基于Spexin的甘丙肽受体2激动剂改善2型糖尿病小鼠的肾损伤。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2023-09-30 eCollection Date: 2023-01-01 DOI:10.1080/19768354.2023.2263067
Jin Joo Cha, Boo Yeon Park, Sung Gi Yoon, Hye Jin Park, Ji Ae Yoo, Jung Yeon Ghee, Dae Ryong Cha, Jae Young Seong, Young Sun Kang
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引用次数: 1

摘要

基于spexin的GALR2激动剂(NS200)是一种新药,在最近的一项实验研究中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。8周龄糖尿病db/db小鼠给予NS200 12周。NS200以1.0的剂量腹膜内给药 mg/kg/天。比较三组肾脏的代谢参数、结构和分子变化:非糖尿病db/m对照组、db/db小鼠和NS200治疗的db/db鼠。在db/db小鼠中,NS200给药不会影响体重、食物和水的摄入量、尿量、空腹血糖水平或HbA1c水平。胰岛素和葡萄糖耐量也不受NS200治疗的影响。然而,NS200改善了糖尿病肾脏的尿白蛋白排泄和肾小球硬化。TGFβ1和胰岛素信号通路的激活,如PI3 K/AKT/ERK均被NS200抑制。总之,一种基于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剂具有相当大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spexin-based galanin receptor 2 agonist improves renal injury in mice with type 2 diabetes.

Spexin-based galanin receptor 2 agonist improves renal injury in mice with type 2 diabetes.

Spexin-based galanin receptor 2 agonist improves renal injury in mice with type 2 diabetes.

Spexin-based galanin receptor 2 agonist improves renal injury in mice with type 2 diabetes.

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 db/db 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 db/m control, db/db mice, and NS200-treated db/db mice. In db/db 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.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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