Molecular mechanism of valine and its metabolite in improving triglyceride synthesis of porcine intestinal epithelial cells.

An insufficient energy supply to intestinal epithelial cells decreases production performance in weaned piglets. Triglycerides are the main energy source for intestinal epithelial cells in piglets. The present study aimed to investigate the effects and mechanisms of valine supplementation on triglyceride synthesis in porcine intestinal epithelial (IPEC-J2) cells. Valine supplementation in the medium significantly increased the content of triglycerides, fat droplets, and long-chain fatty acids (C17:0, C18:0, C20:0, C18:1, C20:1, and C22:1) (P < 0.05). Valine metabolite (3-hydroxyisobutyrate [3-HIB]) concentration increased significantly in the valine-supplemented group (P < 0.05). Silencing of the 3-HIB synthase enzyme 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) in IPEC-J2 cells significantly reduced the triglyceride concentration and lipid droplet synthesis. Further studies found that 3-HIB supplementation in the medium significantly increased the concentration of triglycerides, lipid droplets, and unsaturated fatty acids (C16:1, C18:1, C18:2, C18:3, C20:3, C20:4, and C20:5) (P < 0.05) by upregulating the expression of proteins involved in fatty acid transport (CD36) and fatty acid binding protein 3 (FABP3) or triglyceride synthesis (DGAT1) (P < 0.05), indicating that 3-HIB mediates valine-enhanced triglyceride synthesis in IPEC-J2 cells. In conclusion, our results demonstrated that valine enhanced triglyceride synthesis in IPEC-J2 cells via increasing the 3-HIB concentration, which may promote fatty acid transport via upregulation of proteins related to fatty acid transporter. These findings provide new insights into the mechanisms through which valine participates in lipid metabolism.

Consumption of processed food and risk of nasopharyngeal carcinoma: a systematic review and meta-analysis.

Background: Consumption of processed foods has been associated with nasopharyngeal carcinoma (NPC), but with inconsistent results. Therefore, we conducted a systematic review and meta-analysis to compute results regarding the association between processed foods and risk of NPC in included studies. Methods: Studies exploring the association between consumption of processed food and risk of NPC were included in the present study. All included studies were case-control or cohort designed. PubMed, Web of Science, EMBASE, Medline and Google Scholar databases were searched for articles published before July 2021. We recorded the following data: author, publication year, sample size, study type, study location, years of diagnosis, food item and comparison, and the covariates considered were multivariate adjusted odds ratios (ORs) or relative risks (RRs) with corresponding 95% confidence intervals (CIs) for the highest vs. lowest categories of processed food intake. STATA 12.0 software was used to compute the multivariate ORs or RRs and 95% CIs of the association. Quality appraisal was made using the Cochrane Risk of Bias Tool. Results: A meta-analysis was made for 29 case-control studies (including 14,378 NPC patients and 17,928 controls). The meta-analysis showed that the highest categories of processed food intake were associated with a 65% increase in NPC risk compared with the lowest categories in a random effects model (OR =1.67; 95% CI: 1.56-1.79; P value for Q test <0.001; I2=86.9%). Subgroup study showed significant positive associations regarding consumption of processed food and risk of NPC in both Asians and Caucasians (Asian: OR =1.68, 95% CI: 1.56-1.81; Caucasian: OR =1.36, 95% CI: 1.09-1.71). Conclusions: The association of processed foods with NPC risk might be significant. Further prospective studies and experimental research are needed to explore this relationship.

Uniform and size-tunable mesoporous silica with fibrous morphology for drug delivery.

A family of mesoporous silica microspheres with fibrous morphology and different particle sizes ranging from about 400 to 900 nm has been successfully synthesized through a facile self-assembly process. The structural, morphological, and textural properties of the samples were well characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FT-IR), N(2) adsorption/desorption, and thermal gravimetry (TG). The results reveal that this silica-based mesoporous material exhibits excellent physical properties, including a fibrous spherical morphology, good thermal stability, large pore volume, high specific surface area and narrow size distribution. Additionally, the size and textural properties can be tuned by altering the silica precursor/template molar ratio. The formation and the self-assembly evolution process have also been proposed. The obtained materials were further used as a drug delivery carrier to investigate the in vitro drug release properties using doxorubicin (DOX) as a representative model drug. It was found that this kind of silica exhibits good biocompatibility and obvious sustained drug release properties, suggesting its potential application in biological fields.