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G蛋白偶联受体1通过磷酸化AKT途径参与介导妊娠期糖尿病的机制。

G protein-coupled receptor 1 participating in the mechanism of mediating gestational diabetes mellitus by phosphorylating the AKT pathway.

作者信息

Zhu Yanbin, Huang Shufeng, Chai Dan, Liang Lei

机构信息

Department of Obstetrics and Gynecology, Shenzhen Futian District Maternity & Child Healthcare Hospital, Shenzhen, 518017, Guangdong, China.

Department of Gynecology, Shenzhen Qianhai Shekou Free Trade Zone Hospital, Shenzhen, 518067, Guangdong, China.

出版信息

Open Life Sci. 2024 Aug 23;19(1):20220920. doi: 10.1515/biol-2022-0920. eCollection 2024.

Abstract

Gestational diabetes mellitus (GDM) is a metabolic disease that occurs during pregnancy. Herein, we investigate G protein-coupled receptor 1 (GPR1) in mediating GDM through the phosphorylation of serine/threonine kinase (AKT) pathway. Thirty pregnant SD rats were grouped into: normal pregnancy control group (NC), GDM model group, and GDM model + high-dose GPR1 antagonist treatment (GDM + Ari) group. GDM model was established, and the GDM + Ari group adopted GPR1 antagonist aripiprazole. The blood glucose level, insulin level, and insulin resistance (IR) were detected. The expression and phosphorylation of GPR1, AKT, and extracellular signal-regulated kinase (ERK) in placental tissue were detected using reverse transcription-polymerase chain reaction (RT-PCR) and western blotting (WB). The serum insulin concentration, glucose concentration, and glycated hemoglobin concentration during pregnancy in GDM group SD rats were significantly higher than those in the NC group ( < 0.05). The expression and phosphorylation levels of GPR1, AKT, and ERK in the placental tissue of SD pregnant rats in the GDM group were significantly lower than those in the NC group. Furthermore, compared with the GDM group, the expression of GPR1, AKT, and ERK in placental tissue was significantly reduced in the GDM + Ari group, while simultaneously enhancing the blood glucose level and IR level. In addition, the survival number, body weight, and malformation rate of the offspring of the GDM + Ari group were significantly improved, and there was no significant effect on the number of offspring. The expressions of GPR1, AKT, and ERK in placental tissue exhibited a significant decrease, while the glucose level and IR were observed to increase in the GDM + Ari group. Enhancing the expression of GPR1 may activate AKT phosphorylation to alleviate GDM. GPR1 could potentially serve as a novel target for diabetes treatment, offering new insights into managing GDM.

摘要

妊娠期糖尿病(GDM)是一种在孕期发生的代谢性疾病。在此,我们研究G蛋白偶联受体1(GPR1)通过丝氨酸/苏氨酸激酶(AKT)途径的磷酸化介导妊娠期糖尿病的机制。将30只妊娠SD大鼠分为:正常妊娠对照组(NC)、妊娠期糖尿病模型组和妊娠期糖尿病模型+高剂量GPR1拮抗剂治疗组(GDM+阿立哌唑组)。建立妊娠期糖尿病模型,GDM+阿立哌唑组采用GPR1拮抗剂阿立哌唑。检测血糖水平、胰岛素水平和胰岛素抵抗(IR)。采用逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法(WB)检测胎盘组织中GPR1、AKT和细胞外信号调节激酶(ERK)的表达及磷酸化情况。GDM组SD大鼠孕期血清胰岛素浓度、血糖浓度和糖化血红蛋白浓度显著高于NC组(P<0.05)。GDM组SD妊娠大鼠胎盘组织中GPR1、AKT和ERK的表达及磷酸化水平显著低于NC组。此外,与GDM组相比,GDM+阿立哌唑组胎盘组织中GPR1、AKT和ERK的表达显著降低,同时血糖水平和IR水平升高。另外,GDM+阿立哌唑组后代的存活数量、体重和畸形率显著改善,对后代数量无显著影响。GDM+阿立哌唑组胎盘组织中GPR1、AKT和ERK的表达显著降低,而血糖水平和IR升高。增强GPR1的表达可能激活AKT磷酸化以减轻妊娠期糖尿病。GPR1可能成为糖尿病治疗的新靶点,为管理妊娠期糖尿病提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a230/11365467/bf341a20b110/j_biol-2022-0920-ga001.jpg

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