Relationship between failed mechanism of sevoflurane postconditioning-induced myocardial protection and dynamin-related protein 1 activity in diabetic rats
Aili Fang, Gaoxiang Shi, Chongfang Han, Jiandong He, Xiang Wang, Yinglei Duan
Abstract
Aili Fang, Gaoxiang Shi, Chongfang Han, Jiandong He, Xiang Wang, Yinglei Duan
Abstract
Objective To evaluate the relationship between the failed mechanism of sevoflurane postconditioning-induced myocardial protection and the activity of dynamin-related protein 1(Drp1)in diabetic rats. Methods Pathogen-free healthy adult male Sprague-Dawley rats, weighing 220-280 g, in which diabetes mellitus was induced by combination of high-fat and high-sucrose diet and intraperitoneal injection of streptozotoein 30 mg/kg, were studied.Sixty rats with diabetes mellitus were divided into 5 groups(n=12 each)using a random number table: sham operation group(group Sham), myocardial ischemia/reperfusion(I/R)group(group I/R), sevoflurane postconditioning group(group SP), Drp1 inhibitor mitochondrial division inhibitor-1(Mdivi-1)group(group M)and Mdivi-1 plus sevoflurane postconditioning group(group M-SP). Myocardial I/R was induced by occluding the left anterior descending branch of the coronary artery for 30 min followed by 120 min reperfusion except for group Sham.Mdivi-1 1.2 mg/kg was intraperitoneally injected at 15 min before ischemia in M and M-SP groups, and 2.5% sevoflurane was inhaled starting from 5 min of reperfusion in SP and M-SP groups.Blood samples were collected from the right internal jugular vein at 120 min of reperfusion for measurement of serum cardiac troponin I(cTnI)concentrations(by enzyme-linked immunosorbent assay). Rats were then sacrificed and myocardial specimens were obtained for determination of the myocardial infarct size(by TTC), cell apoptosis(by TUNEL), expression of Bax, Bcl-2 and activated caspase-3(by Western blot)and nicotinamide adenine dinucleotide(NAD+ )content(by spectrophotometry). Apoptosis index(AI)and Bax/Bcl-2 ratio were calculated. Results Compared with group Sham, the percentage of myocardial infarct size, serum concentration of cTnI, AI and Bax/Bcl-2 ratio were significantly increased, the expression of activated caspase-3 was up-regulated, and the NAD+ content was decreased in the other four groups(P 0.05). Compared with group SP, the percentage of myocardial infarct size, serum concentration of cTnI, AI and Bax/Bcl-2 ratio were significantly decreased, the expression of activated caspase-3 was down-regulated, and the NAD+ content was decreased in group M-SP(P 0.05). Conclusion The failed mechanism of sevoflurane postconditioning-induced myocardial protection may be related to the activity of Drp1 in diabetic rats. Key words: Diabetes mellitus; Myocardial reperfusion injury; Anesthetics, inhalation; Apoptosis
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Objective To evaluate the relationship between the failed mechanism of sevoflurane postconditioning-induced myocardial protection and the activity of dynamin-related protein 1(Drp1)in diabetic rats. Methods Pathogen-free healthy adult male Sprague-Dawley rats, weighing 220-280 g, in which diabetes mellitus was induced by combination of high-fat and high-sucrose diet and intraperitoneal injection of streptozotoein 30 mg/kg, were studied.Sixty rats with diabetes mellitus were divided into 5 groups(n=12 each)using a random number table: sham operation group(group Sham), myocardial ischemia/reperfusion(I/R)group(group I/R), sevoflurane postconditioning group(group SP), Drp1 inhibitor mitochondrial division inhibitor-1(Mdivi-1)group(group M)and Mdivi-1 plus sevoflurane postconditioning group(group M-SP). Myocardial I/R was induced by occluding the left anterior descending branch of the coronary artery for 30 min followed by 120 min reperfusion except for group Sham.Mdivi-1 1.2 mg/kg was intraperitoneally injected at 15 min before ischemia in M and M-SP groups, and 2.5% sevoflurane was inhaled starting from 5 min of reperfusion in SP and M-SP groups.Blood samples were collected from the right internal jugular vein at 120 min of reperfusion for measurement of serum cardiac troponin I(cTnI)concentrations(by enzyme-linked immunosorbent assay). Rats were then sacrificed and myocardial specimens were obtained for determination of the myocardial infarct size(by TTC), cell apoptosis(by TUNEL), expression of Bax, Bcl-2 and activated caspase-3(by Western blot)and nicotinamide adenine dinucleotide(NAD+ )content(by spectrophotometry). Apoptosis index(AI)and Bax/Bcl-2 ratio were calculated. Results Compared with group Sham, the percentage of myocardial infarct size, serum concentration of cTnI, AI and Bax/Bcl-2 ratio were significantly increased, the expression of activated caspase-3 was up-regulated, and the NAD+ content was decreased in the other four groups(P 0.05). Compared with group SP, the percentage of myocardial infarct size, serum concentration of cTnI, AI and Bax/Bcl-2 ratio were significantly decreased, the expression of activated caspase-3 was down-regulated, and the NAD+ content was decreased in group M-SP(P 0.05). Conclusion The failed mechanism of sevoflurane postconditioning-induced myocardial protection may be related to the activity of Drp1 in diabetic rats. Key words: Diabetes mellitus; Myocardial reperfusion injury; Anesthetics, inhalation; Apoptosis
Key concepts: Troponin I, Sevoflurane, Streptozotocin, TUNEL assay, Medicine, Myocardial infarction, Internal medicine, Diabetes mellitus