Laser-optical method of stimulation of cell metabolism and its biomedical applications

2007 ◽  
Author(s):  
M. M. Asimov ◽  
R. M. Asimov ◽  
A. N. Rubinov ◽  
S. A. Mamilov ◽  
S. S. Esman ◽  
...  
Keyword(s):  
Optical Method ◽  
Biomedical Applications ◽  
Cell Metabolism ◽  
Stimulation Of

scholarly journals Applications of magnetic and multiferroic core/shell nanostructures and their physical properties

DYNA ◽  
2018 ◽  
Vol 85 (207) ◽  
pp. 29-35
Author(s):  
Claudia Milena Bedoya-Hincapié ◽  
Elisabeth Restrepo-Parra ◽  
Luis Demetrio López-Carreño
Keyword(s):  
Physical Properties ◽  
Biomedical Applications ◽  
Magnetic Behavior ◽  
Core Shell ◽  
Cellular Functions ◽  
Shell Nanostructures ◽  
Biomedical Field ◽  
Core Shell Structure ◽  
Significant Attention ◽  
Stimulation Of

The potential of nanotechnology in the biomedical field has been crucial for contributing to the possibility of efficiently meeting present necessities with novel materials. Over the last few decades, nanostructures with a core/shell structure have attracted significant attention because of the possibility of changing their physical properties by varying their chemistry and geometry. These structures have become relevant in targeted therapy (drug delivery and treatments to complement chemotherapy and radiotherapy), imaging and in the stimulation of cellular functions. Thus in this paper the current development of core/shell nanostructures is reviewed, emphasizing the physical properties of those that have been proposed as potentially having biomedical applications, which are based in a magnetic behavior or in a mixture of magnetic and electric (multiferroic) phenomena.

Optical method of stimulation of the second sound in superfluid helium

1991 ◽  
Vol 161 (2) ◽  
pp. 161-163 ◽  
Author(s):  
Vadim Petrovich Romanov ◽  
Tagaimurod Khaitovich Salikhov
Keyword(s):  
Superfluid Helium ◽  
Optical Method ◽  
Second Sound ◽  
Stimulation Of

scholarly journals Modification by calcium ions of adenine nucleotide translocation in rat liver mitochondria

1972 ◽  
Vol 129 (2) ◽  
pp. 355-365 ◽  
Author(s):  
T. Spencer ◽  
F. L. Bygrave
Keyword(s):  
Rat Liver ◽  
Calcium Ions ◽  
Adenine Nucleotide ◽  
Cell Metabolism ◽  
Liver Mitochondria ◽  
High Energy ◽  
Small Degree ◽  
Metabolic Inhibitors ◽  
Rat Liver Mitochondria ◽  
Stimulation Of

1. Added Ca2+stimulates the translocation of ATP by isolated rat liver mitochondria. 2. The apparent Km for added Ca2+in stimulating the translocation of 200μm-ATP is approx. 160μm (75μm ‘free’ Ca2+). 3. The greatest stimulation of ATP translocation by Ca2+occurs at the lower concentrations of ATP. 4. Sr2+(and to a lesser extent Ba2+) can replace Ca2+whereas Mg2+and Mn2+have only little ability to stimulate ATP translocation. 5. Translocation of dATP is also stimulated by Ca2+whereas that of ADP is stimulated to only a relatively small degree. 6. Studies with metabolic inhibitors and uncouplers provide evidence that stimulation by Ca2+and by uncouplers is additive and that the mechanism of Ca2+stimulation does not seem to involve the high-energy intermediate of oxidative phosphorylation. 7. In the presence of Ca2+, ATP is able to effectively compete with ADP for translocation. 8. Added K+further enhances the ability of Ca2+to stimulate ATP translocation. 9. These findings are discussed in relation to the potential involvement of Ca2+in modifying enzymic reactions involved in the regulation of cell metabolism.

scholarly journals Influence of Extracellular Vesicles Isolated From Osteoblasts of Patients With Cox-Arthrosis and/or Osteoporosis on Metabolism and Osteogenic Differentiation of BMSCs

2020 ◽  
Vol 8 ◽  
Author(s):  
Tanja Niedermair ◽  
Christoph Lukas ◽  
Shushan Li ◽  
Sabine Stöckl ◽  
Benjamin Craiovan ◽  
...  
Keyword(s):  
Gene Expression ◽  
Osteogenic Differentiation ◽  
Extracellular Vesicles ◽  
Bone Structure ◽  
Cell Metabolism ◽  
Marker Gene ◽  
Structural Features ◽  
Alizarin Red ◽  
The Impact ◽  
Stimulation Of

Background: Studies with extracellular vesicles (EVs), including exosomes, isolated from mesenchymal stem cells (MSC) indicate benefits for the treatment of musculoskeletal pathologies as osteoarthritis (OA) and osteoporosis (OP). However, little is known about intercellular effects of EVs derived from pathologically altered cells that might influence the outcome by counteracting effects from “healthy” MSC derived EVs. We hypothesize, that EVs isolated from osteoblasts of patients with hip OA (coxarthrosis/CA), osteoporosis (OP), or a combination of both (CA/OP) might negatively affect metabolism and osteogenic differentiation of bone-marrow derived (B)MSCs.Methods: Osteoblasts, isolated from bone explants of CA, OP, and CA/OP patients, were compared regarding growth, viability, and osteogenic differentiation capacity. Structural features of bone explants were analyzed via μCT. EVs were isolated from supernatant of naïve BMSCs and CA, OP, and CA/OP osteoblasts (osteogenic culture for 35 days). BMSC cultures were stimulated with EVs and subsequently, cell metabolism, osteogenic marker gene expression, and osteogenic differentiation were analyzed.Results: Trabecular bone structure was different between the three groups with lowest number and highest separation in the CA/OP group. Viability and Alizarin red staining increased over culture time in CA/OP osteoblasts whereas growth of osteoblasts was comparable. Alizarin red staining was by trend higher in CA compared to OP osteoblasts after 35 days and ALP activity was higher after 28 and 35 days. Stimulation of BMSC cultures with CA, OP, and CA/OP EVs did not affect proliferation but increased caspase 3/7-activity compared to unstimulated BMSCs. BMSC viability was reduced after stimulation with CA and CA/OP EVs compared to unstimulated BMSCs or stimulation with OP EVs. ALP gene expression and activity were reduced in BMSCs after stimulation with CA, OP, and CA/OP EVs. Stimulation of BMSCs with CA EVs reduced Alizarin Red staining by trend.Conclusion: Stimulation of BMSCs with EVs isolated from CA, OP, and CA/OP osteoblasts had mostly catabolic effects on cell metabolism and osteogenic differentiation irrespective of donor pathology and reflect the impact of tissue microenvironment on cell metabolism. These catabolic effects are important for understanding differences in effects of EVs on target tissues/cells when harnessing them as therapeutic drugs.

scholarly journals Sericin based nanoformulations: a comprehensive review on molecular mechanisms of interaction with organisms to biological applications

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Gitishree Das ◽  
Han-Seung Shin ◽  
Estefânia V. Ramos Campos ◽  
Leonardo Fernandes Fraceto ◽  
Maria del Pilar Rodriguez-Torres ◽  
...  
Keyword(s):  
Tissue Repair ◽  
Biomedical Applications ◽  
Molecular Mechanisms ◽  
Low Cost ◽  
Pharmaceutical Formulations ◽  
Biological Properties ◽  
Regulation Of Transcription ◽  
Main Body ◽  
Silkworm Cocoon ◽  
Stimulation Of

Abstract Background The advances in products based on nanotechnology have directed extensive research on low-cost, biologically compatible, and easily degradable materials. Main body Sericin (SER) is a protein mainly composed of glycine, serine, aspartic acid, and threonine amino acids removed from the silkworm cocoon (particularly Bombyx mori and other species). SER is a biocompatible material with economic viability, which can be easily functionalized due to its potential crosslink reactions. Also, SER has inherent biological properties, which makes possible its use as a component of pharmaceutical formulations with several biomedical applications, such as anti-tumor, antimicrobials, antioxidants and as scaffolds for tissue repair as well as participating in molecular mechanisms attributed to the regulation of transcription factors, reduction of inflammatory signaling molecules, stimulation of apoptosis, migration, and proliferation of mesenchymal cells. Conclusion In this review, the recent innovations on SER-based nano-medicines (nanoparticles, micelles, films, hydrogels, and their hybrid systems) and their contributions for non-conventional therapies are discussed considering different molecular mechanisms for promoting their therapeutic applications.

scholarly journals Influence of chromium (III), cobalt (II) and their mixtures on cell metabolic activity

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Katarzyna Czarnek ◽  
Andrzej K. Siwicki
Keyword(s):  
Cell Proliferation ◽  
Cell Membrane ◽  
Cobalt Chloride ◽  
Cell Metabolism ◽  
Destructive Effect ◽  
Cytotoxic Effects ◽  
Cytotoxicity Assays ◽  
Low Concentrations ◽  
Mtt Reduction ◽  
Stimulation Of

Abstract Chromium (III) and cobalt (II) are necessary elements required for the proper functioning of the organism, but their excess can cause toxic effects. They are the basic components of implants and are also commonly used in medicine as components of dietary supplements, vitamin and mineral products and energy drinks. The aim of this study was to investigate the effect of cobalt (II) and chromium (III) and their combination on BJ cells. In the study, BJ cells were exposed to CoCl2 or CrCl3 at concentrations ranging from 100 to 1400 µM, and the cytotoxicity of chromium (III) and cobalt (II) and their mixtures was assessed by MTT reduction, LDH release and NRU assays. The outcome of this work reveals the cytotoxic effects of chromium (III) and cobalt (II) and their mixtures on BJ cells. In the cytotoxicity assays, at low concentrations of CoCl2 and CrCl3, stimulation of cell proliferation was observed. In higher concentrations, the cell viability decreased for the tested line in all the assays. During the simultaneous incubation of fibroblasts with 200 µM of CrCl3 and 1000 µM of CoCl2, antagonism was observed: chromium (III) at the concentration of 200 µM induced protection from cobalt (II) toxicity; in the case of interaction of chromium chloride at 1000 µm and cobalt chloride at 200 µM, the protective effect of CrCl3 on CoCl2 was not observed. In the latter case, synergism between these elements was noted. Our work indicates that cobalt (II) and chromium (III) show cytotoxic properties. These metals have a destructive effect on the cell membrane, lysosomes and mitochondria, which leads to disorders of cell metabolism.

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