Periostin Acts as a Bridge between Gestational Diabetes Mellitus (GDM) and Chronic Inflammation to Modulate Insulin Resistance by Modulating PPARa/NF-?B/TNF-a Signaling Pathway

Introduction Gestational diabetes mellitus (GDM) is considered an imbalance of glucose metabolism and insulin resistance during pregnancy.Aim/Objective To evaluate the levels of periostin (POSTN) in patients with GDM and investigate the association between POSTN and GDM.Materials and Methods A total of 30 pregnant women (NC group) and 30 pregnant women with GDM (GDM group) were involved. The GDM mouse model was established by intraperitoneally injecting streptozotocin. The oral glucose tolerance test (OGTT), insulin, and insulin resistance indices were tested. An immunohistochemical and Western blot assay was conducted to determine the expression of POSTN, PPARa, TNF-a, and NF-?B. HE staining was performed to evaluate inflammation in the placental tissues of women with GDM and GDM mice. POSTN-siRNA was transfected into glucose-pretreated HTR8 cells, and pAdEasy-m-POSTN shRNA was infected in GDM mice. The RT-PCR assay determined the gene transcription of POSTN, TNF-a, NF-?B, and PPARa.Results Pregnant women in the GDM group demonstrated significantly higher OGTT (p < 0.05), insulin levels (p < 0.05) and insulin resistance (p < 0.05) compared to those of the NC group. The serum levels of POSTN in pregnant women of the GDM group were significantly higher than that of the NC group (p < 0.05). The obvious inflammation was activated in pregnant women in the GDM group. POSTN-siRNA significantly enhanced the cell viability of glucose-treated HTR8 cells compared to that without glucose treatment (p < 0.05). POSTN-siRNA (pAdEasy-m-POSTN shRNA) markedly reduced the glucose level of glucose-treated HTR8 cells (GDM mice) compared to that without treatment (p < 0.05). POSTN-siRNA (pAdEasy-m-POSTN shRNA) promoted PPARa gene transcription (p < 0.05) and inhibited NF-?B/TNF-a gene transcription (p < 0.05) in glucose-treated HTR8 cells (GDM mice) compared to those without treatment. POSTN-siRNA modulated NF-?B/TNF-a pathway mediated inflammation by regulating PPARa in HTR8 cells and GDM mice. PPARa participated in POSTN-associated inflammation. pAdEasy-m-POSTN shRNA inhibited T-CHO/TG levels in GDM mice compared to those without treatment (p < 0.05). All the effects of POSTN-siRNA (pAdEasy-m-POSTN shRNA) were obviously blocked by PPARa inhibitor treatment.Conclusion POSTN levels were significantly higher in pregnant women with GDM and were associated with chronic inflammation and PPARa expression. POSTN may act as a bridge between GDM and chronic inflammation to modulate insulin resistance by modulating PPARa/NF-?B/TNF-a signaling pathway.