Role of JAK2/STAT3 signaling pathway in brain injury induced by myocardial ischemia-reperfusion in diabetic rats
Bo Zhao, Yan Leng, Xiaojing Wu, Jiabao Hou, Yang Wu, Zhongyuan Xia
Abstract
Bo Zhao, Yan Leng, Xiaojing Wu, Jiabao Hou, Yang Wu, Zhongyuan Xia
Abstract
Objective To evaluate the effects of Janus kinase 2/signal transducers and activators of transcription 3 (JAK2/STAT3) signaling pathway on the brain injury induced by myocardial ischemia-reperfusion (I/R) in diabetic rats. Methods Pathogen-free male Sprague-Dawley rats, weighing 200-220 g, were used in this study.Diabetes mellitus was induced by intraperitoneal 1% streptozotocin 60 mg/kg and confirmed by blood glucose level ≥16.7 mmol/L 3 days later.Twenty-four rats with diabetes mellitus were randomly allocated into 3 groups (n=8 each) using a random number table: sham operation group (group S), I/R group, and myocardial I/R + AG490 (JAK inhibitor) group (group IA). Myocardial I/R was induced by occlusion of the anterior descending branch of the left coronary artery for 30 min, followed by 120 min of reperfusion in the rats anesthetized with pentobarbital sodium.AG490 3 mg/kg was injected intravenously at 20 min before reperfusion in group IA.The rats were sacrificed at 120 min of reperfusion, and the brains were removed for determination of caspase-3 and nuclear factor kappa B (NF-κB) activities (using colorimetric method), cell apoptosis (by TUNEL), and expression of interleukin-1 (IL-1), IL-6, IL-8, Bax, Bcl-2, cytochrome C (Cyt c), phosphorylated JAK2 (p-JAK2), and phosphorylated STAT3 (p-STAT3) (by Western blot). Apoptosis index was calculated. Results Compared with group S, the expression of Bax, Cyt c, IL-1, IL-6, IL-8, p-JAK2 and p-STAT3 was significantly up-regulated, the expression of Bcl-2 was down-regulated, and NF-κB and caspase-3 activities and apoptosis index were increased in I/R and IA groups (P<0.05). Compared with group I/R, the expression of Bax, Cyt c, IL-1, IL-6, IL-8, p-JAK2 and p-STAT3 was significantly down-regulated, the expression of Bcl-2 was up-regulated, and NF-κB and caspase-3 activities and apoptosis index were decreased in group IA (P<0.05). Conclusion Inflammatory responses mediated by JAK2/STAT3 signaling pathway are involved in the brain injury induced by myocardial I/R in diabetic rats. Key words: Janus kinase 2; STAT3 transcription factor; Diabetes mellitus; Myocardial reperfusion injury; Brain injuries
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To evaluate the effects of Janus kinase 2/signal transducers and activators of transcription 3 (JAK2/STAT3) signaling pathway on the brain injury induced by myocardial ischemia-reperfusion (I/R) in diabetic rats. Methods Pathogen-free male Sprague-Dawley rats, weighing 200-220 g, were used in this study.Diabetes mellitus was induced by intraperitoneal 1% streptozotocin 60 mg/kg and confirmed by blood glucose level ≥16.7 mmol/L 3 days later.Twenty-four rats with diabetes mellitus were randomly allocated into 3 groups (n=8 each) using a random number table: sham operation group (group S), I/R group, and myocardial I/R + AG490 (JAK inhibitor) group (group IA). Myocardial I/R was induced by occlusion of the anterior descending branch of the left coronary artery for 30 min, followed by 120 min of reperfusion in the rats anesthetized with pentobarbital sodium.AG490 3 mg/kg was injected intravenously at 20 min before reperfusion in group IA.The rats were sacrificed at 120 min of reperfusion, and the brains were removed for determination of caspase-3 and nuclear factor kappa B (NF-κB) activities (using colorimetric method), cell apoptosis (by TUNEL), and expression of interleukin-1 (IL-1), IL-6, IL-8, Bax, Bcl-2, cytochrome C (Cyt c), phosphorylated JAK2 (p-JAK2), and phosphorylated STAT3 (p-STAT3) (by Western blot). Apoptosis index was calculated. Results Compared with group S, the expression of Bax, Cyt c, IL-1, IL-6, IL-8, p-JAK2 and p-STAT3 was significantly up-regulated, the expression of Bcl-2 was down-regulated, and NF-κB and caspase-3 activities and apoptosis index were increased in I/R and IA groups (P<0.05). Compared with group I/R, the expression of Bax, Cyt c, IL-1, IL-6, IL-8, p-JAK2 and p-STAT3 was significantly down-regulated, the expression of Bcl-2 was up-regulated, and NF-κB and caspase-3 activities and apoptosis index were decreased in group IA (P<0.05). Conclusion Inflammatory responses mediated by JAK2/STAT3 signaling pathway are involved in the brain injury induced by myocardial I/R in diabetic rats. Key words: Janus kinase 2; STAT3 transcription factor; Diabetes mellitus; Myocardial reperfusion injury; Brain injuries
Key concepts: TUNEL assay, STAT3, Apoptosis, Endocrinology, Intraperitoneal injection, Medicine, Internal medicine, Streptozotocin