The present study was designed to investigate the acute relaxing effect of phytoestrogen resveratrol on isolated porcine coronary arteries and to determine the mechanisms underlying its vasodilatation. Rings of porcine coronary arteries were suspended in organ baths containing Krebs-Henseleit solution, and then isometric tension was measured. Resveratrol concentration-dependently relaxed arterial rings precontracted with 30 mM KCl. The IC50 value of resveratrol was 38.67±3.21 μM. Incubation with Nω-L-nitro-arginine (L-NNA), endothelium removal or the presence of a potent inhibitor of protein tyrosine phosphatase sodium orthovanadate partly decreased the relaxation induced by resveratrol. However, the relaxation induced by resveratrol was unaffected by the estrogen receptor antagonist tamoxifen, the inhibitor of prostanoid synthesis indomethacin, the antagonist of β-adrenoceptors propranolol or the protein synthesis inhibitor, cycloheximide. In addition, resveratrol significantly decreased the contractile responses of
5-HT, KCl and CaCl2, and shifted their cumulative concentration-response curves to the right. These results suggest that the mechanisms of vasorelaxation induced by resveratrol are heterogeneous, two mechanisms participating partially in the relaxation of porcine coronary artery were detected in the study, one being the nitric oxide released from the endothelium, the other causing inhibition of Ca2+ influx, but estrogen receptors were not involved in resveratrol-induced relaxation.
Hypotonic solution alters ion channel activity, but little attention has been paid to voltage-dependent sodium channels. The aim of this study was to investigate the effects of hypotonic solution on transient sodium currents (INaT) and persistent sodium currents (INaP). We also explored whether the intracellular signal transduction systems participated in the hypotonic modifications of sodium currents. INaT and INaP were recorded by means of whole-cell patch-clamp technique in isolated rat ventricular myocytes. Our results revealed that hypotonic solution reduced INaT and simultaneously augmented INaP with the occurrence of interconversion between INaT and INaP. Hypotonic solution shifted steady-state inactivation to a more negative potential, prolonged the time of recovery from inactivation, and enhanced intermediate inactivation (IIM). Ruthenium red (RR, inhibitor of TRPV4), bisindolylmaleimide VI (BIM, inhibitor of PKC), Kn-93 (inhibitor of Ca/CaMKII) and BAPTA (Ca2+-chelator) inhibited the effects of hypotonic solution on INaT and INaP. Therefore we conclude that hypotonic solution inhibits INaT, enhances INaP and IIM with the effects being reversible. TRPV4 and intracellular Ca2+, PKC and Ca/CaMKII participate in the hypotonic modifications of sodium currents., L. Hu ... [et al.]., and Obsahuje seznam literatury
For an ordered set W = {w1, w2, . . . , wk} of vertices in a connected graph G and a vertex v of G, the code of v with respect to W is the k-vector cW (v) = (d(v, w1), d(v, w2), . . . , d(v, wk)). The set W is an independent resolving set for G if (1) W is independent in G and (2) distinct vertices have distinct codes with respect to W. The cardinality of a minimum independent resolving set in G is the independent resolving number ir(G). We study the existence of independent resolving sets in graphs, characterize all nontrivial connected graphs G of order n with ir(G) = 1, n − 1, n − 2, and present several realization results. It is shown that for every pair r, k of integers with k ≥ 2 and 0 ≤ r ≤ k, there exists a connected graph G with ir(G) = k such that exactly r vertices belong to every minimum independent resolving set of G.