Abstract

Purpose. Retinal vascular changes are associated with retinitis pigmentosa in man and the retinal dystrophy of the Royal College of Surgeons (RCS) rat. Recently we demonstrated that retinal capillary pericytes possess electrical membrane characteristics typical for smooth muscle cells and may thus regulate retinal blood flow in vivo.Methods. In the present study we compared cultured pericytes of 5–7 day old RCS and control rats by measurement of membrane voltage (Vmem) with microelectrodes and currents with the whole-cell configuration of the patch-clamp technique.Results. Resting membrane voltage (–37.6 mV ± 1.0 mV, n = 106 and –36.6 mV ± 0.7 mV, n = 102, respectively) and whole-cell currents, which are mainly determined by a potassium conductance, were comparable in pericytes of control and RCS rats. The electrogenic component of the Na+-K+-ATPase in RCS rat pericytes was reduced, because depolarization of their membrane voltage by Na+-K+-ATPase inhibitor ouabain (10–4 mol · 1–1) or K+ free solution was significantly decreased compared to control pericytes. Norepinephrine (10–5 mol · 1–1) depolarized Vmem of control rat pericytes by ΔDL7.0 mV ± 1.3 mV (n = 7), whereas it hyperpolarized Vmem. of RCS rat pericytes by ΔDL2.0 mV ± 0.8 mV (n = 11). The depolarization of Vmem by histamine (10–5 mol · 1–1) was significantly reduced in pericytes of RCS rats (ΔDL2.6 mV ± 0.4 mV, n = 7) compared to control pericytes (ΔDL4.3 mV ± 0.5 mV, n = 6). In pericytes of RCS rats ATP-induced activation of inward and outward currents and depolarization of membrane voltage were also significantly reduced.Conclusions. The data indicate that there are differences in the electrophysiological properties of retinal capillary pericytes of 5–7 days old RCS and control rats. Whereas resting membrane voltage and K+ conductance are comparable in both groups, there are significant differences in the electrical activity of Na+-K+-ATPase and in the effects of vasoactive substances on the membrane voltage and currents. These differences might contribute to the vascular changes observed in RP, and possibly accelerate the progress of retinal dystrophy.