Previous studies on mangrove carbon utilisation and mineralisation were focused on mangrove sesarmid crabs (Grapsoidea: Sesarmidae) because they are initial processors of mangrove organic carbon. Grapsoid crabs from other families and habitats were generally ignored although they also perform various levels of herbivory. It remains unclear how the herbivorous crabs utilise the production from mangrove or vascular plants because of the high C/N ratio and high structural carbon content of these materials. In this study, production of cellulase and expression of hepatopancreatic glycosyl hydrolase of grapsoid crabs were investigated in a more extensive way in terms of their taxa (15 species) and habitats (i.e., land margin, mangrove, mudflat, and subtidal area). Generally, low gastric endoglucanase (1.46-2.98 μmol min−1 ml−1) and β-glucosidase (0.06-0.61 μmol min−1 ml−1) activity was detected in 15 grapsoid crabs distributed along the land-sea transition. The activity of both enzymes was significantly affected by the taxonomic affiliation and habitat of the crabs: endoglucanase in sesarmids > varunids > grapsids; and land margin, mangrove and limnic habitats > mudflat and subtidal area. For β-glucosidase: sesarmids > varunids and grapsids; and land and limnic > mangrove and subtidal > mudflat. Our detection of gastric cellulases in mudflat and subtidal grapsoid crabs has rarely been reported. These results show that there is a need to re-evaluate the role of crabs from these habitats in mangrove/vascular plant carbon mineralisation. Further, low cellulase activity could be a common trait among crabs along the land-sea transition and the importance of cellulase in vascular plant carbon utilisation could have been previously over-rated. Glycosyl hydrolase family 9 (GH9) genes were identified in the hepatopancreatic transcriptome of all 15 species, indicating endogenous production of cellulase. In addition, the presence of other digestive carbohydrate-active enzymes (CAZymes), including GH5_10, GH13, GH13_24, and GH16, suggests that a capacity for the utilisation of carbon sources other than cellulose by the grapsoid crabs, which may enable sufficient assimilation of vascular plant carbon despite the low cellulase activity.

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Introduction Diabetes mellitus (DM) is characterized by chronic hyperglycemia and diabetic complications. Exacerbated cortical neuronal degeneration was observed in Alzheimer’s disease (AD) patients with DM. In fact, DM is now considered a risk factor of AD, as DM-induced activation of stress responses in the central nervous system (CNS) such as oxidative stress and neuroinflammation may lead to various neurodegenerative disorders. Methylglyoxal (MG) is one of the most reactive advanced glycation end-product (AGE) precursors. Abnormal accumulation of MG is observed in the serum of diabetic patients. As MG is reported to promote brain cells impairment in the CNS, and it is found that AGEs are abnormally increased in the brains of AD patients. Therefore, the effect of MG causing subsequent symptoms of AD was investigated. Methods 5-week-old C57BL/6 mice were intraperitoneally injected with MG solution for 11 weeks. The Morris water maze (MWM) was used to examine the spatial learning ability and cognition of mice. After MG treatment, MTT assay, real-time PCR analyses, and Western blot were performed to assess the harvested astrocytes and hippocampi. Results Significantly longer escape latency and reduced percentage time spent in the target quadrant were observed in the 9-week-MG-treated mice. We have found in both in vitro and in vivo models that MG induced astrogliosis, pro-inflammatory cytokines, AD-related markers, and ERK activation. Further, trend of normalization of the tested markers mRNA expressions were observed after ERK inhibition. Conclusion Our in vivo results suggested that MG could induce AD symptoms and in vitro results implied that ERK may regulate the promotion of inflammation and Aβ formation in MG-induced reactive astrocytes. Taken together, MG may participate in the dysfunction of brain cells resulting in possible diabetes-related neurodegeneration by promoting astrogliosis, Aβ production, and neuroinflammation through the ERK pathway. Our findings provide insight of targeting ERK as a therapeutic application for diabetes-induced AD.

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Abstract. Intertidal benthos link tertiary predators and primary producers in marine food webs as well as directly contribute to sediment CO2 emission. However, current methods for studying food sources of marine benthos are time-consuming and does not allow direct estimates on feeding regime-related CO2 production. We examined the foods of mangrove crabs and gastropods as well as their corresponding CO2 production by using cavity-ring down spectroscopy to measure the δ13C of consumer-respired CO2, considering the effects of feeding regime, benthos taxa, and dominant feeding habit. Benthos taxa and feeding habit have significant impact on δ13C of respired CO2. Particularly, the δ13C of crab (−23.9±0.4 ‰) respired CO2 was significantly lower than that from gastropod (−17.5±1.3 ‰) respiration. The δ13C of deposit-feeder respired CO2 was significantly higher than that from detritivores. There are significant differences in the amount of CO2 emitted and δ13C of crab respired CO2 under different feeding regimes. The differences reflect diet-switching and fuel-switching in the crabs, i.e. you breathe what you eat. Significant differences in CO2 production of crabs also exist between those feeding on microphytobenthos (0.13±0.02 mmol g−1 day−1) and on field collection (0.31±0.03 mmol g−1 day−1). CO2 production of crabs is strongly related to carapace width and length. The δ13C of respired CO2 from mangrove crabs reflects their diet while crab-respired CO2 flux is related to crab size. These relationships enable partitioning the feeding habit and food sources of key benthos, and help incorporate their contribution into the overall sediment-atmosphere CO2 fluxes in mangroves.