Key result
Acute ketone monoester ingestion fails to alter resting heart rate, blood pressure, or sympathetic activity.
Why the study?
Exogenous ketone supplementation can impact cardiovascular regulation, but the effects on muscle sympathetic nerve activity remain unknown.
Does acute oral ketone monoester ingestion modulate heart rate, blood pressure, and muscle sympathetic nerve activity at rest or during stress in healthy adults?
RCT (n=19)
Double-blind
Randomized
No
Does acute oral ketone monoester ingestion modulate heart rate, blood pressure, and muscle sympathetic nerve activity at rest or during stress in healthy adults?
Absolute Event Rate: 72.6% vs 69.6%
p-value: p=0.30
Acute ingestion of a moderate dose of ketone monoester does not significantly alter neuro-cardiovascular regulation at rest or during mental and physical stress in healthy young adults.
Acute ketone monoester leaves neuro-cardiovascular parameters unchanged at rest and during stress; challenges prior reports of altered regulation by exogenous ketones.
Exogenous ketone supplementation can impact cardiovascular regulation, but the effects on muscle sympathetic nerve activity (MSNA) remain unknown. In a randomized, crossover, double-blind design, 19 participants (23 ± 4 years.; female: n = 9) ingested an oral ketone monoester (KME; 0.4 g/kg) or isocaloric, isovolumetric placebo. Blood pressure, heart rate, brachial artery blood flow, and MSNA (microneurography; n = 14) were assessed at rest before and after ingestion and during two laboratory stressors: 2-min static handgrip exercise and 2-min of mental arithmetic. Capillary β-hydroxybutyrate increased 20 and 40 min post KME ingestion versus placebo (both, p < 0.001). Compared to placebo, KME had no effects on resting mean arterial pressure (Placebo: 78.3 ± 9.3 to 80.2 ± 10.5 mmHg; KME: 76.3 ± 8.3 to 79.5 ± 8.8 mmHg; interaction p = 0.32), heart rate (Placebo: 64.6 ± 12.3 to 69.6 ± 11.0 bpm; KME: 65.3 ± 10.6 to 72.6 ± 11.3 bpm; interaction p = 0.30), or MSNA burst frequency (Placebo: 17.7 ± 7.3 to 17.7 ± 6.7 bursts/minute; KME: 17.5 ± 6.1 to 18.2 ± 7.0 bursts/minute; interaction p = 0.72). Resting brachial artery blood flow and vascular conductance changed over time but did not differ between conditions (interactions, both p > 0.40). Neuro-cardiovascular responses during exercise (interactions, all p > 0.72) or mental stress (interactions, all p > 0.44) did not differ between conditions. Compared to placebo, acute KME ingestion did not modulate neuro-cardiovascular measures at rest or during stress in healthy young adults.
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Nardone et al. (2025) conducted an RCT in Healthy adults (n=19). Ketone monoester (KME) vs. Isocaloric, isovolumetric placebo was evaluated on Resting heart rate (bpm) post-ingestion (p=0.30). Compared to placebo, acute ingestion of a ketone monoester did not significantly alter resting heart rate, blood pressure, or muscle sympathetic nerve activity in healthy young adults.
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