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Rubio, W. B.

Publications and source records attributed to Rubio, W. B..

2 recordsLinked to original sources

Metabolic responses to physiological stressors assessed using continuous glucose monitoring integrated with indirect calorimetry in mice

Continuous glucose monitoring (CGM) in rodents has provided unprecedented temporal resolution of glycemic dynamics in vivo. Even in the absence of deliberate perturbation, glucose levels in mice are dynamic, fluctuating in response to the timing and duration of feeding events, changes in neurological and hormonal states, physical activity, and photoperiod. To obtain a comprehensive view of metabolic adaptations under common experimental conditions, we monitored freely moving mice simultaneously using CGM and indirect calorimetry to quantify glucose, food intake, physical activity and metabolic rate. We characterized glycemic and metabolic responses to routine laboratory interventions, including short-term and overnight fasting, refeeding, tail blood sampling during glucose tolerance tests, changes in ambient temperature to cold or thermoneutral conditions, and access to running wheels. We found that food removal induced a robust, transient stress response characterized by increased blood glucose, body temperature, energy expenditure, and physical activity. However, prolonged fasting ultimately led to hypoglycemia and torpor. The magnitude and variability of glycemic responses to insulin tolerance tests were strongly influenced by fasting duration, and tail-tip blood collection itself elicited substantial hyperglycemia. In contrast to prolonged fasting, refeeding produced relatively modest and transient effects on glucose and energy expenditure. Cold exposure elicited increased energy expenditure along with a sustained hyperglycemic response. Voluntary wheel running induced transient increases in glucose and metabolic activity and promoted a shift toward increased fatty acid oxidation. Together, these findings demonstrate that common laboratory manipulations exert dynamic, often substantial effects on glycemia and whole-body metabolism that are readily revealed by CGM and indirect calorimetry.

physiology↗

Microbial metabolism of mannitol as a tracer for the non-invasive measurement of oral-cecal transit

The timing of digestion after a meal reveals information essential for evaluating gastrointestinal function and overall digestive health. Alterations in transit time through the GI tract can reveal abnormalities such as delayed gastric emptying and provide critical insights into nutrient absorption dynamics. This information is particularly valuable for optimizing dietary interventions, managing metabolic conditions such as diabetes, and improving personalized nutrition strategies. Methods for measuring the oral to cecal transit time (OCTT) in murine models have significant limitations. We demonstrate a non-invasive approach in freely-moving non-anesthetized mice which quantifies the microbial digestion of the non-nutritive sweetener mannitol to CO2. We monitor cage air for the production of 13CO2 from 13C-enriched mannitol using Off-Axis Integrated Cavity Output Spectroscopy integrated with multiplexes indirect calorimetry. With this approach, we find mannitol oxidation is absent in mice following commensal depletion of the microbiota. In mice with conventional microbiota, the peak 13C-mannitol oxidation occurs proximal to the mouse cecum, allowing the quantitation of OCTT in mice. By tracking the output of 13CO2, this method provides highly granular, real-time data. We detect delayed OCTT with the use of pharmacological transit-altering compounds loperamide, a gut restricted opioid receptor agonist and also semaglutide, a GLP-1 receptor agonist. This approach may provide more physiologically relevant results in a range of genetic, environmental, and pharmacological research models.

physiology↗