ライフサイエンスコーパス: tetanic

1 Tetanic activation of IpCa by 1 ms depolarizing voltage

2 ate that glutamate spillover caused by brief tetanic activation of mossy fiber terminals remains inta

3 ng of thalamocortical output was mimicked by tetanic activation of retinogeniculate afferent in a fre

4 muscle physiology studies with twitch force, tetanic and eccentric contraction all being normal.

5 SNAC) and spermineNONOate reduced submaximal tetanic and peak twitch forces.

6 NAME, a NOS inhibitor), increased submaximal tetanic and peak twitch forces.

7 x months, exercised mdx mice showed improved tetanic and specific force compared to the sedentary gro

8 CCCP augmented peak tetanic and submaximum [Ca2+]i and force significantly m

9 ability of CNS presynaptic terminals after a tetanic burst of action potentials is important for syna

10 We set out to determine the effects of tetanic burst stimulation in stratum radiatum of region

11 The model simulates tetanic, -burst, pairing-induced, and chemical L-LTP, as

12 caused by strong or prolonged stimuli, like tetanic bursts of afferent fiber discharge at high frequ

13 the peak frequency of AP transmission during tetanic bursts was diminished by ZD7288.

14 Significant differences in tetanic, but not in 4-CmC-evoked, contracture forces wer

15 increased skeletal muscle specific force and tetanic Ca(2+) transients, decreased intracellular Ca(2+

16 Na(+)/K(+) pump determines the magnitude of tetanic [Ca(2+)](i) accumulation and potentiation of exc

17 Peak tetanic [Ca2+]i increased in extraocular muscle with caf

18 pha decreased tetanic force without altering tetanic calcium transients or resting calcium levels.

19 response to either a 400 Hz/10 s episode of tetanic conditioning stimulation of the soleus nerve or

20 During tetanic conditioning, 1000-Hz tones were presented at 11

21 Ca(2+) transients declined in parallel with tetanic contractile force in single intact fibres.

22 nd old (23-30 months) mice were subjected to tetanic contractile protocols in the presence and absenc

23 d male C57BL/6 mice (aged 3-4 months), brief tetanic contraction (100 Hz for 500 ms) evoked rapid ons

24 orders, functional vasodilatation to single tetanic contraction (100 Hz, 500 ms) and to rhythmic twi

25 When applied during the plateau of a tetanic contraction a T-jump induced a tension rise to a

26 ms pulse, 100 Hz for 500 ms) evoked a brief tetanic contraction and produced rapid (<1 s) onset vaso

27 luteus maximus muscle of C57BL/6 mice, brief tetanic contraction evoked rapid onset vasodilatation (R

28 examined the blood flow response to a brief tetanic contraction in which potassium (K(+)) was infuse

29 Tetanic contraction initiates hyperpolarization that con

30 Tetanic contraction produced only a very small backbone

31 nths) and old (24 months) male C57BL/6 mice, tetanic contraction while observing feed arteries and ar

32 eater role in the hyperaemia associated with tetanic contraction.

33 onal reflection (S(M3) and S(M6) ) following tetanic contraction.

34 subjected to electrically induced isometric tetanic contractions (0.25 Hz; 2-min bouts) while peak t

35 rterioles were studied in response to single tetanic contractions (100 Hz, 100-1000 ms).

36 Isometric tetanic contractions (50 Hz; 200 ms duration) via supram

37 In response to single tetanic contractions at 100 Hz (duration, 100-1000 ms),

38 g 3 min of electrically stimulated isometric tetanic contractions corresponding to ~35% of VO2peak .

39 centrations of DHT increases both twitch and tetanic contractions in fast twitch fibres.

40 ibrils in situ, determined from twitches and tetanic contractions in SR-inhibited muscles, showed tha

41 Isometric tetanic contractions of the gastrocnemius complex of six

42 tension and hyperaemic responses: twitch and tetanic contractions were associated with a 3-fold and 2

43 s muscle were recorded; isometric twitch and tetanic contractions were evoked by stimulation of the s

44 during the transition from rest to repeated tetanic contractions.

45 quency for minimum dynamic stiffness) during tetanic contractions.

46 espond to electrical stimuli with twitch and tetanic contractions.

47 actile fatigue testing (3 bouts of 25 100 Hz tetanic contractions; duty cycle = 0.2 s/2 s = 0.1) unde

48 he frog neuromuscular junction, leading to a tetanic contracture in muscle fiber.

49 s in hippocampal CA1 neurons returned to pre-tetanic control levels more rapidly in the presence of n

50 olarizing GABA component underlying the post-tetanic depolarization.

51 er control conditions was replaced by a post-tetanic depression with a slow time course of recovery.

52 LTP varies steeply with the number of brief (tetanic) electrical stimuli.

53 The influence of latrunculin on post-tetanic EPPs depended on its concentration in the bath (

54 ffect in the responses of layer 2/3 cells to tetanic extracellular stimulation in layer 4.

55 antal content and decreased paired-pulse and tetanic facilitation.

56 hese synapses and increased paired-pulse and tetanic facilitation.

57 ays of recovery, maximum tetanic tension and tetanic fade (functional parameters = primary outcome va

58 s muscle mass, decreased fiber diameter, and tetanic fade did not return to normal until day 36, whil

59 aximum tetanic tension, as well as decreased tetanic fade persisted until day 36.

60 Tetanic fade was not affected by inflammation.

61 scle of homozygous HCSMA animals, motor unit tetanic failure is apparent before the appearance of mus

62 sed to observe that, at ages when motor unit tetanic failure is common, the structure of neuromuscula

63 or muscle fibers were apparent at times when tetanic failure is prevalent.

64 ese observations suggest that the motor unit tetanic failure observed in the MG muscle in homozygous

65 tric tetanic force, decline in force after a tetanic fatiguing protocol, and single-fiber-specific fo

66 The maximum isometric tetanic force (P(o)) and power output of limb muscles fr

67 Specific twitch force, specific tetanic force and maximum power were all significantly l

68 um longus muscle showed significantly higher tetanic force and was also more resistant to eccentric c

69 In fact, grip strength and maximum isometric tetanic force are even lower in gamma-sarcoglycan-null/C

70 The tetanic force assay also identified beneficial compound

71 Tetanic force decreased by 14% with assisted ventilation

72 The specific tetanic force decreased significantly in single muscle f

73 SQs is a negative regulator of ECCE and that tetanic force development in slow twitch muscles is supp

74 JP45-CASQ1 and JP45-CASQ2 complexes supports tetanic force development in slow twitch soleus muscles.

75 Mean tetanic force generation was increased significantly at

76 uscles also showed normal peak isometric and tetanic force generation.

77 diac function as well as improved twitch and tetanic force in skeletal muscle.

78 The maximum tetanic force of extensor digitorum longus (EDL) muscles

79 We found that TNF-alpha depressed tetanic force of the diaphragm and FDB to comparable deg

80 he motoneuron, the contraction speed, or the tetanic force of the motor unit.

81 upon external Ca(2+) for maintaining maximal tetanic force output, while young fibres are not.

82 In contrast, there is no decrease in maximal tetanic force production in the mutant diaphragm or sole

83 ecreased voltage-gated Ca2+ release, maximal tetanic force production is decreased and the force freq

84 e was a nonsignificant decrease in diaphragm tetanic force production over the experiment in the vent

85 stimulation at higher frequency for optimal tetanic force production.

86 ucocorticoid family) significantly increased tetanic force relative to placebo-treated controls.

87 requency of 2048 Hz, we show that twitch and tetanic force responses to electric pulses follow the lo

88 was about 8% less than that at which maximum tetanic force was achieved (L0), both in mdx and control

89 forelimb grip strength, and in vivo maximum tetanic force were also reduced.

90 Maximal twitch and isometric tetanic force were reduced at 24 months compared to 6 an

91 isolated muscle fibers, TNF-alpha decreased tetanic force without altering tetanic calcium transient

92 P caused an unexpected decay in nerve-evoked tetanic force, both in wild-type and mdx muscles, withou

93 nction analyses, including maximum isometric tetanic force, decline in force after a tetanic fatiguin

94 h the specific twitch force and the specific tetanic force, when compared to the age-matched control.

95 delayed relaxation and altered generation of tetanic force.

96 nt reduction (-17%) in diaphragmatic maximal tetanic force.

97 show twitch forces of 0.37 +/- 0.15 muN and tetanic forces (100-Hz stimulation frequency) of 2.38 +/

98 olone, deflazacort, and prednisone increased tetanic forces at low doses (EC(50) of 6, 19, and 56 nM,

99 When electrically stimulated, they generated tetanic forces measured with an automated motion trackin

100 aralysis and baclofen, the median motor unit tetanic forces were significantly weaker, twitch half-re

101 uscle force measurements (maximum twitch and tetanic forces) were obtained along with muscle samples

102 3.05 and 2.28 times increases in twitch and tetanic forces, respectively, suggesting that temporally

103 removed, and force generation at twitch and tetanic frequencies as well as fatigue resistance were d

104 ortening (Vmax) at 1 Hz stimulation, and the tetanic fusion frequency.

105 a fast Na(+)/K(+)-ATPase (NKA)-mediated post-tetanic hyperpolarization (PTH) controls the probability

106 The HCNCs are activated by the post-tetanic hyperpolarization occurring during this time.

107 Schaffer collateral-CA1 tetanic long-term potentiation decayed rapidly in acute

108 d determine how neuromodulation, short-burst tetanic microstimulation (sbTetMS), alters multiregional

109 Tetanic muscle contraction was evoked by stimulating L7-

110 The specific single twitch and tetanic muscle force in old transgenic soleus and extens

111 dings indicate that PACAP can be released by tetanic neural stimulation in vitro and increase the exc

112 ptide (PACAP) or substance P released during tetanic neural stimulation modulate cardiac neurone exci

113 muscles, the peak isometric twitch (Pt) and tetanic (Po) tensions, as well as fatigability during 5

114 I) phosphorylation in the expression of post-tetanic potentiation (PTP) and in its modulation by BDNF

115 However, like post-tetanic potentiation (PTP) and long-term potentiation (L

116 tion ([Ca(2+)](i)) in the generation of post-tetanic potentiation (PTP) at crayfish neuromuscular jun

117 CT: High-frequency stimulation leads to post-tetanic potentiation (PTP) at many types of synapses.

118 High-frequency stimulation leads to post-tetanic potentiation (PTP) at many types of synapses.

119 nt for a form of short-term plasticity, post-tetanic potentiation (PTP) at sensory neuron (SN)-motor

120 high-frequency stimulation and mediates post-tetanic potentiation (PTP) in the rat hippocampus.

121 Post-tetanic potentiation (PTP) is a widespread form of short

122 Post-tetanic potentiation (PTP) is a widespread form of synap

123 KEY POINTS: Post-tetanic potentiation (PTP) is attributed mainly to an in

124 Post-tetanic potentiation (PTP) is attributed mainly to an in

125 requency action potential train induces post-tetanic potentiation (PTP) of transmission at many synap

126 The mechanism of the post-tetanic potentiation (PTP) or edrophonium-induced facili

127 Here, we identify a Ca(2+) sensor for post-tetanic potentiation (PTP), a form of plasticity thought

128 er Ca(2+)-dependent vesicle release and post-tetanic potentiation (PTP).

129 litude or the time-constant of decay of post-tetanic potentiation (PTP).

130 hibit a form of intrinsic facilitation: post-tetanic potentiation (PTP).

131 cilitation (F2), augmentation (AUG) and post-tetanic potentiation (PTP).

132 rt-term facilitation and uniquely large post-tetanic potentiation (PTP).

133 short-term enhancement of release like post-tetanic potentiation (PTP).

134 synaptic plasticity induced by tetanus [post-tetanic potentiation (PTP)] or low-frequency stimulation

135 at exogenous adenosine can inhibit both post-tetanic potentiation and long-term potentiation in sympa

136 fragment augmented theta burst-induced post-tetanic potentiation and LTP in mouse hippocampal slices

137 such as facilitation, augmentation, and post-tetanic potentiation at central synapses in the sea slug

138 (2020) reveal that post-tetanic potentiation at dentate gyrus mossy fiber synaps

139 ulse inhibition and increased GABAergic post-tetanic potentiation in both striatal and hippocampal ne

140 Peptidergic vesicle mobilization and post-tetanic potentiation of neuropeptide release are sustain

141 dent capture of transiting vesicles and post-tetanic potentiation of neuropeptide release.

142 RyR and CaMKII are essential for post-tetanic potentiation of neuropeptide secretion.

143 uring mitochondrial depolarization, the post-tetanic potentiation of the EPP observed under control c

144 of short-term homosynaptic plasticity [post-tetanic potentiation or homosynaptic depression (HSD)],

145 nglionic transmission without affecting post-tetanic potentiation or long-term potentiation.

146 ssion, had no significant effect on the post-tetanic potentiation or long-term potentiation.

147 Mutant mice showed less post-tetanic potentiation than wild-type animals, and also sh

148 ll concentration (2 microM) blocked the post-tetanic potentiation without affecting long-term potenti

149 resynaptic activation (augmentation and post-tetanic potentiation), while leaving intact its capacity

150 nduced synapse maturation and abolishes post-tetanic potentiation, a form of synaptic plasticity.

151 utants exhibit loss of facilitation and post-tetanic potentiation, and faster synaptic depression.

152 with decreased facilitation, decreased post-tetanic potentiation, and increased depression.

153 such as facilitation, augmentation, and post-tetanic potentiation, are usually attributed to effects

154 shares components of the mechanisms of post-tetanic potentiation, NMDA- and mGluR-dependent long-ter

155 th and contributes to the generation of post-tetanic potentiation.

156 short-term depression, facilitation and post-tetanic potentiation.

157 ng pronounced synaptic augmentation and post-tetanic potentiation.

158 d-pulse facilitation, LTP induction, or post-tetanic potentiation.

159 manipulations implicate mitochondria in post-tetanic potentiation.

160 n as well as long-term potentiation and post-tetanic potentiation.

161 eled by calcium/synaptotagmin-dependent post-tetanic potentiation.

162 n Sca1 null mice, whereas long-term and post-tetanic potentiations are normal.

163 espectively; P<0.05); maximal Ca2+-activated tetanic pressure was increased significantly by 12% (211

164 TP as induced by a conventional homosynaptic tetanic protocol.

165 [Ca2+]i transients did not fully relax and a tetanic rise of [Ca2+]i was observed.

166 By day 15, post-tetanic, short-term, and long-term potentiation were red

167 l, synaptic potentiation induced by a single tetanic stimulation (100 Hz for 1 s) was enhanced after

168 However, under high-frequency tetanic stimulation (100 Hz; > 100 ms) typically used to

169 was significantly increased following brief tetanic stimulation (18.1 +/- 1.6 to 22.3 +/- 2.0 flashe

170 ynaptic potentiation produced by rather mild tetanic stimulation (20 Hz, 2 sec) at Aplysia sensory-mo

171 n (n=11) and paired-pulse enhancement (n=4); tetanic stimulation (25 Hz, 1.0 s) produced sustained (>

172 A submaximal tetanic stimulation (2x50 Hz/1 s) in control slices elic

173 ashes/1000 mum(2).100 s) following prolonged tetanic stimulation (40 tetani).

174 Tetanic stimulation (50 Hz, 1 s) increases PKA and PKC a

175 halogram recording before and after auditory tetanic stimulation (Pre/Post Blocks).

176 S or TBS gave similar levels of LTP and post tetanic stimulation (PTP), suggesting that the response

177 m potentiation (LTP) induced by one train of tetanic stimulation (TS) in the CA1 region of hippocampa

178 We propose a model where tetanic stimulation activates Syt1-independent mechanism

179 n adult zebra finch brain slices reveal that tetanic stimulation alone does not produce LTP.

180 Following tetanic stimulation an outside-out patch was excised fro

181 EPSPs show little depression in response to tetanic stimulation and, therefore, can be distinguished

182 In neuronal somas, however, tetanic stimulation appears to result in long-lasting in

183 Tetanic stimulation at 50 Hz elicited long-term potentia

184 on CA1 and that LTD was found in response to tetanic stimulation at the trough of the local theta wav

185 actin/G-actin equilibrium, we show here that tetanic stimulation causes a rapid, persistent shift of

186 Tetanic stimulation causes an initial enhancement follow

187 A weak tetanic stimulation consisting of 20 pulses at 100 Hz in

188 Local tetanic stimulation decreased the Zn(2+) signal observed

189 Tetanic stimulation decreases a bicuculline-sensitive fi

190 hypothesis for the mechanism of PTP is that tetanic stimulation elevates presynaptic calcium that in

191 Tetanic stimulation elicited distinct increases in fluor

192 ed from preganglionic nerve terminals during tetanic stimulation enhanced neuronal excitability and e

193 At a maximal tetanic stimulation frequency, intact KO extensor digito

194 Tetanic stimulation in Ca(2+)-free medium elicited an in

195 were compared after low-frequency control or tetanic stimulation in hippocampal slices from postnatal

196 ed vesicle depletion near active zones after tetanic stimulation in staurosporine-treated preparation

197 ation (L-LTP) induced by either forskolin or tetanic stimulation in the hippocampal mossy fiber and S

198 rical activity in response to high-frequency tetanic stimulation in the hippocampus after head injury

199 In both pathways, tetanic stimulation induce significant long-term synapti

200 Tetanic stimulation induced diverse forms of excitatory

201 nist or an endogenous ligand released during tetanic stimulation induced robust rhythms of the subthr

202 nse to theta-burst stimulation and to 100-Hz tetanic stimulation is much reduced.

203 ng presynaptic calcium increases produced by tetanic stimulation may activate these isoforms to produ

204 Here we show that, upon tetanic stimulation of afferents to lateral amygdala, pr

205 Tetanic stimulation of axons terminating in the CA1 regi

206 permeable AMPA receptors exhibited LTD after tetanic stimulation of CA3 excitatory inputs.

207 Here, we report that tetanic stimulation of cerebellar climbing fiber-Purkinj

208 Tetanic stimulation of local circuitry induced effects s

209 Tetanic stimulation of mossy fibers induced long-term po

210 Tetanic stimulation of parallel fibres (PFs) produces a

211 tion takes place in hippocampal slices after tetanic stimulation of Schaffer collateral synapses.

212 was an attenuation of LTP elicited by either tetanic stimulation of Schaffer collaterals or a pairing

213 tic Ca(2+) signaling were also evident after tetanic stimulation of Schaffer collaterals.

214 Moreover, tetanic stimulation of the MD caused a longer-lasting (a

215 Brief tetanic stimulation of the muscle nerve (25 Hz, 90 s) de

216 tion of EPSP and population spike, following tetanic stimulation of the perforant path, was observed

217 icity, homosynaptic potentiation produced by tetanic stimulation of the presynaptic neuron in Aplysia

218 blocked long-lasting potentiation induced by tetanic stimulation of the presynaptic neuron.

219 mporoammonic afferents to CA1 neurons, brief tetanic stimulation of the residual excitatory synapses

220 Here we show that tetanic stimulation of the Schaffer collateral pathway c

221 otential (fEPSP) slope in area CA1 following tetanic stimulation of the Schaffer collaterals.

222 ssed at Aplysia sensorimotor synapses when a tetanic stimulation of the sensory neurons was paired wi

223 Oscillations induced in CA1 in vitro by tetanic stimulation of the stratum radiatum or oriens we

224 In Ca(2+)-free medium, tetanic stimulation of Xenopus motoneurons induced a str

225 receptors (mGluRs), either by high-frequency tetanic stimulation or an agonist, induced eCB-LTD.

226 DNF was of the same order as that induced by tetanic stimulation or substitution of the bathing mediu

227 Both phorbol esters and tetanic stimulation potentiate synaptic strength, and lo

228 hat LTP induced by a theta-burst pairing and tetanic stimulation protocols causes the rapid delivery

229 r superfusion of CO in the presence of ZnPP, tetanic stimulation readily evoked LTP.

230 riple KO mice, calcium transients induced by tetanic stimulation rely on calcium entry via La(3+)- an

231 stable platelet-activating factor analogue, tetanic stimulation that normally induces long-term syna

232 ot on NMDARs, but, when induced by a form of tetanic stimulation that produced prolonged postsynaptic

233 synaptic function and reduces the ability of tetanic stimulation to induce LTP.

234 howed that PBs could be used as an effective tetanic stimulation to study the synaptic plasticity in

235 To induce synaptic plasticity, tetanic stimulation was applied to either continuous or

236 LTP and conventional L-LTP induced by strong tetanic stimulation were completely normal in BDNF-KIV m

237 The effects of tetanic stimulation were examined in each pathway.

238 ty (assessed during re-lengthening following tetanic stimulation).

239 measure the rate of membrane retrieval after tetanic stimulation, and the amount of membrane transfer

240 be reliably induced by specific patterns of tetanic stimulation, and the level of LTD depends on bot

241 ce TrkB was regulated only by high frequency tetanic stimulation, but not by low frequency stimulatio

242 In contrast, LTP induced by 100 Hz tetanic stimulation, which requires Ca(2+) influx throug

243 terminals during and for some minutes after tetanic stimulation, while at the same time the plasma m

244 fter control stimulation to 39% +/- 4% after tetanic stimulation, with a commensurate loss of polyrib

245 ose at specific, repeatable locations during tetanic stimulation.

246 TR) function-blocking antiserum, or previous tetanic stimulation.

247 profiles of ARGs in response to LTP-inducing tetanic stimulation.

248 ablished LTP when applied 1, 3, or 5 h after tetanic stimulation.

249 ion from internalized membrane objects after tetanic stimulation.

250 omuscular transmission, during and following tetanic stimulation.

251 s containing polyribosomes were larger after tetanic stimulation.

252 expressing long-term potentiation induced by tetanic stimulation.

253 air mobilization of synaptic vesicles during tetanic stimulation.

254 gnificantly reduced the effectiveness of the tetanic stimulation.

255 ow-frequency control stimulation or repeated tetanic stimulation.

256 naptic depression after different amounts of tetanic stimulation.

257 h prior to and following 100 or 200 Hz (1 s) tetanic stimulation.

258 ion and endocytosis were slowed by prolonged tetanic stimulation.

259 m a persistent presynaptic [Ca2+]i following tetanic stimulation.

260 aving synaptic inhibition more intact during tetanic stimulation.

261 thening of the ILCx-BNST synapses after ILCx tetanic stimulation.

262 synapses that is dependent on the pattern of tetanic stimulation.

263 ts' appearing in repeatable locations during tetanic stimulation.

264 L-LTP is typically induced by homosynaptic tetanic stimulation; but associative forms of learning a

265 During high-frequency (tetanic) stimulation, somatic synaptic inhibition is sup

266 We investigated whether tetanic-stimulation and activation of metabotropic gluta

267 CA1 pyramidal neurons after weak and strong tetanic stimulations (100 Hz, 400 and 1000 msec, respect

268 Nerves sustained repeated tetanic stimulations (50 Hz or 100 Hz for 1 min) alterna

269 ts (PBs) stimulation are among the effective tetanic stimulations for induction of long-term potentia

270 ous alphaCaMKII and MAP2 proteins induced by tetanic stimulations in hippocampal slices.

271 Tetanic stimulations induce N-methyl-d-aspartate recepto

272 We found that tetanic stimuli coupled to bath application of serotonin

273 d animals, acute exposure to nicotine during tetanic stimuli enhances induction of long-term potentia

274 ong-term potentiation at CA3-CA1 synapses by tetanic stimuli in acute slices, a cellular model of lon

275 be induced in mutant slices by an 'enhanced' tetanic stimulus, implying that the LTP-producing mechan

276 tral index scale, entropy), immobility (limb tetanic stimulus-induced withdrawal reflex) and antinoci

277 Tetanic synaptic stimulation evoked a localized Ca(2+) w

278 Tetanic synaptic stimulation induced a rapid delivery of

279 Low-intensity tetanic synaptic stimulation or uncaging of IP3 increase

280 after 4, 12, or 36 days of recovery, maximum tetanic tension and tetanic fade (functional parameters

281 to 35 degrees C and the relation between the tetanic tension and the reciprocal absolute temperature

282 return to normal until day 36, while maximum tetanic tension had recovered at that time.

283 ously described from other fast muscles; the tetanic tension increased 3- to 4-fold in raising the te

284 The isometric tetanic tension of skeletal muscle increases with temper

285 (3) There was some tendency for maximum tetanic tension of this unit population to separate into

286 t compliance determined by others during the tetanic tension plateau of activated intact muscle.

287 nsion (passive muscle) than at high tension (tetanic tension).

288 lis muscle mass, fiber diameter, and maximum tetanic tension, as well as decreased tetanic fade persi

289 Impaired maximum tetanic tension, decreased tibialis muscle mass, and fib

290 a level which was higher than the prestretch tetanic tension.

291 1.0 mg) of the units correlated with maximum tetanic tension.

292 Maximum twitch and tetanic tensions were similar in WT and TG but force at

293 to the hyperaemia associated with isometric tetanic than isometric twitch contractions and aimed to

294 ion of excitatory transmission, and the post-tetanic time courses of decay of elevated [Ca(2+)](i) an

295 long-term potentiation in CA1 after a single tetanic train.

296 long-term potentiation generated by a single tetanic train.

297 ngle pulses (n=55), paired-pulses (n=15) and tetanic trains (n=11).

298 than does potentiation induced by arbitrary tetanic trains.

299 Na+-Ca2+ exchanger and helps to sustain post-tetanic transmitter release at mouse neuromuscular junct

300 Groups 1 (twitch) and 3 (tetanic) were time controls for Groups 2 and 4, which re