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Although the neurotoxic mechanism of lead (Pb2 +) has been extensively studied, it is not well understood. The effects of Pb2 + on free cytosolic calcium (Ca2 +) concentration and calcium-regulated events have been suggested to be major mechanisms in Pb2 + toxicity. Based on our previous findings that Pb2 + changes calcium release through ryanodine receptors (RyRs), the modulation of endoplasmic reticulum (ER) vesicular RyRs by Pb2 + was investigated further in the present study. The results of [3H]ryanodine binding assays showed that in the presence of a free Ca2 + concentration ([Ca2 +]f) of 100 μM, Pb2 + modulated the equilibrium of [3H]ryanodine binding to brain RyRs, with a U-type dose-response curve, where minimal binding was observed at a free Pb2 + concentration ([Pb2 +]f) of 0.39 μM. This modulation was also observed over a time course. Scatchard analysis indicated that both an increase in Kd and a possible decrease in Bmax were responsible for the decrease in binding induced by low [Pb2 +]f. Moreover, the effects of Pb2 + on the function of ER RyRs in neurons might also be controlled by other RyR modulators. Whole-cell patch-clamp experiments revealed that dynamic calcium oscillations evoked by specific RyR agonists were depressed rapidly and reversibly by exposure to 10 μM Pb2 +. Our study indicates that RyRs are molecular targets of Pb2 +, and this interaction disturbs Ca2 + signals and leads to neurotoxicity.Pb2 + inhibited [3H]ryanodine binding to RyRs with a U-shaped dose-response curve.Modulators of RyRs can change the binding of Pb2 + to RyRs.Calcium oscillation induced by RyR agonists was depressed by Pb2 + exposure.RyRs may be the targets of Pb2 + neurotoxicity through disturbing Ca2 + signaling.