Polychlorinated biphenyls (PCBs) are lipophilic environmental toxicants. Epidemiological studies have established a link between PCBs and both metabolic syndrome and nonalcoholic fatty liver disease (NAFLD). Multiple studies have reported that exposure to both PCB156 and PCB126 among the 12 dioxin-like PCBs leads to the development of NAFLD. However, studies to elucidate whether PCB169 induces the development of NAFLD by constructing in vivo models have not been reported. Therefore, we evaluated the effects of exposure to PCB169 (5 mg/kg-bw) on hepatic lipid metabolism in C57BL/6 mice from control diet and high-fat diet cohorts. The results showed that PCB169 exposure reduced body weight and intraperitoneal fat mass in mice on the control diet, but the liver lipid levels were significantly increased, exacerbating NAFLD in mice on a high-fat diet. Through transcriptomics studies, it was found that PCB169 exposure induced significant up-regulation of Pparγ, Fasn, and Aacs genes involved in hepatic lipogenesis, as well as remarkable up-regulation of Hmgcr, Lss, and Sqle genes involved in cholesterol synthesis. Additionally, there was notable down-regulation of Pparα and Cpt1 genes involved in lipid β-oxidation, leading to abnormal lipid accumulation in the liver. In addition, we found that PCB169 exposure significantly activated the Arachidonic acid metabolism, PPAR signaling pathway, Metabolism of xenobiotics by cytochrome P450, and Retinol metabolism pathways, and so on. Our study suggests that PCB169 can modify gene expression related to lipid metabolism, augument lipid accumulation in the liver, and further contribute to the development of NAFLD, thereby revealing the detrimental effects associated with PCB exposure on animal growth and metabolism.

Background: Cashmere, known as “soft gold”, is a highly prized fiber from Cashmere goats, produced by secondary hair follicles. Dermal papilla cells, located at the base of these follicles, regulate the proliferation and differentiation of hair matrix cells, which are essential for hair growth and cashmere formation. Recent studies emphasize the role of microRNAs (miRNAs) in controlling gene expression within these processes. Methods: This study centered on exploring the targeted regulatory interaction between miR-144 and the Lhx2 gene. Utilizing methodologies like miRNA target prediction, luciferase reporter assays, and quantitative PCR, they assessed the interplay between miR-144 and Lhx2. Dermal papilla cells derived from Cashmere goats were cultured and transfected with either miR-144 mimics or inhibitors to observe the subsequent effects on Lhx2 expression. Results: The results demonstrated that miR-144 directly targets the Lhx2 gene by binding to its mRNA, leading to a decrease in Lhx2 expression. This modulation of Lhx2 levels influenced the behavior of dermal papilla cells, affecting their ability to regulate hair matrix cell proliferation and differentiation. Consequently, the manipulation of miR-144 levels had a significant impact on the growth cycle of cashmere wool. Conclusions: The findings suggest miR-144 regulates hair follicle dynamics by targeting Lhx2, offering insights into hair growth mechanisms. This could lead to innovations in enhancing cashmere production, fleece quality, and addressing hair growth disorders. Future research may focus on adjusting miR-144 levels to optimize Lhx2 expression and promote hair follicle activity.

This study investigated the effects of Rhodopseudomonas palustris (R. palustris) supplementation on the rumen microbiota of Leizhou goats and explored its potential mechanisms. Thirty healthy Leizhou goats of similar weight and age were selected and randomly assigned to five groups (six goats per group) using a completely randomized block design for a 75-day feeding trial. The control group (CONRF) was fed a basal diet, and the Photosynthetic Bacteria Medium (PBMRF) group was fed a basal diet + PBM solution. The low-concentration R. palustris (LRPRF), medium-concentration R. palustris (MRPRF), and high-concentration R. palustris (HRPRF) groups were fed a base diet supplemented with 20.0 mL, 40.0 mL, and 80.0 mL of R. palustris solution, respectively. All supplements were administered by mixing them into the feed. On day 75 of the trial, three goats were randomly selected from each group for slaughter and evisceration. Rumen contents were collected, immediately filtered, aliquoted, quick-frozen in liquid nitrogen, and stored at −80 °C for subsequent analysis of rumen microbial diversity. Rumen microbial community structure was analyzed using high-throughput sequencing. The results showed that R. palustris enriched unique operational taxonomic units (OTUs), particularly in the LRPRF group. At the phylum level, Firmicutes and Bacteroidota were dominant; Firmicutes and Euryarchaeota abundance increased, while Bacteroidota decreased in the experimental groups. In addition, Verrucomicrobiota abundance was significantly elevated (p < 0.05). At the genus level, Prevotella was predominant, whereas Selenomonas abundance was significantly reduced (p < 0.01). Meanwhile, compared to the CONRF, PBMRF, and LRPRF groups, the MRPRF and HRPRF groups exhibited higher relative abundances of Christensenellaceae_R-7 group and Anaeroplasma. LEfSe analysis revealed a greater number of differential taxa in the experimental groups compared with the control, including enrichment of beneficial bacteria, such as Lactobacillus, which may contribute to optimizing the rumen environment by regulating immune and metabolic functions. Functional prediction indicated that rumen microorganisms were mainly involved in carbohydrate and amino acid metabolism. In conclusion, supplementation with R. palustris can beneficially modulate rumen microbial composition and function and promote rumen absorption of nutrients and degradation of crude fiber. This study provides a theoretical basis for green goat farming practices.