Effects of sevoflurane preconditioning on lung injury induced by renal ischemia-reperfusion in rats
Guangjian Jing, Yaoqi Wang, Qianqian Wang
Abstract
Guangjian Jing, Yaoqi Wang, Qianqian Wang
Abstract
Objective To evaluate the effects of sevoflurane preconditioning on lung injury induced by renal ischemia-reperfusion (I/R) in rats.Methods Forty adult male Wistar rats,aged 3 months,weighing 200-250 g,were randomly divided into 5 groups (n =8 each):sham operation group (group S); renal I/R group (group I/R); 1.1% sevoflurane preconditioning group (group SP1); 2.2% sevoflurane preconditioning group (group SP2); and 3.3% sevoflurane preconditioning group (group SP3).Renal I/R was induced by clamping bilateral renal pedicles for 45 min followed by 6 h reperfusion.In SP1-SP3 groups,1.1%,2.2% and 3.3% sevoflurane were inhaled for 1 h,respectively,before ischemia,followed by 10 min washout.The rats were sacrificed by exsanguination at 6 h of reperfusion,and lungs were removed for determination of wet/dry lung weight (W/D) ratio,myeloperoxidase (MPO) activity and expression of angiotensin converting enzyme (ACE) mRNA,and for microscope examination of pathologic changes which were scored.Results Compared with group S,the pathological score,W/D ratio,MPO activity and expression of ACE mRNA were significantly increased in I/R and SP1-SP3 groups (P < 0.05).Compared with group I/R,the pathological score,W/D ratio,MPO activity and expression of ACE mRNA were significantly decreased in SP1-SP3 groups (P < 0.05).Compared with SP1 and SP3 groups,the pathological score,W/D ratio,MPO activity and expression of ACE mRNA were significantly decreased in group SP2 (P < 0.05).Compared with group SP1,the W/D ratio was significantly decreased (P <0.05),and no significant changes were found in the other parameters in group SP3 (P > 0.05).Conclusion Sevoflurane preconditioning can attenuate lung injury induced by renal I/R and inhibition of ACE synthesis is involved in the mechanism. Key words: Anesthetics, inhalation ; Ischemic preconditioning ; Respiratory distress syndrome, adult; Kidney; Reperfusion injury
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Objective To evaluate the effects of sevoflurane preconditioning on lung injury induced by renal ischemia-reperfusion (I/R) in rats.Methods Forty adult male Wistar rats,aged 3 months,weighing 200-250 g,were randomly divided into 5 groups (n =8 each):sham operation group (group S); renal I/R group (group I/R); 1.1% sevoflurane preconditioning group (group SP1); 2.2% sevoflurane preconditioning group (group SP2); and 3.3% sevoflurane preconditioning group (group SP3).Renal I/R was induced by clamping bilateral renal pedicles for 45 min followed by 6 h reperfusion.In SP1-SP3 groups,1.1%,2.2% and 3.3% sevoflurane were inhaled for 1 h,respectively,before ischemia,followed by 10 min washout.The rats were sacrificed by exsanguination at 6 h of reperfusion,and lungs were removed for determination of wet/dry lung weight (W/D) ratio,myeloperoxidase (MPO) activity and expression of angiotensin converting enzyme (ACE) mRNA,and for microscope examination of pathologic changes which were scored.Results Compared with group S,the pathological score,W/D ratio,MPO activity and expression of ACE mRNA were significantly increased in I/R and SP1-SP3 groups (P < 0.05).Compared with group I/R,the pathological score,W/D ratio,MPO activity and expression of ACE mRNA were significantly decreased in SP1-SP3 groups (P < 0.05).Compared with SP1 and SP3 groups,the pathological score,W/D ratio,MPO activity and expression of ACE mRNA were significantly decreased in group SP2 (P < 0.05).Compared with group SP1,the W/D ratio was significantly decreased (P <0.05),and no significant changes were found in the other parameters in group SP3 (P > 0.05).Conclusion Sevoflurane preconditioning can attenuate lung injury induced by renal I/R and inhibition of ACE synthesis is involved in the mechanism. Key words: Anesthetics, inhalation ; Ischemic preconditioning ; Respiratory distress syndrome, adult; Kidney; Reperfusion injury
Key concepts: Sevoflurane, Myeloperoxidase, Ischemic preconditioning, Ischemia, Kidney, Lung, Internal medicine, Endocrinology