Cha Jin Joo, Park Boo Yeon, Yoon Sung Gi, Park Hye Jin, Yoo Ji Ae, Ghee Jung Yeon, Cha Dae Ryong, Seong Jae Young, Kang Young Sun
Department of Nephrology, Korea University Ansan Hospital, Gyeonggi-do, Republic of Korea.
Graduate School of Biomedical Science, Korea University College of Medicine, Seoul, Republic of Korea.
Anim Cells Syst (Seoul). 2023 Sep 30;27(1):187-196. doi: 10.1080/19768354.2023.2263067. eCollection 2023.
The spexin-based GALR2 agonist (NS200) is a novel drug, which has shown antidepressant and anxiolytic action in a recent experimental study. In this study, we investigated the effects of NS200 on renal injury in an animal model of type 2 diabetes. Eight-week-old diabetic mice were administered NS200 for 12 weeks. NS200 was intraperitoneally administered at a dose of 1.0 mg/kg/day. Metabolic parameters and structural and molecular changes in the kidneys were compared among the three groups: non-diabetic control, mice, and NS200-treated mice. In mice, NS200 administration did not impact the body weight, food and water intake, urinary volume, fasting blood glucose level, or HbA1c levels. Insulin and glucose tolerance were also unaffected by NS200 treatment. However, NS200 improved urinary albumin excretion and glomerulosclerosis in diabetic kidneys. Activation of TGFβ1 and insulin signaling pathways, such as PI3 K /AKT/ERK, were inhibited by NS200. In conclusion, a spexin-based GALR2 agonist attenuated diabetic nephropathy by alleviating renal fibrosis in mice with type 2 diabetes. Spexin-based GALR2 agonists have considerable potential as novel treatment agents in diabetic nephropathy.
基于spexin的GALR2激动剂(NS200)是一种新型药物,在最近的一项实验研究中已显示出抗抑郁和抗焦虑作用。在本研究中,我们在2型糖尿病动物模型中研究了NS200对肾损伤的影响。给8周龄的糖尿病小鼠施用NS200,持续12周。NS200以1.0 mg/kg/天的剂量腹腔注射。比较了三组小鼠的代谢参数以及肾脏的结构和分子变化:非糖尿病对照组小鼠和接受NS200治疗的小鼠。在小鼠中,施用NS200对体重、食物和水摄入量、尿量、空腹血糖水平或糖化血红蛋白水平没有影响。NS200治疗对胰岛素和葡萄糖耐量也没有影响。然而,NS200改善了糖尿病肾脏中的尿白蛋白排泄和肾小球硬化。NS200抑制了TGFβ1和胰岛素信号通路(如PI3 K /AKT/ERK)的激活。总之,基于spexin的GALR2激动剂通过减轻2型糖尿病小鼠的肾纤维化来减轻糖尿病肾病。基于spexin的GALR2激动剂作为糖尿病肾病的新型治疗药物具有相当大的潜力。