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1.
J Diabetes Complications ; 38(6): 108743, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38688179

ABSTRACT

AIM: This systematic review and meta-analysis aimed to comprehensively evaluate the impact of glucagon-like peptide 1 receptor agonists (GLP-1RAs) on visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) in individuals with diabetes mellitus and non-alcoholic fatty liver disease (NAFLD) or obesity. METHODS: A search of PubMed, Embase, and Web of Science until October 2023 identified 13 Randomized Controlled Trials (RCTs) meeting the inclusion criteria. Bias risk was assessed using the Cochrane risk-of-bias instrument. Statistical analysis utilized standard mean differences (SMD) in Review Manager 5.4. Heterogeneity and publication bias were assessed. This study used the protocol registered with the Platform of Registered Systematic Review and Meta-analysis Protocols (INPLASY2023110020). RESULTS: GLP-1RA treatment significantly reduced VAT (SMD -0.55, 95 % CI [-0.90, -0.19]), SAT (SMD -0.59, 95 % CI [-0.99, -0.19]), body weight (SMD -1.07, 95 % CI [-1.67, -0.47]), and body mass index (BMI) (SMD -1.10, 95 % CI [-1.74, -0.47]) compared to controls. Heterogeneity was observed for VAT (I2 = 79 %, P < 0.01), SAT (I2 = 73 %, P < 0.01), body weight (I2 = 82 %, P < 0.01), and BMI (I2 = 82 %, P < 0.01). No publication bias was detected for VAT (P = 0.57) and SAT (P = 0.18). GLP-1RA treatment improved fasting blood glucose (FBG), postprandial glucose (PPG), hemoglobin A1c (HbA1c), Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), and fibrosis-4 (FIB-4). CONCLUSIONS: This meta-analysis highlights GLP-1RAs' potential to reduce fat accumulation, body weight, and BMI and improve glycemic control in individuals with diabetes mellitus and NAFLD or obesity. These findings supported using GLP-1RAs as promising therapeutic agents to address abnormal adipose tissue distribution and metabolic dysfunction.


Subject(s)
Diabetes Mellitus, Type 2 , Glucagon-Like Peptide-1 Receptor , Non-alcoholic Fatty Liver Disease , Obesity , Randomized Controlled Trials as Topic , Humans , Non-alcoholic Fatty Liver Disease/drug therapy , Non-alcoholic Fatty Liver Disease/complications , Non-alcoholic Fatty Liver Disease/metabolism , Glucagon-Like Peptide-1 Receptor/agonists , Obesity/complications , Obesity/drug therapy , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/complications , Hypoglycemic Agents/therapeutic use , Intra-Abdominal Fat/drug effects , Intra-Abdominal Fat/metabolism , Adiposity/drug effects , Glucagon-Like Peptide-1 Receptor Agonists
2.
Biofabrication ; 15(2)2023 03 10.
Article in English | MEDLINE | ID: mdl-36791461

ABSTRACT

Topographical cues have been widely used to facilitate cell fusion in skeletal muscle formation. However, an unexpected yet consistent chiral orientation of myotubes deviating from the groove boundaries is commonly observed but has long been unattended. In this study, we report a method to guide the formation of skeletal myotubes into scalable and controlled patterns. By inducing C2C12 myoblasts onto grooved patterns with different widths (from 0.4 to 200µm), we observed an enhanced chiral orientation of cells developing on wide grooves (50 and 100µm width) since the first day of induction. Active chiral nematics of cells involving cell migration and chiral rotation of the cell nucleus subsequently led to a unified chiral orientation of the myotubes. Importantly, these chiral myotubes were formed with enhanced length, diameter, and contractility on wide grooves. Treatment of latrunculin A (Lat A) suppressed the chiral rotation and migration of cells as well as the myotube formation, suggesting the essence of chiral nematics of cells for myogenesis. Finally, by arranging wide grooved/striped patterns with corresponding compensation angles to synergize microtopographic cues and chiral nematics of cells, intricate and scalable patterns of myotubes were formed, providing a strategy for engineering skeletal muscle tissue formation.


Subject(s)
Cues , Muscle Fibers, Skeletal , Cell Differentiation , Muscle, Skeletal , Cell Line
3.
Front Public Health ; 10: 903547, 2022.
Article in English | MEDLINE | ID: mdl-35979473

ABSTRACT

Background: There have been several controversies about the correlation between vitamin D and depression. This study aimed to investigate the relationship between vitamin D supplementation and the incidence and prognosis of depression and to analyze the latent effects of subgroups including population and supplement strategy. Methods: A systematic search for articles before July 2021 in databases (PubMed, EMBASE, Web of Science, and the Cochrane Library) was conducted to investigate the effect of vitamin D supplementation on the incidence and prognosis of depression. Results: This meta-analysis included 29 studies with 4,504 participants, indicating that the use of vitamin D was beneficial to a decline in the incidence of depression (SMD: -0.23) and improvement of depression treatment (SMD: -0.92). Subgroup analysis revealed that people with low vitamin D levels (<50 nmol/L) and females could notably benefit from vitamin D in both prevention and treatment of depression. The effects of vitamin D with a daily supplementary dose of >2,800 IU and intervention duration of ≥8 weeks were considered significant in both prevention and treatment analyses. Intervention duration ≤8 weeks was recognized as effective in the treatment group. Conclusion: Our results demonstrate that vitamin D has a beneficial impact on both the incidence and the prognosis of depression. Whether suffering from depression or not, individuals with low vitamin D levels, dose >2,800 IU, intervention duration ≥8 weeks, and all females are most likely to benefit from vitamin D supplementation.


Subject(s)
Depression , Vitamins , Depression/drug therapy , Depression/epidemiology , Dietary Supplements , Female , Humans , Incidence , Prognosis , Randomized Controlled Trials as Topic , Vitamin D/therapeutic use , Vitamins/therapeutic use
4.
Opt Express ; 27(15): 21999-22016, 2019 Jul 22.
Article in English | MEDLINE | ID: mdl-31510264

ABSTRACT

We present a method to create light field display using a single projector and an array of plane mirrors. Mirrors can reproduce densely arranged virtual projectors regardless of the physical size of the real projector, thus producing a light field display of competitive ray density. We propose an ellipsoidal geometric framework and a design pipeline, and use parametric modelling technique to automatically generate the display configurations satisfying target design parameters. Three units of mirror array light field display systems have been implemented to evaluate the proposed methodologies. More importantly, we have experimentally verified that the high-density light field produced by our method can naturally evoke accommodation of the eyes, thereby reducing the vergence-accommodation conflict. The mirror array approach allows flexible trading between the spatial and angular resolutions for accommodating different applications, thus providing a practical solution to realize projection-based light field display.

5.
J Am Chem Soc ; 141(4): 1498-1505, 2019 01 30.
Article in English | MEDLINE | ID: mdl-30475606

ABSTRACT

The hierarchical control in biogenic minerals, from precise nanomorphology control to subsequent macroscopic assembly, remains a formidable challenge in artificial synthesis. Studies in biomineralization, however, are largely limited to atomic andmolecular scale crystallization, devoting little attention to biomolecular higher-order structures (HOSs) which critically impact long-range assembly of biominerals. Here we demonstrate a biomimetic route and quantitative simulations that explore peptide HOSs on guiding nanocrystal formation and anisotropic assembly into hierarchical structures. It is found that the Pt{100}-specific peptide T7 (Ac-TLTTLTN-CONH2) adopts ST-turn secondary structure, promoting cubic Pt nanocrystal formation at low concentration, and spontaneously transforms into a ß-sheet with increased concentration. The ß-sheet T7-Pt{100} specificity drives cubic Pt nanocrystals to self-assemble into large-area, long-range, [100] linear assemblies. This study provides a robust demonstration for bio/nonbiogenic material specificity, nanoscale synthesis, and long-range self-organization with biomolecular HOSs and opens vast opportunities for multiscale programmable structures.

6.
Sci Adv ; 3(1): e1600615, 2017 Jan.
Article in English | MEDLINE | ID: mdl-28070555

ABSTRACT

Metallic nanoparticles are emerging as an exciting class of heterogeneous catalysts with the potential advantages of exceptional activity, stability, recyclability, and easier separation than homogeneous catalysts. The traditional colloid nanoparticle syntheses usually involve strong surface binding ligands that could passivate the surface active sites and result in poor catalytic activity. The subsequent removal of surface ligands could reactivate the surface but often leads to metal ion leaching and/or severe Ostwald ripening with diminished catalytic activity or poor stability. Molecular ligand engineering represents a powerful strategy for the design of homogeneous molecular catalysts but is insufficiently explored for nanoparticle catalysts to date. We report a systematic investigation on molecular ligand modulation of palladium (Pd) nanoparticle catalysts. Our studies show that ß-functional groups of butyric acid ligand on Pd nanoparticles can significantly modulate the catalytic reaction process to modify the catalytic activity and stability for important aerobic reactions. With a ß-hydroxybutyric acid ligand, the Pd nanoparticle catalysts exhibit exceptional catalytic activity and stability with an unsaturated turnover number (TON) >3000 for dehydrogenative oxidation of cyclohexenone to phenol, greatly exceeding that of homogeneous Pd(II) catalysts (TON, ~30). This study presents a systematic investigation of molecular ligand modulation of nanoparticle catalysts and could open up a new pathway toward the design and construction of highly efficient and robust heterogeneous catalysts through molecular ligand engineering.

7.
ACS Nano ; 8(7): 6934-44, 2014 Jul 22.
Article in English | MEDLINE | ID: mdl-24937767

ABSTRACT

Controlling the morphology of nanocrystals (NCs) is of paramount importance for both fundamental studies and practical applications. The morphology of NCs is determined by the seed structure and the following facet growth. While means for directing facet formation in NC growth have been extensively studied, rational strategies for the production of NCs bearing structure defects in seeds have been much less explored. Here, we report mechanistic investigations of high density twin formation induced by specific peptides in platinum (Pt) NC growth, on the basis of which we derive principles that can serve as guidelines for the rational design of molecular surfactants to introduce high yield twinning in noble metal NC syntheses. Two synergistic factors are identified in producing twinned Pt NCs with the peptide: (1) the altered reduction kinetics and crystal growth pathway as a result of the complex formation between the histidine residue on the peptide and Pt ions, and (2) the preferential stabilization of {111} planes upon the formation of twinned seeds. We further apply the discovered principles to the design of small organic molecules bearing similar binding motifs as ligands/surfactants to create single and multiple twinned Pd and Rh NCs. Our studies demonstrate the rich information derived from biomimetic synthesis and the broad applicability of biomimetic principles to NC synthesis for diverse property tailoring.


Subject(s)
Biomimetics/methods , Nanoparticles/chemistry , Nanotechnology/methods , Colloids , Molecular Conformation , Molecular Dynamics Simulation , Peptides/chemistry , Platinum/chemistry
8.
Nano Lett ; 14(7): 3887-94, 2014 Jul 09.
Article in English | MEDLINE | ID: mdl-24873775

ABSTRACT

Structural defects/grain boundaries in metallic materials can exhibit unusual chemical reactivity and play important roles in catalysis. Bulk polycrystalline materials possess many structural defects, which is, however, usually inaccessible to solution reactants and hardly useful for practical catalytic reactions. Typical metallic nanocrystals usually exhibit well-defined crystalline structure with few defects/grain boundaries. Here, we report the design of ultrafine wavy nanowires (WNWs) with a high density of accessible structural defects/grain boundaries as highly active catalytic hot spots. We show that rhodium WNWs can be readily synthesized with controllable number of structural defects and demonstrate the number of structural defects can fundamentally determine their catalytic activity in selective oxidation of benzyl alcohol by O2, with the catalytic activity increasing with the number of structural defects. X-ray photoelectron spectroscopy (XPS) and cyclic voltammograms (CVs) studies demonstrate that the structural defects can significantly alter the chemical state of the Rh WNWs to modulate their catalytic activity. Lastly, our systematic studies further demonstrate that the concept of defect engineering in WNWs for improved catalytic performance is general and can be readily extended to other similar systems, including palladium and iridium WNWs.

9.
Nat Commun ; 5: 3200, 2014.
Article in English | MEDLINE | ID: mdl-24518643

ABSTRACT

The integration of multiple synergistic catalytic systems can enable the creation of biocompatible enzymatic mimics for cascading reactions under physiologically relevant conditions. Here we report the design of a graphene-haemin-glucose oxidase conjugate as a tandem catalyst, in which graphene functions as a unique support to integrate molecular catalyst haemin and enzymatic catalyst glucose oxidase for biomimetic generation of antithrombotic species. Monomeric haemin can be conjugated with graphene through π-π interactions to function as an effective catalyst for the oxidation of endogenous L-arginine by hydrogen peroxide. Furthermore, glucose oxidase can be covalently linked onto graphene for local generation of hydrogen peroxide through the oxidation of blood glucose. Thus, the integrated graphene-haemin-glucose oxidase catalysts can readily enable the continuous generation of nitroxyl, an antithrombotic species, from physiologically abundant glucose and L-arginine. Finally, we demonstrate that the conjugates can be embedded within polyurethane to create a long-lasting antithrombotic coating for blood-contacting biomedical devices.


Subject(s)
Arginine/metabolism , Aspergillus niger/enzymology , Fibrinolytic Agents/metabolism , Fungal Proteins/metabolism , Glucose Oxidase/metabolism , Glucose/metabolism , Nitrogen Oxides/metabolism , Biomimetic Materials , Catalysis , Fungal Proteins/chemistry , Glucose Oxidase/chemistry , Graphite/chemistry , Hemin/chemistry , Hydrogen Peroxide
11.
Nano Lett ; 13(2): 840-6, 2013 Feb 13.
Article in English | MEDLINE | ID: mdl-23320831

ABSTRACT

Surfactants with preferential adsorption to certain crystal facets have been widely employed to manipulate morphologies of colloidal nanocrystals, while mechanisms regarding the origin of facet selectivity remain an enigma. Similar questions exist in biomimetic syntheses concerning biomolecular recognition to materials and crystal surfaces. Here we present mechanistic studies on the molecular origin of the recognition toward platinum {111} facet. By manipulating the conformations and chemical compositions of a platinum {111} facet specific peptide, phenylalanine is identified as the dominant motif to differentiate {111} from other facets. The discovered recognition motif is extended to convert nonspecific peptides into {111} specific peptides. Further extension of this mechanism allows the rational design of small organic molecules that demonstrate preferential adsorption to the {111} facets of both platinum and rhodium nanocrystals. This work represents an advance in understanding the organic-inorganic interfacial interactions in colloidal systems and paves the way to rational and predictable nanostructure modulations for many applications.


Subject(s)
Biomimetic Materials/chemistry , Metal Nanoparticles/chemistry , Peptides/chemistry , Platinum/chemistry , Adsorption , Biomimetic Materials/chemical synthesis , Models, Molecular , Particle Size , Peptides/chemical synthesis , Phenylalanine/chemistry , Surface Properties
12.
Chem Soc Rev ; 42(7): 2512-27, 2013 Apr 07.
Article in English | MEDLINE | ID: mdl-23079759

ABSTRACT

Biomolecules capable of fabricating complex nanomaterials with required functions in nature have been exploited to artificially control nanomaterial synthesis in all aspects. This tutorial review provides an overview of recent efforts in biomimetic synthesis and the relevant mechanistic studies on biomolecular specificities toward material surfaces. It starts with a discussion of the state-of-the-art progress in colloidal nanocrystal synthesis, wherein the importance of the interfacial control over nanoscale building blocks discloses the potential of exploiting biomolecular recognition properties in nanostructure synthesis. Continued discussions will review the progress in biomimetic syntheses of different classes of nanoscale materials. In vitro biomimetic syntheses with both biomolecules isolated from organisms and material-specific peptide sequences selected from combinatorial molecular evolution processes will be demonstrated. The final part of the review presents the recent research efforts and advances in understanding biomolecule-inorganic material interactions. It is believed that with continued experimental efforts and fundamental understanding of biomolecule-material interactions scientists can one day harvest the ability to rationally design molecules to produce intricate material structures with a similar level of sophistication, precision, and superior functions as those found in nature.


Subject(s)
Biomimetic Materials/chemistry , Nanostructures/chemistry , Metal Nanoparticles/chemistry , Peptides/chemistry , Peptides/metabolism , Platinum/chemistry , Proteins/chemistry , Proteins/metabolism
13.
Nanoscale ; 4(3): 845-51, 2012 Feb 07.
Article in English | MEDLINE | ID: mdl-22159178

ABSTRACT

Bimetallic Pt-Pd core-shell nanocrystals (NCs) are synthesized through a two-step process with controlled Pd thickness from sub-monolayer to multiple atomic layers. The oxygen reduction reaction (ORR) catalytic activity and methanol oxidation reactivity of the core-shell NCs for fuel cell applications in alkaline solution are systematically studied and compared based on different Pd thickness. It is found that the Pd shell helps to reduce the over-potential of ORR by up to 50 mV when compared to commercial Pd black, while generating up to 3-fold higher kinetic current density. The carbon monoxide poisoning test shows that the bimetallic NCs are more resistant to the CO poisoning than Pt NCs and Pt black. It is also demonstrated that the bimetallic Pt-Pd core-shell NCs can enhance the current density of the methanol oxidation reaction, lowering the over-potential by 35 mV with respect to the Pt core NCs. Further investigation reveals that the Pd/Pt ratio of 1/3, which corresponds to nearly monolayer Pd deposition on Pt core NCs, gives the highest oxidation current density and lowest over-potential. This study shows for the first time the systematic investigation of effects of Pd atomic shells on Pt-Pd bimetallic nanocatalysts, providing valuable guidelines for designing high-performance catalysts for fuel cell applications.

14.
Nano Lett ; 11(7): 3040-6, 2011 Jul 13.
Article in English | MEDLINE | ID: mdl-21667927

ABSTRACT

Shape-controlled synthesis requires rigorous kinetic control over both nucleation and growth. For platinum (Pt), to date it is still challenging to generate twinned seeds in nucleation in a controllable fashion. Here, we report that a specific Pt binding peptide BP7A is able to mediate and stabilize single-twinned seeds formation at the nucleation stage under mild conditions. Importantly, it targets the control over nucleation directly. Combining with control over growth, we further demonstrate the rational design and synthesis of single-twinned structures, right bipyramid and {111}-bipyramid, by incorporating targeted facet stabilization over {100} facet and {111} facet, respectively. To the best of our knowledge, this is the first report on the successful synthesis of single-twinned bipyramids for Pt nanocrystals (NCs) with high yields. The work here demonstrates the power of biomolecules in recognizing and mediating inorganic nanomaterials synthesis, guiding the formation of material structures that are otherwise unconventional, and hence presenting one step further toward predictable and programmable biomimetic synthesis.


Subject(s)
Nanoparticles/chemistry , Organoplatinum Compounds/chemical synthesis , Peptides/chemistry , Platinum/chemistry , Kinetics , Models, Molecular , Nanotechnology , Organoplatinum Compounds/chemistry , Particle Size , Surface Properties
15.
Biometrics ; 67(4): 1617-26, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21517790

ABSTRACT

With the prevalence of gene expression studies and the relatively low reproducibility caused by insufficient sample sizes, it is natural to consider joint analysis that could combine data from different experiments effectively to achieve improved accuracy. We present in this article a model-based approach for better identification of differentially expressed genes by incorporating data from different studies. The model can accommodate in a seamless fashion a wide range of studies including those performed at different platforms by fitting each data with different set of parameters, and/or under different but overlapping biological conditions. Model-based inferences can be done in an empirical Bayes' fashion. Because of the information sharing among studies, the joint analysis dramatically improves inferences based on individual analysis. Simulation studies and real data examples are presented to demonstrate the effectiveness of the proposed approach under a variety of complications that often arise in practice.


Subject(s)
Algorithms , Bayes Theorem , Data Interpretation, Statistical , Gene Expression Profiling/methods , Models, Statistical , Oligonucleotide Array Sequence Analysis/methods , Computer Simulation , Reproducibility of Results , Sensitivity and Specificity
16.
Nat Chem ; 3(5): 393-9, 2011 May.
Article in English | MEDLINE | ID: mdl-21505499

ABSTRACT

The properties of a nanocrystal are heavily influenced by its shape. Shape control of a colloidal nanocrystal is believed to be a kinetic process, with high-energy facets growing faster then vanishing, leading to nanocrystals enclosed by low-energy facets. Identifying a surfactant that can specifically bind to a particular crystal facet is critical, but has proved challenging to date. Biomolecules have exquisite specific molecular recognition properties that can be explored for the precise engineering of nanostructured materials. Here, we report the use of facet-specific peptide sequences as regulating agents for the predictable synthesis of platinum nanocrystals with selectively exposed crystal surfaces and particular shapes. The formation of platinum nanocubes and nanotetrahedrons are demonstrated with Pt-{100} and Pt-{111} binding peptides, respectively. Our studies unambiguously demonstrate the abilities of facet-selective binding peptides in determining nanocrystal shape, representing a critical step forward in the use of biomolecules for programmable synthesis of nanostructures.


Subject(s)
Nanoparticles , Peptides/chemistry , Platinum/chemistry , Amino Acid Sequence , Microscopy, Electron, Transmission
17.
Neural Comput ; 23(6): 1605-22, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21395439

ABSTRACT

Finite gaussian mixture models are widely used in statistics thanks to their great flexibility. However, parameter estimation for gaussian mixture models with high dimensionality can be challenging because of the large number of parameters that need to be estimated. In this letter, we propose a penalized likelihood estimator to address this difficulty. The [Formula: see text]-type penalty we impose on the inverse covariance matrices encourages sparsity on its entries and therefore helps to reduce the effective dimensionality of the problem. We show that the proposed estimate can be efficiently computed using an expectation-maximization algorithm. To illustrate the practical merits of the proposed method, we consider its applications in model-based clustering and mixture discriminant analysis. Numerical experiments with both simulated and real data show that the new method is a valuable tool for high-dimensional data analysis.


Subject(s)
Computer Simulation , Models, Statistical , Pattern Recognition, Automated/methods , Algorithms , Cluster Analysis
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