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Objective To investigate whether long-chain non-coding ribonucleic acid HAGLR(LncRNA HAGLR)can affect lipopolysaccharide(LPS)-induced apoptosis and expression of inflammatory factors of retinal pigment epithelium(RPE)cells by targeted regulation of the expression of micro ribonucleic acid-625-5p(miR-625-5p),so as to lay an experi-mental foundation for revealing the mechanism of retinopathy.Methods LPS-induced human retinal pigment epithelial(ARPE-19)cells were set as the LPS group,and normally cultured ARPE-19 cells were assigned to the Con group.Quanti-tative real-time polymerase chain reaction was used to detect the expression levels of LncRNA HAGLR and miR-625-5p.Based on different transfection reagents,the cells were divided into the LPS+sh-NC group,LPS+sh-HAGLR group,LPS+miR-NC group,LPS+miR-625-5p group,LPS+sh-HAGLR+anti-miR-NC group,and LPS+sh-HAGLR+anti-miR-625-5p group.Flow cytometry was used to detect apoptosis rate;enzyme-linked immunosorbent assay was used to detect the lev-els of interleukin-6(IL-6)and interleukin-1β(IL-1β);the targeting relationship between LncRNA HAGLR and miR-625-5p was verified;Western blot was used to detect the protein levels of activated cysteinyl aspartate specific proteinase 3 and 9(cleaved-Caspase 3 and cleaved-Caspase 9).Results Compared with the Con group,the LPS group showed an increase in the expression level of LncRNA HAGLR and a decrease in the expression level of miR-625-5p(both P＜0.05),and there were increases in apoptosis rate,protein levels of cleaved-Caspase 3 and cleaved-Caspase 9,and levels of IL-6 and IL-1β(all P＜0.05).Compared with the LPS+sh-NC group,the LPS+sh-HAGLR group showed decreases in apoptosis rate,protein levels of cleaved-Caspase 3 and cleaved-Caspase 9,and levels of IL-6 and IL-1β(all P＜0.05);LncRNA HAGLR could negatively regulate the expression level of miR-625-5p(P＜0.05).Compared with the LPS+miR-NC group,the LPS+miR-625-5p group showed an increase in the expression level of miR-625-5p and decreases in apoptosis rate,protein levels of cleaved-Caspase 3 and cleaved-Caspase 9,and levels of IL-6 and IL-1β(all P＜0.05).Compared with the LPS+sh-HAGLR+anti-miR-NC group,the LPS+sh-HAGLR+anti-miR-625-5p group showed a decrease in the expression level of miR-625-5p and increases in apoptosis rate,protein levels of cleaved-Caspase 3 and cleaved-Caspase 9,and levels of IL-6 and IL-1β(all P＜0.05).Conclusion Interference on LncRNA HAGLR expression can realize the targeted regulation of miR-625-5p expression to inhibit the apoptosis and inflammatory factor expression,reducing LPS-induced injury of ARPE-19 cells.
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Objective To analyze the GDM of 336 cases with chronic HBV in pregnancy. Methods According to HBV DNA≥1.0 × 103 IU/mL, participants were divided into HBV DNA (+) or (-) group. 409 cases without HBV were selected as control group. Differences on GMD incidence between groups and virus load and OGTT blood sugar correlation were compared. Results The incidence of GDM of HBV DNA (+) or (-) group was 16.77% and 17.71%, which is higher than that in HBV group (10.27%). The difference is significant (P < 0.05). The correlation index between HBV DNA and fasting blood-glucose is r = 0.005, P = 0.610, the result of which is not statistically significant. But correlation index between HBV DNA and blood sugar at 1 h , 2 h are r = 0.082, 0.086; P = 0.000, 0.000, the result of which is statistically significant. Conclusion The oc-currence of GDM were higher in HBV DNA (+) or (-) group. The viral load is positively related with blood sugar of glucose tolerance at 1 h or 2 h.