Affiliations: Department of Orthopaedics, Martin Luther University, Halle‐Wittenberg, Germany
Note: [] Address for correspondence: David Wohlrab, MD, Department of Orthopaedics, Martin Luther University, Halle‐Wittenberg, 06097 Halle, Germany. Tel.: +49 345 557 4802/05; Fax: +49 345 557 4809; E‐mail: david.wohlrab@medizin.uni‐halle.de.
Abstract: The goal of the study was to examine connections between ion channel activity and the proliferation of human chondrocytes. Chondrocytes were isolated form human osteoarthritic knee joint cartilage. In this study the concentration‐dependent influence of the ion channel modulators tetraethylammonium (TEA), 4‐aminopyridine (4‐AP), 4′,4′ diisothiocyanato‐stilbene‐2,2′‐disulfonic acid (DIDS), 4‐acetamido‐4′‐isothiocyano‐2,2′‐disulfonic acid stilbene (SITS), verapamil (vp) and lidocaine (lido) on the membrane potential and the proliferation of human chondrocytes was investigated using flow cytometry and the measurement of 3H‐thymidine incorporation as measure for the cell proliferation. The results show an effect of the used ion channel modulators causing a change of the membrane potential of human chondrocytes. The maximal measurable effects of the membrane potential were listed with 0.25 mmol/l verapamil (−18%) and 0.1 mmol/l lidocaine (+20%). When measuring DNA distribution, it became apparent that the human chondrocytes are diploid cells with a very low proliferation tendency. After 12 days culture duration, lidocaine and 4‐AP cause an increase of the DNA synthesis rate being a limited effect. These results allow the conclusion of an influence of ion channel modulators on chondrocyte proliferation. To gain knowledge of the regulation of chondrocyte proliferation via ion channel modulators could serve the research of new osteoarthritis treatment concepts.
Keywords: Chondrocytes, ion channel modulators, membrane potential, proliferation
Journal: Biorheology, vol. 39, no. 1-2, pp. 55-61, 2002
