digoxin has been researched along with Wounds-and-Injuries* in 2 studies
2 other study(ies) available for digoxin and Wounds-and-Injuries
Article | Year |
---|---|
Synchronization modulation increases transepithelial potentials in MDCK monolayers through Na/K pumps.
Transepithelial potential (TEP) is the voltage across a polarized epithelium. In epithelia that have active transport functions, the force for transmembrane flux of an ion is dictated by the electrochemical gradient in which TEP plays an essential role. In epithelial injury, disruption of the epithelial barrier collapses the TEP at the wound edge, resulting in the establishment of an endogenous wound electric field (∼100 mV/mm) that is directed towards the center of the wound. This endogenous electric field is implicated to enhance wound healing by guiding cell migration. We thus seek techniques to enhance the TEP, which may increase the wound electric fields and enhance wound healing. We report a novel technique, termed synchronization modulation (SM) using a train of electric pulses to synchronize the Na/K pump activity, and then modulating the pumping cycles to increase the efficiency of the Na/K pumps. Kidney epithelial monolayers (MDCK cells) maintain a stable TEP and transepithelial resistance (TER). SM significantly increased TEP over four fold. Either ouabain or digoxin, which block Na/K pump, abolished SM-induced TEP increases. In addition to the pump activity, basolateral distribution of Na/K pumps is essential for an increase in TEP. Our study for the first time developed an electrical approach to significantly increase the TEP. This technique targeting the Na/K pump may be used to modulate TEP, and may have implication in wound healing and in diseases where TEP needs to be modulated. Topics: Animals; Cell Movement; Digoxin; Dogs; Electric Stimulation; Enzyme Inhibitors; Ion Transport; Madin Darby Canine Kidney Cells; Membrane Potentials; Models, Biological; Ouabain; Protein Transport; Sodium-Potassium-Exchanging ATPase; Wound Healing; Wounds and Injuries | 2013 |
Endogenous glycosides in critically ill patients.
To determine the incidence of critically ill patients displaying endogenous digitalis-like-immunoreactive substances (DLIS) and to examine the relationship of these hormones to routine laboratory variables, the underlying disease, myocardial function, hemodynamic status, severity of illness, systemic inflammation, and mortality rate.. Sera of 401 consecutive critically ill patients, not treated with cardiac glycosides, were analyzed for DLIS (digitoxin and digoxin, TDx; Abbott Diagnostics, North Chicago, IL) and endogenous ouabain. Normal values of endogenous ouabain were determined in 62 healthy volunteers. We measured pro- and anti-inflammatory mediators (L-selectin, tumor necrosis factor-alpha, interleukin-1beta, interleukin-2, interleukin-6, interleukin-10), C-reactive protein, and serum amyloid A protein as well as patients' Acute Physiology and Chronic Health Evaluation II and Goris scores. In a subgroup of patients with a pulmonary artery catheter (n = 95), we determined cardiac output, pulmonary artery occlusion pressure, systemic and pulmonary vascular resistance, left ventricular stroke volume, and right and left stroke work.. Two surgical intensive care units of an university hospital.. Sera of 401 consecutive critically ill patients.. Blood sampling.. Of the 401 patients tested, 343 had nonmeasurable DLIS concentrations (DLIS-negative), and 58 (14.5%) had positive digoxin (n = 18) or digitoxin (n = 34) concentrations (DLIS-positive) or were positive in both tests (n = 6). Mean endogenous ouabain concentrations were nine-fold increased in DLIS-positive (3.59 +/- 1.43 nmol/L) and three-fold increased in DLIS-negative (1.34 +/-.81 nmol/L) patients compared with controls (0.38 +/- 0.31 nmol/L). DLIS and ouabain concentrations closely correlated with the Acute Physiology and Chronic Health Evaluation II and Goris score and were associated with increased concentrations of transaminases, bilirubin, aldosterone, cortisol, serum creatinine, fractional sodium excretion, proinflammatory mediators, C-reactive protein, and serum amyloid A (p Topics: Aged; APACHE; C-Reactive Protein; Cardenolides; Cardiac Output; Case-Control Studies; Central Venous Pressure; Critical Illness; Digoxin; Female; Hospital Mortality; Humans; Inflammation; Interleukin-1; Interleukin-10; Interleukin-2; Interleukin-6; L-Selectin; Laparotomy; Male; Middle Aged; Pulmonary Wedge Pressure; Saponins; Serum Amyloid A Protein; Stroke Volume; Thoracic Diseases; Tumor Necrosis Factor-alpha; Wounds and Injuries | 2003 |