Human cerebrospinal fluid net flow enhanced by respiration during the awake state

Cerebrospinal fluid dynamics play a crucial role in maintaining brain homeostasis by delivering nutrients, transmitting immune signals, and clearing waste products. While cardiac activity primarily drives the pulsatile movement of cerebrospinal fluid, respiration has been shown to facilitate low-frequency oscillations and contribute to bulk flow. Recent studies suggest that enhancing respiratory function may be an effective intervention to modulate cerebrospinal fluid dynamics. This study included 20 individuals with long-term formal training in Seokmun Hoheup, a lower belly-centered breathing practice (mean ± SD age, 58.1 ± 17.3 years; 8 females), and 25 controls with no formal long-term breathing practice (mean ± SD age, 49.2 ± 20.2 years; 12 females). All underwent real-time velocity-encoding magnetic resonance imaging to assess cerebrospinal fluid movement at the foramen magnum and lateral ventricle during both regular breathing and deep breathing. Deep breathing enhances cerebrospinal fluid dynamics in both groups, increasing displacement and net flow, particularly at the foramen magnum. Seokmun Hoheup trained participants show greater cerebrospinal fluid movement than controls at both the foramen magnum and lateral ventricle. Even during regular breathing, trained participants show higher cerebrospinal fluid mean speed, displacement, and net flow. Among respiratory factors, inhale length and diaphragm displacement show the strongest correlations with cerebrospinal fluid movement. Respiration modulated cerebrospinal fluid dynamics through both mechanical enhancement of venous outflow and autonomic modulation of the heart, with mechanical effects predominating in the lateral ventricle and both pathways contributing to the foramen magnum. Our findings identify respiration in the awake state as a modifiable, noninvasive mechanism that influences involuntary functions such as cerebrospinal fluid dynamics and may have implications for cerebrospinal fluid-mediated brain homeostasis.