestion, the atria were removed and the cardiac ventricles were collected in a petri dish containing transfer buffer (composition in Supplementary Table S2). The methods describing Langendorff perfusion and tissue digestion can be found in the Supplementary methods online.
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