Abstract
Two pathways have been proposed for Mg2+ transport across the plasma membrane: 1) Na+-Mg2+ exchange and 2) Na+-independent passive Mg2+ pathway in visceral smooth muscle (Nakayama et al. J. Physiol.551.3,843-853,2003). Recently, Nadler et al. (Nature411,590-595,2001) has identified LTRPC7 as a Mg2+ permeable channel in the plasma membrane. In this study, using 31P-nuclear magnetic resonance (NMR), we measured the intracellular free-Mg2+ concentration ([Mg2+]i) in pig carotid artery smooth muscle. [Mg2+]i was estimated from the chemical shift of the β-ATP peak. Intracellular pH (pHi) estimated from the chemical shift of Pi was used to correct the [Mg2+]i value. We found that [Mg2+]i was increased by increasing the extracellular Mg2+ concentration in the absence of Ca2+. This was true when extracellular Na+ was substituted with equimolar K+ or NMDG(N-methyl-D-glucamine). 2-APB is a known potent blocker for LTRPC7. We also examined whether this drug affects the Na+-independent [Mg2+]i rise. [Jpn J Physiol 54 Suppl:S122 (2004)]