Study of durability of diesel vehicle emissions performance based on real driving emission measurement.

Diesel vehicle emissions generally deteriorate with vehicle mileage due to the wear and deterioration of vehicle parts. Most of the experimental studies on vehicle emission durability were carried out based on the standard operation cycles of engine or vehicle, few research investigated vehicle emission deterioration characteristics under real driving conditions. In this research, the real driving emission (RDE) test method was used to investigate and evaluate the emission deterioration characteristics of two China-V diesel vehicles equipped with DOC and SCR systems. The experimental results show the emissions of CO and NOx from the N2 and N3 diesel vehicles increase with the vehicle mileage, showing the tendency of emission deterioration. The calculated deterioration factors of N2 and N3 diesel vehicle CO and NOx emissions are greater than the recommended values in China standard HJ 438-2008, which means experimental study on the vehicle emissions durability is necessary. The vehicle emissions deterioration depends on real driving conditions and the vehicle usage over vehicle lifetime.

Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D.

Vitamin D has been recognized as a potent immunomodulator and its deficiency is common in different population groups including patients with SLE. As miRNAs regulation plays a significant role in SLE, the present study aimed to evaluate the association between vitamin D status and miRNAs levels in patients with SLE. The serum concentrations of vitamin D (25-hydroxyvitamin D) and the levels of six miRNAs in T cells from patients with SLE were measured in 42 SLE cases and 48 healthy controls. Vitamin D treatment was also performed in isolated and cultured T cells from SLE patients in different times and doses. Vitamin D insufficiency (25-hydroxyvitamin D concentration <20 ng/ml) was more common in cases than in controls. Although age and BMI were similar, cases had significantly lower concentrations of miRNA-377, miRNA-342, miRNA-10a, miRNA-374b, miRNA-125a, and miRNA-410 than controls. Furthermore, a significant positive correlation was also observed between 25-hydroxyvitamin D concentrations and measured miRNAs levels. A significant difference in observed miRNAs levels was also observed in patients with 25-hydroxyvitamin D insufficiency compared with patients with 25-hydroxyvitamin D concentration ≥20 ng/ml. And 1α,25(OH)2D3 differentially regulated miRNAs expression in dose- and time- manner in vitro. Lower expressions of miRNA-377, miRNA-342, miRNA-10a, miRNA-374b, miRNA-125a, and miRNA-410 were found in SLE patients. And severe vitamin D deficiency is associated with decreased observed miRNAs levels in SLE patients. A 25-hydroxyvitamin D concentration value <20 ng/ml is suggested as the "cut-off" for such immunological alterations in patients with SLE.