Ketone Monoester and Blood Pressure

The goal of this clinical trial is to determine the effect of acute consumption of a ketone monoester supplement in healthy male adults. The main questions it aims to answer are: * To determine if acute consumption of a ketone monoester supplement modulates diurnal (measured in lab) and nocturnal blood pressure (assessed by ambulatory blood pressure monitoring; ABPM) compared to a taste-matched placebo. The investigators hypothesize that a ketone monoester supplement will acutely decrease systolic and diastolic blood pressure compared to the placebo. The same results are expected for diurnal and nocturnal blood pressure. * To determine if acute consumption of a ketone monoester supplement improves glucose control measured with continuous glucose monitoring (CGM) following a standardized meal consumed 90 minutes after ingestion of the ketone supplement. The investigators hypothesize that a ketone monoester supplement, consumed 90 minutes before a meal, will decrease the 2-hour postprandial glucose incremental area under the curve (iAUC) and peak glucose compared to a placebo. * To assess IL-10's ability to inhibit proinflammatory cytokine production (TNF- α and IL-1β) in LPS-stimulated whole blood cultures following the ingestion of β-OHB and placebo. The investigators hypothesize that β-OHB will augment the ability of IL-10 to inhibit TNF-α and IL-1β production compared to placebo. Using a double-blind placebo-controlled randomized crossover study design, 15 adults will participate in two experimental conditions. Participants will be recruited using a local recruitment database (Nabû), during presentations in community organizations, with posters at the University of Sherbrooke and from word of mouth. Following screening, eligible participants will be invited for one baseline and two experimental conditions at the Research Centre on Aging (CdRV). During the baseline visit, the following assessments and tests will be conducted: 1) resting heart rate (HR) and blood pressure; 2) anthropometry and body composition; 3) medical history and questionnaires on physical activity levels, dietary habits and anxiety symptoms; 4) explanation of the dietary and physical activity logs; 5) installation of accelerometers to control physical activity levels and sedentary behaviours over 10 days and CGM to assess glucose control over the subsequent 10 consecutive days. Informed consent will be obtained from all participants involved in the study before participating in any assessments or tests. The participant will then be invited to our lab for two non-consecutive days for the experimental condition (at least 48 hours apart). The first visit will take place at the CdRV (Sherbrooke, QC) on a Thursday or Friday morning. Once the informed consent has been obtained, a medical history and a physical activity questionnaire (International Physical Activity Questionnaire) will be completed by the participant. Body weight, height, and waist circumference will then be measured using standardized procedures. Body composition will be assessed using Dual Energy X-ray absorptiometry (DXA). A CGM will be installed at the abdominal region by the participant himself with the supervision of an experienced exercise physiologist. To limit compensatory behaviours in response to observed blood glucose levels, CGM will be blinded to participants. Finally, participants will be outfitted with a thigh-worn activPAL4 and a hip-worn ActiGraph wGT3X-BT accelerometer to wear for the following 10 days. Wearing the accelerometers will allow for comparing physical activity levels and sedentary behaviours on the days before and after each condition. To ensure that both accelerometers provide reliable data, standardized tests will be performed in our laboratory during the baseline condition. While wearing the activPAL4 and ActiGraph, participants will walk on the treadmill (Life Fitness, Club Series, FlexDeck®; Rosemont, IL, USA) at 3.0, 5.0 and 7.0 km/h for 6 minutes at each intensity. Participants will also have to be in a seated, recline and lying position for 5 minutes each and perform non-ambulatory tasks (washing dishes - 6 minutes and setting the table - 3 minutes). All participants will wear the Xsens motion system during these tasks to capture movement and inform us of the activity profile for better data analysis. During the week following the baseline visit, participants will be invited to the CdRV for the first experimental condition (duration = 240 minutes). Participants will come to the lab in a fasted state (at least 12-hour overnight) to the lab at 8:00 am where resting blood pressure will be measured in a standardized manner. HR will be continuously monitored for the duration of the visit in the lab (from 8:00 am to 12:00 pm) using a heart rate monitor (Polar H10, Kempele, Finland). At 8:20 am, blood samples will be collected by a certified research nurse. A total of 35 mL of blood will be collected in EDTA tubes for whole blood culture and CPT sodium heparin tubes for PBMC isolation and subsequent transcriptomic analyses. Capillary β-OHB levels will be measured using the Abbot Freestyle Precision Neo® ketone meter before the ingestion of the ketone monoester supplement drink or the taste-matched placebo. At 8:30 am participants will be allowed 2 minutes to consume the oral ketone supplement or placebo drink (liquid form; \~80 - 120 mL depending on to the participant's body weight). β-OHB concentration will then be measured at 30, 60, and 90 minutes after ingestion (\~9:00, 9:30, and 10:00 am). Participants will remain seated for 90 minutes following ingestion of the ketone supplement while standardized blood pressure measures will be performed every 20 minutes. At 9:30 am (i.e., 60 minutes after β-OHB ingestion), another blood sample collection will be done (25 mL). Five minutes after the blood sample collection, and right before the blood pressure challenge (i.e., cold pressor test), resting blood pressure and HR will be measured. The cold pressor test will allow the evaluation of the vascular response following an external stressor in a controlled setting, which can occur in everyday life, following the consumption of β-OHB. Ninety minutes after ketone or placebo ingestion, participants will consume a standardized breakfast consisting of a meal replacement drink, granola bars, and orange juice, which is representative of a realistic mixed meal (MMTT) and provides 490 kcal (68g CHO, 12g FAT, 29g PRO; 55%, 22%, and 23% respectively). Participants will then remain seated for 120 minutes after the MMTT to assess glucose response (CGM) in the postprandial state, and blood pressure will be measured every 20 minutes. Additionally, participants will be asked to complete visual analog scales assessing gastrointestinal (GI) discomfort at -10, 0, 30, 60 and 90 minutes after ketone supplement consumption to monitor for GI distress. Participants will also be asked to complete visual analog scales for hunger and fullness at -10, 0, 60 and 90 minutes after the standardized meal. At 12:00 pm, participants will then be outfitted with the ABPM (IEM PWA Mobil-o-graph; I.E.M. GmbH, Germany) on the non-dominant arm with the appropriate cuff size as suggested by the manufacturer. Participants will also receive instructions on how to fill the logbook, which asks participants to record bedtime hours, physical activity, and sleep quality (assessed via a visual analogue scale). Nutritional intake will be estimated by using the Keenoa app. Another ketone supplement or placebo drink will be provided to consume directly before going to bed. Participants will be asked to refrain from structured exercise, alcohol, and caffeine consumption, limit physical activity to their activities of daily living on the day before and during each trial, and replicate their dietary intake 24 hours before and 24 hours after both experimental visits. Furthermore, participants will also be asked to refrain from taking any medications that could affect glucose metabolism or blood pressure and any short-term analgesics (acetaminophen, ibuprofen, etc.). While being conducted in free-living settings, standardizing the experimental conditions as outlined above will allow for controlling any potentially confounding factors between both conditions that could affect our variables of interest and therefore improve measurement rigour. Forty-eight hours later, participants will complete the same experimental condition with the alternate supplement (ketone or placebo) according to their randomization.