Immediate effects of systemic administration of normal and high O2-affinity haemoglobin vesicles as a transfusion alternative in a rat pneumonectomy model. Issue 1 (10th June 2020)
- Record Type:
- Journal Article
- Title:
- Immediate effects of systemic administration of normal and high O2-affinity haemoglobin vesicles as a transfusion alternative in a rat pneumonectomy model. Issue 1 (10th June 2020)
- Main Title:
- Immediate effects of systemic administration of normal and high O2-affinity haemoglobin vesicles as a transfusion alternative in a rat pneumonectomy model
- Authors:
- Hashimoto, Ryo
Kohno, Mitsutomo
Oiwa, Kana
Onozawa, Hiroto
Watanabe, Masazumi
Horinouchi, Hirohisa
Sakai, Hiromi
Kobayashi, Koichi
Iwazaki, Masayuki - Abstract:
- Abstract : Background: Haemoglobin vesicles (HbVs) are red blood cell (RBC) substitutes with a phospholipid bilayer membrane and a polyethylene modified surface (diameter=250 nm; P50 =28 Torr). They can be preserved for years and can be used in patients of all blood types without the risk of infection. Their oxygen affinity can be modified by changing the allosteric effectors. Methods: Left pneumonectomy was performed under mechanical ventilation on rats, followed by rapid exsanguination of ~30% of the total circulating blood volume. Rat RBCs shed in 5% human serum albumin (HSA) solution (rat RBC), HbV with high oxygen affinity in 5% albumin solution (low-P50 HbV, P50 =9 Torr), normal HbV suspended in 5% albumin (HbV, P50 =28 Torr) or 5% HSA was infused for resuscitation. Haemodynamics and oxygenation were evaluated. Results: Systemic arterial blood pressure significantly decreased after exsanguination and increased after each infusion. In the HbV, low-P50 HbV and rat RBC groups, all rats were liberated from mechanical ventilation and blood pressure was stabilised, whereas 50% of the rats in the HSA group died within 1 hour after weaning from mechanical ventilation. The PaO2 in arterial blood for 1 hour after liberation from mechanical ventilation in the rat RBC, HbV and low-P50 HbV groups was 59.4±12.5, 58.3±10.1 and 70.5±14.5 mm Hg, respectively. The PaO2 in the low-P50 HbV group was significantly higher than those in the rat RBC and HbV groups (p=0.05 for both). SerumAbstract : Background: Haemoglobin vesicles (HbVs) are red blood cell (RBC) substitutes with a phospholipid bilayer membrane and a polyethylene modified surface (diameter=250 nm; P50 =28 Torr). They can be preserved for years and can be used in patients of all blood types without the risk of infection. Their oxygen affinity can be modified by changing the allosteric effectors. Methods: Left pneumonectomy was performed under mechanical ventilation on rats, followed by rapid exsanguination of ~30% of the total circulating blood volume. Rat RBCs shed in 5% human serum albumin (HSA) solution (rat RBC), HbV with high oxygen affinity in 5% albumin solution (low-P50 HbV, P50 =9 Torr), normal HbV suspended in 5% albumin (HbV, P50 =28 Torr) or 5% HSA was infused for resuscitation. Haemodynamics and oxygenation were evaluated. Results: Systemic arterial blood pressure significantly decreased after exsanguination and increased after each infusion. In the HbV, low-P50 HbV and rat RBC groups, all rats were liberated from mechanical ventilation and blood pressure was stabilised, whereas 50% of the rats in the HSA group died within 1 hour after weaning from mechanical ventilation. The PaO2 in arterial blood for 1 hour after liberation from mechanical ventilation in the rat RBC, HbV and low-P50 HbV groups was 59.4±12.5, 58.3±10.1 and 70.5±14.5 mm Hg, respectively. The PaO2 in the low-P50 HbV group was significantly higher than those in the rat RBC and HbV groups (p=0.05 for both). Serum lactate elevations due to hypoxic damage were minimised by HbV, low-P50 HbV as well as rat RBCs. Conclusions: The oxygen-carrying ability of HbV was comparable to that of rat RBCs, even under impaired lung function after pneumonectomy. HbVs with high oxygen affinity may have more beneficial effects on oxygenation in pulmonary resection. … (more)
- Is Part Of:
- BMJ open respiratory research. Volume 7:Issue 1(2020)
- Journal:
- BMJ open respiratory research
- Issue:
- Volume 7:Issue 1(2020)
- Issue Display:
- Volume 7, Issue 1 (2020)
- Year:
- 2020
- Volume:
- 7
- Issue:
- 1
- Issue Sort Value:
- 2020-0007-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-06-10
- Subjects:
- thoracic surgery
Respiratory organs -- Diseases -- Periodicals
Respiratory organs -- Diseases -- Treatment -- Periodicals
Respiratory therapy -- Periodicals
616.2005 - Journal URLs:
- http://www.bmj.com/archive ↗
http://bmjopenrespres.bmj.com/content/by/year ↗ - DOI:
- 10.1136/bmjresp-2019-000476 ↗
- Languages:
- English
- ISSNs:
- 2052-4439
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- Legaldeposit
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