![]() ![]() Right now it has an intriguing story, FANTASTIC renders, interesting characters and a few problematic elements, (Unskippable voyeurism), which are being worked on by the Dev. Will it have a harem and incest? Fuck yeah it will! 405 ( Suppl.I think the tags are jumping the gun right now and should be removed.ĭoes it have a harem and incest right now? Fuck no it doesnt! Volume regulation and basolateral co-transport of sodium, potassium, and chloride ions in frog skin epithelium. Volume regulation of frog skin epithelium. Basolateral membrane chloride transport in isolated epithelia of frog skin. Voltage dependence of cellular current and conductances in frog skin. Contribution of junctional conductance to the cellular voltage-divider ratio in frog skins. Basolateral membrane ionic conductance in frog skin. Effects of anions on cellular volume and transepithelial Na + transport across toad urinary bladder. Apical Na + permeability of frog skin during seasonal Cl − replacement. Osmoregulatory salt transporting mechanisms: Control of cell volume in anisotonic media. Basolateral membrane potential and conductance in frog skin exposed to high serosal potassium. The XXX Congress of the International Union of Physiological Sciences, Vancouver, Canada Decreased K conductance at the basolateral membrane in frog skin bathed in serosal Cl free solutions. Intracellular chloride activity and membrane potential in stripped frog skin ( Rana temporaria). Cell sodium activity and sodium pump function in frog skin. Cell K activity in frog skin in the presence and absence of cell current. The cell membrane resistance and the effect of amiloride. Electrical properties of amphibian urinary bladder epithelia: III. The regulation of volume and ion composition in frog skin. Microelectrode study of intracellular pH in frog skin: Dependence on serosal chloride. E., Kelepouris, E., Peterson-Yantorno, K., Civan, M. Effect of changes in extracellular Cl on intracellular Cl activity in frog skin. Cl transport across the basolateral membrane in frog skin epithelium. Apical sodium entry in split frog skin: Current-voltage relationship. Effects of ouabain and furosemide on basolateral membrane Na efflux of frog skin. Calcium ion activity in physiological salt solution: Influence of anions substituted for chloride. Sodium washout kinetics across inner and outer barriers of the isolated frog skin epithelium. Intracellular Cl activity changes of frog skin. The concurrent decrease of both a c K and a c Na following serosal substitution of SO 4 for Cl raises questions concerning mechanisms of osmoregulation.īiber, T. Serosal sulfate lowered the cell Na activity a c Na, but the electrochemical potential difference for Na across the apical surface was unaffected. Nor was it the result of decrease of the K equilibrium potential E K: exposure to serosal SO 4-Ringer decreased cell K activity a c K from 104☖ to 58±4 mm ( n=5), but E K was reduced only slightly exposure to serosal gluconate increased a c K and E K. Depolarization on removal of serosal Cl was not attributable to inhibition of the pump. Equilibration in serosal gluconate-Ringer enhanced polarization on serosal restoration of Cl or removal of Na, again indicating a time-dependent change in the basolateral conductance pattern. Following prolonged exposure to serosal SO 4-Ringer, the extent of depolarization induced by raising the serosal K concentration decreased, indicating diminution of basolateral K conductance and the existence of other basolateral conductances. With the use of gluconate or NO 3 in place of Cl, the effects on cellular current and conductance were minimal or insignificant, despite changes of the cell potential, fractional resistance, and basolateral conductance similar to those seen with sulfate. Similar effects were obtained with isolated epithelia. Apical membrane slope conductance was unaffected. After 30 to 45 min, however, the transcellular current had decreased and the cell electrical potential had depolarized, in association with decrease of the apical membrane fractional resistance and basolateral membrane conductance. Despite prompt changes of transepithelial measurements, initial cellular effects were slight. The effects of serosal substitution of isosmotic Na 2SO 4-Ringer solution for NaCl-Ringer solution were studied in the short-circuited frog skin ( Rana pipiens, Northern variety). ![]()
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