SARM1 Promotes Neurodegeneration and Memory Impairment in Mouse Models of Alzheimer's Disease.

Neuroinflammation plays a crucial role in the pathogenesis and progression of Alzheimer's disease (AD). The Sterile Alpha and Toll Interleukin Receptor Motif-containing protein 1 (SARM1) has been shown to promote axonal degeneration and is involved in neuroinflammation. However, the role of SARM1 in AD remains unclear. In this study, we found that SARM1 was reduced in hippocampal neurons of AD model mice. Interestingly, conditional knockout (CKO) of SARM1 in the central nervous system (CNS, SARM1Nestin-CKO mice) delayed the cognitive decline in APP/PS1 AD model mice. Furthermore, SARM1 deletion reduced the Aß deposition and inflammatory infiltration in the hippocampus and inhibited neurodegeneration in APP/PS1 AD model mice. Further investigation into the underlying mechanisms revealed that the signaling of tumor necrosis factor-α (TNF-α) was downregulated in the hippocampus tissues of APP/PS1;SARM1Nestin-CKO mice, thereby alleviating the cognitive decline, Aß deposition and inflammatory infiltration. These findings identify unrecognized functions of SARM1 in promoting AD and reveal the SARM1-TNF-α pathway in AD model mice.

Virgin coconut oil attenuates lipopolysaccharide-induced depression-like behaviors: Integrating network pharmacology analysis and molecular mechanism evaluation.

Depression is a mental disease that seriously affects the quality of life. Its pathophysiology is complex and includes neuroinflammation and apoptosis. Virgin coconut oil (VCO) is a natural food that has been found to have remarkable anti-inflammatory and antiapoptotic properties. We assessed the effects of VCO on depression and the related mechanisms by performing network pharmacology analysis and evaluating depressive-like behaviors in rat model and found that VCO-treatment alleviated the depressive-like behaviors, inhibited microglial and astrocytic activation and reduced neuronal loss in the hippocampus, possibly by decreasing neuronal apoptosis. In addition, network pharmacology analysis and western blotting showed that VCO might exert neuroprotective effects by activating Protein Kinase B (AKT)-related pathway. Taken together, our results revealed the previously unrecognized effects of VCO on depression, and further explored the underlying mechanism of depression.

One-Pot, Open-Air Synthesis of Flexible and Degradable Multifunctional Polymer Composites with Adhesion, Water Resistance, Self-Healing, Facile Drug Loading, and Sustained Release Properties.

Developing proper wound management via wound dressings represents a global challenge. Ideal wound dressings shall encompass multiple integrated functionalities for variable, complex scenarios; however, this is challenging due to the complex molecular design and synthesis process. Herein, polymer composites, cross-linked poly(styrene oxide-co-hexaphenylcyclotrisiloxane)/crosslinked poly(hexaphenylcyclotrisiloxane) (cP(SO-co-HPCTS)/cPHPCTS) with multiple functionalities are prepared by a one-step, open-air method using catalytic ring-opening polymerization. The introduction of a mobile polymer cP(SO-co-HPCTS) endows the composite with good flexibility and self-healing properties at human body temperature. The hydrophobic groups in the main chain provide hydrophobicity and good water resistance, while the hydroxyl groups contained in the end groups enable good adhesion properties. Drugs can be efficiently loaded by blending and then sustainably release from the polymer composite. The material can rapidly degrade in a tetrahydrofuran solution of tetrabutylammonium fluoride due to its SiOSi bonds. The facile, one-step, open-air synthesis procedure and multiple functional properties integrated into the composites provide good prospects for their extensive application and batch production as wound dressing materials.

Amphiphilically Modified Porous Polymeric Nanosandwich-Based Membranes for Rapid and Efficient Water Treatment.

Low removal efficiency, long treatment time, and high energy consumption hinder advanced and eco-friendly use of traditional adsorbents and separation membranes. Here, a class of amphiphilically modified 2D porous polymeric nanosandwich is designed and is subsequently assembled into adsorptive membranes. The 2D nanosandwich is gifted with high porosity and excellent pore accessibility, demonstrating rapid adsorption kinetics. The as-assembled membrane integrates unimpeded interlayer channels and well-developed, amphiphilic, and highly accessible intralayer nanopores, leading to ultrafast water permeation (1.2 × 104  L m-2  h-1  bar-1 ), high removal efficiency, and easy regeneration. The family of the membrane can be expanded by changing amphiphilic functional groups, further providing treatment of a wide-spectrum of pollutants, including aromatic compounds, pesticide, and pharmaceuticals. It is believed that the novel amphiphilically modified adsorptive membrane offers a distinct water treatment strategy with ultrahigh water permeation and efficient pollutants removal performances, and provides a multiple-in-one solution to the detection and elimination of pollutants.

Investigation of the Water Damage Resistance and Storability of a SEBS-Modified Cold-Patching Asphalt Mixture.

At present, achieving good storability and water damage resistance remains challenging for cold-patching asphalt mixtures (CAMs). To address this issue, this study selects styrene-ethylene-butadiene-styrene copolymer (SEBS) and diesel as a modifier and diluent, respectively, to improve the water stability and storability of CAMs. The diesel oil content is determined through the Brookfield rotational viscosity test, and the modifier content is obtained through the Marshall stability test. With the empirical formula method, paper trail test, and modified Marshall test, mixed designs of CAMs modified with and without SEBS are established to determine the best cold-patching asphalt content. On this basis, the modification effect of SEBS is verified by comparing the test results of the modified and unmodified CAMs, and the water stability and Marshall stability tests are conducted before and after CAM storage, respectively. Results show that the optimum contents of SEBS and diesel oil are 7.5% and 40% of the base asphalt weight, respectively, and the best modified asphalt content is 4.6% of the mineral material weight in CAM. The Marshall residual stability and freeze-thaw splitting strength ratio of the 7.5% SEBS-modified CAM are increased by 20.1% and 15.7%, respectively, relative to the unmodified CAM, and the storage performance requirement of at least two months can be guaranteed.

A robust all-organic protective layer towards ultrahigh-rate and large-capacity Li metal anodes.

The low cycling efficiency and uncontrolled dendrite growth resulting from an unstable and heterogeneous lithium-electrolyte interface have largely hindered the practical application of lithium metal batteries. In this study, a robust all-organic interfacial protective layer has been developed to achieve a highly efficient and dendrite-free lithium metal anode by the rational integration of porous polymer-based molecular brushes (poly(oligo(ethylene glycol) methyl ether methacrylate)-grafted, hypercrosslinked poly(4-chloromethylstyrene) nanospheres, denoted as xPCMS-g-PEGMA) with single-ion-conductive lithiated Nafion. The porous xPCMS inner cores with rigid hypercrosslinked skeletons substantially increase mechanical robustness and provide adequate channels for rapid ionic conduction, while the flexible PEGMA and lithiated Nafion polymers enable the formation of a structurally stable artificial protective layer with uniform Li+ diffusion and high Li+ transference number. With such artificial solid electrolyte interphases, ultralong-term stable cycling at an ultrahigh current density of 10 mA cm-2 for over 9,100 h (>1 year) and unprecedented reversible lithium plating/stripping (over 2,800 h) at a large areal capacity (10 mAh cm-2) have been achieved for lithium metal anodes. Moreover, the protected anodes also show excellent cell stability when paired with high-loading cathodes (~4 mAh cm-2), demonstrating great prospects for the practical application of lithium metal batteries.

Molecular Engineering toward High-Crystallinity Yet High-Surface-Area Porous Carbon Nanosheets for Enhanced Electrocatalytic Oxygen Reduction.

Carbon-based nanomaterials have been regarded as promising non-noble metal catalysts for renewable energy conversion system (e.g., fuel cells and metal-air batteries). In general, graphitic skeleton and porous structure are both critical for the performances of carbon-based catalysts. However, the pursuit of high surface area while maintaining high graphitization degree remains an arduous challenge because of the trade-off relationship between these two key characteristics. Herein, a simple yet efficient approach is demonstrated to fabricate a class of 2D N-doped graphitized porous carbon nanosheets (GPCNSs) featuring both high crystallinity and high specific surface area by utilizing amine aromatic organoalkoxysilane as an all-in-one precursor and FeCl3 ·6H2 O as an active salt template. The highly porous structure of the as-obtained GPCNSs is mainly attributed to the alkoxysilane-derived SiOx nanodomains that function as micro/mesopore templates; meanwhile, the highly crystalline graphitic skeleton is synergistically contributed by the aromatic nucleus of the precursor and FeCl3 ·6H2 O. The unusual integration of graphitic skeleton with porous structure endows GPCNSs with superior catalytic activity and long-term stability when used as electrocatalysts for oxygen reduction reaction and Zn-air batteries. These findings will shed new light on the facile fabrication of highly porous carbon materials with desired graphitic structure for numerous applications.

Molecular Level Design of Nitrogen-Doped Well-Defined Microporous Carbon Spheres for Selective Adsorption and Electrocatalysis.

Nitrogen-doped porous carbon spheres have attracted great interest in diversified fields owing to their unique physical and chemical properties. However, the synthesis of nitrogen-doped porous carbon spheres with hierarchical superstructures and refined micropore structures is still a challenge. Herein, we develop a molecular-scale silica templating strategy to prepare nitrogen-doped microporous carbon spheres (MCSSs) with high porosity and a well-defined micropore structure. Octa(aminophenyl) polyhedral oligomeric silsesquioxane is used as a building block in MCSS precursors to provide precise molecular-scale templating and nitrogen doping. The morphology of MCSSs can be easily tuned by choosing the proper solvent. The as-synthesized MCSS with a large surface area (2036 m2 g-1), narrow micropore size distribution, nitrogen doping, and hierarchical geometry can serve as an efficient selective adsorbent for CO2 and organic pollutants. Furthermore, the MCSS decorated with Fe-N-C active sites (MCSS-Fe) shows enhanced electrocatalytic ORR activity in alkaline solution. This novel approach may open a new avenue for controllable fabrication of porous carbon spheres with desired geometry and well-designed pore structure and show potential applications in selective adsorption and catalysis.

FeS/FeNC decorated N,S-co-doped porous carbon for enhanced ORR activity in alkaline media.

A novel strategy is developed to produce an FeS-FeNC-decorated hierarchical porous N,S-co-doped carbon (FeS-FeNC@NSC) electrocatalyst via introducing volatile FeCl3 into a porphyrin polymer framework followed by carbonization. The synergistic effect between the FeS nanoparticles and FeNC active sites in FeS-FeNC@NSC is beneficial for enhancing the ORR activity.

All-in-One Porous Polymer Adsorbents with Excellent Environmental Chemosensory Responsivity, Visual Detectivity, Superfast Adsorption, and Easy Regeneration.

It remains a formidable challenge to construct advanced adsorbents with superb adsorption, environmental stimuli response, and real-time detection capability for efficiently treating contaminants from complex environmental systems. A novel class of an all-in-one microporous adsorbent that simultaneously has excellent environmental chemosensory responsivity, visual detectivity, superfast micropollutant adsorption, as well as easy regeneration is reported herein. The advanced microporous adsorbent discussed in this study presents a hairy nanospherical morphology composed of a hairy stimuli-responsive polymeric shell and a shell-assisted superadsorptive microporous core. The adsorbent not only exhibits a valuable capability of pollutant detection by visible fluorescence quenching, but can also remove organic micropollutants from polluted water with super-rapid speed (79%, 98%, and 100% of its equilibrium uptake in 7 s, 10 s, and 2 min, respectively) and excellent recyclability (>96%). More importantly, the adsorbent still shows unimpeded adsorption performance in the flow-through adsorption tests (15 mL min-1 ), indicating a very appealing application prospect.

Construction of 3D carbon networks with well-dispersed SiO x nanodomains from gelable building blocks for lithium-ion batteries.

Nonstoichiometric silicon oxide (SiO x ) with high theoretical capacity is a promising anode material for lithium-ion batteries (LIBs). However, volume changes and poor electronic conductivity of SiO x are major impediments to its practical application. The modification of SiO x with carbonaceous materials to accommodate volume variations and improve conductivity is a valuable strategy. Nanonetwork-structured (NNS) carbons have been paid great attention because of their unique three-dimensional structure, and high electronic and ionic conductivity. Incorporating SiO x with well-designed NNS carbons is a promising method to prepare high quality electrode materials for lithium-ion batteries. In this work, a fabrication approach is developed to synthesize a 3D carbon network composed of carbonaceous hybrid nanotubes with well-dispersed SiO x nanodomains (CNT@SiO x -C) from 1D gelable bottlebrushes as network building blocks based on molecular-scale interface engineering technology. Herein, nano-sized SiO x particles are embedded into the carbonaceous matrix to prevent their volume change during cycling. The experimental results indicated that the CNT@SiO x -C presents high reversible capacity, remarkable cycle life and high rate capability due to the high dispersion of nano-sized SiO x and conductive 3D carbon nanonetwork.