ライフサイエンスコーパス: isosmotic

1 -min hypoxia followed by reoxygenation under isosmotic (293 mOsm) conditions.

2 llecting duct (mIMCD) were exposed to either isosmotic (300 mosmol/kg) or hyperosmotic medium (isosmo

3 Isosmotic addition of 50 mM propionate to the standard H

4 cell swelling, which could be blocked by an isosmotic addition of a pore-impermeable solute (sucrose

5 -19755 (50 microM) completely protected both isosmotic and hyposmotic (233 mOsm) slices against hypox

6 le whole-cell currents were elicited by both isosmotic and hyposmotic cell swelling.

7 rane potential (Em) was -58 and -32 mV under isosmotic and hyposmotic conditions, respectively.

8 ile during I- influx, together with Em under isosmotic and hyposmotic conditions, were used to calcul

9 O3- Ringer's were exposed to I- pulses under isosmotic and, subsequently, hyposmotic conditions.

10 gh water permeabilities, consistent with the isosmotic ASL theory, and the capacity to restore water

11 and CF airway epithelia, consistent with an isosmotic ASL.

12 For resuspension in isosmotic buffer (osmotic upshift, or Delta, of 0), the

13 Importantly, isosmotic cell swelling obtained by parallel activation

14 ity under hyposmotic condition to that under isosmotic condition (termed enhancement ratio or ER) was

15 entration (1.8 to </=1.6 mM) in an otherwise isosmotic condition, real-time AFM imaging revealed a si

16 Jdw was determined in control isosmotic conditions and after either changes in osmolar

17 erved under both hyperosmotic conditions and isosmotic conditions associated with osmotic stress.

18 , ICl,swell was persistently activated under isosmotic conditions in CHF myocytes, and 9AC increased

19 (Cir,swell) was persistently activated under isosmotic conditions in CHF myocytes, and Gd3+ decreased

20 Under isosmotic conditions or with activation of the kinases S

21 However, the function of NFAT5 under isosmotic conditions present in vivo remains unknown.

22 ificantly faster under hyposmotic than under isosmotic conditions.

23 posmotic media (170 mosmol kg-1) relative to isosmotic control (300 mosmol kg-1) values, it decreased

24 h after onset of hyperosmolality, but not in isosmotic controls, growth arrest and DNA damage-inducib

25 ring moderate hyperosmotic stress but not in isosmotic controls.

26 greater in the hyperosmotic papilla than the isosmotic cortex but was not affected by the animal's hy

27 ignificantly increased after 6 h exposure to isosmotic EtOH, but not hyperosmotic EtOH.

28 Isosmotic exposure of MMDD1 cells to low NaCl (60 mm) ca

29 egulate ASL volume by modulating the flow of isosmotic fluid across the epithelium, whereas an altern

30 Acute dynamic exercise and isosmotic fluid ingestion each seem to change IOP throug

31 rformed after dehydration and hydration with isosmotic fluid.

32 go reversible volume changes when exposed to isosmotic glucose-fructose exchange.

33 go reversible volume changes when exposed to isosmotic glucose-fructose exchange.

34 d by a return of extracellular osmolality to isosmotic levels.

35 dehydration, and after hydration with 946 ml isosmotic liquid (345 mOsM).

36 otic (300 mosmol/kg) or hyperosmotic medium (isosmotic medium + 150 mM NaCl) after seeding.

37 ckle cell disease (SCD) lyse in deoxygenated isosmotic non-electrolyte solutions.

38 nsport after brief exposure to hypo-osmotic, isosmotic or hyperosmotic medium (170, 300 and 430 mosmo

39 up to 7%, but 9AC had no effect on volume in isosmotic or hyperosmotic solutions.

40 Strain on the TM induced by isosmotic PEG solutions of different molecular masses wa

41 In normoxia and in hypoxia, an isosmotic reduction in [Na+]o caused a proportional decr

42 The isosmotic replacement of NaCl with choline chloride had

43 ium chloride in the bathing fluid and during isosmotic replacement of sodium chloride with mannitol.

44 erosmotic samples were shifted compared with isosmotic samples showing a gap of 18 h but had the same

45 llular physiological calcium in an otherwise isosmotic situation.

46 of the antagonist provided no protection to isosmotic slices (51% vs. 57% recovery rate) while affor

47 to hyposmotic conditions as 57% of control (isosmotic) slices showed recovery compared with 51%, 35%

48 l myocytes, osmotic swelling in 0.9x to 0.6x isosmotic solution (296 mOsm/L) was required to elicit a

49 Osmotic shrinkage in 1.1x to 1.5x isosmotic solution inhibited both I(Cir,swell) and Gd3+-

50 9T to 0.6T solution (T, relative osmolarity; isosmotic solution, 296 mOsmol/L) was required to elicit

51 ely 10%, but Gd3+ had no effect on volume in isosmotic solution.

52 y extrapolation of osmolalities of predicted isosmotic state at 8,000-8,500 m may indicate a possible

53 ies from bathyal and abyssal fishes, predict isosmotic state at 8,200 m.

54 Although isosmotic substitution of extracellular Na(+) ions block

55 iated inward current, which was sensitive to isosmotic substitution of Na(+) or Cl(-) ion.

56 Neither isosmotic substitution of sucrose for NaCl in the medium

57 als showed progressive lysis in deoxygenated isosmotic sucrose solution at pH 7.4 to a level greater