ライフサイエンスコーパス: reinstatement

1 pretreatment) also suppressed E2-potentiated reinstatement.

2 of alcohol approach behaviors and attenuates reinstatement.

3 cient mutant of AKAP150 also impairs cocaine reinstatement.

4 ing to a reduction in subsequent cue-induced reinstatement.

5 also correlate with the level of hippocampal reinstatement.

6 ck-out mice prevented foot-shock-induced CPP reinstatement.

7 mental area are necessary for these forms of reinstatement.

8 is necessary for stress-induced nicotine CPP reinstatement.

9 ited in a dopamine-dependent manner to drive reinstatement.

10 acellular mechanism by which stress leads to reinstatement.

11 d neurotransmitter systems in stress-induced reinstatement.

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

13 y results from rat studies on stress-induced reinstatement.

14 cimol and baclofen decreased context-induced reinstatement.

15 ine, followed by cue-induced and drug-primed reinstatement.

16 ) blockade in the AId similarly reduced cued reinstatement.

17 statement or sucrose self-administration and reinstatement.

18 ppocampal pattern completion and neocortical reinstatement.

19 PIc activity does not influence cue-induced reinstatement.

20 ex to the nucleus accumbens is implicated in reinstatement.

21 ially to reduce drug self-administration and reinstatement.

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

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

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

25 activation is necessary for E2 to potentiate reinstatement.

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

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

28 o LS specifically attenuated context-induced reinstatement.

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

30 mpulsive-like context-driven methamphetamine reinstatement.

31 is during abstinence in compulsive-like drug reinstatement.

32 elf-administration but before extinction and reinstatement.

33 variectomized to isolate estrogen effects on reinstatement.

34 uorescence-activated cell sorting to isolate reinstatement-activated Fos-positive neurons from Fos-ne

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

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

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

38 creased responding during drug prime-induced reinstatement-an effect that was normalized by inhibitin

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

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

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

42 tablish conditions that favor stress-induced reinstatement and increase the risk for addiction.

43 etics, we show modulation of context-induced reinstatement and reacquisition of alcohol seeking via d

44 p the VP output pathways for context-induced reinstatement and reacquisition of alcohol seeking.

45 -> STN pathways is sufficient to reduce both reinstatement and reacquisition of alcohol seeking.

46 A and VP --> STN pathways in context-induced reinstatement and reacquisition we used a chemogenetic d

47 involved in the regulation of cocaine-primed reinstatement, and activation of both brain regions is s

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

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

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

51 C pathway positively correlated with cocaine reinstatement behavior, unlike BLA or vSub inputs to NAc

52 ral overexpression of Brg1 enhanced, cocaine-reinstatement behavior.

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

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

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

56 ry mediating the facilitation of cue-induced reinstatement by NPS involves structures critically invo

57 O mice showed recovery from hyperalgesia and reinstatement by NTX; (3) there was no MOR internalizati

58 Participant's degree of incidental reinstatement correlates with their hippocampal activity

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

60 e effects of vmPFC activation on cue-induced reinstatement depended on prior extinction training, con

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

62 hippocampal activity, which predict pattern reinstatement during later free recall.

63 , the strength of a memory's unique episodic reinstatement during retrieval was inversely related to

64 on-related brain activity showed evidence of reinstatement during subsequent periods of neutral stimu

65 Together, these findings suggest that Ube3a reinstatement early in development may be necessary to p

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

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

68 ntral pallidal neurons blocked the augmented reinstatement elicited by chemogenetic regulation of eit

69 experiments) and a test of outcome-specific reinstatement (Experiments 1 and 3).

70 ons are (1) The phenomenon of stress-induced reinstatement, first shown with an intermittent footshoc

71 Ic inactivation had no effect on cue-induced reinstatement for cocaine seeking.

72 binoid-mediated mechanism in the cue-induced reinstatement for different drugs of abuse.

73 ppocampus and compared the extent of pattern reinstatement for different mnemonic outcomes.

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

75 being a common locus for different forms of reinstatement, fundamental aspects of neural circuitry f

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

77 eurons was sufficient to induce nicotine CPP reinstatement, identifying an anatomically specific intr

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

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

80 Motor deficits were rescued by Ube3a reinstatement in adolescent mice, whereas anxiety, repet

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

82 th rimonabant and AM4113 reduced cue-induced reinstatement in monkeys trained to self-administer coca

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

84 nephrine failed to potentiate cocaine-primed reinstatement in OCT3-deficient mice.

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

86 uation of nicotine and THC reinforcement and reinstatement in squirrel monkeys by the CB1-receptor in

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

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

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

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

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

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

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

94 , we correlated regional Fos expression with reinstatement induced by the most effective U50,488 dose

95 We show that memory reinstatement is accompanied by a decrease of low-freque

96 eval manipulation on cocaine-priming-induced reinstatement is mediated by regulation of AMPA-receptor

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

98 eat episodes were associated with subsequent reinstatement magnitude.

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

100 We used a rodent self-administration/reinstatement model of relapse to show that cue-induced

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

102 either the temporal precision of study-phase reinstatement nor the processing stage at which the rein

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

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

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

106 Cue-induced reinstatement of alcohol seeking activates a subset of m

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

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

109 and Hcrt-1/Ox-A systems interact to modulate reinstatement of alcohol seeking in rats.

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

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

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

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

114 to study brain mechanisms of U50,488-induced reinstatement of alcohol seeking.

115 f NPS facilitated discriminative cue-induced reinstatement of alcohol seeking.

116 n, as well as stress-induced and cue-induced reinstatement of alcohol seeking.

117 mg/kg) was tested in a model of cue-induced reinstatement of alcohol-seeking behavior in post-depend

118 -705253 dose-dependently reduced cue-induced reinstatement of alcohol-seeking behavior.

119 aving no impact on context- plus cue-induced reinstatement of alcohol-seeking behavior.

120 aving no impact on context- plus cue-induced reinstatement of alcohol-seeking responses.

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

122 We found that the reinstatement of assembly patterns representing a novel,

123 The context-dependent reinstatement of assembly patterns whose expression did

124 that reactivation was only required for the reinstatement of assembly patterns whose expression was

125 ory retrieval-extinction procedure decreases reinstatement of cocaine and heroin seeking in rats and

126 This stress-induced reinstatement of cocaine CPP depends on type 1 orexin re

127 eading to VTA dopaminergic disinhibition and reinstatement of cocaine CPP.

128 ative subunits of AMPK increased cue-induced reinstatement of cocaine seeking and enhanced mTORC1 and

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

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

131 This disconnection attenuated cue-induced reinstatement of cocaine seeking but had no effect on re

132 of vmPFC neurons with the Gq-DREADD reduced reinstatement of cocaine seeking elicited by cocaine-ass

133 d corticosterone, potentiates cocaine-primed reinstatement of cocaine seeking following self-administ

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 administration of CNO inhibited cue-induced reinstatement of cocaine seeking in rats extinguished fr

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

138 rum corticosterone and significantly greater reinstatement of cocaine seeking than the control group,

139 rgic inputs to nucleus accumbens during cued reinstatement of cocaine seeking versus sucrose seeking.

140 found to differentially promote cue-induced reinstatement of cocaine seeking via the ventral pallidu

141 Reinstatement of cocaine seeking was then tested after f

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

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

144 arker of neural activity) during cue-induced reinstatement of cocaine seeking, but only subpopulation

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

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

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

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

149 hell, but not the lateral core, enhanced the reinstatement of cocaine seeking.

150 re responsible for the decreased cue-induced reinstatement of cocaine seeking.

151 ing persistent cocaine-seeking and increased reinstatement of cocaine seeking.

152 lateral core or medial shell attenuated the reinstatement of cocaine seeking.

153 n dopamine signaling, neuronal activity, and reinstatement of cocaine seeking.

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

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

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

157 essive ratio schedule of reinforcement), and reinstatement of cocaine taking in rats allowed either s

158 Further, reinstatement of cocaine tolerance was accompanied by de

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

160 e examined Fos expression during cue-induced reinstatement of cocaine- and sucrose-seeking in prelimb

161 significant attenuation of yohimbine-induced reinstatement of cocaine-seeking after intra-CeA SB-3348

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

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

164 n the nucleus accumbens is necessary for the reinstatement of cocaine-seeking behavior, an animal mod

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

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

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

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

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

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

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

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

173 Reinstatement of DLX3 function is sufficient to attenuat

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

175 the shell attenuated cocaine priming-induced reinstatement of drug seeking and was associated with in

176 system has been implicated in stress-induced reinstatement of drug seeking for other commonly abused

177 tem plays a conserved role in stress-induced reinstatement of drug seeking for prototypical substance

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

179 ished lever pressing and tested the rats for reinstatement of drug seeking induced by cocaine-paired

180 and the roles of these VP output pathways in reinstatement of drug seeking remain poorly understood.

181 ural circuitry for these VP contributions to reinstatement of drug seeking remain unknown.

182 ls to both prevent extinction and facilitate reinstatement of drug seeking to drive relapse.

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

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

185 reas and circuits controlling stress-induced reinstatement of drug seeking.

186 he reinforcing effects of drugs of abuse and reinstatement of drug seeking.

187 accumbens attenuated cocaine priming-induced reinstatement of drug seeking.

188 studied using a rat model of stress-induced reinstatement of drug seeking.

189 a critical node in the neural circuitry for reinstatement of drug seeking.

190 ressor specific and not all stressors induce reinstatement of drug seeking.

191 r, including stress-, drug-, and cue-induced reinstatement of drug seeking.

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

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

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

195 ine intake, the motivation for the drug, and reinstatement of drug taking after extinction.

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

197 ng behavior, and (2) priming- or cue-induced reinstatement of drug-seeking behavior in abstinent subj

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

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

200 ding the mechanisms by which stress triggers reinstatement of drug-seeking behaviors is particularly

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

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

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

204 Reinstatement of dynamic memories requires the replay of

205 ognition (AR) yields enhanced event-specific reinstatement of encoding patterns compared to non-assoc

206 or STN are recruited during context-induced reinstatement of extinguished alcohol seeking in rats.

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

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

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

210 d for self-administered intravenous meth and reinstatement of extinguished meth seeking in male and f

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

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

213 AId inactivation had no effect on reinstatement of food-seeking behavior induced by cues,

214 been shown to contribute to context-induced reinstatement of heroin, cocaine, and alcohol seeking, b

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

216 nduced by miR-150 deficiency were rescued by reinstatement of miR-150.

217 nt with the antibiotic, ceftriaxone, blocked reinstatement of morphine-evoked conditioned place prefe

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

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

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

221 Converging evidence suggests that reinstatement of neural activity underlies our ability t

222 Several studies suggest that the reinstatement of neural encoding patterns is beneficial

223 esults are consistent with the proposal that reinstatement of neural oscillations during retrieval su

224 endent memory effects can be captured by the reinstatement of neural patterns.

225 al stressor yohimbine (2 mg/kg, i.p.) induce reinstatement of nicotine CPP in a norbinaltorphimine (n

226 -coupled intracellular signaling cascades on reinstatement of nicotine CPP.

227 e basolateral amygdala during stress-induced reinstatement of nicotine preference.

228 is both necessary and sufficient to produce reinstatement of nicotine preference.

229 on, and mechanisms that this system plays in reinstatement of nicotine seeking has not been character

230 intravenous nicotine self-administration and reinstatement of nicotine seeking induced by nicotine pr

231 nt with reduced nicotine reward; (3) blocked reinstatement of nicotine seeking induced by reexposure

232 se, we hypothesized that stress would induce reinstatement of nicotine seeking-like behavior in a KOR

233 Reinstatement of PEXEL to its original location restores

234 wing for coordinated shutdown and subsequent reinstatement of photosynthesis.

235 Memory reactivation--the reinstatement of processes and representations engaged w

236 tial patterns of brain activity has revealed reinstatement of recently-experienced events throughout

237 t after the clearance phase leads to a rapid reinstatement of robust tau pathology once soluble tau e

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

239 nisms governing the initiation, closure, and reinstatement of sensitive period plasticity has emerged

240 ment of cocaine seeking but had no effect on reinstatement of sucrose seeking.

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

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

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

244 Moreover, reinstatement of Syt1 expression partially restored syna

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

246 However, reinstatement of the original encoding context is not al

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

248 this hypothesis through cerebellum-specific reinstatement of Ube3a, which ameliorated cerebellar lea

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

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

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

252 inction training, rats underwent cue-induced reinstatement or an 'inactivation-alone' extinction test

253 reinstatement, with no effect on cue-induced reinstatement or sucrose self-administration and reinsta

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

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

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

257 Using a conditioned place preference (CPP) reinstatement procedure in mice, we show that both foot-

258 Here, we used the rat extinction-reinstatement procedure to test the hypothesis that the

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

260 ion showed that oxytocin reduced cue-induced reinstatement response in dependent rats-an effect that

261 As Long-Evans rats did not show a robust reinstatement response to nicotine, we used alcohol-pref

262 rring rats (P-rats) that display much higher reinstatement responses to nicotine than Long-Evans rats

263 or intra-VTA) before a single extinction or reinstatement session, while having no immediate effect

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

265 During subsequent cued reinstatement sessions, rats that had previously receive

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

267 tement nor the processing stage at which the reinstatement supported subsequent memory [12].

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

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

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

271 After reinstatement testing, we visualized robust c-fos expres

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

273 Before each reinstatement, the PIc or the more anterior dorsal agran

274 tivation significantly decreased cue-induced reinstatement to both cues, indicative of reconsolidatio

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

276 ith CRF1 receptors in this region, regulates reinstatement to cocaine seeking, but not food seeking,

277 inactivated to determine their roles in the reinstatement to cocaine seeking.

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

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

280 rst discuss the generality of stress-induced reinstatement to different drugs of abuse, different str

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

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

283 g behavior, pretreatment with E2 potentiated reinstatement to the ordinarily subthreshold cocaine dos

284 or in response to an ordinarily subthreshold reinstatement trigger.

285 the neuropeptide S (NPS) system exacerbates reinstatement vulnerability to cocaine and alcohol via s

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

287 After extinction training, reinstatement was assessed following re-exposure to thes

288 Context-induced reinstatement was associated with increased expression o

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

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

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

292 Memory reinstatement was not observed during the sequential enc

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

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

295 Corticosterone effects on reinstatement were attenuated by intra-PL injections of

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

297 t not food seeking, depending on the type of reinstatement, whereas PIc activity does not influence c

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

299 ffects of cocaine and attenuated drug-primed reinstatement, with no effect on cue-induced reinstateme

300 BLA prevented yohimbine-induced nicotine CPP reinstatement without affecting CPP acquisition.