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1.
Biorheology ; 51(4-5): 305-14, 2014.
Article in English | MEDLINE | ID: mdl-25381135

ABSTRACT

BACKGROUND: Injection of xanthan gum (XG) has been demonstrated to reduce the symptoms and progression of osteoarthritis (OA) in experimental models. Due to its high viscosity and stability, it may restore the rheological homeostasis of osteoarthritic synovial fluid (SF), and avoid numerous intra-articular injections. OBJECTIVE: The present study investigated the effect of XG on the rheological properties of SF, and determined its residence time in the rabbit joint cavity. METHODS: Rabbit knees were subject to intra-articular injection with XG or XG labeled with green fluorescence, and the SF was collected at different time. Rheological properties of SF with XG injected were compared with those with sodium hyaluronate injected. Resistance to oxidant damage was tested by adding H2O2 to the viscosupplement. Fluorescence intensity was measured for the SF with XG labeled with green fluorescence. RESULTS: Results showed that XG could significantly improve the SF viscosity at 24, 96, 168 h, and increase the storage moduli (G') and loss moduli (G″) tested at frequency of 0.5 and 2.5 Hz. SF with XG injection exhibited a gel-like behavior at 24 h, in that G' exceed G″ over the entire oscillation frequency range. XG preparation had a high resistance to oxidant damage. Half-life of XG in the joint cavity was 35.9 h, with clearance obeying first-order kinetics. CONCLUSIONS: Intra-articular injection of XG could improve the rheological properties of SF, and this effect could last for several days.


Subject(s)
Knee Joint/physiopathology , Osteoarthritis/physiopathology , Polysaccharides, Bacterial/chemistry , Synovial Fluid/physiology , Animals , Hyaluronic Acid/chemistry , Hydrogen Peroxide/chemistry , Injections, Intra-Articular , Male , Oxidants/chemistry , Polysaccharides, Bacterial/pharmacokinetics , Rabbits , Rheology/methods , Stress, Mechanical , Viscosity
2.
J Trace Elem Electrolytes Health Dis ; 4(3): 157-61, 1990 Sep.
Article in English | MEDLINE | ID: mdl-2136132

ABSTRACT

Selenium (Se) is a trace element variously distributed in the human body and especially concentrated in certain organs, such as the renal cortex. We report results obtained during a ten weeks' oral Se supplementation. Experiments were devised to evaluate previous preliminary observations which suggested a possible effect of Se addition on the renal glomerular filtration rate. Eleven healthy volunteers have given increasing oral Se (as a sodium selenite solution) as follows: on the first week they have given 100 micrograms Se per day; this was progressively increased 100 micrograms per day for each of the following 6 weeks; the last dose (700 micrograms per day) was maintained for three further weeks. Serum and 24-hour urine were collected weekly for creatinine determination by kinetic Jaffé reaction and Se measurement by proton-induced X ray emission (PIXE). The final mean serum creatinine concentration was 13% lower than the initial mean value (p less than 0.01). Mean creatinine clearance increased significantly (p less than 0.05) and showed a direct correlation with mean Se clearance (r = 0.79; p less than 0.001). As the increase of creatinine clearance was concomitant with a reduction of serum creatinine levels, we excluded the possibility of toxic effects. Our results seem to suggest a positive influence of Se supplementation on the rate of glomerular filtration and we hypothesize that Se might be involved in the vascular regulatory mechanism of the kidney.


Subject(s)
Glomerular Filtration Rate/drug effects , Selenium/pharmacology , Adult , Creatinine/blood , Creatinine/urine , Humans , Male , Metabolic Clearance Rate , Selenium/administration & dosage , Selenium/pharmacokinetics
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