ライフサイエンスコーパス: superfuse

1 50 microm thickness) of rat neostriatum were superfused (400 ml/h) with an artificial cerebrospinal f

2 neurons that might mediate these effects of superfused 5-HT are unknown, one pair of 5-HT-immunoreac

3 Although superfused 5HT inhibits the spontaneous firing of these

4 We developed a method for isolating and superfusing a nasal segment in dogs.

5 sists of 15 channel networks each capable of superfusing a single islet and mixing superfusate from e

6 n of the mossy fibres), tonic inhibition and superfused ACh are 1:3:12, indicating that tonic and ACh

7 In the presence of 2 nM externally superfused alpha-dendrotoxin (alpha-DTX), or 50 nM super

8 Preparations were superfused and stimulated at 100 beats per minute.

9 serotonin (5HT) were briefly applied in the superfusing artificial cerebrospinal fluid.

10 1-AM were paced at 3 Hz at 36 degrees C and superfused at [Ca2+]o of 0.6, 1.2, and 3.0 mmol/L.

11 The cells were superfused at a rate of 6.2 ml x h-1 with Media 199 (pH

12 atic microsomes were loaded with 45Ca2+, and superfused at high flow rates to provide precise control

13 When tissue was superfused at pH 3, the 25 microm adjacent to the epithe

14 ed to the stroma of deepithelialized corneas superfused at the endothelial surface with the same medi

15 Superfused ATP in retina or noradrenaline in cerebellum

16 When exchange activity was initiated by superfusing Ba(2+)-containing solutions over the cells f

17 ned by applying histamine to a dark-adapted, superfused baboon eye cup preparation while making extra

18 When superfused before tetanus, the 5-HT1A receptor agonist 8

19 ole-cell currents were reversibly blocked by superfused beta-bungarotoxin (beta-BuTX; apparent KD = 4

20 used alpha-dendrotoxin (alpha-DTX), or 50 nM superfused beta-BuTX, unitary currents were recorded (ou

21 x, insulin, and cAMP release of continuously superfused beta-HC9 cells encapsulated in microscopic ag

22 When we superfused both cell types with a buffer containing 5 mM

23 lease of corticotropin-releasing factor from superfused brain slice preparations containing hypothala

24 m-stimulated [3H]ACh release was measured in superfused brain slices, either in the absence or the pr

25 Superfusing brain slices with ACSF containing 'physiolog

26 and spinal segments C(5)-D(1) was blocked by superfusing C(2)-C(4) with Na(+)-free solution.

27 The data show EAD formation in superfused canine pulmonary veins, enhanced by an increa

28 a2+ transient) recordings were obtained from superfused canine pulmonary veins.

29 n of impulse propagation in eight flecainide-superfused canine Purkinje fibers was examined with a du

30 The epicardial surfaces of 19 isolated and superfused canine right ventricular slices (4x4 cm and <

31 sensory discharge and tissue PO2 of perfused-superfused cat carotid body before and during flow inter

32 Superfusing cells with U-73122, an inhibitor of phosphol

33 TNF alpha superfused corneas had significantly higher permeabiliti

34 igate vasomotor control in arterioles of the superfused cremaster muscle preparation of anesthetized

35 Superfusing CXCL1 over venules promoted neutrophil migra

36 Superfused cystine increased tonic glutamate release, an

37 ct tonic glutamate release in the absence of superfused cystine.

38 Further assessment with an in vitro superfused electrically stimulated guinea-pig tracheal-s

39 dykinin and NO donor released adenosine from superfused endothelial cells in vitro; L-NAME attenuated

40 were made from flatmounted, isolated retina, superfused eyecup, and living retinal slice preparations

41 on of 1 micromol isoproterenol to flecainide-superfused fibers at physiological Vm increased theta2 b

42 r, if antibodies were also included with the superfused fMLP, stopping was inhibited, and detachment

43 oxygenated Krebs buffer (KRB) (120 min) then superfused for 10 min with KRB (control), or KRB contain

44 than doubled in amplitude after slices were superfused for 30 min with 100 nM rotenone.

45 ted [Ca(2+)](i) in ECL and parietal cells of superfused gastric glands, but only the parietal cell si

46 oaded N-methyl-4-[(3)H]phenylpyridinium from superfused hDAT cells.

47 d, and stimulated NE release is decreased in superfused hippocampal slices isolated at day 8 post-lig

48 Using superfused hippocampal slices, we tested the hypothesis

49 Compared to controls, superfused hypothalamic slices of fasted birds treated w

50 When CCAP was superfused in a low Ca2+ saline that blocked chemical tr

51 rent times of the day or night, retinas were superfused in darkness for 90 min ("prolonged darkness")

52 were prepared, preloaded with [3H]GABA, and superfused in order to measure [3H]GABA overflow in resp

53 hypercapnia and asphyxia were examined in a superfused in vitro rat carotid body preparation.

54 In superfused in vitro rat carotid body, we recorded chemor

55 r tachyarrhythmias at the time of study were superfused in vitro with normal Tyrode solution (extrace

56 pothesis using cat carotid body perfused and superfused in vitro with Po2 of about 100 Torr.

57 cose intravenously and in neocortical slices superfused in vitro with the same isotope.

58 rom rat and cat carotid bodies, perfused and superfused in vitro.

59 proved force-frequency relations of isolated superfused LV trabeculae (P=0.01) but not RV trabeculae.

60 Reducing the Ca2+ concentration of the superfusing medium caused time-dependent increases in pe

61 harmacologic agents or as a component of the superfusing medium.

62 ibition electrophysiologically using rapidly superfused membrane patches expressing mouse muscle nACh

63 ation-induced suppression of inhibition when superfusing mouse hippocampi with amyloid-beta.

64 In well-superfused myocytes, exofacial CA activity is superfluou

65 because PDAc enhanced the currents evoked by superfused NMDA to the same extent that it did the NMDA

66 prevent lactate generation, or with only 20% superfused O(2) to mimic physiological O(2) levels.

67 seen on the maintenance phase when ZnPP was superfused on ganglia with established LTP.

68 orcine aortic endothelial cells cultured and superfused on microcarriers.

69 charybdotoxin (20-40 nM) in vitro (perfused/superfused) on the cat carotid chemosensory discharge, a

70 uency activity in sensory nerves, QX-314 was superfused over isolated rat vagus nerves during stimula

71 ne (5-50 microM), a glycine antagonist, were superfused over the anterior spinal hindlimb enlargement

72 Superfused P7 rat cerebrocortical slices (350 mum) were

73 In superfused PA myocytes, diphenyleneiodonium, rotenone, a

74 mM) were significantly lower than TNF alpha superfused pairs at all concentrations, although only si

75 ficantly lower permeabilities than TNF alpha superfused pairs.

76 In vitro experiments were performed with superfused-perfused cat CBs, measuring chemosensory disc

77 pCO in the carotid chemosensory response, we superfused-perfused in vitro cat carotid bodies using HE

78 The superfused preparations were stimulated for 60 s with el

79 ular microelectrode recordings (n = 56) in a superfused PV preparation.

80 trodes were used to record activation in the superfused rabbit AV junction.

81 The release of SP from superfused rabbit carotid body was determined by an enzy

82 of [3H]dopamine were measured from isolated superfused rabbit retinas.

83 Here we show that, in the intact superfused rat CB, basal sensory neuronal activity was s

84 in the tissue temperature and pH of isolated superfused rat dental pulp regulate capsaicin-induced re

85 The present study used isolated superfused rat dental pulp to test the hypothesis that c

86 ced by kainic acid in a novel preparation of superfused rat hippocampus in vivo.

87 ibited GHRH-induced GH release in vitro in a superfused rat pituitary system than their parent compou

88 uced GH release were evaluated in vitro in a superfused rat pituitary system, as well as in vivo afte

89 duced GH release was evaluated in vitro in a superfused rat pituitary system, as well as in vivo afte

90 fflux of endogenous dopamine was measured in superfused rat striatal slices; dopamine was measured by

91 rfusing with 100 microM noradrenaline and by superfusing rat venules with the nitric oxide synthase i

92 ratified AII amacrine cells in the isolated, superfused retina-eyecup of the rabbit.

93 recordings were obtained from neurons in the superfused retina-eyecup preparation of the rabbit under

94 e P and calcitonin gene-related peptide from superfused segments of the dorsal horn of the spinal cor

95 e sum of ADO increase and ACh increase, when superfused separately, was less than the increase when t

96 The effect of superfused serotonin (5-HT; 50 microns) on the synaptic

97 pacing in 9 isolated, coronary perfused, and superfused sheep ventricular slabs (3x3 cm(2)).

98 s investigated using electrically stimulated superfused slices of rat corpus striatum.

99 and the addition of 10 microM A23187 to the superfusing solution reduced the time to complete globul

100 r I, E-64, or pepstatin (0.5 mM each) to the superfusing solution, increased tg to 105 +/- 3.5, 84.2

101 s even in the absence of Na+ and Ca2+ in the superfusing solution.

102 the NO-mediated release was NMDA-driven, we superfused spinal cord slices with competitive and non-c

103 In superfused striatal slices from wild-type mice, the non-

104 (DA) obtained following DA infusion into the superfused striatal tissue fragments of male and female

105 of a combined infusion of TMX and MA within superfused striatal tissue fragments of male mice as an

106 Action potentials (APs) were recorded from superfused SVC and PV sleeves using microelectrode techn

107 To "superfuse" sympathetic nerves innervating the ventricles

108 Using superfused synaptosomes, we have studied the readily rel

109 ors on fictive lung and gill ventilation, we superfused the isolated brainstems with agonists, antago

110 us oocytes, inward currents were elicited by superfusing the cell with 5-HT (in the presence of Na(+)

111 nic content by rapidly changing the solution superfusing the cilia.

112 rease of IPSCs; this effect was nullified by superfusing the slices with haemoglobin or NO-Arg.

113 The depolarization was not prevented by superfusing the slices with tetrodotoxin (0.3 microM) or

114 Superfusing the slices with the NO precursor L-arginine

115 run" events can be increased to over 80% by superfusing the synapses with hypertonic solution.

116 When CCAP was superfused, the membrane potentials of these neurons beg

117 funiculus (DLF) in spinal cord slices while superfusing them with peptidase inhibitors to prevent op

118 Vasopressin was superfused topically on the cremaster muscle resistance

119 administered ragweed antigen to an isolated, superfused tracheal segment of ragweed-sensitized dogs.

120 Contracting cardiomyocytes were superfused under controlled O2 conditions while fluoresc

121 n with 2 mumol/L cytochalasin D (cytD), were superfused, under first-order conditions, to steady stat

122 lly by using carboxy-SNARF-1, AM-loaded into superfused ventricular myocytes isolated from guinea-pig

123 Enzymatically isolated, superfused ventricular myocytes were exposed to betaAR a

124 ere isolated and the endothelial surface was superfused while thickness was measured with the specula

125 When the outer segment was superfused with 0 Ca2+, 0 Mg2+,0 Na+ solution just befor

126 Addition of glutamine (0.5 mM) to slices superfused with 10 mM of glucose did not enhance populat

127 The tissue was constantly superfused with 36.5 degrees C oxygenated Tyrode's solut

128 acellular pH of the in vitro goldfish retina superfused with a bicarbonate-based Ringer solution in t

129 In cultured NPE superfused with a CO(2)/HCO(3)(-)-free HEPES buffer, exp

130 release studies, carotid bodies (n=56) were superfused with a modified Tyrode medium containing Hepe

131 of terminals on one muscle fibre was locally superfused with a physiological saline containing barium

132 ning barium; the rest of the preparation was superfused with a physiological saline containing calciu

133 Bovine adrenal chromaffin cells were superfused with a variety of GABA(A)-selective drugs to

134 Isolated nuclei were superfused with an internal solution containing the Ca(2

135 f terminals on one muscle fibre were locally superfused with barium.

136 estigated with use of rat hippocampal slices superfused with bicuculline, with or without increasing

137 n this model, the exteriorized mesentery was superfused with ferric chloride and the accumulation of

138 aged with a scanning confocal microscope and superfused with glutamate (30 micromter to 1 mm), kainat

139 specular microscope, and the endothelium was superfused with glutathione bicarbonate Ringer's solutio

140 In slices superfused with H(2)O(2) for 10 min, there was a signifi

141 Slices were superfused with HCO(3)(-)-aCSF or with HEPES-aCSF (witho

142 cle was incised and raised, forming a cradle superfused with heparinized blood (activated clotting ti

143 the stimulus-response at rat carotid bodies superfused with high potassium concentrations, during no

144 Cells shrank when superfused with hypertonic solutions to a minimum relati

145 Mitochondria were attached to coverslips and superfused with K(+)-based HEPES-buffer medium supplemen

146 In PA and CA myocytes dialysed and superfused with K+ -free media, pipette solutions contai

147 between a force transducer and a motor arm, superfused with Krebs-Henseleit (K-H) solution (pH 7.4,

148 d leukocytes (P<0.01 vs. control mesenteries superfused with Krebs-Henseleit buffer).

149 ([Ca(2+)]i) were measured in rat trabeculae superfused with Krebs-Henseleit solution, with or withou

150 superior cervical ganglion (SCG) of the rat (superfused with Locke solution containing 100 microM cho

151 45Ca2+ efflux from permeabilised hepatocytes superfused with medium in which the [Ca2+] was clamped w

152 in a flow-through chamber, and continuously superfused with medium, and Ca2+ responses to nucleotide

153 epileptiform activity in neocortical slices superfused with Mg(2+)-free medium (IC(50) approximately

154 nergic stimulation (beta effect), cells were superfused with norepinephrine (10 mumol/L) in the prese

155 the beta-adrenergic stimulation, cells were superfused with norepinephrine alone (alpha 1 + beta eff

156 lls cultured from several vascular beds were superfused with normoxic (equilibrated with room air; PO

157 th propranolol (5 mumol/L) were continuously superfused with PE at 37 degrees C on the stage of an in

158 were evaluated in the gluteus maximus muscle superfused with physiological saline solution (35 degree

159 ice (3-5 months old), the GM was exposed and superfused with physiological saline solution (35 degree

160 junum was exteriorized and an MA network was superfused with physiological salt solution (pH 7.4, 37

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

162 of its original magnitude when the cell was superfused with Ringer solution during the 5 s interval

163 T:(g) of fiber cells superfused with Ringer's solution containing 2 x 10(-)(3

164 was abolished when they were simultaneously superfused with strychnine, consistent with the presence

165 Corneas superfused with the f-actin stabilizing agent phallacidi

166 polarization were abolished when slices were superfused with the tyrosine hydroxylase inhibitor alpha

167 Permeabilities of corneas superfused with TNF alpha plus 8-bromo-cAMP (0.01 to 3 m

168 x 3.2 cm) were mounted in a tissue bath and superfused with Tyrode's solution containing 10 to 15 mu

169 cells expressing sensors in the cytosol were superfused with up to 20 mM glutamate, consistent with a

170 egments from human, dog, and rat antrum were superfused with various concentrations of somatostatin 1

171 reversibly abolished in frog capillaries by superfusing with 100 microM noradrenaline and by superfu

172 ory glutamatergic currents were abolished by superfusing with a combination of tetrodotoxin, 6-cyano-

173 bolished by tetrodotoxin (0.5 microM) and by superfusing with low Ca(2+)-high Mg(2+)-containing solut