Effects of pulsing electromagnetic fields on cultured cartilage cells

• Published in: International orthopaedics Vol. 15; no. 4; pp. 341 - 346
• Main Authors: SAKAI, A, SUZUKI, K, NAKAMURA, T, NORIMURA, T, TSUCHIYA, T
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01-01-1991
• Subjects: Animals; Biological and medical sciences; Cartilage - cytology; Cartilage - drug effects; Cartilage - radiation effects; Cartilage, Articular - cytology; Cell Division - radiation effects; Cells, Cultured; DNA - biosynthesis; Doxorubicin - pharmacology; Electromagnetic Fields; Glycosaminoglycans - biosynthesis; Glycosaminoglycans - radiation effects; Investigative techniques, diagnostic techniques (general aspects); Lidocaine - pharmacology; Male; Medical sciences; Rabbits; Ribs; Cartilage; Electrodiagnosis; Animal; Diseases of the osteoarticular system; Exploration; Electromagnetic field; Experimental study; Result
• ISSN: 0341-2695; 1432-5195
• DOI: 10.1007/BF00186874

In order to evaluate the effects of pulsing electromagnetic fields (PEMFs) on cell proliferation and glycosaminoglycan (GAG) synthesis and to study the action site of PEMF stimulation in the cells, we performed a series of experiments on rabbit costal growth cartilage cells and human articular cartilage cells in culture. A PEMF stimulator was made using a Helmholz coil. Repetitive pulse burst electric currents with a burst width of 76 ms, a pulse width of 230 microseconds and 6.4 Hz were passed through this coil. The magnetic field strength reached 0.4 mT (tesla) on the average. The syntheses of DNA and GAG were measured by 3H-thymidine and 35S-sulfuric acid incorporations. The effects on the cells treated with lidocaine, adriamycin and irradiation were also measured using a colony forming assay. The PEMF stimulation for the duration of 5 days promoted both cell proliferation and GAG synthesis in growth cartilage cells and intermittent stimulation on and off alternatively every 12 h increased them most significantly, while, in articular cartilage cells, the stimulation promoted cell proliferation, but did not enhance GAG synthesis. PEMF stimulation promoted cells treated with lidocaine more significantly than with other agents. These results present evidence that intermittent PEMF stimulation is more effective on both cell proliferation and GAG synthesis of cartilage cells than continuous stimulation, and that the stimulation could exert effects not by nucleus directly, but by the cellular membrane-dependent mechanism. This study provides further basic data to encourage the clinical application of PEMF stimulation on bone and cartilage disorders.