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1.
Healthcare (Basel) ; 11(12)2023 Jun 12.
Article in English | MEDLINE | ID: mdl-37372836

ABSTRACT

The relationship between asymmetrical occlusion and surface electromyographic activity (sEMG) in people with different chewing preferences is not clear. In this study, the 5 s sEMG changes in the masseter muscle (MM), sternocleidomastoid (SCM), lateral (LGA), and medial (MGA) gastrocnemius muscles were recorded in controls, and subjects with chewing side preference (CSP) during clench with bilateral (BCR), left (LCR), and right (RCR) posterior teeth placement of cotton rolls. The images of the middle 3 s were selected and expressed as the root mean square (unit: µV/s). The EMG waves of bilateral muscles were compared by computing the percentage overlapping coefficient (POC). Only the POCMM of the CSP showed gender differences at BCR and RCR. Between the control group and the CSP group, there were significant differences in the POCMM and the POCLGA at BCR. In addition, there was a significant difference in POCMM and POCSCM between the two populations in different occlusal positions. The change in the POCSCM correlated with the change in the POCMM (r = 0.415, p = 0.018). The experiment-induced asymmetrical occlusion showed that the altered symmetry of the MM correlated with the altered symmetry of the SCM. Long-term asymmetrical occlusion (i.e., CSP) not only affects MM but also has potential effects on other superficial muscles (e.g., LGA).

2.
Mater Today Bio ; 20: 100659, 2023 Jun.
Article in English | MEDLINE | ID: mdl-37229212

ABSTRACT

Proteoglycans (PGs), also known as a viscous lubricant, is the main component of the cartilage extracellular matrix (ECM). The loss of PGs is accompanied by the chronic degeneration of cartilage tissue, which is an irreversible degeneration process that eventually develops into osteoarthritis (OA). Unfortunately, there is still no substitute for PGs in clinical treatments. Herein, we propose a new PGs analogue. The Glycopolypeptide hydrogels in the experimental groups with different concentrations were prepared by Schiff base reaction (Gel-1, Gel-2, Gel-3, Gel-4, Gel-5 and Gel-6). They have good biocompatibility and adjustable enzyme-triggered degradability. The hydrogels have a loose and porous structure suitable for the proliferation, adhesion, and migration of chondrocytes, good anti-swelling, and reduce the reactive oxygen species (ROS) in chondrocytes. In vitro experiments confirmed that the glycopolypeptide hydrogels significantly promoted ECM deposition and up-regulated the expression of cartilage-specific genes, such as type-II collagen, aggrecan, and glycosaminoglycans (sGAG). In vivo, the New Zealand rabbit knee articular cartilage defect model was established and the hydrogels were implanted to repair it, the results showed good cartilage regeneration potential. It is worth noting that the Gel-3 group, with a pore size of 122 â€‹± â€‹12 â€‹µm, was particularly prominent in the above experiments, and provides a theoretical reference for the design of cartilage-tissue regeneration materials in the future.

3.
ACS Appl Mater Interfaces ; 14(49): 54431-54438, 2022 Dec 14.
Article in English | MEDLINE | ID: mdl-36445947

ABSTRACT

Porous scaffolds have widely been exploited in cartilage tissue regeneration. However, it is often difficult to understand how the delicate hierarchical structure of the scaffold material affects the regeneration process. Graphene materials are versatile building blocks for robust and biocompatible porous structures, enabling investigation of structural cues on tissue regeneration otherwise challenging to ascertain. Here, we utilize a graphene hydrogel with stable and tunable structure as a model scaffold to examine the effect of porous structure on matrix remodeling associated with ingrowth of chondrocytes on scaffolds. We observe much-accelerated yet balanced cartilage remodeling correlating the ingrowth of chondrocytes into the graphene scaffold with an open pore structure on the surface. Importantly, such an enhanced remodeling selectively promotes the expression of collagen type II fibrils over proteoglycan aggrecan, hence clearly illustrating that chondrocytes maintain a stable phenotype when they migrate into the scaffold while offering new insights into scaffold design for cartilage repair.


Subject(s)
Cartilage, Articular , Graphite , Hydrogels/chemistry , Porosity , Graphite/pharmacology , Graphite/metabolism , Tissue Scaffolds/chemistry , Cartilage , Chondrocytes/metabolism , Tissue Engineering
4.
APL Bioeng ; 6(3): 031503, 2022 Sep.
Article in English | MEDLINE | ID: mdl-36061076

ABSTRACT

Platelet concentrates (PCs) are easily obtained from autogenous whole blood after centrifugation and have evolved through three generations of development to include platelet-rich plasma, platelet-rich fibrin, and concentrated growth factor. Currently, PCs are widely used for sinus floor elevation, alveolar ridge preservation, periodontal bone defects, guided bone regeneration, and treatment of gingival recession. More recently, PCs have been leveraged for tissue regeneration to promote oral soft and hard tissue regeneration in implant dentistry and regenerative periodontology. PCs are ideal for this purpose because they have a high concentration of platelets, growth factors, and cytokines. Platelets have been shown to release extracellular vesicles (P-EVs), which are thought to be essential for PC-induced tissue regeneration. This study reviewed the clinical application of PCs and P-EVs for implant surgery and periodontal tissue regeneration.

5.
Colloids Surf B Biointerfaces ; 208: 112090, 2021 Dec.
Article in English | MEDLINE | ID: mdl-34507071

ABSTRACT

In this study, graphene coating was introduced to the modified titanium surface to prevent bacterial infection in oral implants. We modified the titanium surface through SLA and silanization treatment and then coated the surface with graphene. The structure and surface properties were characterized by XPS and SEM. Graphene-coated titanium sheet was incubated with bacteria to test the antibacterial property, which was enhanced by adsorption and release of levofloxacin. We further implanted the graphene-coated titanium sheet loaded with levofloxacin into rabbits to test the antibacterial properties in vivo. The graphene coating exhibited inherent antibacterial properties through membrane stress and the generation of reactive oxygen species (ROS). When loaded with levofloxacin, the graphene coating exhibited a synergistic antibacterial effect and effectively prevented bacterial infections following the implantation. The graphene coating is promising to improve the antibacterial functions of oral implant surfaces to prevent bacterial infection.


Subject(s)
Graphite , Titanium , Animals , Anti-Bacterial Agents/pharmacology , Coated Materials, Biocompatible/pharmacology , Levofloxacin/pharmacology , Rabbits , Staphylococcus aureus , Surface Properties , Titanium/pharmacology
6.
Biomed Res Int ; 2021: 8094932, 2021.
Article in English | MEDLINE | ID: mdl-33628814

ABSTRACT

Platelet aggregates, such as PRP, PRF, and CGF, have been used alone or in combination with other grafting materials to enhance restoration outcomes. The process for preparing these autografting materials requires two-step centrifugation or specific centrifuges. In this study, we obtained an injectable fibrin scaffold (IFS) rich in growth factors by one-step centrifugation of whole blood from rabbits. The purpose of this study is to introduce some characteristics of IFS. This scaffold was characterized using various techniques, including Masson's trichrome staining, scanning electron microscopy, porosity measurements, and cell counting. The sustained release of growth factors, including PDGF, VEGF, TGF-ß1, IGF, FGF, and EGF, was quantified using ELISA assay. The obtained IFS was tested for its effects on cell proliferation, extracellular matrix deposition, and full-thickness skin defect repair. The prepared IFS is characterized by a loose fibrin network structure with white blood cells and platelets that slowly release growth factors and can promote the healing of skin defects via the promotion of cell proliferation, collagen deposition, and tissue revascularization. In addition, its liquid properties and porous structure are conducive to its application as a therapeutic component in tissue engineering.


Subject(s)
Fibrin/pharmacology , Intercellular Signaling Peptides and Proteins/pharmacology , Platelet-Rich Fibrin , Skin , Tissue Scaffolds , Wound Healing/drug effects , Animals , Humans , Rabbits , Skin/injuries , Skin/metabolism , Skin/pathology
7.
Biomed Res Int ; 2020: 1487681, 2020.
Article in English | MEDLINE | ID: mdl-32190649

ABSTRACT

BACKGROUND: The healing process following tooth extraction results in alveolar ridge resorption. The dimensional changes may complicate the subsequent implant procedure. Socket preservation using absorbable collagen membranes or a combination of membranes with calcium phosphate cement (CPC) particles might ensure that the alveolar ridge retains a suitable morphology for implant placement. OBJECTIVE: To evaluate the quality and quantity of new bone regenerated after application of either collagen membranes alone covering the sockets or a combination of membranes with CPC particles added into the sockets in dogs. Materials and Methods. Six dogs were included in this study. The mandibular premolars were extracted. For each hemimandible, three premolar extraction sites were randomly assigned to one of the following treatments: a covering collagen membrane, CPC with a covering collagen membrane, and a socket left empty. Cone-beam computed tomography (CBCT) measurements, polyfluorochrome sequential labeling, and histological assessments were performed to investigate the healing ability and repair processes within a 6-month observation period. RESULTS: Buccal bone height in the membrane group was significantly higher than that in the membrane+CPC and blank groups at 4 and 6 months after extraction. The mineral apposition rate over 2-4 months and the alizarin red-stained area in the membrane group were significantly higher than those in the other two groups. Histological analysis after 6 months of healing showed significantly higher amounts of newly formed bone in the membrane group than in the other groups. CONCLUSION: Extraction sites treated with collagen barrier membranes showed better protection than sites not covered with membranes. And the buccal bone wall of the socket was well preserved by collagen membrane without extra CPC materials. Socket preservation using absorbable membranes alone yielded better quality and quantity of regenerated bone inside the socket site.


Subject(s)
Alveolar Bone Loss/prevention & control , Alveolar Ridge Augmentation/methods , Bone Regeneration , Collagen/therapeutic use , Tooth Socket , Alveolar Bone Loss/pathology , Alveolar Process/pathology , Alveolar Process/surgery , Animals , Bicuspid , Cone-Beam Computed Tomography , Dogs , Male , Mandible , Membranes , Membranes, Artificial , Minerals , Tooth Extraction , Tooth Socket/diagnostic imaging , Tooth Socket/pathology
8.
J Comput Assist Tomogr ; 41(4): 535-540, 2017.
Article in English | MEDLINE | ID: mdl-28722697

ABSTRACT

OBJECTIVE: The aim of this study was to analyze the rate, location, and characteristics of bifid mandibular canals (BMCs) in the population of the Shanghai area using cone beam computed tomography to avoid complications during surgical procedures. METHODS: Two hundred eighty patients were recruited for this study, and the presence and morphology of BMCs were evaluated. RESULTS: The occurrence rate of BMCs in the Shanghai area was relatively high compared with that in other populations, reaching 31.1%. In addition, the study also found some far less-common trifid mandibular canals, as well as a peculiarly shaped special type, which we called v-type canal that has yet to be described. CONCLUSIONS: Our study underlined the different characteristics and occurrence rates of BMCs in the population of the Shanghai area and the importance of using cone beam computed tomography for a reliable detection, providing useful information to help prevent presurgery and postsurgery complications.


Subject(s)
Cone-Beam Computed Tomography , Mandible/abnormalities , Mandible/diagnostic imaging , Adolescent , Adult , Aged , China , Female , Humans , Incidence , Male , Middle Aged , Young Adult
9.
Curr Pharm Biotechnol ; 18(1): 85-94, 2017.
Article in English | MEDLINE | ID: mdl-27915981

ABSTRACT

The lack of supporting hard and soft tissues always prevents the rehabilitation with dental implants. Among various hard and soft tissue augmentation procedures, autologous grafts have been considered to be the gold standard. Autologous mesenchymal stem cells (MSCs) from bone marrow, dental tissue and adipose tissue have been described as promising alternatives for bone regeneration in the field of dental implantation. Mucosal cells, gingival fibroblasts and dental progenitor cells (DPS) can enhance peri-implant soft tissue augmentation and regenerate periodontal tissues around dental implants. Obtained from patients, platelet-rich plasma (PRP) and platelet-rich fibrin (PRF) are enriched in autologous platelets, which contain a great deal of growth factors and cytokines that are conducive to the regeneration of both hand and soft tissues around dental implants. Pharmaceutical treatments for osteoporosis and diabetes should be locally applied with implant procedures to restrict the resorption of autologous bone grafts and reduction of bone volume. Although autografts hold great potentials for dental implants, new approaches should also be explored with minimally invasion donor sites methods such as tissue engineering combined with autologous three factors and bio-3D printing involving selfassembling cell aggregates.


Subject(s)
Autografts , Bone Regeneration/physiology , Bone Transplantation/methods , Dental Implants , Mesenchymal Stem Cell Transplantation/methods , Tissue Engineering/methods , Humans , Platelet-Rich Fibrin , Platelet-Rich Plasma
10.
Adv Mater ; 28(21): 4025-31, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27031209

ABSTRACT

A multilayered graphene hydrogel (MGH) membrane is used as an excellent barrier membrane for guided bone regeneration. The unique multilayered nanostructure of the MGH membrane results in improved material properties, which benefits protein adsorption, cell adhesion, and apatite deposition, and allows higher quality and fast bone regeneration.


Subject(s)
Graphite/chemistry , Apatites , Bone Regeneration , Guided Tissue Regeneration , Hydrogels , Membranes, Artificial
12.
PLoS One ; 10(12): e0143377, 2015.
Article in English | MEDLINE | ID: mdl-26629988

ABSTRACT

This study was designed to explore the effects of tobacco smoke on gene expression through bioinformatics analyses. Gene expression profile GSE17913 was downloaded from the Gene Expression Omnibus database. The differentially expressed genes (DEGs) in buccal mucosa tissues between 39 active smokers and 40 never smokers were identified. Gene Ontology Specifically, the DEG distribution in the pathway of Metabolism of xenobiotics by cytochrome P450 was shown in Fig 2[corrected] were performed, followed by protein-protein interaction (PPI) network, transcriptional regulatory network as well as miRNA-target regulatory network construction. In total, 88 up-regulated DEGs and 106 down-regulated DEGs were identified. Among these DEGs, cytochrome P450, family 1, subfamily A, polypeptide 1 (CYP1A1) and CYP1B1 were enriched in the Metabolism of xenobiotics by cytochrome P450 pathway. In the PPI network, tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta (YWHAZ), and CYP1A1 were hub genes. In the transcriptional regulatory network, transcription factors of MYC associated factor X (MAX) and upstream transcription factor 1 (USF1) regulated many overlapped DEGs. In addition, protein tyrosine phosphatase, receptor type, D (PTPRD) was regulated by multiple miRNAs in the miRNA-DEG regulatory network. CYP1A1, CYP1B1, YWHAZ and PTPRD, and TF of MAX and USF1 may have the potential to be used as biomarkers and therapeutic targets in tobacco smoke-related pathological changes.


Subject(s)
Computational Biology , Nicotiana/chemistry , Smoke/adverse effects , Transcriptome/drug effects , Adult , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Female , Gene Ontology , Gene Regulatory Networks/drug effects , Humans , Male , MicroRNAs/genetics , Middle Aged , Mouth Mucosa/cytology , Oligonucleotide Array Sequence Analysis , Protein Interaction Mapping
13.
ACS Appl Mater Interfaces ; 7(36): 20245-54, 2015 Sep 16.
Article in English | MEDLINE | ID: mdl-26323463

ABSTRACT

Graphene and its derivatives have received increasing attention from scientists in the field of biomedical sciences because of their unique physical properties, which are responsible for their interesting biological functions. With a range of extraordinary properties such as high surface area, high mechanical strength, and ease of functionalization, graphene is considered highly promising for application in bone tissue engineering. Here, we examined the effect of using a self-supporting graphene hydrogel (SGH) film to induce the osteogenic differentiation of human adipose-derived stem cells (hADSCs). In comparison to conventional graphene and carbon fiber films, the SGH film had higher mechanical strength and flexibility. Moreover, we found that the SGH film was nontoxic and biocompatible. Of particular interest is the fact that the film alone could stimulate the osteogenic differentiation of hADSCs, independent of additional chemical inducers. Such effects are stronger for the SGH film than for graphene or carbon fiber films, although the induction capacity of the SGH film is not as high as that of the osteogenic-induced medium. The excellent osteoinductivity of the SGH film is closely related to its remarkable physical properties that include specific nanostructures, surface morphology, strong cell adherence, reasonable surface hydrophilicity, and high protein absorption.


Subject(s)
Adipose Tissue/cytology , Graphite/chemistry , Methylgalactosides/chemistry , Stem Cells/cytology , Adipose Tissue/metabolism , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Bone Morphogenetic Protein 2/genetics , Bone Morphogenetic Protein 2/metabolism , Cell Adhesion/drug effects , Cell Differentiation/drug effects , Cell Survival/drug effects , Cells, Cultured , Core Binding Factor Alpha 1 Subunit/genetics , Core Binding Factor Alpha 1 Subunit/metabolism , Humans , Osteocalcin/genetics , Osteocalcin/metabolism , Osteogenesis/drug effects , Stem Cells/metabolism , Stress, Mechanical
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