高脂肪食を負荷した糖尿病モデルマウスで生じる網膜神経細胞の脱落に対するAPJアゴニストの保護作用

• Published in: 日本薬理学会年会要旨集 p. 2-P-213
• Main Authors: 前田, 定秋, 柴垣, 郁弥, 赤井, 喜一, 山室, 晶子, 石丸, 侑希, 徳田, 華奈, 吉岡, 靖啓
• Format: Journal Article
• Language: Japanese
• Published: 公益社団法人 日本薬理学会 2020
• Subjects: hyperglycemia; neurodegeneration; retina
• ISSN: 2435-4953
• DOI: 10.1254/jpssuppl.93.0_2-P-213

Diabetic retinopathy is a leading cause of blindness and leads to retinal neuronal cell death at the early stage. We have previously shown that an apelin receptor (APJ) agonist suppresses the reduction of the retinal neuronal function observed in a mouse model of diabetes fed a high-fat diet (HFD). In the present study, we investigated the protective effect of endogenous apelin and ML233, an APJ agonist, against retinal neuronal cell death in the diabetes model mice fed the HFD by immunohistochemistry. We used Ins2 mutant (Ins2+/-) mouse (Akita mouse), which is a mouse model of type 1 diabetes. Akita mouse was fed the HFD from 5 to 9 weeks after birth. ML233 (5 mg/kg) was administered intraperitoneally on every other day for 4 weeks. Immunohistochemical staining showed that intraperitoneal injection of ML233 prevented the loss of retinal ganglion cells, bipolar cells, and cone cells in Akita mice fed the HFD for 4 weeks. The loss of these retinal neuronal cells was accelerated by deletion of apelin. These results suggest that systemic administration of APJ agonists could protect against retinal neuronal cell death in diabetic retinopathy.