Variability in Tidal Volume Affects Lung and Cardiovascular Function Differentially in a Rat Model of Experimental Emphysema

• Published in: Frontiers in physiology Vol. 8; p. 1071
• Main Authors: Wierzchon, Caio G R S, Padilha, Gisele, Rocha, Nazareth N, Huhle, Robert, Coelho, Mariana S, Santos, Cintia L, Santos, Raquel S, Samary, Cynthia S, Silvino, Fernanda R G, Pelosi, Paolo, Gama de Abreu, Marcelo, Rocco, Patricia R M, Silva, Pedro L
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 18.12.2017
• Subjects: cardiorespiratory function; inflammation; lung morphometry; Physiology; respiratory system elastance; surfactant protein-D; variable ventilation; cardiorespiratory function; surfactant protein-D; variable ventilation; respiratory system elastance; inflammation; lung morphometry
• ISSN: 1664-042X; 1664-042X
• DOI: 10.3389/fphys.2017.01071

In experimental elastase-induced emphysema, mechanical ventilation with variable tidal volumes (V ) set to 30% coefficient of variation (CV) may result in more homogenous ventilation distribution, but might also impair right heart function. We hypothesized that a different CV setting could improve both lung and cardiovascular function. Therefore, we investigated the effects of different levels of V variability on cardiorespiratory function, lung histology, and gene expression of biomarkers associated with inflammation, fibrogenesis, epithelial cell damage, and mechanical cell stress in this emphysema model. Wistar rats ( = 35) received repeated intratracheal instillation of porcine pancreatic elastase to induce emphysema. Seven animals were not ventilated and served as controls (NV). Twenty-eight animals were anesthetized and assigned to mechanical ventilation with a V CV of 0% (BASELINE). After data collection, animals ( = 7/group) were randomly allocated to V CVs of 0% (VV ); 15% (VV ); 22.5% (VV ); or 30% (VV ). In all groups, mean V was 6 mL/kg and positive end-expiratory pressure was 3 cmH O. Respiratory system mechanics and cardiac function (by echocardiography) were assessed continuously for 2 h (END). Lung histology and molecular biology were measured post-mortem. VV and VV decreased respiratory system elastance, while VV had no effect. VV , VV , and VV , but not VV , increased pulmonary acceleration time to pulmonary ejection time ratio. VV decreased the central moment of the mean linear intercept (D2 of Lm) while increasing the homogeneity index (1/β) compared to NV (77 ± 8 μm vs. 152 ± 45 μm; 0.85 ± 0.06 vs. 0.66 ± 0.13, < 0.05 for both). Compared to NV, VV was associated with higher interleukin-6 expression. Cytokine-induced neutrophil chemoattractant-1 expression was higher in all groups, except VV , compared to NV. IL-1β expression was lower in VV and VV compared to VV . IL-10 expression was higher in VV than NV. Club cell protein 16 expression was higher in VV than VV . SP-D expression was higher in VV than NV, while SP-C was higher in VV and VV than VV In conclusion, VV improved respiratory system elastance and homogeneity of airspace enlargement, mitigated inflammation and epithelial cell damage, while avoiding impairment of right cardiac function in experimental elastase-induced emphysema.