Deficiency of leucine-rich repeat kinase 2 aggravates thioacetamide-induced acute liver failure and hepatic encephalopathy in mice.

BACKGROUND: Hepatic encephalopathy (HE) is closely associated with inflammatory responses. However, as a crucial regulator of the immune and inflammatory responses, the role of leucine-rich repeat kinase 2 (LRRK2) in the pathogenesis of HE remains unraveled. Herein, we investigated this issue in thioacetamide (TAA)-induced HE following acute liver failure (ALF). METHODS: TAA-induced HE mouse models of LRRK2 wild type (WT), LRRK2 G2019S mutation (Lrrk2G2019S) and LRRK2 knockout (Lrrk2-/-) were established. A battery of neurobehavioral experiments was conducted. The biochemical indexes and pro-inflammatory cytokines were detected. The prefrontal cortex (PFC), striatum (STR), hippocampus (HIP), and liver were examined by pathology and electron microscopy. The changes of autophagy-lysosomal pathway and activity of critical Rab GTPases were analyzed. RESULTS: The Lrrk2-/--HE model reported a significantly lower survival rate than the other two models (24% vs. 48%, respectively, p < 0.05), with no difference found between the WT-HE and Lrrk2G2019S-HE groups. Compared with the other groups, after the TAA injection, the Lrrk2-/- group displayed a significant increase in ammonium and pro-inflammatory cytokines, aggravated hepatic inflammation/necrosis, decreased autophagy, and abnormal phosphorylation of lysosomal Rab10. All three models reported microglial activation, neuronal loss, disordered vesicle transmission, and damaged myelin structure. The Lrrk2-/--HE mice presented no severer neuronal injury than the other genotypes. CONCLUSIONS: LRRK2 deficiency may exacerbate TAA-induced ALF and HE in mice, in which inflammatory response is evident in the brain and aggravated in the liver. These novel findings indicate a need of sufficient clinical awareness of the adverse effects of LRRK2 inhibitors on the liver.

Effects of zeolite imidazole frameworks on rice seedlings (Oryza sativa L.): Phytotoxicity, transformation, and bioaccumulation.

Zeolite imidazole frameworks (ZIFs), a class of the metal organic framework, have been extensively studied in environmental applications. However, their environmental fate and potential ecological impact on plants remain unknown. Here, we investigated the phytotoxicity, transformation, and bioaccumulation processes of two typical ZIFs (ZIF-8 and ZIF-67) in rice (Oryza sativa L.) under hydroponic conditions. ZIF-8 and ZIF-67 in the concentration of 50 mg/L decreased root and shoot dry weight maximally by 55.2% and 27.5%, 53.5% and 37.5%, respectively. The scanning electron microscopy (SEM) imaging combined with X-ray diffraction (XRD) patterns revealed that ZIFs on the root surface gradually collapsed and transformed into nanosheets with increasing cultivation time. The fluorescein isothiocyanate (FITC) labeled ZIFs were applied to trace the uptake and translocation of ZIFs in rice. The results demonstrated that the transformed ZIFs were mainly distributed in the intercellular spaces of rice root, while they cannot be transported to culms and leaves. Even so, the Co and Zn contents of rice roots and shoots in the ZIFs treated groups were increased by 1145% and 1259%, 145% and 259%, respectively, compared with the control groups. These findings suggested that the phytotoxicity of ZIFs are primarily attributed to the transformed ZIFs and to a less extent, the metal ions and their ligands, and they were internalized by rice root and increased the Co and Zn contents of shoots. This study reported the transformation of ZIFs and their biological effectiveness in rice, highlighting the potential environmental hazards and risks of ZIFs to crop plants.

Paint sludge derived activated carbon encapsulating with cobalt nanoparticles for non-radical activation of peroxymonosulfate.

Industrial solid waste management and recycling are important to environmental sustainability. In this study, cobalt (Co) nanoparticles encapsulated in paint sludge-derived activated carbon (AC) were fabricated. The Co-AC possessed high conductivity, magnetic properties and abundant metal oxide impurities (TiAlSiOx), which was applied as multifunctional catalyst for peroxymonosulfate (PMS) activation. Compared to pure AC, the Co-AC exhibited significant enhanced performance for degradation of tetracycline hydrochloride (TCH) via PMS activation. Mechanism studies by in situ Raman spectroscopy, Fourier infrared spectroscopy, electrochemical analysis and electron paramagnetic resonance suggested that surface-bonded PMS (PMS*) and singlet oxygen (1O2) are the dominant reactive species for TCH oxidation. The non-radical species can efficiently oxidize electron-rich pollutants with high efficiency, which minimized the consumption of PMS and the catalyst. The removal percentages of TCH reached 97 % within 5 min and âˆ¼ 99 % within 15 min in the Co-AC/PMS system. The Co active sites facilitated PMS adsorption to form the PMS* and the TiAlSiOx impurities provided abundant oxygen vacancy for generation of the 1O2. In addition, the Co-AC/PMS system achieved high efficiency and stability for oxidation of the target pollutants over a long-term continuous operation. This work not only offers a cost-effective approach for recycling industrial waste but also provides new insights into the application of waste-derived catalyst for environmental remediation.

Graphitic carbon nitride nanosheets mitigate cadmium toxicity in Glycine max L. by promoting cadmium retention in root and improving photosynthetic performance.

Cadmium (Cd) pollution poses a serious threat to plant growth and yield. Nanomaterials have shown great application potential for alleviation of Cd toxicity to plants. In this study, we applied graphitic carbon nitride nanosheets (g-C3N4 NSs) for alleviation of Cd-toxicity to soybean (Glycine max L.). The g-C3N4 NSs supplementation significantly improved plant growth and reduced oxidative damage in the Cd-toxicated soybean seedlings through hydroponic culture. Particularly, the g-C3N4 NSs dynamically regulated the root cell wall (RCW) components by increasing pectin content and modifying its demethylation via enhancing pectin methylesterase (PME) activity, therefore greatly enhanced stronger RCW-Cd retention (up to 82.8%) and reduced Cd migration to the shoot. Additionally, the g-C3N4 NSs reversed the Cd-induced chlorosis, increased photosynthetic efficiency because of enhancement in Fv/Fm ration, Y(II) and sugars content. These results provide new insights into the alleviation of Cd toxicity to plants by g-C3N4 NSs, and shed light on the application of low-cost and environmental-friendly carbon-based NMs for alleviating heavy metal toxicity to plants.

Directional and Ultrafast Charge Transfer in Oxygen-Vacancy-Rich ZnO@Single-Atom Cobalt Core-Shell Junction for Photo-Fenton-Like Reaction.

In photosynthesis, solar energy is harvested by photosensitizers, and then, the excited electrons transfer via a Z-Scheme mode to enzymatic catalytic centers to trigger redox reactions. Herein, we constructed a core-shell Z-scheme heterojunction of semiconductor@single-atom catalysts (SACs). The oxygen-vacancy-rich ZnO core and single-atom Co-N4 sites supported on nitrogen-rich carbon shell (SA-Co-CN) act as the photosensitizer and the enzyme-mimicking active centers, respectively. Driven by built-in electric field across the heterojunction, photoexcited electrons could rapidly (2 ps) transfer from the n-type ZnO core to the p-type SA-Co-CN shell, finally boosting the catalytic performance of the surface-exposed single-atom Co-N4 sites for peroxymonosulfate (PMS) activation under light irradiation. The synergies between photocatalysis and heterogeneous Fenton-like reaction lead to phenomenally enhanced production of various reactive oxygen species for rapid degradation of various microcontaminants in water. Experimental and theoretical results validate that the interfacial coupling of SA-Co-CN with ZnO greatly facilitates PMS adsorption and activation by reducing the adsorption energy and enhancing the cascade electron transfer processes for the photo-Fenton-like reaction.

Hollow-structured amorphous prussian blue decorated on graphitic carbon nitride for photo-assisted activation of peroxymonosulfate.

Heterogeneous activation of peroxymonosulfate (PMS) is one of the most promising techniques for wastewater treatment. Herein, an ingenious system by coupling of photocatalysis and PMS activation was developed, using hollow-structured amorphous prussian blue (A-PB) decorated on graphitic carbon nitride (g-C3N4) as the catalyst. Degradation of bisphenol A (BPA) via the A-PB-g-C3N4 mediated PMS activation under visible light (Vis) was systematically investigated. Astonishingly, it was found that ~ 82.0%, 92.6%, 98.2% and 99.3% of BPA (40 mg/L) were removed within 2, 4, 6 and 7 min, respectively, suggesting the extremely strong oxidizing capacity of the A-PB-g-C3N4/PMS/Vis system. Synergistic effect between the decorated A-PB and the g-C3N4 substrate promoted the Fe(III)/Fe(II) redox cycling and facilitated the charge transfer at the A-PB/g-C3N4 heterojunction interface. As a result, both photocatalysis and heterogeneous activation of PMS were boosted in the A-PB-g-C3N4/PMS/Vis system, leading to the production of large amount of reactive oxygen species (ROS). The various ROS (SO4•-, HO•, •O2- and 1O2) was responsible for the ultrafast degradation of BPA. Moreover, the A-PB-g-C3N4 catalyst also exhibited outstanding reusability and stability, retaining 98.9% of the removal percentage for BPA after five consecutive reaction cycles. This study suggests that the A-PB-g-C3N4 can be an all-rounder to bridge photocatalysis and PMS activation, and shed a new light on the application of multiple ROS for the ultrafast elimination of micropollutants from wastewater.

Stable and recyclable Fe3C@CN catalyst supported on carbon felt for efficient activation of peroxymonosulfate.

Stable and recyclable catalysts are crucial to the peroxymonosulfate (PMS) based advanced oxidation process (AOPs) for wastewater treatment. Herein, nitrogen-rich carbon wrapped Fe3C (Fe3C@CN) on carbon felt (CF) substrate was synthesized by using Prussian blue (PB) loaded CF as the precursors. The obtained Fe3C@CN/CF catalyst was applied for degradation of bisphenol A (BPA) via the heterogeneous catalytic activation of PMS. Results showed that ~91.7%, 95.2%, 98.1% and 99.1% of BPA (20 mg/L) were eliminated in the Fe3C@CN/CF + PMS system within 4, 10, 20 and 30 min, respectively. The fast degradation kinetics is attributed to the production of abundant reactive species (OH, SO4- and 1O2) in the Fe3C@CN/CF + PMS system, as demonstrated by the electron paramagnetic resonance spectroscopy and quench experiments. The Fe3C@CN/CF catalyst was stable and can be easily recycled by using an external magnet. The results indicated that the nanoconfined Fe3C endowed Fe3C@CN/CF with high stability and magnetic property and enabled the efficient electron transfer for PMS activation. This study provides a cost-effective approach for the fabrication of stable and recyclable Fe3C@CN/CF catalyst, and shed a new light on the rational design of multifunctional catalyst for advanced water remediation.

Effects of molecular weight distribution of soluble microbial products (SMPs) on membrane fouling in a membrane bioreactor (MBR): Novel mechanistic insights.

While molecular weight distribution (MWD) is one of the most important properties of soluble microbial products (SMPs), mechanisms underlying effects of MWD of SMPs on membrane fouling have not well unveiled. In this study, it was found that, the supernatant of sludge suspension in a membrane bioreactor (MBR) for wastewater treatment can be fractionated into a series of SMPs samples with different molecular weight (MW) fraction. The real gel sample mainly formed by the rejected SMPs on membrane surface had a high specific filtration resistance (SFR) of 1.21 × 1016 m-1 kg-1. The SFR of SMPs samples and the model foulants of polyethylene glycol (PEG) increased with their MW. The change trend of SFR with MW cannot be sufficiently explained by three-dimensional excitation-emission matrix (EMM) and chemical compositions. Tyndall effect analysis indicated that gelating ability of SMPs and PEG in the solution increased with their MW. Scanning electron microscope (SEM) confirmed gel structure changes with the PEG MW. Accordingly, mechanisms based on Carman-Kozeny equation and Flory-Huggins lattice theory were proposed to interpret SFR of SMPs with low and high MW, respectively. Simulating these two mechanistic models on PEG samples resulted in the comparable SFR data to the experimental ones, indicating the correctness and feasibility of the proposed mechanisms. The proposed mechanisms provided in-depth understanding of membrane fouling regarding MW, facilitating to develop effective membrane fouling mitigation strategies.

One-Pot and Surfactant-Free Synthesis of Ultrafine PtSn Nanoparticles Supported on Onion-Like Nanocarbons Toward Efficient Methanol and Ethylene Glycol Oxidation Reactions.

New synthetic method toward carbon supported catalysts with improved performance is of great importance in direct alcohol fuel cells (DAFCs). Herein, onion-like nanocarbons (OLNCs) were fabricated by using cheap and readily available candle as the raw material. And a facile one-pot and surfactant-free solvothermal approach was developed for the fabrication of PtSn nanoparticles supported on the OLNCs. Transmission electron microscopy (TEM) images showed the highly crystalline PtSn nanoparticles with size of ~2-5 nm were evenly deposited on the surface of the OLNCs. The obtained PtSn/OLNCs nanocomposites with Pt loading of about 10.1% exhibited excellent electrocatalytic activity toward both methanol oxidation reactions (MOR) and ethylene glycol oxidation reactions (EGOR). The current density of PtSn/OLNCs is 2.6 and 2.7 times of the commercial 20 wt% Pt/C toward the MOR and EGOR, respectively, suggesting the great application potential of the PtSn/OLNCs catalyst in DAFCs. The highly electrocatalytic activity of the PtSn/OLNCs may arise from the ultra-small size of the PtSn NPs as well as the large surface area and good electric conductivity of the OLNCs support. This study not only provides an example of the cost-effective fabrication and application of the OLNCs based catalysts and also sheds a new light on the application of the PtSn/OLNCs catalyst in DAFS.

Dual active sites of the Co2N and single-atom Co-N4 embedded in nitrogen-rich nanocarbons: a robust electrocatalyst for oxygen reduction reactions.

The development of low-cost, highly efficient and durable non-precious-metal (NPM) electrocatalysts for the oxygen reduction reaction (ORR) is of great significance. Herein, we report an ingenious two-step strategy for the fabrication of NPM electrocatalysts containing multifarious cobalt species embedded in nitrogen-rich nanocarbons (Co-N-C). Firstly, Co ions were fixed by coordination with 1H-Imidazo[4,5-f][1,10]phenanthroline (Hip), and secondly the Co-Hip precursor with abundant Co, C and N sources was subjected to calcination at various temperatures (700-900 °C). The obtained Co-N-C catalysts exhibited excellent activity in terms of the ORR in alkaline conditions, with a half-wave potential of 0.82 eV versus the reversible hydrogen electrode, which is close to that of commercial Pt/C. Moreover, the Co-N-C exhibited an unexpected catalytic activity with long-term stability and immunity to methanol which is better than commercial Pt/C catalyst, suggesting that Co-N-C with dual active sites of the single-atom Co sites (Co-N4) and Co2N can be a promising alternative to replace Pt-based electrocatalysts in fuel cells. This work can provide a new route to designing promising catalysts with dual active sites for ORR.

Insight into the mechanisms for hexavalent chromium reduction and sulfisoxazole degradation catalyzed by graphitic carbon nitride: The Yin and Yang in the photo-assisted processes.

As robust polymeric catalysts, graphitic carbon nitride (g-C3N4) has been known to have great application potential in environmental remediation. However, the mechanisms in the photo-assisted catalytic processes during the reduction or oxidation of pollutants are still difficult to discern and therefore not well studied. In this work, visible-assisted catalytic reduction of hexavalent chromium (Cr(VI)) or oxidation of sulfisoxazole (SIZ) by g-C3N4 with the addition of formic acid (FA) or potassium peroxydisulfate (PS) were systematically investigated. Effects of operation parameters such as g-C3N4 dosage, FA concentration, Cr(VI) concentration, solution pH, PS concentration were studied. The results showed g-C3N4 can be effective and robust catalyst for both the reduction (Yin) and oxidation (Yang) reactions in the environmental remediation. Mechanisms were studied by using electron spin resonance (ESR) spectroscopy. The results revealed the CO 2- is the predominant radical for Cr(VI) reduction in the g-C3N4/FA/Vis system and the SO4- and OH are all the main radicals for the oxidation of SIZ in the g-C3N4/PS/Vis system. The photo-generated carriers by g-C3N4, act as radical initiator, were responsible for the production of the reactive radical species in aqueous solution. This work not only shed a new light on the application of semiconductor polymers for the removal of micropollutants and also will expand the applicability of the polymeric photocatalysts for environmental remediation.

Nitrogen Doped Nanoporous Carbon Derived from Zizania Latifolia for Adsorptive Removal of Bisphenol A.

Nitrogen doped nanoporous activated carbon (N-NPAC) was prepared via the facile and effective KOH activation method using Zizania latifolia (ZL), a common Chinese aquatic vegetable, as the raw material. The biomass derived N-NPAC exhibited high content of nitrogen (18.4 at%), large surface area (1493.4 m²/g) and abundant nanopores. The unique physical-chemical structure endows the N-NPAC with great application potential in adsorbents. The performance of the N-NPAC for the adsorptive removal of bisphenol A (BPA) was studied. The results showed the adsorption processes were barely affected by solution pH. The adsorption kinetics are well-fitted by the pseudo-second-order kinetic model and the adsorption isotherms followed the Langmuir isotherm model. The maximum adsorption capacity calculated by the Langmuir isotherm model is 555.5 mg/g at 313 K, demonstrating the promise of the N-NPAC for the application in water cleanup. This study provides an example using the inexpensive and abundantly available biomass as the raw materials for the large scale production of nanocarbons and paves an avenue for the development of bio-derived nanomaterials.

New insights into bisphenols removal by nitrogen-rich nanocarbons: Synergistic effect between adsorption and oxidative degradation.

In this work, nitrogen-rich graphene-like carbon sheets (N-GLCS) with high specific surface area (488.4m2/g), narrow pore distribution and high N-doping (18.4 at%) were prepared and applied as both adsorbent and catalyst for the removal of bisphenols. Adsorption experiments demonstrated the high adsorption capacities of the N-GLCS toward bisphenol F (BPF) (222.9mg/g), bisphenol A (BPA) (317.8mg/g), and bisphenol C (BPC) (540.4mg/g). Results showed that about 98.6% of BPA (70mg/L) was removed at pH 7.0 within 80min after the adsorption-catalytic degradation process. The N-GLCS also showed a superb reusability for the catalytic oxidative degradation of BPA (70mg/L) with the removal percentage maintains over 83% after 5 cycles. With the synergistic combination of the excellent adsorption and catalytic properties of the N-GLCS, trace amount of pollutants can be preconcentrated and immobilized at the surface of N-GLCs, at the same time, active radicals were also produced at the surface of the N-GLCS by the activation of peroxydisulfate (PS), and finally the pollutants can be degraded in-situ by the active radicals. These findings provide a new avenue towards the efficient removal of trace-level EDCs from water solution by using the coupled adsorption-advanced oxidation processes.

Tau-mediated Neurodegeneration and Potential Implications in Diagnosis and Treatment of Alzheimer's Disease.

OBJECTIVE: To review recent research advances on tau, a major player in Alzheimer's disease (AD) pathogenesis, a biomarker for AD onset, and potential target for AD therapy. DATA SOURCES: This review was based on a comprehensive search using online literature databases, including PubMed, Web of Science, and Google Scholar. STUDY SELECTION: Literature search was based on the following keywords: Alzheimer's disease, tau protein, biomarker, cerebrospinal fluid (CSF), therapeutics, plasma, imaging, propagation, spreading, seeding, prion, conformational templating, and posttranslational modification. Relevant articles were carefully reviewed, with no exclusions applied to study design and publication type. RESULTS: Amyloid plaques enriched with extracellular amyloid beta (Aß) and intracellular neurofibrillary tangles comprised of hyperphosphorylated tau proteins are the two main pathological hallmarks of AD. Although the Aß hypothesis has dominated AD research for many years, clinical Aß-targeting strategies have consistently failed to effectively treat AD or prevent AD onset. The research focus in AD has recently shifted to the role of tau in AD. In addition to phosphorylation, tau is acetylated and proteolytically cleaved, which also contribute to its physiological and pathological functions. Emerging evidence characterizing pathological tau propagation and spreading provides new avenues for research into the molecular and cellular mechanisms underlying AD pathogenesis. Techniques to detect tau at minute levels in CSF and blood have been developed, and improved tracers have facilitated tau imaging in the brain. These advances have potential to accurately determine tau levels at early diagnostic stages in AD. Given that tau is a potential therapeutic target, anti-tau immunotherapy may potentially be a viable treatment strategy in AD intervention. CONCLUSION: Detecting changes in tau and targeting tau pathology represent a promising lead in the diagnosis and treatment of AD.

Green-assembly of three-dimensional porous graphene hydrogels for efficient removal of organic dyes.

Herein, a facile and straightforward green-assembly approach was developed for preparation of nitrogen and sulphur co-doped three-dimensional (3D) graphene hydrogels (N/S-GHs) with the assistance of glutathione. Specifically, graphene oxide is reduced and assembled into 3D porous nanostructures with glutathione as the reducing agent and modifier for its intrinsic structure, along with the nitrogen and sulphur sources in the synthetic process. As expected, the as-obtained N/S-GHs demonstrated superior adsorption performances for organic dyes (e.g., methylene blue, malachite green, and crystal violet) in aqueous media. This work provides new insight for the green-assembly of 3D porous nanomaterials as adsorbent and their promising applications in water treatment.

Amyloid ß Protein Aggravates Neuronal Senescence and Cognitive Deficits in 5XFAD Mouse Model of Alzheimer's Disease.

BACKGROUND: Amyloid ß (Aß) has been established as a key factor for the pathological changes in the brains of patients with Alzheimer's disease (AD), and cellular senescence is closely associated with aging and cognitive impairment. However, it remains blurred whether, in the AD brains, Aß accelerates the neuronal senescence and whether this senescence, in turn, impairs the cognitive function. This study aimed to explore the expression of senescence-associated genes in the hippocampal tissue from young to aged 5XFAD mice and their age-matched wild type (WT) mice to determine whether senescent neurons are present in the transgenic AD mouse model. METHODS: The 5XFAD mice and age-matched wild type mice, both raised from 1 to 18 months, were enrolled in the study. The senescence-associated genes in the hippocampus were analyzed and differentially expressed genes (DEGs) were screened by quantitative real-time polymerase chain reaction. Cognitive performance of the mice was evaluated by Y-maze and Morris water maze tests. Oligomeric Aß (oAß) (1-42) was applied to culture primary neurons to simulate the in vivo manifestation. Aging-related proteins were detected by Western blotting analysis and immunofluorescence. RESULTS: In 5XFAD mice, of all the DEGs, the senescence-associated marker p16 was most significantly increased, even at the early age. It was mainly localized in neurons, with a marginal expression in astrocytes (labeled as glutamine synthetase), nil expression in activated microglia (labeled as Iba1), and negatively correlated with the spatial cognitive impairments of 5XFAD mice. oAß (1-42) induced the production of senescence-related protein p16, but not p53 in vitro, which was in line with the in vivo manifestation. CONCLUSIONS: oAß-accelerated neuronal senescence may be associated with the cognitive impairment in 5XFAD mice. Senescence-associated marker p16 can serve as an indicator to estimate the cognitive prognosis for AD population.

Early-life stress leads to impaired spatial learning and memory in middle-aged ApoE4-TR mice.

BACKGROUND: Apolipoprotein E (ApoE) is a major lipid carrier that supports lipid transport and injury repair in the brain. The APOE ε4 allele is associated with depression, mild cognitive impairment (MCI) and dementia; however, the precise molecular mechanism through which ApoE4 influences the risk of disease development remains unknown. To address this gap in knowledge, we investigated the potential effects of chronic unpredictable mild stress (CUMS) on ApoE3 and ApoE4 target replacement (ApoE3-TR and ApoE4-TR) mice. RESULTS: All ApoE-TR mice exposed to CUMS at 3 months old recovered from a depression-like state by the age of 12 months. Of note, ApoE4-TR mice, unlike age-matched ApoE3-TR mice, displayed impaired spatial cognitive abilities, loss of GABAergic neurons, decreased expression of Reelin, PSD95, SYN and Fyn, and reduced phosphorylation of NMDAR2B and CREB. CONCLUSION: These results suggest that early-life stress may mediate cognitive impairment in middle-age ApoE4-TR mice through sustained reduction of GABAergic neurons and Reelin expression, which might further diminish the activation of the Fyn/NMDAR2B signaling pathway.

Self-templated synthesis of novel carbon nanoarchitectures for efficient electrocatalysis.

The cost-efficient large-scale production of novel carbon nanostructure with high performance is still a challenge, restricting their applications in catalysis. Herein, we present a low-cost one-pot and one-step approach for the synthesis of both N-doped graphene (NG) and N-doped carbon nanotubes (NCNTs) from self-templated organic nanoplates. By varying the FeCl3 concentration in the precursor, we can control the formation of graphene or CNTs. To the best of our knowledge, this is the first example for the controllable synthesis of graphene or CNTs by varying the precursors' compositions. This provides a simple and cost-effective route for the large-scale production of both NG and NCNTs for applications in catalysis. By example, we show how these unique structured nanocarbons can be applied in electrocatalysis for oxygen reduction reaction (ORR). The obtained NG and NCNTs show excellent ORR activities with long-term stability under alkaline conditions. The unique porous nanostructure, abundant defects, homogeneous N-doping and high N-content in the NG and NCNTs can provide abundant active sites, leading to the excellent ORR performance. This research not only displayed a simple and cost-effective approach for the large-scale production of novel carbon nanoarchitectures, but also revealed the exceptional application potential of these nanocarbons for electrocatalysis.

Reduction of Glucose Metabolism in Olfactory Bulb is an Earlier Alzheimer's Disease-related Biomarker in 5XFAD Mice.

BACKGROUND: Early diagnosis assumes a vital role in an effective treatment of Alzheimer's disease (AD). Most of the current studies can only make an AD diagnosis after the manifestation of typical clinical symptoms. The present study aimed to investigate typical and other biomarkers of AD to find a possible early biomarker. METHODS: A total of 14 5XFAD mice (at 3 and 6 months old), with 14 age-matched wild-type (WT) mice as control, were enrolled in this case-control study. Morris water maze test was performed to evaluate the cognitive function; buried food pellet test and olfactory maze test were employed to investigate the olfactory function; immunofluorescence to detect amyloid deposition and positron emission tomography to examine 2-deoxy-2-(18F) fluoro-D-glucose ([18F]-FDG) uptake in the hippocampus and cerebral cortex. RESULTS: With the increasing age, cognitive performance (P = 0.0262) and olfactory function were significantly deteriorated (day 1 P = 0.0012, day 2 P = 0.0031, day 3 P = 0.0160, respectively) and the (18F)-FDG uptake was markedly decreased in multi-cerebral regions including the olfactory bulb (P < 0.0001), hippocampus (P = 0.0121), and cerebral cortex (P < 0.0001). Of note, in 3-month-old 5XFAD mice, a significant decline of (18F)-FDG uptake in the olfactory bulb was found when compared with that of age-matched WT mice (P = 0.023) while no significant difference was present when the uptakes in other cerebral regions were compared. CONCLUSIONS: The decline of (18F)-FDG uptake in the olfactory bulb occurs earlier than other incidents, serving as an earlier in vivo biological marker of AD in 5XFAD mice and making early diagnosis of AD possibly.