Loss-of-function mutations of Na(V)1.1 channels cause severe myoclonic epilepsy in infancy (SMEI), which is accompanied by severe ataxia that contributes substantially to functional impairment and premature deaths. Mutant mice lacking Na(V)1.1 channels provide a genetic model for SMEI, exhibiting severe seizures and premature death on postnatal day 15. Behavioral assessment indicated severe mot...

We sought to determine whether the impairment of sodium pump activity and Na+/H+ exchange reported in tumorigenic cells was specific to these cells or more general. Sodium pump activity and Na+/H+ exchange were measured in erythrocytes from 49 cancer patients and 51 healthy subjects. Cancer patients with a newly detected cancer or in relapse and without associated pathologies known to modify th...

The kinetics of Na/succinate cotransport across renal brush-borders was studied using membrane vesicles. Initial rates of succinate uptake (Js) were estimated from 1-s uptakes measured under voltage-clamped conditions. Lowering the external (cis) sodium concentration reduced the succinate Kt without affecting the Jsmax. Increasing the intravesicular (trans) sodium concentration reduced both Jsm...

Herein, the nitridophosphate Na3V(PO3)3N is synthesized by solid state method. X-ray diffraction (XRD) and Rietveld refinement confirm the cubic symmetry with P213 space group. The material exhibits very good thermal stability and high operating voltage of 4.0 V vs. Na/Na+ due to V3+/V4+ redox couple. In situ X-ray diffraction studies confirm the two-phase (de-)sodiation process to occur with v...

Amiloride-sensitive Na+/H+ exchange in plasma membrane vesicles prepared by sucrose density gradient centrifugation of mitochondria-rich posterior gill cells in two species of crabs (Callinectes sapidus and Carcinus maenas) was examined by acridine orange fluorescence quenching. Sodium-loaded vesicles injected into sodium-free incubation medium (pHout = pHin) caused a quench in fluorescence ind...

Nephrotic syndrome is often accompanied by sodium retention and generalized edema. However, the molecular basis for the decreased renal sodium excretion remains undefined. We hypothesized that epithelial Na channel (ENaC) subunit dysregulation may be responsible for the increased sodium retention. An experimental group of rats was treated with puromycin aminonucleoside (PAN; 180 mg/kg iv), wher...

The uptake of glucose and the nutrient coupled transcellular sodium traffic across epithelial cells in the small intestine has been an ongoing topic in physiological research for over half a century. Driving the uptake of nutrients like glucose, enterocytes must have regulatory mechanisms that respond to the considerable changes in the inflow of sodium during absorption. The Na-K-ATPase membran...

background: today, in many countries, wastewater treatment plants effluent is an important part of the renewable water resources. in this case, the effluent quality standards are developed and used is important. the aim of this study was to investigate the potential use of wastewater plants effluent restricted irrigation. methods: in this descriptive - analytical study, samples was collected fr...

The benzophenone dianion [diphenyloxidomethanide, (Ph(2)CO)(2-)], which occurs in the well known deeply violet sodium/benzophenone tetrahydrofuran solutions, was crystallised with sodium cations in form of the two polymeric chain compounds [Na(2)(Ph(2)CO)(tetraglyme)](infinity) and [Na(2)(Ph(2)CO)(thf)(2)](infinity). It was found to aggregate with its conjugated acid, the alcoholate (Ph(2)CHO)(...

BACKGROUND Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel (Na(v)1.5). We previously reported that the function of a trafficking-deficient BrS Na(v)1.5 mutation, R282H, could be restored by coexpression with the sodium channel polymorphism H558R. Here, we tested the hypothesis that peptide fragments from Na(v)1.5, spanning the H558R polymorphism, can be used to...