Anthropogenic debris pollution in peri-urban mangroves of South China: Spatial, seasonal, and environmental drivers in Hong Kong.

Excessive mismanaged debris along tropical coasts pose a threat to vulnerable mangrove ecosystems. Here, we examined the spatial, seasonal and environmental drivers of anthropogenic debris abundance and its potential ecological impact in peri-urban mangroves across Hong Kong. Seasonal surveys were conducted in both landward and seaward zones, with identification, along belt transects, of macrodebris (>5 mm) based on material type and use. Our results indicate spatial variability in debris abundance and distribution, with plastic being the predominant material type identified. Both plastic and non-plastic domestic items covered the most surface area. Debris aggregation was highest at the landward zones, consistent with the literature. In the dry season, more debris accumulated and covered greater surface area in both seaward and landward zones. These results confirm that land-derived debris from mismanaged waste, rather than debris coming from the Pearl River, is the primary source of anthropogenic debris pollution threatening Hong Kong's mangroves.

Fate of plastic in the environment: From macro to nano by macrofauna.

Plastic ingestion has been widely investigated to understand its adverse harms on fauna, but the role of fauna itself in plastic fragmentation has been rarely addressed. Here, we review and discuss the available experimental results on the role of terrestrial and aquatic macrofauna in plastic biofragmentation and degradation. Recent studies have shown how biting, chewing, and stomach contractions of organisms shatter ingested plastic along their digestive tracts. Gut microbial communities can play a role in biodegradation and their composition can shift according to the type of plastic ingested. Shifts in molecular weights, chemical bond forming and breaking, and changes in thermal modification detected in the plastic debris present in the faeces also suggest active biodegradation. A few studies have also shown interactions other than ingestion, such as burrowing, may actively or passively promote physical plastic fragmentation by fauna. We suggest that further investigations into the role of fauna in physical fragmentation and chemical degradation linked to active ingestion and gut associated microbiota metabolism, respectively, should be conducted to better evaluate the impact of these mechanisms on the release of micro- and nano-plastic in the environment. Knowledge on macrofauna other than marine invertebrates and terrestrial soil dwelling invertebrates is particularly lacking, as well as focus on broader types of plastic polymers.

Analysis of time-dependent adaptations in whole-body energy balance in obesity induced by high-fat diet in rats.

BACKGROUND: High-fat (HF) diet has been extensively used as a model to study metabolic disorders of human obesity in rodents. However, the adaptive whole-body metabolic responses that drive the development of obesity with chronically feeding a HF diet are not fully understood. Therefore, this study investigated the physiological mechanisms by which whole-body energy balance and substrate partitioning are adjusted in the course of HF diet-induced obesity. METHODS: Male Wistar rats were fed ad libitum either a standard or a HF diet for 8 weeks. Food intake (FI) and body weight were monitored daily, while oxygen consumption, respiratory exchange ratio, physical activity, and energy expenditure (EE) were assessed weekly. At week 8, fat mass and lean body mass (LBM), fatty acid oxidation and uncoupling protein-1 (UCP-1) content in brown adipose tissue (BAT), as well as acetyl-CoA carboxylase (ACC) content in liver and epidydimal fat were measured. RESULTS: Within 1 week of ad libitum HF diet, rats were able to spontaneously reduce FI to precisely match energy intake of control rats, indicating that alterations in dietary energy density were rapidly detected and FI was self-regulated accordingly. Oxygen consumption was higher in HF than controls throughout the study as whole-body fat oxidation also progressively increased. In HF rats, EE initially increased, but then reduced as dark cycle ambulatory activity reached values ~38% lower than controls. No differences in LBM were detected; however, epidydimal, inguinal, and retroperitoneal fat pads were 1.85-, 1.89-, and 2.54-fold larger in HF-fed than control rats, respectively. Plasma leptin was higher in HF rats than controls throughout the study, indicating the induction of leptin resistance by HF diet. At week 8, UCP-1 content and palmitate oxidation in BAT were 3.1- and 1.5-fold higher in HF rats than controls, respectively, while ACC content in liver and epididymal fat was markedly reduced. CONCLUSION: The thermogenic response induced by the HF diet was offset by increased energy efficiency and time-dependent reduction in physical activity, favoring fat accumulation. These adaptations were mainly driven by the nutrient composition of the diet, since control and HF animals spontaneously elicited isoenergetic intake.

Prolonged AICAR-induced AMP-kinase activation promotes energy dissipation in white adipocytes: novel mechanisms integrating HSL and ATGL.

This study was designed to investigate the effects of prolonged activation of AMP-activated protein kinase (AMPK) on lipid partitioning and the potential molecular mechanisms involved in these processes in white adipose tissue (WAT). Rat epididymal adipocytes were incubated with 5'-aminoimidasole-4-carboxamide-1-beta-d-ribofuranoside (AICAR;0.5 mM) for 15 h. Also, epididymal adipocytes were isolated 15 h after AICAR was injected (i.p. 0.7 g/kg body weight) in rats. Adipocytes were utilized for various metabolic assays and for determination of gene expression and protein content. Time-dependent in vivo plasma NEFA concentrations were determined. AICAR treatment significantly increased AMPK activation, inhibited lipogenesis, and increased FA oxidation. This was accompanied by upregulation of peroxisome proliferator-activated receptor (PPAR)alpha, PPARdelta, and PPARgamma-coactivator-1alpha (PGC-1alpha) mRNA levels. Lipolysis was first suppressed, but then increased, both in vitro and in vivo, with prolonged AICAR treatment. Exposure to AICAR increased adipose triglyceride lipase (ATGL) content and FA release, despite inhibition of basal and epinephrine-stimulated hormone-sensitive lipase (HSL) activity. Here, we provide evidence that prolonged AICAR-induced AMPK activation can remodel adipocyte metabolism by upregulating pathways that favor energy dissipation versus lipid storage in WAT. Additionally, we show novel time-dependent effects of AICAR-induced AMPK activation on lipolysis, which involves antagonistic modulation of HSL and ATGL.

Kinetic capillary electrophoresis-based affinity screening of aptamer clones.

DNA aptamers are single stranded DNA (ssDNA) molecules artificially selected from random-sequence DNA libraries for their specific binding to a certain target. DNA aptamers have a number of advantages over antibodies and promise to replace them in both diagnostic and therapeutic applications. The development of DNA aptamers involves three major stages: library enrichment, obtaining individual DNA clones, and the affinity screening of the clones. The purpose of the screening is to obtain the nucleotide sequences of aptamers and the binding parameters of their interaction with the target. Highly efficient approaches have been recently developed for the first two stages, while the third stage remained the rate-limiting one. Here, we introduce a new method for affinity screening of individual DNA aptamer clones. The proposed method amalgamates: (i) aptamer amplification by asymmetric PCR (PCR with a primer ratio different from unity), (ii) analysis of aptamer-target interaction, combining in-capillary mixing of reactants by transverse diffusion of laminar flow profiles (TDLFP) and affinity analysis using kinetic capillary electrophoresis (KCE), and (iii) sequencing of only aptamers with satisfying binding parameters. For the first time we showed that aptamer clones can be directly used in TDLFP/KCE-based affinity analysis without an additional purification step after asymmetric PCR amplification. We also demonstrated that mathematical modeling of TDLFP-based mixing allows for the determination of K(d) values for the in-capillary reaction of an aptamer and a target and that the obtained K(d) values can be used for the accurate affinity ranking of aptamers. The proposed method does not require the knowledge of aptamer sequences before screening, avoids lengthy (3-5 h) purification steps of aptamer clones, and minimizes reagent consumption to nanoliters.