ライフサイエンスコーパス: reinstatement

1 ial encoding of misleading details (cortical reinstatement).

2 -RMTg pathway during cue- or cocaine-induced reinstatement.

3 O(2) and CH(4)) prior to and following tidal reinstatement.

4 NST cFOS immunoreactivity and stress-induced reinstatement.

5 kes and predicting the fidelity of EC object reinstatement.

6 not prevent fear conditioning itself or fear reinstatement.

7 ex to the nucleus accumbens is implicated in reinstatement.

8 during context-induced, but not cue-induced reinstatement.

9 pha(2a)-AR heteroreceptors to stress-induced reinstatement.

10 ng activity in D2-MSNs augmented cue-induced reinstatement.

11 ially to reduce drug self-administration and reinstatement.

12 n the dose-response curve for cocaine-primed reinstatement.

13 ially mimicked the drug's systemic effect on reinstatement.

14 activation is necessary for E2 to potentiate reinstatement.

15 ic prefrontal cortex (PrL-PFC) to potentiate reinstatement.

16 se sessions, but had no effect on subsequent reinstatement.

17 o LS specifically attenuated context-induced reinstatement.

18 in the DG and produced compulsive-like drug reinstatement.

19 mpulsive-like context-driven methamphetamine reinstatement.

20 is during abstinence in compulsive-like drug reinstatement.

21 elf-administration but before extinction and reinstatement.

22 variectomized to isolate estrogen effects on reinstatement.

23 pretreatment) also suppressed E2-potentiated reinstatement.

24 of alcohol approach behaviors and attenuates reinstatement.

25 which predicted susceptibility to later fear reinstatement.

26 ommon mediator of cocaine- and stress-primed reinstatement.

27 cC pathway during cocaine- and stress-primed reinstatement.

28 capitulation of encoding-related EMs or gaze reinstatement.

29 e BNST activity, but prevents stress-induced reinstatement.

30 rojections to RMTg in inhibiting cue-induced reinstatement.

31 s expression in several regions critical for reinstatement.

32 anfacine on BNST activity and stress-induced reinstatement.

33 ojection in Ca(v)1.2-deficient mice restores reinstatement.

34 r (nonsignificant) effect on context-induced reinstatement.

35 i)-DREADD activation is sufficient to induce reinstatement.

36 to intra- and extrahippocampal circuits for reinstatement, a feature critical to memory indexing.

37 Prior to orchestrating reinstatement, a separate population of hippocampal neur

38 ircuits distinct from those recruited during reinstatement after experimenter-imposed abstinence, or

39 e after 1 week of abstinence and cue-induced reinstatement after extinction.

40 nstated sucrose seeking, nor was potentiated reinstatement after mGluR2/3 blockade reduced by blockin

41 re we examine the role of AKAP150 in cocaine reinstatement, an animal model of relapse.

42 GluR5 antagonist MTEP blocked cocaine-primed reinstatement and corresponding depotentiation, whereas

43 n of the mGluR5 agonist CHPG itself promoted reinstatement and depotentiated synaptic strength in the

44 kdown prevented ceftriaxone from attenuating reinstatement and from upregulating GLT-1 and resulted i

45 also prevented ceftriaxone from attenuating reinstatement and from upregulating xCT expression, with

46 algorithm, we quantify the timescale of the reinstatement and identify brain regions that show signi

47 activation, we blocked cued-induced cocaine reinstatement and increased spine head diameter (d(h)).

48 e retrieval, (c) older age weakened cortical reinstatement and its relationship to memory behaviour.

49 mber changes and weaker associations between reinstatement and memory performance.

50 Our findings provide evidence linking gaze reinstatement and pattern completion and advance a funct

51 ies in sub-Saharan Africa in response to the reinstatement and subsequent repeal of the Mexico City P

52 electrophysiology showed that cocaine-primed reinstatement and synaptic depotentiation were disrupted

53 Thus, cocaine-paired cues initiate cocaine reinstatement and synaptic enlargement through a signali

54 eroreceptor deletion disrupts stress-induced reinstatement and that BNST G(i)-DREADD activation is su

55 to alcohol-seeking: renewal (context-induced reinstatement) and reacquisition.

56 fects of cocaine, reduced stress-potentiated reinstatement, and altered behavioral strategies for coc

57 required for both cocaine- and stress-primed reinstatement, and that activation of this projection in

58 fidence judgments, sparse coding, contextual reinstatement, and the ventral tegmental area (VTA)-hipp

59 urther suggesting that garcinol's effects on reinstatement are through reconsolidation-based mechanis

60 ese areas also show evidence of anticipatory reinstatement as subjects listen to a familiar narrative

61 We also found that the onset of memory reinstatement at boundary onset was accompanied by a lef

62 ch that SB was most effective in attenuating reinstatement behavior in highly motivated rats.

63 cued reinstatement of fentanyl seeking; this reinstatement behavior was attenuated by SB administrati

64 Alcohol self-administration and cue-induced reinstatement behavior was measured after intracerebrove

65 mpletion and coordination of cortical memory reinstatement between 500 and 1500 ms.

66 inactivation markedly increased cue-induced reinstatement, but did not increase cocaine-induced rein

67 showed beneficial effects in preventing fear reinstatement, but differed in the groups they targeted.

68 at corticosterone potentiates cocaine-primed reinstatement by blockade of OCT3.

69 h the induction of escape deficits and their reinstatement by brief re-exposure to IES up to 20 days

70 ciated memories, we find that cocaine drives reinstatement by increasing the duration that mice spend

71 Potentiated sucrose reinstatement by mGluR2/3 blockade was reversed by antag

72 Three measures of t-SP were assayed during reinstatement: dendritic spine morphology, alpha-amino-3

73 The induction of t-SP during cued reinstatement depends on activating matrix metalloprotei

74 reat of misinformation can modulate cortical reinstatement during memory retrieval and reduce misinfo

75 to measure hippocampal activity and cortical reinstatement during retrieval of trial-unique associati

76 dle temporal gyrus and the left hippocampus, reinstatement effects between the retrieval phases corre

77 erved widespread within- and between-subject reinstatement effects within a posterior midline core me

78 trength of hippocampal activity and cortical reinstatement explained unique variance in performance a

79 trends when assessing the efficacy of tidal reinstatement for GHG emission control.

80 d that neural oscillations may be crucial to reinstatement for successful memory retrieval.

81 mory should be restabilized had no effect on reinstatement, further suggesting that garcinol's effect

82 inistered prior to E2 and cocaine suppressed reinstatement in a dose-dependent manner.

83 whether PACAP is also involved in producing reinstatement in a model of stress-induced relapse to dr

84 reproduced stress-potentiated cocaine-primed reinstatement in both sexes.

85 However, restraint potentiated reinstatement in both sexes.

86 ed the role of LHAad PNNs/ECM in cue-induced reinstatement in cocaine self-administering (SA) rats an

87 ilitated extinction and blunted drug-induced reinstatement in female mice, it had the opposite effect

88 nsities, failed to potentiate cocaine-primed reinstatement in females.

89 Neural activity pattern reinstatement in medial temporal lobe (MTL) during the r

90 provide support for the role of oscillatory reinstatement in memory retrieval.SIGNIFICANCE STATEMENT

91 normetanephrine to potentiate cocaine-primed reinstatement in OCT3-deficient and wild-type mice.

92 d extinction, but each treatment potentiates reinstatement in response to an otherwise subthreshold c

93 with cocaine, and was sufficient to promote reinstatement in the absence of a cocaine challenge.

94 S interneurons, we recapitulated cue-induced reinstatement in the absence of cues.

95 f mGluR5 in NAcore recapitulated cue-induced reinstatement in the absence of drug-associated cues.

96 rexanolone infusion without anesthetic agent reinstatement in the following 24 hours.

97 However, the temporal dynamics of reinstatement in the human cortex remain poorly understo

98 mpal pattern completion inducing information reinstatement in the neocortex during memory retrieval.

99 Reinstatements in posterior medial cortex (PMC) addition

100 , progressive ratio, extinction, cue-induced reinstatement) in wild-type (WT) and Npas2 mutant mice a

101 However, ketamine administered before reinstatement increased the number of rearing bouts in a

102 bens shell of Sprague-Dawley rats attenuates reinstatement induced by either cocaine or a D1DR agonis

103 nduced reinstatement of alcohol seeking, and reinstatement induced by injections of U50,488 (0, 0.3,

104 einstatement of cocaine-seeking and assessed reinstatement-induced Fos expression in several regions

105 f cocaine + alcohol also altered patterns of reinstatement-induced Fos expression.

106 ssical extinction-reinstatement model, where reinstatement is induced by reexposure to the self-admin

107 The increase in stress-induced reinstatement is paralleled by heightened anxiety measur

108 e seeking in the rat self-administration and reinstatement model of addiction.

109 ing, as assessed in the classical extinction-reinstatement model, where reinstatement is induced by r

110 g-induced cocaine-seeking in the rat cocaine reinstatement model.

111 , has well-established roles in conventional reinstatement models tested following extinction trainin

112 e drinking-related behaviors and cue-induced reinstatement, motivating human studies of mGlu5 recepto

113 Remarkably, reinstatement of 11beta-HSD2 expression, or AMFR loss, r

114 appearance of hypo-phosphorylated RB and the reinstatement of a G1 checkpoint.

115 ed that verbal memory retrieval leads to the reinstatement of activity across regions of the brain th

116 ting to NAc, but not BLA, blocks cue-induced reinstatement of alcohol seeking and neither pathway is

117 BNST is a critical site for U50,488-induced reinstatement of alcohol seeking and suggest that KOR/dy

118 U50,488-induced reinstatement of alcohol seeking was associated with inc

119 The yohimbine-induced reinstatement of alcohol seeking was prevented by infusi

120 s of nor-BNI (4 mug/side) on U50,488-induced reinstatement of alcohol seeking, and reinstatement indu

121 C-->NAc pathway is necessary for cue-induced reinstatement of alcohol seeking, expand our understandi

122 ct of U50,488 (0, 1.25, 2.5, and 5 mg/kg) on reinstatement of alcohol seeking.

123 euronal activation induced by stress-induced reinstatement of alcohol-seeking using c-Fos immunohisto

124 come associations in the hippocampus and the reinstatement of anticipated outcomes in visual cortex.

125 ach'), neurons in the hippocampus coordinate reinstatement of associated memories ('cocktail') in cor

126 d BNST G(i)-GPCR signaling in stress-induced reinstatement of cocaine conditioned place preference (C

127 Here, using cocaine- and stress-primed reinstatement of cocaine conditioned place preference to

128 d BNST G(i)-GPCR signaling in stress-induced reinstatement of cocaine CPP and provide insight into th

129 cocaine self-administration and cue-induced reinstatement of cocaine seeking after drug extinction.

130 ctive subunits of AMPK decreased cue-induced reinstatement of cocaine seeking and inhibited the mamma

131 bility of ceftriaxone to prevent cue-induced reinstatement of cocaine seeking and normalize glutamate

132 pocampus (DH) is involved in context-induced reinstatement of cocaine seeking but the role of the DH

133 While decreasing stress-induced reinstatement of cocaine seeking in animal models and st

134 We also attempted to block the reinstatement of cocaine seeking in cocaine self-adminis

135 Ifenprodil also mitigated cue-induced reinstatement of cocaine seeking in mice self-administer

136 SA and prolonged (over 5 weeks) increases in reinstatement of cocaine seeking induced by foot-shock s

137 Reinstatement of cocaine seeking was then tested after f

138 rm treatment with ceftriaxone attenuates the reinstatement of cocaine seeking while increasing the fu

139 e findings elucidate the importance of LS in reinstatement of cocaine seeking, and indicate that dors

140 vation is necessary for and potentiates cued reinstatement of cocaine seeking, and MMP-induced cataly

141 egmental nucleus (RMTg) may instead suppress reinstatement of cocaine seeking, due to the role of RMT

142 lity of ceftriaxone to attenuate cue-induced reinstatement of cocaine seeking, each protein uniquely

143 re have been shown to be involved in driving reinstatement of cocaine seeking, PL projections to the

144 the NAc core is critical for the cue-induced reinstatement of cocaine seeking, which may be mediated

145 effects of G-CSF treatment on extinction and reinstatement of cocaine seeking.

146 necessary and sufficient for stress-induced reinstatement of cocaine seeking.

147 on learning and promoted the subsequent cued reinstatement of cocaine seeking.

148 ers of drug relapse-context- and cue-induced reinstatement of cocaine seeking.

149 to LS mediate context-, but not cue-induced, reinstatement of cocaine seeking.

150 ons attenuated both context- and cue-induced reinstatement of cocaine seeking.

151 during seeking, extinction, and drug-induced reinstatement of cocaine self-administration.

152 FICANCE STATEMENT Ceftriaxone attenuates the reinstatement of cocaine, alcohol, and heroin seeking.

153 h-ABC) blocked the expression of cue-induced reinstatement of cocaine- but not sucrose-seeking behavi

154 ic cortex is a critical factor in triggering reinstatement of cocaine-primed conditioned approach beh

155 the ability of ceftriaxone to attenuate the reinstatement of cocaine-seeking and assessed reinstatem

156 he role of G-CSF in affecting extinction and reinstatement of cocaine-seeking and perform detailed ch

157 results suggest that AKAP150 facilitates the reinstatement of cocaine-seeking behavior by amplifying

158 the NpHR-mCherry groups disrupted CS-induced reinstatement of cocaine-seeking behavior relative to (i

159 s to the ventral tegmental area (VTA) in the reinstatement of cocaine-seeking behavior, an animal mod

160 tinctly contributes to cue- and drug-induced reinstatement of cocaine-seeking behavior.

161 tinctly contributes to cue- and drug-induced reinstatement of cocaine-seeking behavior.

162 lidation and subsequent drug context-induced reinstatement of cocaine-seeking behavior.

163 sion, would block BDNF's ability to suppress reinstatement of cocaine-seeking in rats with a cocaine

164 lack of increase in glutamate efflux during reinstatement of cocaine-seeking.

165 ion immediately before cue- and drug-induced reinstatement of cocaine-seeking.

166 cocaine SA session results in attenuation of reinstatement of cocaine-seeking.

167 n the nucleus accumbens (NA) core during the reinstatement of cocaine-seeking.

168 to ventral pallidum may promote cue-induced reinstatement of cocaine-seeking.

169 ore, both true and false memory entailed the reinstatement of concept-related information at varying

170 igated a causal link between cocaine-induced reinstatement of conditioned place preference and rapid

171 Our data suggest that temporally compressed reinstatement of cortical activity is a feature of cued

172 l events is thought to depend on coordinated reinstatement of cortical representations by the medial

173 ntaneous recollections and orchestrating the reinstatement of cortical representations during free ep

174 We show that reinstatement of distributed patterns of high gamma acti

175 L-DOPA reinstatement of dopamine normalized HCN activity, but S

176 er extinction of the learned preference, the reinstatement of drug seeking after operant drug self-ad

177 WIN), in order to assess measures of relapse/reinstatement of drug seeking and long-term effects on c

178 opamine D3 receptor (D3R) is involved in the reinstatement of drug seeking and motivation for drugs o

179 itioned place preference, and cocaine-primed reinstatement of drug seeking in rats.

180 mory processes and that nuclear HDAC5 limits reinstatement of drug seeking independent of NPAS4.

181 hether they reduce drug self-administration, reinstatement of drug seeking, and incubation of drug cr

182 se consequences, and very robust cue-induced reinstatement of drug seeking, especially in a subset of

183 dministration, without affecting cue-induced reinstatement of drug seeking.

184 aOR regulation that plays a critical role in reinstatement of drug seeking.

185 f-administration, extinction responding, and reinstatement of drug seeking.

186 sponding under extinction and cocaine-primed reinstatement of drug seeking.

187 FC, and decreased cocaine intake and blocked reinstatement of drug seeking.

188 the importance of multiple neuropeptides in reinstatement of drug use, we formulated intranasal insu

189 ite-specific epigenetic manipulations on the reinstatement of drug-conditioned place preference after

190 tenuated heroin-primed, but not cue-induced, reinstatement of drug-seeking behavior, whereas inhibiti

191 ine self-administration, and cocaine-induced reinstatement of drug-seeking behavior, whereas R-MOD in

192 It also failed to induce reinstatement of drug-seeking behavior.

193 al behavior in the absence of Meth triggered reinstatement of drug-seeking in concurrent animals.

194 io responding for cocaine and stress-induced reinstatement of drug-seeking.

195 m has been implicated in drug-taking and the reinstatement of drug-seeking.

196 ng cocaine self-administration (SA) underlie reinstatement of drug-seeking.

197 s well as contributing to relatively greater reinstatement of encoding-related patterns for recollect

198 rease cocaine-induced reinstatement or drive reinstatement of extinguished cocaine seeking in the abs

199 Reinstatement of extinguished cocaine seeking was elicit

200 ist, PACAP 6-38, prevented footshock-induced reinstatement of extinguished cocaine seeking.

201 a concentrations) potentiated cocaine-primed reinstatement of extinguished cocaine-induced conditione

202 was more effective than 2 in attenuating the reinstatement of extinguished cocaine-seeking behavior i

203 ed place preference (CPP) and stress-induced reinstatement of extinguished morphine-CPP in mouse mode

204 Conditioned place preference, extinction and reinstatement of extinguished preference in response to

205 ntions would be more effective to reduce the reinstatement of fear in subjects genetically predispose

206 ing context memories and to context-specific reinstatement of fear.

207 ne alpha values predicted the amount of cued reinstatement of fentanyl seeking; this reinstatement be

208 dMSNs and iMSNs in encoding vulnerability to reinstatement of heroin-seeking and provide insight into

209 iMSNs is capable of suppressing cue-induced reinstatement of heroin-seeking in high- but not low-ris

210 nactivation of iMSNs exacerbates cue-induced reinstatement of heroin-seeking in high- but not low-ris

211 partial-cue recognition memory task to index reinstatement of lure images behaviorally via the recapi

212 male and female rats, meth demand predicted reinstatement of meth seeking, and systemic oxytocin dec

213 ve to less memorable ones, results in faster reinstatement of neural activity in the anterior tempora

214 Our data therefore provide a link between reinstatement of neural activity in the cortex and spont

215 tive memory recall is thought to involve the reinstatement of neural activity patterns that occurred

216 that episodic memory retrieval involves the reinstatement of neural activity that was present when w

217 r, whether these pathways similarly regulate reinstatement of opioid-seeking remains unknown, as is t

218 range using measures such as phase reset and reinstatement of oscillatory activity.SIGNIFICANCE STATE

219 Furthermore, reinstatement of oscillatory patterns in the hippocampus

220 t B (extinction responding), context-induced reinstatement of oxycodone seeking in context A, and rea

221 educed oxycodone self-administration and the reinstatement of oxycodone-seeking behavior in rats.

222 nuated oxycodone self-administration and the reinstatement of oxycodone-seeking behavior without affe

223 nhibited oxycodone extinction responding and reinstatement of oxycodone-seeking behavior.

224 ledge building is suggested to occur through reinstatement of prior knowledge during new learning, yi

225 tive learning and are critically involved in reinstatement of psychostimulant-seeking.

226 aling in remifentanil demand and cue-induced reinstatement of remifentanil seeking in male rats.

227 (VP) in remifentanil demand and cue-induced reinstatement of remifentanil seeking.

228 icroinjected intra-VP attenuated cue-induced reinstatement of remifentanil seeking.

229 We proposed that reinstatement of respiratory sinus arrhythmia would impr

230 We tested if reinstatement of respiratory-modulated heart rate (RMH)

231 urons in the human cortex participate in the reinstatement of semantic representations.

232 ctivity during or prior to the induction and reinstatement of stress-induced behavioral deficits.

233 aine-induced adaptations and potentiate cued reinstatement of sucrose seeking.

234 ce preference for high-fat food, cue-induced reinstatement of sucrose-seeking, and motivation to work

235 ally in the bronchial epithelium resulted in reinstatement of susceptibility to fungal allergen-induc

236 Neural replay is characterized by the reinstatement of temporal patterns from encoding(2,3).

237 nd that event boundaries triggered the rapid reinstatement of the just-encoded movie event EEG patter

238 of event boundaries triggered a rapid memory reinstatement of the just-encoded sequence episode.

239 d memory retrieval is thought to involve the reinstatement of those representations.

240 c neurons, and it was rescued by pancellular reinstatement of Ube3a at postnatal day 21 (P21), but no

241 be amenable to therapies leveraging juvenile reinstatement of UBE3A.

242 deprivation and the subsequent weakening by reinstatement of visual experience were prevented in the

243 Rats exhibited significant cue-induced reinstatement of WIN seeking that increased with 21 days

244 eeking behavior, they do not directly induce reinstatement on their own.

245 ior, whereas R-MOD inhibited cocaine-induced reinstatement only at the high dose of 100 mg/kg.

246 f-administration, extinction responding, and reinstatement only in females as well as reinforcement a

247 tement, but did not increase cocaine-induced reinstatement or drive reinstatement of extinguished coc

248 ct the propensity to approach drug cues, and reinstatement or relapse, even after relatively brief pe

249 Rats were tested 24 h later for cue-induced reinstatement, or LA slices were prepared for electrophy

250 study, we use a conditioned place preference/reinstatement paradigm in mice to directly test the hypo

251 Using a novel modification of the reinstatement paradigm, we show that achieving cocaine u

252 ed with reinstatement strength, (b) cortical reinstatement partially mediated the relationship betwee

253 Here, we used a modified self-administration/reinstatement procedure combined with anatomical, pharma

254 abstinence using a modified context-induced reinstatement procedure, a rat relapse model.

255 ment sessions using different extinction and reinstatement protocols in 4 separate studies.

256 Prior to reinstatement, rats received microinjections of the GABA

257 ocedures and cocaine self-administration and reinstatement (relapse) procedures.

258 ontextual extinction behavior and subsequent reinstatement remain poorly understood.

259 Importantly, both forms of reinstatement require Ca(v)1.2 L-type Ca(2+) channels (L

260 P administration in the nucleus accumbens on reinstatement (RI) of cocaine seeking, a rodent model of

261 IP infused into the nucleus accumbens on the reinstatement (RI) of cocaine seeking.

262 L inhibition after lever presses during cued reinstatement sessions increased cocaine seeking during

263 sured during cue reactivity, extinction, and reinstatement sessions using different extinction and re

264 th 3 mg/kg of ADX71441 before stress-induced reinstatement significantly decreased c-Fos expression i

265 ed that (a) hippocampal activity scaled with reinstatement strength, (b) cortical reinstatement parti

266 and a corresponding decrease in cue-induced reinstatement, suggesting that calcineurin may be a pote

267 e affect (NA)) followed by an analog smoking reinstatement task for which participants could earn mon

268 responding in Group CONTRA, but only in the reinstatement test.

269 ine across progressive ratio, extinction and reinstatement testing, but had no effect on food reinfor

270 anced cocaine seeking measured in extinction/reinstatement tests following an extended 3 week withdra

271 xtinction sessions, and cue- or Meth-induced reinstatement tests.

272 splayed a lower threshold for cocaine-primed reinstatement than males.

273 Rats were later tested on cue-induced reinstatement to both cues.

274 ependently inhibited cue- and cocaine-primed reinstatement to cocaine, but did not affect locomotor a

275 e activity of kappaORs governs the prolonged reinstatement to cocaine-seeking observed after cold wat

276 nd was effective in blocking cocaine-induced reinstatement to drug seeking.

277 cin decreased demand for meth and attenuated reinstatement to meth seeking.

278 ne, but did not affect locomotor activity or reinstatement to sucrose seeking.

279 , and that older adults are less able to use reinstatement to update memory for changed features.

280 ockdown attenuates extinction responding and reinstatement triggered by either cocaine-priming inject

281 This viral-mediated attenuation of cocaine reinstatement was accompanied by decreased phosphorylati

282 Enhanced cue-induced reinstatement was also observed with ipsilateral inactiv

283 t compulsive, punishment-resistant rats, and reinstatement was associated with neural activity in ana

284 Morphine-CPP reinstatement was associated with the D2R-mediated hyper

285 U50,488-induced reinstatement was blocked by BNST nor-BNI injections, an

286 spase strategy, the intensity of cue-induced reinstatement was correlated with the extent of selectiv

287 Furthermore, reinstatement was driven by an mGluR5-dependent reductio

288 After extinction, reinstatement was initiated by 10 minutes of cue-induced

289 s following degraded retrieval cues and this reinstatement was negatively correlated with accuracy fo

290 d across the estrous cycle; CORT-potentiated reinstatement was only observed during diestrus and proe

291 gulated by presynaptic mGluR2/3, and sucrose reinstatement was potentiated following mGluR2/3 blockad

292 erone treatment to potentiate cocaine-primed reinstatement was recapitulated by intra-PL injection of

293 seeking provoked by renewal (context-induced reinstatement), we found that VP Gad1 and parvalbumin (P

294 s during tests of extinction, or cue-induced reinstatement were observed between the groups.

295 nput to the NAc shell blocked cocaine-primed reinstatement, whereas low-frequency stimulation (10 Hz)

296 ng showed an overall effect in reducing fear reinstatement, whereas pharmacological memory enhancemen

297 phomutant mice failed to show cocaine-primed reinstatement which can be reversed by chemogenetic mani

298 ction or reconsolidation reduced cue-induced reinstatement, which was blocked by co-infusion of the C

299 lasminogen activator potentiated cue-induced reinstatement, which was prevented by beta3 integrin kno

300 ts demonstrate that riluzole impairs cocaine reinstatement while rectifying several cellular adaptati