Characterization of Thyroid Hormone Effects on Na Channel Synthesis in Cultured Skeletal Myotubes: Role of Ca2+*

Abstract

Thyroid hormones (TH) cause an increase in spontaneous electical activity fo cultured rat skeletal myotubes. This activity is associated with tetrodotoxin (TTX)-sensitive Na channels. In addition, the initial effect of TH on Na-K pump synthesis has been shown to be TTX dependent. Accordingly, we have studied effects of TH on expression of TTX-sensitive Na channels in cultured skeletal muscle. Expression of Na channels was determined by measurements of the binding of [3H]saxitoxin (STX). The frequency and rate of rise of spontaneously occurring action potentials, which are related to the density of TTX-sensitive Na channels, were also determined. TH caused dose-dependent increases in Na channels as well as in action potential frequency and rate of rise. The increases were detectable as early as 12 ha after treatment with TH was begun, and levels reached a maximum plateau after 36-48 h. The effects of TH were blocked by inhibitors of protein synthesis. Scatchard analysis showed the channels in TH-treated myotubules to have lower affinity for STX than those in control cells. The effect of TH to up-regulate Na channels was reduced by growth of the cells in elevated calcium. In contrast, treatment with TTX or verapamil, which lower cytosolic Ca2+, resulted in a marked increase in the effect of TH over that in control myotubes. Thus, TH appears to regulate Na channels in cultured myotubes by two opposing mechanisms; 1) direct stimulation of Na channel synthesis, and 2) indirect decrease in synthesis mediated by an increase in cytosolic Ca2+. The results indicate that TH may play an important role in developmental expression of Na channels in excitable tissue.