ArticleEuropean journal of applied physiology2026
The impact of mild hypohydration and sex on the cardiovascular responses to progressive lower-body negative pressure.
Article in European journal of applied physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
The arterial baroreflex maintains blood pressure during mild-to-moderate orthostatic stress, but the roles of hydration status and sex in this response are unclear. This study used progressive lower-body negative pressure (LBNP) to examine how both fluid restriction and sex influence blood pressure regulation during central hypovolemia. Twenty-eight healthy young adults (15 females) completed two visits, in a counterbalanced order: 24-hr fluid restriction (hypohydrated) or 24-hr ad libitum fluid intake (euhydrated). Hydration status was assessed by changes in body mass and urine specific gravity. Beat-by-beat blood pressure, heart rate, stroke volume, and cardiac output were measured during progressive LBNP to presyncope, defined as systolic blood pressure < 90 mmHg for three consecutive cardiac cycles. 24-hr fluid restriction reduced body mass (Δ - 1.27 ± 0.70 kg; p < 0.01) and elevated urine specific gravity (Δ + 0.013; p < 0.01), confirming that participants were mildly hypohydrated after 24-hr of fluid restriction. Mild hypohydration did not affect tolerance time to presyncope (p = 0.48), blood pressure (all p > 0.39), stroke volume (p = 0.87), or cardiac output (p = 0.21), but heart rate was borderline elevated during LBNP when hypohydrated (p = 0.051). Females exhibited lower tolerance to LBNP than males (12.8 ± 4.2 min vs. 16.7 ± 5.7 min; p = 0.037), and a distinct cardiac response, characterized by a higher heart rate (~ 4.3 bpm) and a greater reduction in stroke volume (~ 2.6 mL) during LBNP (both p < 0.01). However, no significant interactions were observed between sex and hydration status for any cardiovascular responses to LBNP (all p > 0.05). These data indicate that sex and hydration status influence cardiac function in response to LBNP.
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