ライフサイエンスコーパス: Ringer solution

1 the presence of basolateral bicarbonate-rich Ringer solution.

2 ed to a third or less of its normal value in Ringer solution.

3 delivered by pressure ejections of odor-free Ringer solution.

4 seen when returning immediately to IBMX-free Ringer solution.

5 ontrol and received a continuous infusion of Ringer solution.

6 lished when cells were bathed in an alkaline Ringer solution.

7 s, which could be observed even from rods in Ringer solution.

8 to changes in pH(o) in bicarbonate-buffered Ringer solution.

9 i which normally accompanies illumination in Ringer solution.

10 th the oscillation period when stimulated in Ringer solution.

11 extran 2000 reduced flows in comparison with Ringer solution.

12 g lumen and bath perfusion with an HCO(3)(-)-Ringer solution.

13 g sympathetic ganglion neurones in 2.0 mM K+ Ringer solution.

14 fluid had a similar effect to hyaluronan in Ringer solution.

15 etal muscle fibres by exposure to hypertonic Ringer solutions.

16 H2O-1 (mean +/- s.e.m.), was 1/39th that for Ringer solution (1.94 +/- 0.01 microliter 2O-1 ).

17 control (90% propylene glycol + 10% lactated Ringer solution); (2) 20 mm capsazepine to inhibit TRPV-

18 Compartments #1, #2 and #5 contained frog Ringer solution, #4 was filled with Vaseline and formed

19 her in contralateral joints expanded by 2 ml Ringer solution (5.80 +/- 0.84 micrograms h-1, n = 5, P

20 When the cilia were returned to Ringer solution after a period in reduced-Na(+) solution

21 , instead, the outer segment was returned to Ringer solution after the bleach, thereby allowing [Ca2+

22 crodialysis fibres for the local delivery of Ringer solution and 20 mm ascorbic acid (AA).

23 Ringer solution and 214 microM VIP(10-28) were each perf

24 erved by comparing trains of EPSCs in normal Ringer solution and atropine.

25 lined at a rate that was much slower than in Ringer solution and consistent with previous physiologic

26 its replacement by an isotonic Ca(2+)-Mg(2+) Ringer solution and cooling sharply reduced such access.

27 ng VIP(10-28) at the three concentrations or Ringer solution and perfusion was continued for 45-60 mi

28 esponses had a longer latency than in normal Ringer solution and were blocked by [D-pGlu1, D-Phe2, D-

29 studied in Cl(-)-free, normal and Na(+)-free Ringer solutions and in the presence of bumetanide, chlo

30 ide and replacement of Na+ by choline in the Ringer solution, and irreversibly by both fetal and mate

31 nto the knees of anaesthetized rabbits, with Ringer solution as control in the contralateral joint.

32 Preparations were superfused with rat Ringer solution at 25 degrees C.

33 ight of much lower intensity if delivered in Ringer solution but not if delivered in 0 Ca(2+), 0 Na(+

34 ifts in E(m) in fibres studied in Cl(-)-free Ringer solution consistent with the Goldman-Hodgkin-Katz

35 In Ringer solution containing both Cl- and HCO3-, the magni

36 Ringer solution containing enzyme was injected into the

37 troqinoxaline-2,3-dione (CNQX; 10 microM) in Ringer solution containing physiological concentrations

38 Vessels, microperfused with frog Ringer solutions containing 0.1% bovine serum albumin an

39 vessels were perfused via micropipettes with Ringer solutions containing bovine serum albumin (1 mg m

40 ng and 10 older subjects for infusion of (1) Ringer solution (control), (2) 0.5 mm L-tyrosine, (3) 5

41 older (O) human subjects for infusion of (1) Ringer solution (control), (2) 5 mM BH(4), (3) 5 mM BH(4

42 rodialysis sites were perfused with lactated Ringer solution (Control), 40 pm, 4 nm or 400 nm ET-1; i

43 2 (n = 11) sites were perfused with lactated Ringer solution (Control), 400 nm ET-1, 10 mm N(G) -nitr

44 ion, microdialysis fibres were perfused with Ringer solution (control), a ATP-sensitive potassium cha

45 ays, microdialysis fibres were perfused with Ringer solution (control), a non-specific NO synthase in

46 onium (TEA), (3) EMLA + TEA (Combo), and (4) Ringer solution (Control).

47 (L-NAME), (3) Keto + l-NAME (Combo), and (4) Ringer solution (Control).

48 intradermal microdialysis with: (1) lactated Ringer solution (Control); (2) 10 mm ascorbate (Ascorbat

49 e other 24 degrees C site served as control (Ringer solution + cooling).

50 magnitude when the cell was superfused with Ringer solution during the 5 s interval between odour ex

51 bicarbonate Ringer (KBR) with Hepes-buffered Ringer solution exhibited basolateral, but not apical, r

52 xposed to 110 mM hydroxylamine in a low-Ca2+ Ringer solution for a period of 10-50 s beginning 10-17

53 induced by infusion of 0.2 M HCl in lactated Ringer solution in the acid group.

54 With Na(+)-containing Ringer solution in the bath and K(+)-containing Ringer s

55 ger solution in the bath and K(+)-containing Ringer solution in the pipette, both currents were selec

56 h retina superfused with a bicarbonate-based Ringer solution in the subjective day and night; that is

57 ked by 20 Hz nerve firing occurred in normal Ringer solution, in ryanodine, and in caffeine with a pe

58 sites were then heated to 42 degrees C, with Ringer solution infused in one probe and N-nitro-L-argin

59 on of neurones with zero calcium (1 mM EGTA) Ringer solution inhibited depolarization-induced calcium

60 exposure of muscles to a hypertonic glycerol-Ringer solution, its replacement by an isotonic Ca(2+)-M

61 also unchanged when the cone was exposed to Ringer solution made up from heavy water, whose solvent

62 intradermal microdialysis sites: control (C, Ringer solution), NO synthase inhibited (NOS-I, 10 mm l-

63 mmHg) men and women to serve as: control (C, Ringer solution), NOS inhibited (NOS-I, 10 mM L-NAME), A

64 ears) human subjects, serving as control (C, Ringer solution), NOS-inhibited (10.0 mM NG-nitro-L-argi

65 In contrast, fibres exposed to hypertonic Ringer solutions of normal ionic composition showed no s

66 s evoked by continuous stimulation in normal Ringer solution or by bursts of stimuli in hexamethonium

67 llumination, whether the bleach was given in Ringer solution or in 0Ca(2+)/0Na(+) solution.

68 fluid drainage rate was reduced relative to Ringer solution (P < 0.001, ANOVA) but increased steeply

69 l pH was observed at two different values of Ringer solution pH, indicating that the circadian phenom

70 Acidification of Ringer solution resulted in a reduced antagonism by Zn2+

71 + solution before the flash and returning to Ringer solution shortly before the normal time of recove

72 n isotonic Cl(-)-free, normal and Na(+)-free Ringer solutions showed similar E(m) values consistent w

73 In normal Ringer solution, TEP was 20-90 mV with the basolateral (

74 polarization produced by a high K(+) (40 mM) Ringer solution that was delivered rapidly and briefly t

75 In Ringer solution, the Ca2+ in the light-releasable pool c

76 When the cell was bathed in Ca2+-free Ba2+ Ringer solution, the K+ currents were blocked and large

77 When a cone was exposed in normal Ringer solution to bright light bleaching a significant

78 m or amplitude when rods were pre-exposed in Ringer solution to light which was bright enough to supp

79 milar average mass (2000 kDa; n = 7) or with Ringer solution vehicle (n = 2).

80 Ringer solution was infused into the knee joint cavity o

81 + P), bretylium tosylate (BT), and lactated Ringer solution were infused via intradermal microdialys

82 declined exponentially towards its value in Ringer solution with a time constant of around 1 s.

83 Applications of Ringer solutions with added NH(4)Cl induced rapid reduct

84 H (pHi) or Na(+) ([Na(+)](i)) in response to Ringer solutions with/without B(OH)(4)(-) or HCO(3)(-) a

85 edium was prepared by supplementing isotonic Ringers solution with sucrose.

86 The contralateral joint received Ringer solution without enzyme as a control.