ライフサイエンスコーパス: seeking behavior

1 until some individuals developed compulsive seeking behavior.

2 gion that controls the expression of cocaine-seeking behavior.

3 uch as ethanol, can trigger craving and drug-seeking behavior.

4 te or pathogen, the host may respond by cold-seeking behavior.

5 ic valuation systems, in driving information-seeking behavior.

6 n information and motivates this information-seeking behavior.

7 xual context appears to enhance further drug-seeking behavior.

8 pecific ALDH2 inhibition can prevent alcohol-seeking behavior.

9 he released glutamate from synapses and drug seeking behavior.

10 ocognitive mechanisms underlying information-seeking behavior.

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

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

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

14 d forebrain nuclei known to regulate cocaine-seeking behavior.

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

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

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

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

19 mechanisms underlying extinction of cocaine-seeking behavior.

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

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

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

23 educed responding under simpler schedules of seeking behavior.

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

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

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

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

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

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

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

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

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

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

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

35 extinction sessions showed increased cocaine-seeking behavior.

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

37 resentation of punishment risk during reward-seeking behavior.

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

39 innervation that mediate noncompulsive food-seeking behavior.

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

41 ne, and it facilitated extinction of cocaine-seeking behavior.

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

43 oned responses and control compulsive reward-seeking behavior.

44 lie contextual stimulus control over cocaine-seeking behavior.

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

46 ntly dampened seasonal cycles in information-seeking behavior.

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

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

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

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

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

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

53 rovement is necessary to induce intervention-seeking behavior.

54 icothalamic projections did not alter heroin-seeking behavior.

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

56 icotine nor reinstated extinguished nicotine-seeking behavior.

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

58 ifting from habitual to goal-directed reward-seeking behavior.

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

60 onserved neuromodulator that stimulates food-seeking behavior.

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

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

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

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

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

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

67 increased palatable food preference and food-seeking behavior.

68 mine invigorates environmentally cued reward-seeking behavior.

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

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

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

72 built through experience that are linked to seeking behavior.

73 ganglia region functionally linked to reward-seeking behavior.

74 mportant real-time insights into health-care seeking behavior.

75 ble rates of responding and conditioned drug-seeking behavior.

76 tinx participants' knowledge and information-seeking behavior.

77 irectionally altered rats' subsequent reward-seeking behavior.

78 inhibition of this circuit potentiates food-seeking behavior.

79 rug context-induced reinstatement of cocaine-seeking behavior.

80 rons orchestrate glucoprivation-induced food seeking behavior.

81 chanisms that give rise to aberrant cannabis-seeking behavior.

82 n the nucleus accumbens, and reduced cocaine-seeking behavior.

83 or the acquisition of cue-controlled cocaine-seeking behavior.

84 lopment and persistence of compulsive opioid-seeking behavior.

85 which were effective in attenuating cocaine-seeking behavior.

86 ed reinstatement of cocaine- but not sucrose-seeking behavior.

87 relevant inputs to accurately inform reward-seeking behavior.

88 aversive stimuli and plays a role in ethanol-seeking behavior.

89 subsequent development of compulsive alcohol-seeking behavior.

90 s "novelty-seeking" predicts compulsive drug-seeking behavior.

91 on responding and reinstatement of oxycodone-seeking behavior.

92 as been implicated in stress-induced alcohol seeking behavior.

93 pective community screenings, and healthcare seeking behaviors.

94 primary and non-redundant role in human host-seeking behaviors.

95 oped either habitual or goal-directed reward-seeking behaviors.

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

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

98 nfluence motivational states and elicit food-seeking behaviors.

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

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

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

102 c disorders associated with abnormal novelty-seeking behaviors.

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

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

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

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

107 standing the neural basis of mosquito nectar-seeking behaviors.

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

109 ty of postingestive signals to modulate food-seeking behaviors.

110 aptive plasticity that drives food- and drug-seeking behaviors.

111 ism by which VTA activity can support reward-seeking behaviors.

112 dministration and reduce cue-induced cocaine-seeking behaviors.

113 ABA neurons facilitates adaptation in reward-seeking behaviors.

114 xperience-dependent neuroplasticity and drug-seeking behaviors.

115 with the potential to reduce drug craving or seeking behaviors.

116 d insulin secretion, food intake, and reward-seeking behaviors.

117 motivational properties and initiate reward-seeking behaviors.

118 ng that disinhibiting iMSNs decreases reward-seeking behaviors.

119 cocaine-conditioned cues and relapse to drug seeking behaviors.

120 rticipates in learning of conditioned reward-seeking behaviors.

121 somedial striatum (DMS) contribute to reward-seeking behaviors.

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

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

124 idation reduced drug context-induced cocaine-seeking behavior 3 d, but not three weeks, later.

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

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

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

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

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

130 sequent enhanced locomotor response and drug seeking behavior after repeated cocaine administration.

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

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

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

134 l area (VTA) in the reinstatement of cocaine-seeking behavior, an animal model of relapse.

135 rons prevented cues from invigorating reward-seeking behavior, an effect that was mediated by activat

136 mulus-control over both drug taking and drug seeking behavior and are difficult to extinguish.

137 Drug seeking behavior and chronic drug use are associated wit

138 d efficiently protects the mice from cocaine-seeking behavior and cocaine overdose.

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

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

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

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

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

144 We examined changes in healthcare seeking behavior and outputs for sick-child care among c

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

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

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

148 of exendin-4 that reduced opioid-taking and -seeking behaviors and did not produce adverse feeding ef

149 tion includes the evolution of enhanced food seeking behaviors and loss of defensive responses.

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

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

152 ated education effort can improve transplant-seeking behaviors and waitlisting rates.

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

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

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

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

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

158 essive effects of GLP-1R agonists on cocaine-seeking behavior are largely unknown.

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

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

161 (1) subsequent drug context-induced cocaine-seeking behavior as well as (2) cellular adaptations and

162 Cues can also promote dysfunctional reward-seeking behavior, as in overeating.

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

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

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

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

167 150 facilitates the reinstatement of cocaine-seeking behavior by amplifying D1DR/PKA-dependent AMPA t

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

169 Biases in such information-seeking behavior can contribute to the maintenance of in

170 displayed a significant reduction in cocaine-seeking behavior compared to rats housed in isolation.

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

172 ncrease in serum osmolality reinstates water-seeking behavior, demonstrating preservation of the phys

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

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

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

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

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

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

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

180 ry 2017 and February 2019, to ascertain care-seeking behavior for individuals with 1) fever for >=3 c

181 tum (DMS) in regulating goal-directed reward-seeking behavior has been long appreciated.

182 The influence of social cues on drug-seeking behavior has garnered attention recently, but fe

183 ng the acquisition of cue-controlled cocaine-seeking behavior have not been elucidated.

184 iated contextual memories can reduce cocaine-seeking behavior, however the molecular mechanisms withi

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

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

187 In a GWAS meta-analysis of sun-seeking behavior in 261,915 subjects of European ancestr

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

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

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

191 ch conditioned stimuli (CS) can guide reward-seeking behavior in adaptive (e.g., locating food) and m

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

193 where Fos expression correlated with alcohol seeking behavior in Context B after prolonged abstinence

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

195 Here we show that information-seeking behavior in humans is driven by subjective value

196 vey was administered to ascertain healthcare-seeking behavior in individuals with recent suspected en

197 , 90, and 120 mg/kg) were used to assess the seeking behavior in mice.

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

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

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

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

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

203 owed an insignificant attenuation of cocaine seeking behavior in rats, most likely due to its limited

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

205 itazone reduces alcohol drinking and alcohol-seeking behavior in rats.

206 istration and the reinstatement of oxycodone-seeking behavior in rats.

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

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

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

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

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

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

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

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

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

216 s a robust intervention for reducing cocaine-seeking behaviors in animals when given during forced ab

217 nd significantly reduced cue-induced cocaine-seeking behaviors in rats.

218 through monitoring the real-time information-seeking behaviors in the search engine queries, which ar

219 The target article addresses increased food-seeking behaviors in times of instability, particularly

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

221 well balanced for all covariates and health-seeking behavior indicators.

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

223 Synaptic plasticity and seeking behavior induced by drug-paired cues depends not

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

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

226 Habitual reward-seeking behavior is a hallmark of addictive behavior.

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

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

229 Therefore, cold-seeking behavior is beneficial to F. occidentalis when i

230 ces of excessive sun exposure, modifying sun-seeking behavior is challenging because it appears to be

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

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

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

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

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

236 ade of MORs in the VTA counteracted two drug-seeking behaviors, locomotor activity and place preferen

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

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

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

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

241 -19 symptoms and prevention) and information-seeking behavior (number of web links demanded out of 10

242 is manuscript, we summarized the health-care seeking behavior of FNY participants who reported influe

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

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

245 T2) neurons have contrasting effects on drug-seeking behavior, our data may indicate a complex role f

246 he large apparent increases observed in care seeking behavior, particularly for antenatal care, refle

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

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

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

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

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

252 urst and an increase in cue-induced cannabis-seeking behavior relative to VEH.

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

254 However, those roles for ethanol-seeking behaviors remain unknown.

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

256 designer drugs) during a variety of cocaine-seeking behaviors, revealing nuanced, pathway-specific r

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

258 and iMSNs regulate ethanol-containing reward-seeking behaviors.SIGNIFICANCE STATEMENT Our findings hi

259 t of volitional cannabis intake and cannabis-seeking behaviors.SIGNIFICANCE STATEMENT The evolving le

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

261 This cold-seeking behavior suppressed the growth of B. bassiana in

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

263 incentive salience attribution and sensation-seeking behavior that were not previously apparent.

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

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

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

267 ability of METH-associated memories and METH-seeking behavior to NMII inhibition within the BLA.

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

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

270 strumental- and non-instrumental information seeking behaviors to resolve uncertainty about future ou

271 The amplification of reward-seeking behavior under uncertainty described by Anselme

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

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

274 sition from habitual to goal-directed reward-seeking behaviors upon astrocyte activation, while resto

275 lters the ethanol-containing reward (10E10S) seeking behaviors using the combination of pharmacologic

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

277 d hyperkatifeia, which drive pronounced drug-seeking behavior via processes of negative reinforcement

278 Shelter-seeking behavior was decreased by dilbit and conventiona

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

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

281 e from cocaine self-administration, and drug seeking behavior was measured.

282 However, drug-seeking behavior was significantly higher in concurrent

283 ing responses for alcohol; (2) after alcohol-seeking behavior was well established; and (3) after the

284 tly established models of opioid-taking and -seeking behaviors, we showed that systemic administratio

285 To investigate ethanol-seeking behaviors, we used an ethanol-containing reward

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

287 Next, drug-seeking behaviors were measured during cue reactivity, e

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

289 ork also plays a key role in adapting reward-seeking behavior when the contingencies linked to a cue

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

291 , but not cue-induced, reinstatement of drug-seeking behavior, whereas inhibition of SNr GABA neurons

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

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

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

297 stigated the role of glutamate in pregabalin-seeking behavior with ceftriaxone (CEF), a potent GLT-1

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

299 aby's bedside as a driver of maternal health-seeking behaviors, with women not seeking or delaying me

300 istration and the reinstatement of oxycodone-seeking behavior without affecting ad libitum food intak