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 though 4AP increased peak forces during unit tetanic activation, tetanic force failure was not elimin

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

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

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

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 ile forces during a single twitch and during tetanic conditions.

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

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

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

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

31 eater role in the hyperaemia associated with tetanic contraction.

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

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

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

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

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

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

38 Isometric tetanic contractions of the gastrocnemius complex of six

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

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

41 during the transition from rest to repeated tetanic contractions.

42 quency for minimum dynamic stiffness) during tetanic contractions.

43 espond to electrical stimuli with twitch and tetanic contractions.

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

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

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

47 olarizing GABA component underlying the post-tetanic depolarization.

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

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

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

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

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

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

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

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

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

57 Tetanic fade was not affected by inflammation.

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

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

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

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

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

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

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

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

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

67 The tetanic force assay also identified beneficial compound

68 Tetanic force decreased by 14% with assisted ventilation

69 The specific tetanic force decreased significantly in single muscle f

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

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

72 peak forces during unit tetanic activation, tetanic force failure was not eliminated.

73 Mean tetanic force generation was increased significantly at

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

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

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

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

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

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

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

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

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

83 stimulation at higher frequency for optimal tetanic force production.

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

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

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

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

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

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

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

91 delayed relaxation and altered generation of tetanic force.

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

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

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

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

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

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

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

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

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

101 Tetanic muscle contraction was evoked by stimulating L7-

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

103 osis in frog motor nerve terminals following tetanic nerve stimulation, and we used fura-2 imaging of

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

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

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

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

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

109 Moreover, transmission augmentation and post-tetanic potentiation (PTP) are disrupted in the mutant.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

131 the periphery (perhaps attributable to post-tetanic potentiation at the neuromuscular junction), and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

148 ng pronounced synaptic augmentation and post-tetanic potentiation.

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

150 manipulations implicate mitochondria in post-tetanic potentiation.

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

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

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

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

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

156 TP as induced by a conventional homosynaptic tetanic protocol.

157 x after contraction, consequently leading to tetanic responses at lower stimulation frequencies.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 Tetanic stimulation at 50 Hz elicited long-term potentia

175 scillations were evoked in the CA1 region by tetanic stimulation at one or two sites simultaneously,

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

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

178 Tetanic stimulation causes an initial enhancement follow

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

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

181 Tetanic stimulation decreases a bicuculline-sensitive fi

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

183 Tetanic stimulation elicited distinct increases in fluor

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

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

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

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

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

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

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

191 ed in induction of long-term potentiation by tetanic stimulation in the hippocampus.

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

193 Tetanic stimulation induced diverse forms of excitatory

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

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

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

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

198 Tetanic stimulation of axons terminating in the CA1 regi

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

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

201 Brief tetanic stimulation of granule cell parallel fibers acti

202 Tetanic stimulation of local circuitry induced effects s

203 Tetanic stimulation of mossy fibers induced long-term po

204 Tetanic stimulation of parallel fibres (PFs) produces a

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

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

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

208 rge and the contractile tension generated by tetanic stimulation of single motor units.

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

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

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

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

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

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

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

216 We suggest that tetanic stimulation of the Schaffer collateral pathway m

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

236 Thirty minutes after tetanic stimulation, autophosphorylated CaM kinase II (P

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

238 s PKC isozymes in slices subjected to low or tetanic stimulation, or perfused with phorbol esters (PD

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

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

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

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

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

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

245 ion from internalized membrane objects after tetanic stimulation.

246 omuscular transmission, during and following tetanic stimulation.

247 s containing polyribosomes were larger after tetanic stimulation.

248 expressing long-term potentiation induced by tetanic stimulation.

249 air mobilization of synaptic vesicles during tetanic stimulation.

250 gnificantly reduced the effectiveness of the tetanic stimulation.

251 ow-frequency control stimulation or repeated tetanic stimulation.

252 naptic depression after different amounts of tetanic stimulation.

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

254 ion and endocytosis were slowed by prolonged tetanic stimulation.

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

256 sticity, or LTP induced by several trains of tetanic stimulation.

257 aving synaptic inhibition more intact during tetanic stimulation.

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

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

260 ts' appearing in repeatable locations during tetanic stimulation.

261 ose at specific, repeatable locations during tetanic stimulation.

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

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

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

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

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

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

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

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

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

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

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

273 Tetanic stimuli that were strong enough to induce oscill

274 l level by applying a second, high-frequency tetanic stimulus to the dorsal root, indicating that LTD

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