Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia; Department of Biochemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
Biomed Pharmacother. 2018 Nov;107:347-358. doi: 10.1016/j.biopha.2018.07.126. Epub 2018 Aug 9.
The present study aimed to investigate the protective effect of sitagliptin, a dipeptidyl peptidase-4 inhibitor, on diabetic cardiomyopathy (DCM)-associated apoptosis and if this effect is mediated via modulating the activity of the survival kinases; AMP-activated protein kinase (AMPK) and Akt & the apoptotic kinases; glycogen synthase kinase-3 β (GSK-3β) and p38 mitogen-activated protein kinase (p38MAPK). Diabetes was induced by a single intraperitoneal injection of streptozotocin (55 mg/kg). Diabetic rats were treated with sitagliptin (10 mg/kg/day, p.o.) and metformin (200 mg/kg/day, p.o. as positive control) for six weeks. Chronic hyperglycemia resulted in elevation of serum cardiac biomarkers reflecting cardiac damage which was supported by H&E stain. The mRNA levels of collagen types I and III were augmented reflecting cardiac fibrosis and hypertrophy which was supported by Masson trichome stain and enhanced phosphorylation of p38MAPK. Cardiac protein levels of cleaved casapse-3, BAX were elevated, whereas, the levels of Bcl-2 and p-BAD were reduced indicating cardiac apoptosis which could be attributed to the diabetes-induced reduced phosphorylation of Akt and AMPK with concomitant augmented activation of GSK-3β and p38MAPK. Protein levels of liver kinase B-1, the upstream kinase of AMPK were also supressed. Sitagliptin administration alleviated the decreased phosphorylation of AMPK and Akt, inactivated the GSK-3β and p38 AMPK, therefore, attenuating the apoptosis and hypertrophy induced by hyperglycemia in the diabetic heart. In conclusion, sitagliptin exhibits valuable therapeutic potential in the management of DCM by attenuating apoptosis. The underlying mechanism may involve the modulating activity of AMPK, Akt, GSK-3β and p38MAPK.
本研究旨在探讨二肽基肽酶-4 抑制剂西他列汀对糖尿病心肌病(DCM)相关细胞凋亡的保护作用,以及这种作用是否通过调节存活激酶 AMP 激活的蛋白激酶(AMPK)和 Akt 的活性和凋亡激酶糖原合成酶激酶-3β(GSK-3β)和 p38 丝裂原激活蛋白激酶(p38MAPK)来介导。通过单次腹腔注射链脲佐菌素(55mg/kg)诱导糖尿病。糖尿病大鼠用西他列汀(10mg/kg/天,口服)和二甲双胍(200mg/kg/天,口服作为阳性对照)治疗 6 周。慢性高血糖导致血清心脏标志物升高,反映心脏损伤,这一结果得到 H&E 染色的支持。I 型和 III 型胶原的 mRNA 水平增加,反映了心脏纤维化和肥大,这一结果得到 Masson 三色染色的支持,并伴有 p38MAPK 的磷酸化增强。心脏 cleaved casapse-3、BAX 的蛋白水平升高,而 Bcl-2 和 p-BAD 的水平降低,表明心脏凋亡,这可能归因于糖尿病诱导的 Akt 和 AMPK 磷酸化减少,同时 GSK-3β 和 p38MAPK 的激活增加。AMPK 的上游激酶肝激酶 B-1 的蛋白水平也受到抑制。西他列汀的给药减轻了 AMPK 和 Akt 的磷酸化减少,使 GSK-3β 和 p38MAPK 失活,从而减轻高血糖引起的糖尿病心脏中的凋亡和肥大。总之,西他列汀通过减轻凋亡显示出在 DCM 管理中的有价值的治疗潜力。其潜在机制可能涉及调节 AMPK、Akt、GSK-3β 和 p38MAPK 的活性。