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Published on: May 26, 2023
Dexmedetomidine Dose-Dependent Modulation of Lung Function and AQP1 Expression During One-Lung Ventilation in Adults
YuanQiang Li1, BenJing Gong1, SongLiu He1
1Department of Anesthesiology, Nanxishan Hospital of Guangxi Zhuang Autonomous Region (The Second Peoples Hospital of Guangxi Zhuang Autonomous Region), Guilin, Guangxi, China.
Abstract:
BACKGROUND This randomized controlled trial evaluated the dose-dependent effects of dexmedetomidine (DEX) on pulmonary function and aquaporin-1 (AQP1) expression during one-lung ventilation (OLV) in thoracoscopic surgery. MATERIAL AND METHODS Sixty patients were randomized into 3 groups in this single-center, double-blind trial: Control (Group C, saline), DEX 0.3 µg/kg/h (Group D1), and DEX 0.5 µg/kg/h (Group D2). Serum TNF-alpha/IL-8 levels were measured at 5 perioperative timepoints. Respiratory indices [respiratory index (RI), oxygenation index (OI), and dynamic lung compliance (Cdyn)] were calculated. Post-resection AQP1 expression in isolated lung tissue was assessed via semi-quantitative immunohistochemistry by 2 blinded pathologists (excellent agreement, kappa=0.82). Pearson correlation analysis was performed to assess relationships between AQP1 scores and TNF-alpha/IL-8 levels at OLV90 min. RESULTS Compared to Groups C and D1, Group D2 exhibited lower IL-8 and RI starting at OLV90 min and TNF-a at OLV120 min and 30 min after reinstitution of two-lung ventilation (ReTLV30 min), while OI improved after OLV60 min, and Cdyn increased at OLV90 min and OLV120 min (P<0.05). AQP1 expression in Group D2 exceeded Groups C and D1 (P<0.05). Pearson correlation analysis revealed negative correlations between AQP1 expression and both TNF-alpha (r=-0.672) and IL-8 (r=-0.744) levels at OLV90 min (P<0.001). CONCLUSIONS Dexmedetomidine dose-dependently attenuates OLV-induced lung injury and improves pulmonary function, concomitant with reduced inflammatory cytokines and preserved AQP1 expression. The 0.5 µg/kg/h dose demonstrated superior efficacy without increasing adverse events. This protection likely involves concurrent suppression of inflammation and modulation of alveolar fluid clearance pathways.
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