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Cerebral O(2) and CO(2) transport in isovolumic haemodilution: Compensation of cerebral delivery of O(2) and maintenance of cerebrovascular reactivity to CO(2)

This study investigated the influence of acute reductions in arterial O(2) content (CaO(2)) via isovolumic haemodilution on global cerebral blood flow (gCBF) and cerebrovascular CO(2) reactivity (CVR) in 11 healthy males (age; 28 ± 7 years: body mass index; 23 ± 2 kg/m(2)). Radial artery and interna...

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Detalles Bibliográficos
Autores principales: Carr, Jay MJR, Ainslie, Philip N, MacLeod, David B, Tremblay, Joshua C, Nowak-Flück, Daniela, Howe, Connor A, Stembridge, Mike, Patrician, Alexander, Coombs, Geoff B, Stacey, Benjamin S, Bailey, Damian M, Green, Daniel J, Hoiland, Ryan L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875354/
https://www.ncbi.nlm.nih.gov/pubmed/36131560
http://dx.doi.org/10.1177/0271678X221119442
Descripción
Sumario:This study investigated the influence of acute reductions in arterial O(2) content (CaO(2)) via isovolumic haemodilution on global cerebral blood flow (gCBF) and cerebrovascular CO(2) reactivity (CVR) in 11 healthy males (age; 28 ± 7 years: body mass index; 23 ± 2 kg/m(2)). Radial artery and internal jugular vein catheters provided measurement of blood pressure and gases, quantification of cerebral metabolism, cerebral CO(2) washout, and trans-cerebral nitrite exchange (ozone based chemiluminescence). Prior to and following haemodilution, the partial pressure of arterial CO(2) (PaCO(2)) was elevated with dynamic end-tidal forcing while gCBF was measured with duplex ultrasound. CVR was determined as the slope of the gCBF response and PaCO(2). Replacement of ∼20% of blood volume with an equal volume of 5% human serum albumin (Alburex® 5%) reduced haemoglobin (13.8 ± 0.8 vs. 11.3 ± 0.6 g/dL; P < 0.001) and CaO(2) (18.9 ± 1.0 vs 15.0 ± 0.8 mL/dL P < 0.001), elevated gCBF (+18 ± 11%; P = 0.002), preserved cerebral oxygen delivery (P = 0.49), and elevated CO(2) washout (+11%; P = 0.01). The net cerebral uptake of nitrite (11.6 ± 14.0 nmol/min; P = 0.027) at baseline was abolished following haemodilution (−3.6 ± 17.9 nmol/min; P = 0.54), perhaps underpinning the conservation of CVR (61.7 ± 19.0 vs. 69.0 ± 19.2 mL/min/mmHg; P = 0.23). These findings demonstrate that the cerebrovascular responses to acute anaemia in healthy humans are sufficient to support the maintenance of CVR.