Kim Dong-Hyun, Choi Bo-Hyun, Ku Sae-Kwang, Park Jeong-Hyeon, Oh Euichaul, Kwak Mi-Kyoung
College of pharmacy, The Catholic University of Korea, Bucheon, Gyeonggi-do, 420-743, Republic of Korea.
College of Korean Medicine, Daegu Haany University, Gyeongsan, Gyeonsangbuk-do, 712-715, Republic of Korea.
PLoS One. 2016 Apr 20;11(4):e0153965. doi: 10.1371/journal.pone.0153965. eCollection 2016.
Chronic kidney disease (CKD) is a major complication of metabolic disorders such as diabetes mellitus, obesity, and hypertension. Comorbidity of these diseases is the factor exacerbating CKD progression. Statins are commonly used in patients with metabolic disorders to decrease the risk of cardiovascular complications. Sarpogrelate, a selective antagonist of 5-hydroxytryptamine (5-HT) 2A receptor, inhibits platelet aggregation and is used to improve peripheral circulation in diabetic patients. Here, we investigated the effects of sarpogrelate and rosuvastatin on CKD in mice that were subjected to a high fat diet (HFD) for 22 weeks and a single low dose of streptozotocin (STZ, 40 mg/kg). When mice were administrated sarpogrelate (50 mg/kg, p.o.) for 13 weeks, albuminuria and urinary cystatin C excretion were normalized and histopathological changes such as glomerular mesangial expansion, tubular damage, and accumulations in lipid droplets and collagen were significantly improved. Sarpogrelate treatment repressed the HFD/STZ-induced CD31 and vascular endothelial growth factor receptor-2 expressions, indicating the attenuation of glomerular endothelial proliferation. Additionally, sarpogrelate inhibited interstitial fibrosis by suppressing the increases in transforming growth factor-β1 (TGF-β1) and plasminogen activator inhibitor-1 (PAI-1). All of these functional and histological improvements were also seen in rosuvastatin (20 mg/kg) group and, notably, the combinatorial treatment with sarpogrelate and rosuvastatin showed additive beneficial effects on histopathological changes by HFD/STZ. Moreover, sarpogrelate reduced circulating levels of PAI-1 that were elevated in the HFD/STZ group. As supportive in vitro evidence, sarpogrelate incubation blocked TGF-β1/5-HT-inducible PAI-1 expression in murine glomerular mesangial cells. Taken together, sarpogrelate and rosuvastatin may be advantageous to control the progression of CKD in patients with comorbid metabolic disorders, and particularly, the use of sarpogrelate as adjunctive therapy with statins may provide additional benefits on CKD.
慢性肾脏病(CKD)是糖尿病、肥胖症和高血压等代谢紊乱的主要并发症。这些疾病的合并症是加剧CKD进展的因素。他汀类药物常用于患有代谢紊乱的患者,以降低心血管并发症的风险。沙格雷酯是5-羟色胺(5-HT)2A受体的选择性拮抗剂,可抑制血小板聚集,用于改善糖尿病患者的外周循环。在此,我们研究了沙格雷酯和瑞舒伐他汀对高脂饮食(HFD)22周并单次低剂量注射链脲佐菌素(STZ,40mg/kg)的小鼠CKD的影响。当给小鼠口服沙格雷酯(50mg/kg)13周时,蛋白尿和尿胱抑素C排泄恢复正常,肾小球系膜扩张、肾小管损伤以及脂滴和胶原蛋白积聚等组织病理学变化得到显著改善。沙格雷酯治疗可抑制HFD/STZ诱导的CD31和血管内皮生长因子受体-2表达,表明肾小球内皮细胞增殖减弱。此外,沙格雷酯通过抑制转化生长因子-β1(TGF-β1)和纤溶酶原激活物抑制剂-1(PAI-1)的增加来抑制间质纤维化。所有这些功能和组织学改善在瑞舒伐他汀(20mg/kg)组中也可见,值得注意的是,沙格雷酯和瑞舒伐他汀联合治疗对HFD/STZ引起的组织病理学变化显示出相加的有益效果。此外,沙格雷酯降低了HFD/STZ组中升高的循环PAI-1水平。作为体外支持证据,沙格雷酯孵育可阻断TGF-β1/5-HT诱导的小鼠肾小球系膜细胞中PAI-1的表达。综上所述,沙格雷酯和瑞舒伐他汀可能有利于控制合并代谢紊乱患者的CKD进展,特别是将沙格雷酯作为他汀类药物的辅助治疗可能会为CKD带来额外益处。