During all surgical procedures, mice were maintained at the body temperature of 37°C.
An anaesthetized rat (with 1.5 2.5 % isoflurane) was immobilized in a multimodal animal carrier unit (MACU; medres® medical research GmbH, Cologne, Germany) and maintained at a body temperature of 37 °C throughout the whole experiment.
Here, the experimenter asked the participant to place the right hand including the wrist into a tub of warm water, which was maintained at normal body temperature (35 37° Celsius), and to keep the computer screen in view.
Seven of the endotoxic mice were maintained at their original body temperature post-LPS injection, while eight were maintained at 37°C using a homeothermic heating mat.
The expired CO2 was maintained at 3.3 4.0%, body temperature at 37 38°C, and heart rate was constantly monitored.
Six melatonin implants were individually immersed in 1 mL physiological buffer maintained at 37°C (shrews' body temperature), and renewed every day for 130 days.
Twelve to fourteen days following the end of the exercise period, rats (Naïve, n = 8; DMSO, n = 7; LY294002, n = 8) were anesthetized with urethane carbamate (1.5 mg/kg), placed in a stereotaxic frame, and maintained at a constant body temperature of 37°C.
The dose was maintained at 0.1 ml/100 g body mass for each successive imaging session.
In contrast, in endotoxemic animals, which were maintained at a core body temperature of 37°C, thrombus formation was markedly accelerated, as indicated by significantly reduced arteriolar and venular occlusion times of 255 ± 35 s and 238 ± 58 s, respectively.
