scholarly journals Synthesis of Silver Nanoparticles Using L.Rosa Flowers Extracts: Thermodynamic and Kinetic Studies on the Inhibitoty Effects of Nanoparticles on Creatine Kinase Activity

2021 ◽  
pp. 2486-2500
Author(s):  
Riyam Lateef Khalaf ◽  
Elham Majeed Ahmed ◽  
Thikra Hasan Mathkor ◽  
Hadeel Y. AL-Zubaidi
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Creatine Kinase ◽  
Silver Nitrate ◽  
Kinase Activity ◽  
Biological Activities ◽  
Kinetic Studies ◽  
Creatine Kinase Activity ◽  
Full Potential ◽  
Scale Production

      The present work investigates the synthesis of silver nanoparticles (AgNPs) by a biological method using L.Rosa flower extract and silver nitrate as precursors. Optimum conditions of synthesis were studies, such as pH, temperature, concentration of extract, concentration of silver nitrate, and stability with time. Characterization of AgNPs was carried out using UV-visible Spectroscopy, Scanning Electron Microscopy, X-Ray Diffraction, Fourier Transform Infrared and Transmission Electron Microscopy. The biosynthesized AgNPs exhibited inhibitory effects on creatine kinase activity in the sera of patients with myocardial infarction, compared with control subjects. Thermodynamic and kinetic studies of creatine kinase were performed. Further studies on other biological activities were performed to exploit AgNPs full potential. In conclusions, the present study utilize a simple, cheap and environmentally green method to synthesize silver nanoparticles. This single step procedure is more suitable for large scale production as it is rapid and eliminates the elaborate processes employed in the other bio-based protocols (e.g. by using fungi and bacteria).  

scholarly journals In vitro effect of silver nanoparticles on creatine kinase activity

2009 ◽  
Vol 20 (8) ◽  
pp. 1556-1560 ◽  
Author(s):  
Marcos Marques da Silva Paula ◽  
Cláudio Sérgio da Costa ◽  
Mario César Baldin ◽  
Giselli Scaini ◽  
Gislaine Tezza Rezin ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Creatine Kinase ◽  
Kinase Activity ◽  
Creatine Kinase Activity ◽  
Vitro Effect

Kinetic studies on the inhibition of creatine kinase activity by branched‐chain α‐amino acids in the brain cortex of rats

2003 ◽  
Vol 21 (3) ◽  
pp. 145-151 ◽  
Author(s):  
Carmen Pilla ◽  
Rui Felipe Oliveira Cardozo ◽  
Paula Karine Barcelos Dornelles ◽  
Carlos Severo Dutra‐Filho ◽  
Angela Terezinha Souza Wyse ◽  
...  
Keyword(s):  
Amino Acids ◽  
Creatine Kinase ◽  
Brain Cortex ◽  
Kinase Activity ◽  
Kinetic Studies ◽  
Creatine Kinase Activity ◽  
Branched Chain ◽  
The Brain

Kinetic studies on the inhibition of creatine kinase activity by 3-butyl-1-phenyl-2-(phenyltelluro)oct-en-1-one in the cerebral cortex of rats

2012 ◽  
Vol 50 (10) ◽  
pp. 3468-3474 ◽  
Author(s):  
Rodrigo Binkowski de Andrade ◽  
Tanise Gemelli ◽  
Robson Brum Guerra ◽  
Cláudia Funchal ◽  
Clovis Milton Duval Wannmacher
Keyword(s):  
Creatine Kinase ◽  
Cerebral Cortex ◽  
Kinase Activity ◽  
Kinetic Studies ◽  
Creatine Kinase Activity

Distribution of serum creatine kinase activity in young healthy persons

1999 ◽  
Vol 279 (1-2) ◽  
pp. 107-115 ◽  
Author(s):  
Eli I. Lev ◽  
Ilan Tur-Kaspa ◽  
Isaac Ashkenazy ◽  
Anat Reiner ◽  
David Faraggi ◽  
...  
Keyword(s):  
Creatine Kinase ◽  
Kinase Activity ◽  
Creatine Kinase Activity ◽  
Serum Creatine Kinase ◽  
Healthy Persons

scholarly journals Ability of adenovirus 5 E1A proteins to suppress differentiation of BC3H1 myoblasts correlates with their binding to a 300 kDa cellular protein.

1992 ◽  
Vol 3 (10) ◽  
pp. 1107-1115 ◽  
Author(s):  
J S Mymryk ◽  
R W Lee ◽  
S T Bayley
Keyword(s):  
Creatine Kinase ◽  
Kinase Activity ◽  
Cellular Protein ◽  
Creatine Kinase Activity ◽  
Cellular Proteins ◽  
Deletion Mutants ◽  
Transcriptional Enhancers ◽  
Actin Mrna ◽  
Alpha Actin ◽  
Adenovirus 5

We have used deletion mutants to define the regions in Ad5 E1A proteins necessary to suppress differentiation of mouse BC3H1 myoblasts. We examined the differentiation of cells infected at a low multiplicity with viruses containing the E1A deletions and constructed so as to produce only the smaller of the two major E1A proteins. Only four of the mutant viruses containing deletions within the N-terminal 69 residues failed to suppress differentiation as judged by changes in morphology and in levels of muscle-specific alpha-actin mRNA and creatine kinase activity. The results were confirmed by analyses of lines of cells stably transfected with representative E1A mutants. The mouse cellular proteins to which mutant E1A proteins bound were identified by immunoprecipitating E1A proteins specifically from infected BC3H1 cells and by analyzing the precipitates on denaturing gels. Bands of proteins of 300, 130, 107, 105 (the retinoblastoma product), and 60 kDa (cyclin A) were distinguished. Failure to suppress differentiation correlated with loss of binding to the 300-kDa protein but not to any of the others. The regions of E1A defined in this way have been shown to be required for several other activities, including enhancer repression and transformation. One function of the 300-kDa protein appears to be to facilitate the action of transcriptional enhancers of differentiation-specific genes.

Skeletal muscle collagen content in humans after high-force eccentric contractions

2004 ◽  
Vol 97 (1) ◽  
pp. 197-203 ◽  
Author(s):  
Abigail L. Mackey ◽  
Alan E. Donnelly ◽  
Taina Turpeenniemi-Hujanen ◽  
Helen P. Roper
Keyword(s):  
Creatine Kinase ◽  
Kinase Activity ◽  
Staining Intensity ◽  
Creatine Kinase Activity ◽  
Serum Creatine Kinase ◽  
Muscle Contractions ◽  
Tissue Inhibitors Of Metalloproteinases ◽  
Eccentric Contractions ◽  
Knee Extensors ◽  
Type Iv

The purpose of this study was to investigate the effects of high-force eccentric muscle contractions on collagen remodeling and on circulating levels of matrix metalloproteinases (MMP) and tissue inhibitors of metalloproteinases (TIMP) in humans. Nine volunteers [5 men and 4 women, mean age 23 (SD 4) yr] each performed a bout of 100 maximum voluntary eccentric contractions of the knee extensors. Muscle biopsies were taken before exercise and on days 4 and 22 afterward. Image analysis of stained tissue sections was used to quantify endomysial collagen staining intensity. Maximum voluntary contractile isometric force was recorded preexercise and on days 1, 2, 3, 4, 8, 11, and 14 postexercise. Venipuncture blood samples were also drawn on these days for measurement of serum creatine kinase activity and concentrations of MMP-9, TIMP-1, TIMP-2, and the MMP-2/TIMP-2 complex. Maximum voluntary contractile force declined by 39 ± 23% (mean ± SD) on day 2 postexercise and recovered thereafter. Serum creatine kinase activity peaked on day 4 postexercise ( P < 0.01). Collagen type IV staining intensity increased significantly on day 22 postexercise to 126 ± 29% (mean ± SD) of preexercise values ( P < 0.05). Serum MMP-9 levels increased on day 8 postexercise ( P < 0.01), and serum TIMP-1 was also significantly elevated on days 1, 2, 3, 4, and 14 postexercise ( P < 0.05). These results suggest that a single bout of eccentric muscle contractions results in remodeling of endomysial type IV collagen, possibly via the MMP pathway.

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