ライフサイエンスコーパス: transmembrane potential

1 ger conductance is observed under a positive transmembrane potential).

2 larization by using fluorescent reporters of transmembrane potential.

3 ionic strength of the aqueous phase, and the transmembrane potential.

4 he pore will compromise the integrity of the transmembrane potential.

5 nt flowing through the pore under an applied transmembrane potential.

6 charged residues in response to a change in transmembrane potential.

7 ATP coincident with a loss of mitochondrial transmembrane potential.

8 tween the inner and outer bath establishes a transmembrane potential.

9 H(2)O(2) depends on the mitochondrial inner transmembrane potential.

10 a2+] gradient, and strongly dependent on the transmembrane potential.

11 s Bak and Bax, and reduces the mitochondrial transmembrane potential.

12 microscopy was used to verify mitochondrial transmembrane potential.

13 st H2O2-mediated disruption of mitochondrial transmembrane potential.

14 to open and close in response to changes in transmembrane potential.

15 pha-hydroxyryanodine complex is sensitive to transmembrane potential.

16 dissociation of the ligand are sensitive to transmembrane potential.

17 chondrial network with varying mitochondrial transmembrane potential.

18 Occlusion was dependent upon a cis-negative transmembrane potential.

19 ocaspases 8 and 3, and loss of mitochondrial transmembrane potential.

20 efront and perpendicular to gradients in the transmembrane potential.

21 net current flows along the gradient in the transmembrane potential.

22 poptosis and preserved cardiac mitochondrial transmembrane potential.

23 rs to originate from a reduced mitochondrial transmembrane potential.

24 oupling and ATP synthesis, Ca(2+) uptake and transmembrane potential.

25 nalization and collapse of the mitochondrial transmembrane potential.

26 duced changes in intramembrane potential and transmembrane potential.

27 s H(2)O(2)-induced loss of the mitochondrial transmembrane potential.

28 , like As(2)O(3), disrupts the mitochondrial transmembrane potential.

29 iated with ROS-induced loss of mitochondrial transmembrane potential.

30 brane permeability changes, or mitochondrial transmembrane potential.

31 ng that the ions decreased the mitochondrial transmembrane potential.

32 molecule photoactivatable optical sensors of transmembrane potential.

33 a cells leads to alteration of mitochondrial transmembrane potential.

34 volved the early disruption of mitochondrial transmembrane potential.

35 betaCD complex varies continuously with the transmembrane potential.

36 ex environment, which includes a substantial transmembrane potential.

37 pecies production, and drop in mitochondrial transmembrane potential.

38 l cardiolipin, and loss of the mitochondrial transmembrane potential.

39 electrical low-pass filtering of the cell's transmembrane potential.

40 tio of OHC displacement to the change in its transmembrane potential.

41 give large and fast responses to changes in transmembrane potential.

42 ich is then able to record the intracellular transmembrane potential.

43 er the cell, inducing a fast upstroke of the transmembrane potential.

44 of their modification rates by Ag(+) to the transmembrane potential.

45 nditions could induce VDAC closure at <10 mV transmembrane potentials.

46 frequent and prolonged closures, even at low transmembrane potentials.

47 mparison reveals the existence of a critical transmembrane potential above which delivery with the se

48 of electroporation is related to the maximum transmembrane potential achieved.

49 The dependence of the maximum transmembrane potential across the cell membrane on cell

50 By focusing the transmembrane potential across the selectivity filter, t

51 Free energy calculations of the fractional transmembrane potential, acting upon key charged residue

52 ma membrane asymmetry, loss of mitochondrial transmembrane potential, activation of caspase-3, and in

53 (DN) Akt-1 resulted in loss of mitochondrial transmembrane potential, activation of caspases-9 and -3

54 uncouple channel opening from changes in the transmembrane potential, allowing current activation at

55 cal current injected into the cochlea induce transmembrane potential along the outer hair cell (OHC)

56 oppositely charged, a combination of a large transmembrane potential and a large nanotube diameter ca

57 This in turn changes the resting transmembrane potential and affects the excitability of

58 IN cells undergo a decrease in mitochondrial transmembrane potential and an increase in annexin V bin

59 TPCs are activated by a decrease in transmembrane potential and an increase in cytosolic cal

60 open or close in response to changes in the transmembrane potential and are essential for generating

61 asmic cytochrome c to maintain mitochondrial transmembrane potential and ATP production.

62 l plasma membrane is a sigmoidal function of transmembrane potential and bathing media osmolality.

63 sis was defined by the loss of mitochondrial transmembrane potential and by DNA fragmentation.

64 Simultaneous optical mapping of transmembrane potential and Ca(2+) transients was perfor

65 Mitochondrial transmembrane potential and Ca2+ fluxing were assessed b

66 lide antibiotic that regulates mitochondrial transmembrane potential and Ca2+ fluxing, has been used

67 idate this model, we used optical mapping of transmembrane potential and calcium transients.

68 IAP-2; and induced loss of the mitochondrial transmembrane potential and caspase-independent, calpain

69 y in Rb cells leads to loss of mitochondrial transmembrane potential and caspase-independent, calpain

70 ed H(2)O(2)-induced changes in mitochondrial transmembrane potential and cell death.

71 r domains in these channels sense changes in transmembrane potential and control ion flux across memb

72 alysis, theory, and mathematical modeling of transmembrane potential and currents have been an integr

73 o blocks depolarization of the mitochondrial transmembrane potential and cytochrome c release.

74 athway of apoptosis, as evidenced by loss of transmembrane potential and cytoplasmic release of cytoc

75 SMCs through depolarization of mitochondrial transmembrane potential and down-regulated PH-PASMC prol

76 ition state; this includes a decrease in the transmembrane potential and elevated generation of react

77 In vivo, TCL1 stabilizes the mitochondrial transmembrane potential and enhances cell proliferation

78 uced a substantial drop in the mitochondrial transmembrane potential and increases in cytosolic heme

79 Disruption of the CcO complex caused loss of transmembrane potential and induction of Ca2+/Calcineuri

80 ent with the disruption of the mitochondrial transmembrane potential and induction of cytochrome c re

81 er the influence of acidic pH and a positive transmembrane potential and initiates translocation in a

82 We simultaneously mapped transmembrane potential and intracellular Ca in Langendo

83 Optical mapping of transmembrane potential and intracellular Ca(2+) was per

84 lated by two distinct physiological signals, transmembrane potential and intracellular Ca(2+), each a

85 is not associated with loss of mitochondrial transmembrane potential and is blocked by overexpression

86 We studied the transmembrane potential and magnetic fields from electri

87 Mitochondrial transmembrane potential and mTOR were assessed by flow c

88 In addition to transmembrane potential and nanotube diameter, solution

89 preceded the reduction of the mitochondrial transmembrane potential and nuclear chromatin condensati

90 evaluation of the effects on the cytoplasmic transmembrane potential and on the respiration of isolat

91 related with protection of the mitochondrial transmembrane potential and prevention of cytochrome c r

92 -Darpp expression enforces the mitochondrial transmembrane potential and protects against ceramide-in

93 Bid and caspase-3, decrease in mitochondrial transmembrane potential and release of cytochrome c from

94 ding Bid cleavage, decrease in mitochondrial transmembrane potential and release of cytochrome c from

95 domain (VSD), which is critical for sensing transmembrane potential and subsequent gating.

96 The model enables calculation of the transmembrane potential and the fraction of the cell mem

97 he ionic current passing through a pore in a transmembrane potential and thereby provides both the co

98 p-32 and t-Darpp preserved the mitochondrial transmembrane potential and was associated with increase

99 d that glutamate binding is dependent on the transmembrane potential and, thus, is electrogenic.

100 ocardium using high-speed optical mapping of transmembrane potentials and calcium concentrations in t

101 induced NAD depletion, loss of mitochondrial transmembrane potential, and cell death, demonstrating a

102 from mitochondria, decrease in mitochondrial transmembrane potential, and cleavage of poly(ADP-ribose

103 Basal mitochondrial respiration, transmembrane potential, and electron transport system e

104 the mycobacterial membrane, equilibrates the transmembrane potential, and is localized within both th

105 ectron transport chain function, collapse of transmembrane potential, and loss of dehydrogenase activ

106 s, including elevated mitochondrial calcium, transmembrane potential, and reactive oxygen species (RO

107 poptotic protein Noxa, loss of mitochondrial transmembrane potential, and release of cytochrome c in

108 truct also allows the measurement of E. coli transmembrane potential, and the determination of the pr

109 m an alpha-helix, dissipated the cytoplasmic transmembrane potential, and uncoupled the respiration o

110 f NaCl on polarization of interfacial water, transmembrane potentials, and mechanisms for ion transpo

111 Frequency-dependent transmembrane potentials are modeled for spherical, weak

112 Without the transmembrane potential as a countermeasure, water will

113 Membranes flex with changes in transmembrane potential as a result of changes in interf

114 We have also found that a transmembrane potential as small as 20 mV strongly biase

115 ed by loss of cytochrome c and mitochondrial transmembrane potential as well as by induction of caspa

116 abilization which, in turn, are modulated by transmembrane potential, as well as peptide concentratio

117 izing Jurkat cells with 7-ns pulses produces transmembrane potentials associated with increased membr

118 tify the influence of synaptic inputs on the transmembrane potential at the axon initial segment.

119 of shock-induced activation depended on the transmembrane potential at the end of the shock.

120 The binding is enhanced at increased transmembrane potentials, because the free energy contri

121 els attenuated the loss of the mitochondrial transmembrane potential, blocked mitochondrial fission,

122 the cytosol; (b) reduction in mitochondrial transmembrane potential; (c) proteolytic processing of c

123 inhibits ara-C-induced loss of mitochondrial transmembrane potential, caspase-3 activation, and apopt

124 of intracellular ATP, loss of mitochondrial transmembrane potential, caspase-3/7 activation, and LDH

125 ociated with the loss of mitochondrial inner transmembrane potential, caspases activation, the transl

126 y observed negative bias in the asymmetry of transmembrane potential changes (DeltaVm) induced by str

127 es that can simultaneously respond to pH and transmembrane potential changes.

128 ane were marked by 160 min and mitochondrial transmembrane potential collapsed over roughly the same

129 water pores is then seen; it discharges the transmembrane potential, considerably reduces the size o

130 on pathway, leading to loss of mitochondrial transmembrane potential, cytochrome c release and activa

131 tion of caspase-8; (c) loss of mitochondrial transmembrane potential; (d) release of cytochrome c; an

132 xicity of Fe + AA, because the mitochondrial transmembrane potential decreased early in the process,

133 Mitochondria rapidly lose their transmembrane potential (Delta Psi m) and generate react

134 t sHA 14-1 triggered a loss of mitochondrial transmembrane potential (Delta psi m) and weak caspase-9

135 sociated with elevation of the mitochondrial transmembrane potential (Delta psi(m)) and increased pro

136 Bid processing, dissipation of mitochondrial transmembrane potential (Delta Psi(m)), and cytochrome c

137 channel (VDAC3) and alter the mitochondrial transmembrane potential (Delta Psi(m)).

138 principally exhibit increased mitochondrial transmembrane potential (DeltaPsi(m)) and altered metabo

139 duced a time-dependent loss of mitochondrial transmembrane potential (DeltaPsi(m)) and DNA fragmentat

140 d macrophages, we investigated mitochondrial transmembrane potential (DeltaPsi(m)) and the mitochondr

141 A loss of mitochondrial transmembrane potential (Deltapsi(m)) beginning at 24 h

142 eactive oxygen species (ROS) and disrupt the transmembrane potential (DeltaPsi(m)) but does not perme

143 and chemically induced loss of mitochondrial transmembrane potential (Deltapsi(m)) caused recruitment

144 in resulted in a rapid loss of mitochondrial transmembrane potential (Deltapsi(m)) in a subpopulation

145 species (ROS) and lowering of mitochondrial transmembrane potential (DeltaPsi(m)) in in vitro HCV-in

146 lent H37Rv induces significant mitochondrial transmembrane potential (Deltapsi(m)) loss caused by mit

147 ymphocytes is regulated by the mitochondrial transmembrane potential (Deltapsi(m)) through controllin

148 with BHA also induced loss of mitochondrial transmembrane potential (Deltapsi(m)), cytochrome c, and

149 e victorin-induced collapse in mitochondrial transmembrane potential (Deltapsi(m)), indicative of a m

150 thin the mitochondrial compartment preserved transmembrane potential (DeltaPsi(m)), NAD(+) content, a

151 ation of caspases, the loss of mitochondrial transmembrane potential (Deltapsi(m)), the cleavage of B

152 depends on maintenance of the mitochondrial transmembrane potential (Deltapsi(m)), which is generate

153 rylation, and increases in the mitochondrial transmembrane potential (deltaPsi(m)), which were preced

154 t to contribute to the loss of mitochondrial transmembrane potential (Deltapsi(m)).

155 ly member, A1, and the loss of mitochondrial transmembrane potential (Deltapsi(m)).

156 st, both these agents decrease mitochondrial transmembrane potential (Deltapsi(m)).

157 gradient, which underlies the mitochondrial transmembrane potential (DeltaPsi(mem)), is harnessed fo

158 oxic side by a gradual rise of mitochondrial transmembrane potential (Deltapsi) and reactive oxygen s

159 rations (1 to 3 M), coupled with its loss of transmembrane potential (DeltaPsi) during postexponentia

160 nes based upon negative charge, disrupts the transmembrane potential (Deltapsi) in mitochondria, and

161 e model was tested by estimating the pHi and transmembrane potential (DeltaPsi) of cells acid stresse

162 nce vs absence of pH gradients (DeltapH) and transmembrane potentials (DeltaPsi).

163 ctivities, followed by reduced mitochondrial transmembrane potential, DeltaPsi(M).

164 hich also served to report the mitochondrial transmembrane potential, DeltaPsi.

165 which can be regulated through mitochondrial transmembrane potential (Deltapsim) and mammalian target

166 y biochemical checkpoints, the mitochondrial transmembrane potential (deltapsim) and production of re

167 vels, apoptosis, ER tress and, mitochondrial transmembrane potential (DeltaPsim) decline.

168 Mitochondrial transmembrane potential (DeltaPsim) was measured as a fu

169 tion of caspase 8, the loss of mitochondrial transmembrane potential (DeltaPsim), and apoptotic cell

170 pendent manner, caused quantitative loses in transmembrane potential (DeltaPsim), and induced both ea

171 of electron transport, loss of mitochondrial transmembrane potential (DeltaPsim), decline in ATP leve

172 roteases and disruption of the mitochondrial transmembrane potential (Deltapsim).

173 rillation is due to shock-induced changes of transmembrane potential (DeltaV(m)) in the bulk of ventr

174 n shocks induce complex nonlinear changes of transmembrane potential (DeltaV(m)).

175 rillation shocks induce nonlinear changes of transmembrane potential (DeltaVm) that determine the out

176 ion of charges at the membrane surfaces; the transmembrane potential, determined by imbalance of char

177 esults are compatible with the proposal that transmembrane potentials, determined mainly by extracell

178 l division, was independent of the organelle transmembrane potential, did not require the chaperone H

179 etween two electrolyte solutions, applying a transmembrane potential difference, and measuring the re

180 ctance of ion channels can be modulated by a transmembrane potential difference, due to alterations o

181 ondrial dysfunction, as indicated by loss of transmembrane potential, diminished mitochondrial mass,

182 ial), which is the sum of contributions from transmembrane potential, dipole potential, and the diffe

183 n apoptosis, causing mitochondrial swelling, transmembrane potential dissipation, membrane blebbing,

184 Numerical simulation of the initial transmembrane potential distribution and propidium iodid

185 at with low ac frequencies (10Hz-10kHz), the transmembrane potential does not vary with the frequency

186 currently eliminated the depolarizing sag of transmembrane potential during hyperpolarizing current i

187 p confers drug resistance through changes in transmembrane potential (E(m)) or ion conductance, we st

188 Microelectrodes were used to record transmembrane potentials from isolated epicardial and en

189 brane conductance regulator, which shunt the transmembrane potential generated by movement of protons

190 hannel in the AM also functions to shunt the transmembrane potential generated by proton pumping and

191 gnetic action field and optically imaged the transmembrane potentials generated by planar wavefronts

192 e area for postshock propagation but smaller transmembrane potential gradients to initiate new wavefr

193 how that under the condition of high applied transmembrane potential (>100 mV) and low ionic strength

194 spectral shift associated with the change in transmembrane potential has been used for continuous mem

195 UC1 attenuated (i) the loss of mitochondrial transmembrane potential, (ii) mitochondrial cytochrome c

196 2C12 cells with TCDD disrupted mitochondrial transmembrane potential in a time-dependent fashion and

197 is elaborated to account for the effect of a transmembrane potential in computer simulations.

198 fluorescent protein 2.3 (VSFP2.3) to monitor transmembrane potential in either myocytes or nonmyocyte

199 al shift response can be used to measure the transmembrane potential in single cells.

200 multisite high-resolution optical mapping of transmembrane potential in strands of cells of mixed Cx4

201 igh-frequency cut-off of the outer hair cell transmembrane potential in vivo may be necessary for coc

202 A fragmentation, and decreased mitochondrial transmembrane potential in VSMC while decreasing PP1cgam

203 Applied DC electric fields change transmembrane potentials in CA3 pyramidal cell somata by

204 ict that at short cell-to-tip distances, the transmembrane potential increases significantly while th

205 nnexin V binding and a drop in mitochondrial transmembrane potential indicative of apoptotic cell dea

206 udy, we investigated the distribution of OHC transmembrane potential induced along the cell perimeter

207 The OHC transmembrane potential induced by the EEF is shown to b

208 Mitochondrial dysfunction and altered transmembrane potential initiate a mitochondrial respira

209 h gives successive values of the prestimulus transmembrane potential instead of successive values of

210 tical systems for multiparametric mapping of transmembrane potential, intracellular calcium dynamics

211 However, the transmembrane potential is an incomplete metric.

212 of the action potential foot, even when the transmembrane potential is measured 150 microm below the

213 foot with propagation direction, even if the transmembrane potential is measured 150 microm below the

214 At the microscopic level, the transmembrane potential is thought to decay nonlinearly

215 simulations at different concentrations and transmembrane potentials is presented.

216 TOR), which is a sensor of the mitochondrial transmembrane potential, is increased in lupus T cells.

217 in reactive oxygen species and mitochondrial transmembrane potential loss, but does not cleave bid or

218 hydrolyzes ATP to maintain the mitochondrial transmembrane potential (mdeltapsi).

219 and capacitance, the EEF-induced nonuniform transmembrane potential measured in this study suggests

220 Mitochondrial transmembrane potential (MTP) was measured by a cationic

221 ecording steady-state and dynamic changes in transmembrane potential noninvasively across an intact c

222 The model determines transmembrane potential, number of pores, and distributi

223 mmetric conductance upon the polarity of the transmembrane potential observed experimentally is repro

224 ilter that defines the region over which the transmembrane potential occurs.

225 at rates from 10 V/s to 1 kV/s, to a maximum transmembrane potential of +/-1000 mV.

226 s a proton flux of 3100 +/- 500 H+/s/FO at a transmembrane potential of 106 mV (25 degrees C and pH 6

227 with the model's prediction that a critical transmembrane potential of 250 mV is achieved when the c

228 t broad-spectrum antibiotic that reduces the transmembrane potential of Gram-positive and Gram-negati

229 In the last assay the mitochondrial transmembrane potential of Jkt cells was measured with t

230 ed cells were resistant to a decrease in the transmembrane potential of mitochondria induced by staur

231 pecifically, we determine the sensitivity to transmembrane potential of second harmonic generation by

232 The resulting changes in the transmembrane potential of the cell initiates a process

233 for PEGs with 15 to 45 monomers, at applied transmembrane potentials of -40 to -80 mV and for three

234 DOPC mixed bilayers in 1 M KCl solution with transmembrane potentials of 0, +/-25, +/-50, +/-75, and

235 energy that is modified by the action of the transmembrane potential on dipole moments held by the do

236 be inside diameter, solution pH, and applied transmembrane potential on the rate and selectivity of p

237 The patterns of transmembrane potential on the whole heart during and im

238 onsists of a simple difference of the sum of transmembrane potentials on one side of a tissue sheet a

239 IL-1beta to cause a decline in mitochondrial transmembrane potential or ATP depletion.

240 vage, and DNA fragmentation, but not loss of transmembrane potential or viability, indicating that ce

241 ular wire to create a Berkeley Red Sensor of Transmembrane potential, or BeRST 1 ("burst").

242 r, emergent phenomena, such as mitochondrial transmembrane potential oscillations or propagating wave

243 For ion channels, the transmembrane potential plays a critical role by acting

244 r changes that include loss of mitochondrial transmembrane potential, production of reactive oxygen s

245 ion potential (MAP) is a near replica of the transmembrane potential recorded when an electrode is pu

246 Potassium concentration and transmembrane potential recordings showed that AC stimul

247 e propagation using the ionic current versus transmembrane potential relationship fit from the experi

248 DIM #34 induced loss of mitochondrial inner transmembrane potential, release of cytochrome c into th

249 Transmembrane potential responses of single cardiac cell

250 translocation is driven only by the negative transmembrane potential resulting from the asymmetric bi

251 rchitecture and dissipation of mitochondrial transmembrane potential revealed a functional link betwe

252 in this study we experimentally explore the transmembrane potential's distribution across the open p

253 electrostatic computations indicate that the transmembrane potential sensed by the charged residues i

254 a 4-h exposure to CDDO, mitochondrial inner transmembrane potential-sensitive dyes revealed mitochon

255 idal electric fields have smaller effects on transmembrane potentials: sensitivity drops as an expone

256 resulted in a 50% decrease in mitochondrial transmembrane potential, sequential activation of caspas

257 single cells in response to step changes in transmembrane potentials set with a patch electrode, usi

258 cantly even at high atrial rates because the transmembrane potential spends little time at voltages a

259 m, varied linearly with the amplitude of the transmembrane potential step between -80 and +60 mV.

260 hia coli has been suggested to dissipate the transmembrane potential, such that the depletion of ATP

261 cell membrane, with subsequent alteration of transmembrane potential that is a function of cell bioph

262 es can be described by three parameters: the transmembrane potential, the membrane surface potential,

263 In contrast, at zero transmembrane potential, the peptides bind weakly to the

264 NaSal resulted in the loss of mitochondrial transmembrane potential, the release of cytochrome c and

265 At high transmembrane potentials, the alanine-based peptides, wh

266 of cell membrane integrity and mitochondrial transmembrane potential through unknown mechanisms.

267 ition pore, which in turn causes the loss of transmembrane potential, thus initiating apoptotic degra

268 Many approaches for studying the transmembrane potential (TMP) induced during the treatme

269 As K(+) channels, they drive the transmembrane potential toward E(K) when open and thus d

270 turn, was followed by loss of mitochondrial transmembrane potential, translocation of cytochrome c t

271 agocytic clearance, and retain mitochondrial transmembrane potential until constitutive platelet deat

272 Previous measurements of transmembrane potential using the electrochromic probe d

273 y charged arginines, caused by the change of transmembrane potential V, further drag the S4 segment a

274 ding nonexcitable cells, maintain a discrete transmembrane potential (V (mem)), and have the capacity

275 When spatial maps of transmembrane potential (V(m)) are available, pECG can b

276 y use of optical recordings of shock-induced transmembrane potential (V(m)) changes (DeltaV(m)) measu

277 Transmembrane potential (V(m)) was significantly less ne

278 e and the relationship with local changes of transmembrane potential (V(m)) were determined in geomet

279 ernal electrodes to induce sustained VT, and transmembrane potentials (V(m)) were compared with synth

280 cteristics of ventricular fibrillation (VF), transmembrane potentials (V(m)) were recorded from multi

281 nts across their plasma membranes, producing transmembrane potentials (V(mem)).

282 ted parameters (e.g., ion concentrations and transmembrane potential, V(m)) drift in time, never atta

283 ew the effects of electrical currents on the transmembrane potential, V(m), as a shock is applied to

284 In our experiments, the transmembrane potential, V(m), was first measured optica

285 We tested the responses of plasma transmembrane potential (Vm) depolarization, voltage gat

286 We tested the responses of plasma transmembrane potential (Vm) depolarization, voltage gat

287 The lack of transmembrane potential (Vm) distribution data makes it

288 h involved recording high-fidelity (200 kHz) transmembrane potential (Vm) signals with glass microele

289 ; disruption of this spatial gradient of the transmembrane potential (Vmem) diminishes or eliminates

290 s effects, we show that hyperpolarization of transmembrane potential (Vmem) in ventral cells outside

291 treatment with bFGF, a loss of mitochondrial transmembrane potential was accompanied by down-regulati

292 A transmembrane potential was applied across a single nano

293 A loss of mitochondrial transmembrane potential was detected in vivo, although n

294 Mitochondrial transmembrane potential was determined by JC-1 fluoresce

295 lthough no mitochondrial swelling or loss of transmembrane potential was observed in isolated mitocho

296 Transmembrane potentials were recorded from right ventri

297 er respiratory inhibitors, which perturb the transmembrane potential, were equally efficient in induc

298 lds were applied to this system to model the transmembrane potential, which proved to be important.

299 uses a rapid depolarization of mitochondrial transmembrane potential, which recovers to original leve

300 atment induced the collapse of mitochondrial transmembrane potential within 2 h, indicating a MPT.

301 of events: dissipation of the mitochondrial transmembrane potential within 30 min, release of mitoch