|
|
|
| Study on the Establishment of a Rat Model for Transfusion-related Acute Lung Injury with Coronary Heart Disease and its Oxygen Balance |
| QIU Qi-dong, QIU Xiao-lan, CHEN Wei-mei |
| Department of Blood Transfusion, Longyan First Affiliated Hospital of Fujian Medical University, Longyan Fujian 364000, China |
|
|
|
|
Abstract Objective: To establish a rat model of transfusion-related acute lung injury (TRALI) with coronary heart disease (CHD), and to analyze the safety of blood transfusion through oxygen balance. Methods: Forty-five 10-day-old male Wistar rats were purchased, and 35 of them were fed with high-fat diet to establish coronary heart disease rat models, and then 20 of them were selected to establish rat models of transfusion-related acute lung injury with coronary heart disease (model group, 10 rats),positive acute lung injury group (positive group, 5 rats) and negative acute lung injury group (negative group, 5 rats),and the lung histomorphology, pathological score and wet/dry weight ratio were compared. Then, another 15 rats with coronary heart disease were selected and infused with mutant Hb, rHb1.1 and rHb2.0 with the same osmotic pressure through femoral vein catheterization, respectively, and were divided into mutant Hb group, rHb1.1 group and rHb2.0 group, with 5 rats in each group, and 5 healthy rats were combined as control group. The MAP, HR and blood gas values of mesenteric artery of rats were compared at 0, 30, 60 and 90 min after infusion. Results: (1) Rats in the model group and the positive group showed symptoms such as irregular and shallow breathing, increased oral and nasal secretions, and audible wheezing, which were consistent with the symptoms of acute lung injury. Comparison of lung histological score and lung tissue wet/dry ratio in three groups: There was no significant difference in lung histological score and lung tissue wet/dry ratio (P>0.05), but they were higher than those in the negative group (P<0.05). (2)During hemoglobin infusion, the MAP of mutant Hb group, rHb1.1 group and rHb2.0 group was higher than that of the control group, while the pH and PaCO2 were lower than those of the control group (P<0.05), and there was no significant difference in QSMA(P>0.05). In the mutant Hb group, MAP returned to normal at 30-60 min after infusion (P>0.05), but MAP increased again at 90 min after infusion (P<0.05), and QSMAincreased significantly at 60 min after transfusion (P<0.05). The pH value was lower than the normal value and the PaCO2 was higher than the normal value within 90 min of infusion (P<0.05), and the HCO3- level returned to normal after 30 min of infusion (P>0.05). In rHb 1.1 group, MAP returned to normal, QSMA remained at normal level(P>0.05), and pH, PaCO2 and HCO3- returned to normal after 60 min of infusion (P>0.05); In rHb 2.0 group, the levels of MAP, pH, PaCO2 and HCO3- returned to normal after 30 min of infusion(P>0.05), and QSMA remained normal during infusion(P>0.05). Conclusion: The rat model of transfusion-relatted acute lung injury with coronary heart disease can be successfully established by injecting LPS into the rat model of coronary heart disease, and the infusion of recombinant hemoglobin can improve the balance of blood supply in rats, in which the infusion of rHb2.0 can better correct the metabolic acidosis.
|
|
Received: 23 September 2022
|
|
|
|
Corresponding Authors:
CHEN Wei-mei
|
|
|
|
[1] Vlaar APJ, Toy P, Fung M, et al.A consensus redefinition of transfusion-related acute lung injury[J].Transfusion: The Journal of the American Association of Blood Banks, 2019, 59(7):2465-2476.
[2] Meyer DE, Reynolds JW, Pommerening MJ,et al.The incidence of transfusion-related acute lung injury at a large, urban tertiary medical center: A decade's experience[J].Anesthesia & Analgesia: Journal of the International Anesthesia Research Society,2018, 127(2):444-449.
[3] Johan R, Semple JW, Kapur R.The pathogenic involvement of neutrophils in acute respiratory distress syndrome and transfusion-related acute lung injury[J].Transfus Med Hemother,2018, 45(5).290-298.
[4] Minh VCN, Masson D, Bardy B, et al.Transfusion-related acute lung injury:critical neutrophil activation by anti-HLA-A2 antibodies for endothelial permeability[J].Transfusion: The Journal of the American Association of Blood Banks,2017, 57(7):1699-1708.
[5] Sofiane T, Hind H-C, Sandrine L, et al.Evidence of CD40L/CD40 pathway involvement in experimental transfusion-related acute lung injury[J].Scientific Reports,2019, 9(1):12536.
[6] Alexander PJ, Vlaar SK.An update of the transfusion-related acute lung injury(TRALI) definition[J].Transfusion & Apheresis Science: Official Journal of the World Apheresis Association: Official Journal of the European Society for Haemapheresis,2019, 58(5):632-633.
[7] Rick K, Michael K, Johan R, et al.Gastrointestinal microbiota contributes to the development of murine transfusion-related acute lung injury[J].Blood Advances,2018, 2(13):1651-1663.
[8] Hechler B, Maitre B, Magnenat S,et al.Platelets are dispensable for antibody-mediated transfusion-related acute lung injury in the mouse[J].Journal of Thrombosis & Haemostasis: JTH,2016, 14(6). |
|
|
|
