{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,31]],"date-time":"2026-03-31T09:47:40Z","timestamp":1774950460376,"version":"3.50.1"},"reference-count":23,"publisher":"American Physiological Society","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Heart and Circulatory Physiology"],"published-print":{"date-parts":[[2005,4]]},"abstract":"<jats:p>The oxygen transport capacity of phospholipid vesicles encapsulating purified Hb (HbV) produced with a Po<jats:sub>2<\/jats:sub>at which Hb is 50% saturated (P 50 ) of 8 (HbV<jats:sub>8<\/jats:sub>) and 29 mmHg (HbV<jats:sub>29<\/jats:sub>) was investigated in the hamster chamber window model by using microvascular measurements to determine oxygen delivery during extreme hemodilution. Two isovolemic hemodilution steps were performed with 5% recombinant albumin (rHSA) until Hct was 35% of baseline. Isovolemic exchange was continued using HbV suspended in rHSA solution to a total [Hb] of 5.7 g\/dl in blood. P<jats:sub>50<\/jats:sub>was modified by coencapsulating pyridoxal 5\u2032-phosphate. Final Hct was 11% for the HbV groups, with a plasma [Hb] of 2.1 \u00b1 0.1 g\/dl after exchange with HbV<jats:sub>8<\/jats:sub>or HbV<jats:sub>29<\/jats:sub>. A reference group was hemodiluted to Hct 11% with only rHSA. All groups showed stable blood pressure and heart rate. Arterial oxygen tensions were significantly higher than baseline for the HbV groups and the rHSA group and significantly lower for the HbV groups compared with the rHSA group. Blood pressure was significantly higher for the HbV<jats:sub>8<\/jats:sub>group compared with the HbV<jats:sub>29<\/jats:sub>group. Arteriolar and venular blood flows were significantly higher than baseline for the HbV groups. Microvascular oxygen delivery and extraction were similar for the HbV groups but lower for the rHSA group ( P &lt; 0.05). Venular and tissue Po<jats:sub>2<\/jats:sub>were statistically higher for the HbV<jats:sub>8<\/jats:sub>vs. the HbV<jats:sub>29<\/jats:sub>and rHSA groups ( P &lt; 0.05). Improved tissue Po<jats:sub>2<\/jats:sub>is obtained when red blood cells deliver oxygen in combination with a high- rather than low-affinity oxygen carrier.<\/jats:p>","DOI":"10.1152\/ajpheart.01004.2004","type":"journal-article","created":{"date-parts":[[2004,11,25]],"date-time":"2004-11-25T01:13:54Z","timestamp":1101345234000},"page":"H1885-H1892","source":"Crossref","is-referenced-by-count":42,"title":["Oxygen transport by low and normal oxygen affinity hemoglobin vesicles in extreme hemodilution"],"prefix":"10.1152","volume":"288","author":[{"given":"Pedro","family":"Cabrales","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiromi","family":"Sakai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amy G.","family":"Tsai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shinji","family":"Takeoka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eishun","family":"Tsuchida","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marcos","family":"Intaglietta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"24","reference":[{"key":"R1","unstructured":"Altman DGand Bland JM.Statistics notes: how to randomise.BMJ319: 703\u2013704,1999."},{"key":"R2","doi-asserted-by":"crossref","unstructured":"Baines ADand Drangova R.Does dopamine use several signal pathways to inhibit Na-Pi transport in OK cells?J Am Soc Nephrol9: 1604\u20131612, 1998.","DOI":"10.1681\/ASN.V991604"},{"key":"R3","doi-asserted-by":"publisher","DOI":"10.1152\/japplphysiol.00223.2003"},{"key":"R4","doi-asserted-by":"publisher","DOI":"10.1152\/ajpheart.00146.2004"},{"key":"R5","doi-asserted-by":"publisher","DOI":"10.1152\/ajpheart.01039.2003"},{"key":"R6","doi-asserted-by":"publisher","DOI":"10.1007\/BF01851841"},{"key":"R7","doi-asserted-by":"publisher","DOI":"10.1152\/jappl.1991.70.6.2656"},{"key":"R8","doi-asserted-by":"publisher","DOI":"10.1016\/0026-2862(75)90004-7"},{"key":"R9","doi-asserted-by":"publisher","DOI":"10.1016\/S0026-2862(02)00027-4"},{"key":"R10","doi-asserted-by":"publisher","DOI":"10.1152\/ajpheart.1986.250.6.H908"},{"key":"R11","doi-asserted-by":"publisher","DOI":"10.1016\/0026-2862(78)90009-2"},{"key":"R12","doi-asserted-by":"publisher","DOI":"10.1152\/ajpheart.2000.279.3.H908"},{"key":"R13","doi-asserted-by":"publisher","DOI":"10.1097\/01.CCM.0000109774.99665.22"},{"key":"R14","doi-asserted-by":"publisher","DOI":"10.1021\/bc990173h"},{"key":"R15","unstructured":"Sakai H, Tsai AG, Intaglietta M, and Tsuchida E.Hemoglobin encapsulation with polyethylene glycol-modified and unmodified vesicles: systemic and microvascular hemodynamics at 80% blood substitution. 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