The cervical cancer related distribution, coinfection and risk of 15 HPV types in Baoan, Shenzhen, in 2017-2023.

Cervical cancer is one of the most common malignant tumours. Human papillomavirus (HPV) infection is the main cause of this cancer so that it could be prevented by screening and early treatment. Developing reginal screen protocols of maximum public health efficacy requires in-depth understandings of local HPV distribution and consequential cancer risks. Therefore, test results of HPV genotyping, cytology testing (TCT) and colposcopy inspection with biopsy were collected in this retrospective research. Data included by this research involved 63,906 women received screen related tests from Shenzhen Baoan Shiyan People's Hospital and the subsidiary institutes between 2017.01 and 2023.05. 10,238 colposcopies were performed in this period collecting 8,716 samples and 814 high-grade CIN were discovered. Within the 763 high-grade CIN cases with both TCT and HPV testing results, 232 were tested cytologically normal but only 30 were negative in HPV test. Besides, the rates of high-grade CIN observed in coinfection were all lower than the estimated rates generated from related single infection. HPV 52, 58 and 16 were found to be the most common types in Baoan, Shenzhen. The result also suggested that HPV coinfections should not increase risk for cervical cancers.

Development and Performance Evaluation of an Asphalt Regenerant Derived from Waste Engine Oil Residue.

This study assessed the fundamental physical properties and chemical composition of three specific waste engine oil residue (WEORs) asphalt regenerants. Through dynamic shear rheometer and rolling thin-film oven tests, the performance of aged asphalt was evaluated using three key indicators. Thin-layer chromatography investigations probed the WEOR-induced changes in the aging asphalt components, leading to the creation of two novel asphalt regenerants, WEOR-H and WEOR-G. WEOR-G was developed from WEOR-1, liquid rubber, ultraviolet absorber, light shielding agent, and antioxidant, while WEOR-H was formulated from WEOR-2, aromatic oil, and liquid rubber. The study employed differential scanning calorimetry and conventional laboratory tests to analyze the road performance attributes of Ingevity J type regenerant (J), WEOR-G, and WEOR-H. The results indicated that WEORs increase the saturate and aromatic content in asphalt and partially replenish the missing lightweight components of aged asphalt, moderately improving the three key indicators, though the regenerative effect is restricted. Achieving a full restoration of component proportions within aged asphalt to their initial levels proved unattainable, and direct application of any of the three WEORs as asphalt regenerants is impractical. WEOR-H and WEOR-G demonstrated potential in enhancing aged asphalt binder road performance, outpacing three other WEORs. At a 14% dosage, WEOR-G and WEOR-H could increase the 10 °C ductility to 23.5 and 21.4 cm, respectively, effectively counterbalancing the insufficient ability of WEOR-1 and WEOR-2 to restore the low-temperature performance of aged asphalt. Among the regenerants, WEOR-G, possessing superior regenerative effects, the lowest glass transition temperature, and optimal low-temperature deformation resistance, emerged as the most efficacious. This inquiry furnishes vital data support for future applications of WEOR-G asphalt regenerant.

Preparation of Wax-Based Warm Mixture Additives from Waste Polypropylene (PP) Plastic and Their Effects on the Properties of Modified Asphalt.

The production of high-performance, low-cost warm mix additives (WMa) for matrix asphalt remains a challenge. The pyrolysis method was employed to prepare wax-based WMa using waste polypropylene plastic (WPP) as the raw material in this study. Penetration, softening point, ductility, rotational viscosity, and dynamic shear rheological tests were performed to determine the physical and rheological properties of the modified asphalt. The adhesion properties were characterized using the surface free energy (SFE) method. We proved that the pyrolysis temperature and pressure play a synergistic role in the production of wax-based WMa from WPPs. The product prepared at 380 °C and 1.0 MPa (380-1.0) can improve the penetration of matrix asphalt by 61% and reduce the viscosity (135 °C) of matrix asphalt by 48.6%. Furthermore, the modified asphalt shows favorable elasticity, rutting resistance, and adhesion properties; thus, it serves as a promising WMa for asphalt binders.

Sumatriptan inhibits the electrophysiological activity of ASICs in rat trigeminal ganglion neurons.

Sumatriptan, a selective serotonin 5-HT1 receptor agonist, is an effective therapeutic for migraine attacks. However, the molecular mechanisms underlying sumatriptan migraine relief are still not fully understood. Here, we found that acid-sensing ion channels (ASICs), pH sensors, are peripheral targets of sumatriptan against migraine. Sumatriptan can inhibit the electrophysiological activity of ASICs in the trigeminal ganglion (TG) neurons. In the present study, sumatriptan decreased proton-gated currents mediated by ASICs in a concentration-dependent manner. In addition, sumatriptan shifted concentration-response curves for protons downwards, with a decrease of 37.3 ±â€¯4.6% in the maximum current response but with no significant change in the pH0.5 value. Sumatriptan inhibition of ASIC currents was blocked by 5-HT1D receptor antagonist BRL 15572, but not by 5-HT1B antagonist SB 224289. Moreover, the sumatriptan inhibition of ASICs can be mimicked by the 5-HT1D receptor agonist L-694,247, but not by the 5-HT1B agonist CP-93129. Sumatriptan inhibition of ASIC currents was also reversed by G-protein αi subunit inhibitor PTX and 8-Br-cAMP, suggesting the inhibition may involve the intracellular signal transduction. Finally, sumatriptan decreased the number of action potentials induced by acid stimuli in rat TG neurons. Our results indicated that the anti-migraine drug, sumatriptan, inhibited ASICs in rat TG neurons via 5-HT1D receptor subtype and a cAMP-dependent signal pathway. These observations add to the understanding of the mechanisms that underlie the clinical effectiveness of anti-migraine sumatriptan.