ライフサイエンスコーパス: seeking behavior

1 r that is associated with compulsive alcohol-seeking behavior.

2 oin self-administration and cue-induced drug-seeking behavior.

3 n on subsequent drug context-induced cocaine-seeking behavior.

4 nt drug context-induced instrumental cocaine-seeking behavior.

5 s to fuel later escalated cocaine taking and seeking behavior.

6 food plays an important role in cue-induced seeking behavior.

7 ver new therapeutic candidates to treat drug-seeking behavior.

8 rovement is necessary to induce intervention-seeking behavior.

9 high-effort cost behavior, but not by reward-seeking behavior.

10 ed group showed low attachment and attention-seeking behavior.

11 icotine nor reinstated extinguished nicotine-seeking behavior.

12 an important role in stress-induced cocaine-seeking behavior.

13 t- plus cue-induced reinstatement of alcohol-seeking behavior.

14 onserved neuromodulator that stimulates food-seeking behavior.

15 users, and are thought to facilitate a drug-seeking behavior.

16 n the environment is critical for their host-seeking behavior.

17 ine play a critical role in voluntary reward-seeking behavior.

18 ll (AcbSh) facilitates extinction of cocaine-seeking behavior.

19 ese brain regions mediate CS-induced cocaine-seeking behavior.

20 ects on an addict's emotional state and drug-seeking behavior.

21 (mPFC) is implicated in the relapse of drug-seeking behavior.

22 increased palatable food preference and food-seeking behavior.

23 arning and the active suppression of cocaine-seeking behavior.

24 mine invigorates environmentally cued reward-seeking behavior.

25 such cues can instigate and invigorate drug-seeking behavior.

26 NAc cue-evoked neuronal activity, and reward-seeking behavior.

27 ay be a successful strategy to abate ethanol-seeking behavior.

28 ine-dependent signal is necessary for reward-seeking behavior.

29 and reduced the motivation to engage in food-seeking behavior.

30 reviously self-administered to renew cocaine-seeking behavior.

31 ing stress prevents reinstatement of cocaine-seeking behavior.

32 ia infection status also mediate vector host-seeking behavior.

33 n of stress-induced reinstatement of cocaine-seeking behavior.

34 ncreased resistance to extinction of ethanol-seeking behavior.

35 mechanisms underlying extinction of cocaine-seeking behavior.

36 synaptic transmission in the VTA and reward-seeking behavior.

37 DH may similarly control contextual cocaine-seeking behavior.

38 at promote behavioral sensitization and drug-seeking behavior.

39 e- and drug-induced reinstatement of cocaine-seeking behavior.

40 ry processes that promote contextual cocaine-seeking behavior.

41 ory processes involved in extinction of drug-seeking behavior.

42 c HDAC is involved in the extinction of drug-seeking behavior.

43 ventral pallidum (VP) is necessary for drug-seeking behavior.

44 nversely correlated with cue-induced cocaine-seeking behavior.

45 ses the most evidence linking it to nicotine seeking behavior.

46 ng") that instigates and/or invigorates drug-seeking behavior.

47 ong-lasting increases in cue-elicited reward-seeking behavior.

48 n cocaine self-administration versus cocaine-seeking behavior.

49 translating conditioned stimuli into cocaine-seeking behavior.

50 cal responses, craving, withdrawal, and drug-seeking behavior.

51 ed motivation for cocaine-taking and cocaine-seeking behavior.

52 e ability of a drug-paired cue to drive drug-seeking behavior.

53 tudy of anxiogenesis and stress-induced drug-seeking behavior.

54 lso attenuated the reinstatement of nicotine-seeking behavior.

55 of drug-predictive cues to precipitate drug-seeking behavior.

56 responding, suggesting a blockade of cocaine-seeking behavior.

57 and cocaine-primed reinstatement of cocaine-seeking behavior.

58 n dependence and their association with drug seeking behavior.

59 early- and late-stage performance of cocaine-seeking behavior.

60 test (FUST), a measure of sex-related reward-seeking behavior.

61 te signaling plays an essential role in drug-seeking behavior.

62 c connections, to promote CS-induced cocaine-seeking behavior.

63 and may have a role in the etiology of drug-seeking behavior.

64 educed responding under simpler schedules of seeking behavior.

65 factors and orchestrate an increase in food-seeking behavior.

66 e- and drug-induced reinstatement of cocaine-seeking behavior.

67 late to the timing of a visually cued reward-seeking behavior.

68 during extinction of cue-conditioned alcohol-seeking behavior.

69 sentations of the DS(+) to reinstate cocaine seeking behavior.

70 CSs intact and able to continue driving drug-seeking behavior.

71 also failed to induce reinstatement of drug-seeking behavior.

72 is attenuation was due to a blockade of cold-seeking behavior.

73 the thalamus (pPVT) participates in cocaine-seeking behavior.

74 mportance of the VP in context-driven reward-seeking behavior.

75 activation and a test of cue-induced cocaine-seeking behavior.

76 he DG that could directly contribute to drug-seeking behavior.

77 extinction sessions showed increased cocaine-seeking behavior.

78 onal states that instigate and maintain drug-seeking behavior.

79 resentation of punishment risk during reward-seeking behavior.

80 cocaine self-administration (SA) and cocaine-seeking behavior.

81 innervation that mediate noncompulsive food-seeking behavior.

82 roduction and loss, as well as dramatic cold-seeking behavior.

83 reduced cue-induced reinstatement of alcohol-seeking behavior.

84 oned responses and control compulsive reward-seeking behavior.

85 lie contextual stimulus control over cocaine-seeking behavior.

86 emories that can precipitate relapse to drug-seeking behavior.

87 ntly dampened seasonal cycles in information-seeking behavior.

88 iction involves an inability to control drug-seeking behavior.

89 l reward-predictive cues can motivate reward-seeking behaviors.

90 on both voluntary alcohol-intake and alcohol-seeking behaviors.

91 h hormone secretion, food intake, and reward-seeking behaviors.

92 that may contribute to the memory of alcohol-seeking behaviors.

93 erences in extinction and incubation of drug-seeking behaviors.

94 mesolimbic reward circuits to control reward-seeking behaviors.

95 (VTA) plays a key role in regulating reward-seeking behaviors.

96 n a way that may facilitate maladaptive food-seeking behaviors.

97 ulator that potentially plays a role in drug-seeking behaviors.

98 ive stress- or cue-induced drug- and alcohol-seeking behaviors.

99 ons to rewarding stimuli, to modulate reward-seeking behaviors.

100 are powerful triggers for compulsive opiate-seeking behaviors.

101 gulates orexin neuronal activity during drug-seeking behaviors.

102 ite-host combinations and for different host-seeking behaviors.

103 d propensities to engage in drug and alcohol seeking behaviors.

104 nfluence motivational states and elicit food-seeking behaviors.

105 ections between BLA and NAc, mediate alcohol-seeking behaviors.

106 n 5-HT neuron firing, contributes to cocaine-seeking behaviors.

107 n regions involved in the extinction of drug-seeking behaviors.

108 c disorders associated with abnormal novelty-seeking behaviors.

109 elated with cocaine-seeking, but not sucrose-seeking, behavior.

110 er to drive cocaine-seeking, but not sucrose-seeking, behavior.

111 mories.SIGNIFICANCE STATEMENT Continued drug-seeking behavior, a defining characteristic of cocaine a

112 escents are notorious for engaging in reward-seeking behaviors, a tendency attributed to heightened a

113 significantly enhanced extinction of alcohol-seeking behavior across multiple extinction sessions, an

114 acotherapy (oxytocin) in attenuating cocaine-seeking behaviors across individuals, demonstrating that

115 Here we report consistent novelty-seeking behavior, across different contexts, among honey

116 h the ability of multiple cues to drive drug-seeking behavior after just one reactivation and treatme

117 l and eliminated the maintenance of morphine-seeking behavior after morphine withdrawal.

118 Rats were assessed for cocaine-seeking behaviors after either intra-accumbal injections

119 ht into how the nervous system mediates food-seeking behavior amid oxidative stress and suggest that

120 Few data exist describing healthcare-seeking behaviors among persons with influenza-like illn

121 s necessary for the reinstatement of cocaine-seeking behavior, an animal model of drug craving and re

122 Uncertain level and consistency of health-seeking behavior and access and uncertain accuracy of di

123 ndent intensification of cue-induced cocaine-seeking behavior and an impaired extinction of this beha

124 s a critical mediator of instrumental reward seeking behavior and appears to have a particularly impo

125 sed binge-like eating and fully blocked food-seeking behavior and compulsive eating, selectively in t

126 OCT3 mediates corticosterone effects on drug-seeking behavior and establish OCT3 function as an impor

127 Mosquito host-seeking behavior and heterogeneity in host distribution

128 a foundation for understanding mosquito host-seeking behavior and identifies odors that are potential

129 sure to drug-related cues reinstated cocaine-seeking behavior and increased AMPK and p70s6k phosphory

130 roadaptations underlying stress-induced drug-seeking behavior and may be useful in the treatment of c

131 investigate the correlation between cocaine-seeking behavior and mGluR5 receptor binding.

132 s associated with confounding by health-care-seeking behavior and misclassification of cases.

133 novel mu-opioid receptor antagonist, on food-seeking behavior and on binge-like eating of a highly pr

134 pulation, and it influences dental treatment-seeking behavior and oral and systemic health.

135 ical costs, which may influence their health-seeking behavior and potentially affect health outcomes.

136 accumbens (NAc) facilitate conditioned drug-seeking behavior and primarily originate from medial pre

137 e a useful way to encourage appropriate care-seeking behavior and reduce health system surge in epide

138 dolescents exhibit greater levels of novelty-seeking behavior and risk-taking relative to adults, beh

139 Data on health-seeking behavior and school attendance were recorded.

140 eptive neurons is necessary for both novelty-seeking behavior and the abstinence-induced escalation o

141 to consider the motivations for information-seeking behavior and to study it in its ethological cont

142 in adaptive patterns of food consumption and seeking behaviors and a consideration of how these could

143 s as a common molecular substrate of novelty-seeking behaviors and behaviors associated with alcohol

144 ide released into the VTA that promotes drug-seeking behaviors and potentiates excitatory synaptic tr

145 GS6) as a critical regulator of both alcohol-seeking behaviors and the associated cardiac and hepatic

146 blance with reward-seeking behavior, novelty-seeking behavior, and addictive behavior, we hypothesize

147 caine prime-induced reinstatement of cocaine-seeking behavior, and cocaine self-administration using

148 ical symptoms, malaria microscopy, treatment-seeking behavior, and compliance with referral advice we

149 e developed a model of TB transmission, care-seeking behavior, and diagnostic/treatment practices in

150 depression, the propensity to engage in drug-seeking behavior, and drug craving.

151 inil (S-MOD) on nicotine-taking and nicotine-seeking behavior, and mechanisms underlying such actions

152 bias action selection and invigorate reward-seeking behaviors, and appear to do so through distinct

153 Behavioral manifestations of drug-seeking behavior are causally linked to alterations of s

154 ocardial infarction symptoms and timely care-seeking behavior are critical to optimize acute medical

155 Overall, these data suggest that drug-seeking behaviors are, in part, attributable to a DNA me

156 c dopamine neurons, known to promote cocaine-seeking behavior, are strongly inhibited by a newly char

157 ine doses used were capable of inducing drug-seeking behaviors as measured by place preference condit

158 d found the strongest representation of cold-seeking behavior at the ventral border of the dorsomedia

159 hock stress did not by itself reinstate drug-seeking behavior but potentiated reinstatement in respon

160 no immediate effects on cue-induced cocaine-seeking behavior but produced residual effects on a subs

161 ronal activation both increased operant food-seeking behavior, but only activation of LHA (GABA) neur

162 as been shown to negatively regulate cocaine-seeking behavior, but the precise conditions by which vm

163 IL) contributes to the extinction of cocaine-seeking behavior, but the precise relationship among IL

164 ial self-stimulation (ICSS) and other reward-seeking behaviors, but it is not yet known where dopamin

165 150 facilitates the reinstatement of cocaine-seeking behavior by amplifying D1DR/PKA-dependent AMPA t

166 ng new possibility is the extinction of drug-seeking behavior by manipulation of epigenetic mechanism

167 by which mPFC modulates expression of reward-seeking behavior, by regulating the dynamical interactio

168 e role of the LH to VTA projection in reward-seeking behavior can be informed by using optogenetic te

169 Furthermore, drug-seeking behavior continued to require dopamine neurotran

170 The decision to engage in food-seeking behavior depends not only on homeostatic signals

171 ociated cue was sufficient to reinstate drug-seeking behavior, despite the continued presence of the

172 frontal cortex and amygdala regulate alcohol-seeking behaviors differentially, adding to our understa

173 in difficulties in learning to suppress drug-seeking behavior during abstinence.

174 led to long-lasting facilitation of cocaine-seeking behavior during extinction tests conducted after

175 Cocaine-seeking behavior during the first 20 min of the test ses

176 Adolescents demonstrated more reward-seeking behavior during the previously inhibitory Pavlov

177 We hypothesized that alcohol-seeking behavior elicited by a discrete CS that predicte

178 ed for reinstatement of extinguished cocaine-seeking behavior elicited by response-contingent present

179 m memory, increased risk taking and stimulus seeking behavior, enhanced susceptibility to stress and

180 at contributes to the development of alcohol-seeking behavior following a history of dependence.

181 rug context-induced reinstatement of cocaine-seeking behavior following extinction training in an alt

182 xtinguished and spontaneous recovery of drug-seeking behavior following presentation of previously dr

183 We (i) report robust seasonal information-seeking behavior for chicken pox using Google data from

184 ut the role that astrocytes may play in drug-seeking behavior for commonly abused substances.

185 Cocaine can elicit drug-seeking behavior for drug-predicting stimuli, even after

186 ich in turn is associated with improved help-seeking behaviors for symptoms of mental ill-health.

187 ed carcinogen, yet evidence suggests that UV-seeking behavior has addictive features.

188 high levels of novelty-seeking and sensation-seeking behavior have been associated with increased sus

189 in/hypocretin system is important for reward-seeking behaviors, however less is known about its funct

190 lves a new form of learning, reduces cocaine-seeking behavior; however, the molecular mechanisms unde

191 Furthermore, we replicated this entropy-seeking behavior in a control task with no explicit util

192 n shown to facilitate the extinction of drug-seeking behavior in a manner resistant to reinstatement.

193 of palatable food, as well as palatable food-seeking behavior in a second-order schedule of reinforce

194 riming- or cue-induced reinstatement of drug-seeking behavior in abstinent subjects (models of relaps

195 To better model drug-seeking behavior in addicts, we first developed a novel

196 scence increases the risk of relapse to drug-seeking behavior in adulthood.

197 CH23390, dose-dependently attenuated cocaine-seeking behavior in an anatomically selective manner, wi

198 rug context-induced reinstatement of cocaine-seeking behavior in an animal model of drug relapse.

199 t of the analogues successfully reduced drug-seeking behavior in an animal model of drug-relapse with

200 rtex (mPFC) critically contribute to cocaine-seeking behavior in humans and rodents.

201 e exists for a role of dopamine in sensation-seeking behavior in humans.

202 nt, and nicotine-associated cue-induced drug-seeking behavior in P-rats.

203 odel of cue-induced reinstatement of alcohol-seeking behavior in post-dependent Wistar rats and in an

204 hat moderate stress increased social support-seeking behavior in rat cagemates and facilitated long-t

205 We modeled flexible drug-seeking behavior in rats by requiring animals to solve d

206 ng the reinstatement of extinguished cocaine-seeking behavior in rats, demonstrating the potential of

207 erent subregions regulate relapse to cocaine-seeking behavior in rats.

208 y involved in learning to extinguish cocaine-seeking behavior in rats.

209 l target to facilitate extinction of alcohol-seeking behavior in rats.

210 atal addiction circuitry and attenuated drug-seeking behavior in rats.

211 ested whether an estrogen could augment drug-seeking behavior in response to an ordinarily subthresho

212 d basolateral amygdala (BLA) promote cocaine-seeking behavior in response to drug-associated conditio

213 re more likely to promote maladaptive reward-seeking behavior in STs than GTs.

214 work identifies the neural substrate of cold-seeking behavior in systemic inflammation and expands th

215 tion of heat and odor cues likely drive host-seeking behavior in the absence of CO2 detection.

216 n reinstated previously extinguished cocaine-seeking behavior in the absence of footshock.

217 e discrete alcohol CS triggered more alcohol-seeking behavior in the alcohol context than the non-alc

218 uron stimulation is sufficient to drive food-seeking behavior in the continued presence of a competin

219 Here, we analyze a complex food seeking behavior in the nematode Caenorhabditis elegans

220 Naive water-seeking behavior in thirsty flies did not require water

221 ockdown of CeA GluA1 eliminated the morphine-seeking behavior in withdrawn rats of the pain group.

222 d that many of these odorants stimulate host-seeking behaviors in a species-specific manner.

223 cess in both development and relapse of drug-seeking behaviors in drug addiction.

224 As estimates for care-seeking behaviors in LMICs have not been studied, this r

225 question of how these animals modulate food-seeking behaviors in tune with physiological needs.

226 ated subsequent drug context-induced cocaine-seeking behavior, in a memory reactivation-dependent man

227 is a paucity of data regarding newborn care-seeking behaviors; in South Asia, care seeking is low fo

228 ostingestive contact with food, whereas food-seeking behavior independent of food consumption is only

229 ation had no effect on reinstatement of food-seeking behavior induced by cues, a food-prime, or cues+

230 NorBNI did not induce or potentiate cocaine-seeking behavior induced by OrxA but reversed DynA effec

231 ngs suggest that the exploratory and novelty-seeking behaviors induced by dietary fat may be mediated

232 Initiating a reward-seeking behavior involves deciding on an action, how fas

233 ted cold seeking.SIGNIFICANCE STATEMENT Cold-seeking behavior is a life-saving response that occurs i

234 This salt-seeking behavior is also observed when the animal is pre

235 Moreover, yohimbine-induced cocaine-seeking behavior is BNST-dependent.

236 Reward-seeking behavior is fundamental to survival, but suppres

237 circuitry necessary for context-driven salt-seeking behavior is unknown.

238 which stress triggers reinstatement of drug-seeking behaviors is particularly pertinent to nicotine.

239 motor learning, memory formation, and reward-seeking behavior, is a major target of cocaine and metha

240 ficantly inhibits cocaine-taking and cocaine-seeking behavior likely by interfering with cocaine bind

241 function as a likely mechanism for morphine-seeking behavior maintained by long-lasting affective pa

242 Further understanding of stimulation-seeking behavior may shed light on the etiology of psych

243 initiation of multiple components of reward-seeking behavior, most prominently when valid reward-pre

244 osted anticipation significantly drives risk-seeking behaviors, most pertinently in gambling.

245 -like eating) and appetitive (cue-controlled seeking) behavior motivated by chocolate-flavored sucros

246 Cocaine-seeking behavior (non-reinforced active lever pressing)

247 hy consumption bears resemblance with reward-seeking behavior, novelty-seeking behavior, and addictiv

248 We conclude that the nectar-seeking behavior of P. falciparum-infected An. gambiae a

249 We observed decreased drug-seeking behavior on ED1 following 10 mg/kg S-propranolol

250 , mNTS leptin administration suppressed food-seeking behavior only in chronically food-restricted rat

251 xpression and attenuated cue-induced cocaine-seeking behavior only in rats exposed to long withdrawal

252 ncluded estimates of attack rate, healthcare-seeking behavior, prescription rates, adherence, disease

253 .p.) alone were sufficient to reinstate drug-seeking behavior, pretreatment with E2 potentiated reins

254 a conserved role in the regulation of reward-seeking behavior, providing cellular and anatomical iden

255 or-activating effects of cocaine and on drug-seeking behavior, rats receiving methyl supplementation

256 isrupted CS-induced reinstatement of cocaine-seeking behavior relative to (i) no optogenetic inhibiti

257 l BLA disrupted drug context-induced cocaine-seeking behavior relative to vehicle, while independent

258 rug context-induced reinstatement of cocaine-seeking behavior relative to vehicle, without altering i

259 oved preventive health care, and prompt care-seeking behaviors represent important target for this po

260 Relapse to cocaine-seeking behavior requires an increase in nucleus accumbe

261 turn have a positive impact on future health seeking behavior, service utilization and reduction in m

262 acilitate long-lasting extinction of alcohol-seeking behavior.SIGNIFICANCE STATEMENT Alcohol use diso

263 s enhanced learning and promoted information-seeking behaviors; specifically, infants learned more ef

264 ns shell (NAS) has been implicated in reward-seeking behaviors, such as binge eating, which contribut

265 vate-sector treatment patterns, patient care-seeking behavior, symptoms, and infectiousness over time

266 d significantly more exploratory and novelty-seeking behavior than the wild-type mice.

267 ch to facilitate learned suppression of drug-seeking behavior that may aid drug abstinence.

268 esulting in the increase of impulsive reward-seeking behaviors that are often observed during puberty

269 idating the molecular details of vector host-seeking behavior, the susceptibility of disease vectors

270 Although estrogens can enhance drug-seeking behavior, they do not directly induce reinstatem

271 Although such cues may influence drug-seeking behavior through multiple routes, it is their pu

272 ns in the regulation of emotional and reward-seeking behaviors; thus, dysfunctional interactions betw

273 d seasonal cycles in chicken pox information-seeking behavior to VZV vaccine-induced reduction of sea

274 nfective juveniles (IJs) of EPNs employ host-seeking behaviors to locate suitable hosts for infection

275 tive relationships between patient treatment-seeking behavior, treatment coverage, and the effects of

276 Cocaine-seeking behavior triggered by drug-paired environmental

277 , we tested the effects of memantine on food-seeking behavior, under a second-order schedule of reinf

278 caine and prevented reinstatement of cocaine-seeking behavior up to 6 months in rats.

279 IA1, a glutamatergic gene implicated in drug-seeking behavior, verified the increased enrichment of l

280 ent inducers of the reinstatement of cocaine-seeking behavior via activation of multiple adrenergic r

281 Shelter-seeking behavior was decreased by dilbit and conventiona

282 ffect of the introduction of the ADF on drug-seeking behavior was examined.

283 ment, in which a prolonged period of alcohol-seeking behavior was maintained by contingent presentati

284 Shelter-seeking behavior was monitored using digital tracking so

285 bon dioxide (CO2) detection to mosquito host-seeking behavior, we mutated the AaegGr3 gene, a subunit

286 viors, additional experiments examining food-seeking behavior were also conducted.

287 Furthermore, effects of OSU6162 on ethanol seeking behavior were evaluated with the progressive rat

288 orcement, in which prolonged periods of food-seeking behavior were maintained by contingent presentat

289 Cocaine-seeking behaviors were not affected by RO5166017 when mi

290 at the therapeutic target (SERT) and shelter-seeking behavior when fish plasma levels exceeded human

291 NF in extinction memory for fear and cocaine-seeking behaviors, where extinction circuits overlap in

292 Inactivation of the VMHvl reduced aggression-seeking behavior, whereas optogenetic stimulation of the

293 n, and cocaine-induced reinstatement of drug-seeking behavior, whereas R-MOD inhibited cocaine-induce

294 ement in rats trained and tested for sucrose-seeking behavior, whereas rats trained and tested with t

295 ignificantly reduced exploratory and novelty-seeking behaviors, whereas the chow-consuming rats exhib

296 re considerable ingenuity and flexibility in seeking behavior, which, by definition, precludes the de

297 itability of AcbSh neurons, enhances cocaine-seeking behavior while producing depression-like behavio

298 This is the first work to modulate drug-seeking behavior with astrocyte-specific DREADDs.

299 nduced reinstatement of instrumental cocaine-seeking behavior, with a focus on the NACc and on the ba

300 OrxA reinstated cocaine- and SCM-seeking behavior, with a greater effect in cocaine anima