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Fig 1.

Experimental outline of the study.

Lungs from donor rats were randomly assigned to one of four experimental groups (n = 7/group): 1) healthy, directly procured lungs, 2) lungs procured from rats subjected to 3 hours of brain death (BD) and 1 hour cold storage (CS), 3) healthy, directly procured lungs subjected to 6 hours ex vivo lung perfusion (EVLP) and 4), lungs procured from rats subjected to 3 hours of BD, 1 hour CS and 6 hours EVLP.

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Fig 1 Expand

Fig 2.

Schematic overview of the rat ex vivo lung perfusion model.

Lungs from healthy or brain-dead donor rats were subjected to 6 hours ex vivo lung perfusion (EVLP). The EVLP circuit consisted of a (1) graft humidity chamber, (2) reservoir, (3) roller pump, (4) leukocyte filter, (5) deoxygenator, (6) heat exchanger, (7) funnel, (8) pressure sensor, (9) ventilator, and a (10) water bath.

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Table 1.

List of reagents for ex vivo lung perfusion.

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Table 1 Expand

Table 2.

List of instruments for the ex vivo lung perfusion model.

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Table 2 Expand

Fig 3.

Experimental groups with number of rats utilized and rationale for exclusion.

Lungs from donor rats were randomly assigned to one of four experimental groups (n = 7/group): 1) healthy, directly procured lungs, 2) lungs procured from rats subjected to 3 hours of brain death (BD) and 1 hour cold storage (CS), 3) healthy, directly procured lungs subjected to 6 hours ex vivo lung perfusion (EVLP) and 4), lungs procured from rats subjected to 3 hours of BD, 1 hour CS and 6 hours EVLP. In total, 38 rats were utilized for the establishment of a stable BD and EVLP protocol, of which 10 rats were excluded. Eventually, 7 rats per group were included in the final protocol.

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Fig 4.

Ventilation parameters and inflammatory status after lung procurement.

Lungs were procured from either healthy rats (experimental group 1) or rats subjected to 3 hours of brain death (BD, experimental group 2). (A) Pulmonary Inspiratory Pressure (PIP) required to maintain tidal volume at 7 ml/kg of bodyweight and dynamic compliance (Cdyn) of healthy donor lungs 1) versus donor lungs subjected to 3 hours of BD, at time of lung procurement. (B) Pro-inflammatory gene expressions of TNF-α, IL-1β, IL-6, MCP-1 and C3 of healthy donor lungs versus donor lungs subjected to 3 hours of BD. ** p<0.01 in healthy donor lungs versus lungs from brain-dead donors.

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Fig 5.

Lung morphology after lung procurement.

Lungs were procured from either healthy rats (experimental group 1) or rats subjected to 3 hours of brain death (BD, experimental group 2). Histological lung injury was scored after staining for hematoxylin and eosin (H&E). (A) Quantification of lung injury scores in H&E-stained lung slides. (B-C) Representative H&E-stained slices of healthy donor lungs and lungs from brain-dead donors. ** p<0.01 in healthy donor lungs versus lungs from brain-dead donors.

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Fig 6.

Ventilation and perfusion performance during ex vivo lung perfusion.

Lungs from healthy donor rats or rats subjected to 3 hours of brain death (BD) and 1 hour cold storage (CS) were ex vivo perfused for 6 hours (EVLP, experimental group 3 and 4). (A) Positive Inspiratory Pressure (PIP) required to maintain tidal volume at 7 ml/kg of bodyweight over time, during EVLP. (B) Dynamic compliance (Cdyn) of donor lungs over time, during EVLP. (C) Oxygenation capacity of donor lungs as reflected by PaO2/FiO2 ratio. (D) Perfusion flow of donor lungs over time, during EVLP. * p<0.05 in healthy donor lungs versus lungs from brain-dead donors subjected to EVLP. ** p<0.01 in healthy donor lungs versus lungs from brain-dead donors subjected to EVLP.

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Fig 7.

Metabolic profile and inflammatory status after ex vivo lung perfusion.

Lungs from healthy donor rats or rats subjected to 3 hours of brain death (BD) and 1 hour cold storage (CS) were ex vivo perfused for 6 hours (EVLP, experimental group 3 and 4). (A) Cumulative glucose consumption of healthy donor lungs versus lungs from brain-dead rats, during EVLP. (B) Cumulative lactate production of healthy donor lungs versus lungs from brain-dead rats, during EVLP. (C) Pro-inflammatory gene expressions of TNF-α, IL-1β, IL-6, MCP-1 and C3 in donor lungs, after 6 hours of EVLP. * p<0.05 in healthy donor lungs versus lungs from brain-dead donors subjected to EVLP. ** p<0.01 in healthy donor lungs versus lungs from brain-dead donors subjected to EVLP.

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Fig 8.

Lung morphology after ex vivo lung perfusion.

Lungs from healthy donor rats or rats subjected to 3 hours of brain death (BD) and 1 hour cold storage (CS) were ex vivo perfused for 6 hours (EVLP, experimental group 3 and 4). Histological lung injury was scored after staining for hematoxylin and eosin (H&E). (A) Quantification of lung injury scores after EVLP in H&E-stained lung slides. (B-C) Representative H&E-stained slices of healthy donor lungs and lungs from brain-dead donors, after EVLP. ** p<0.01 in healthy donor lungs versus lungs from brain-dead donors subjected to EVLP.

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Table 3.

Donor type characteristics of reported rat ex vivo lung perfusion models.

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