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1 on corticosterone secretion, body weight, or conditioned taste aversion.
2 rs, increased feeding and the formation of a conditioned taste aversion.
3 t due to sickness as icv TTR did not cause a conditioned taste aversion.
4 ves intact the development of a LiCl-induced conditioned taste aversion.
5 itched from "good" to "bad" as occurs during conditioned taste aversion.
6 or memory, since they successfully expressed conditioned taste aversion.
7 rtical lesions had no impact on LiCl-induced conditioned taste aversion.
8 ecreases food intake in rats without causing conditioned taste aversion.
9 epting or avoiding taste stimuli following a conditioned taste aversion.
10 inducing agent used in laboratory studies of conditioned taste aversion.
11 sed with respect to the neural substrates of conditioned taste aversion.
12 e acquisition of latent inhibition (LI) of a conditioned taste aversion.
13 endocrine responses including development of conditioned taste aversion.
14 2, or 4 g/kg) aversive effects as indexed by conditioned taste aversion.
15 duce food intake, induce pica, and produce a conditioned taste aversion.
16 finds as evidence that drugs of abuse induce conditioned taste aversions.
17 depletion, induces pica, and produces robust conditioned taste aversions.
18  two TPN classes are absolutely required for conditioned taste aversion, a learned behavior.
19                          The impairment of a conditioned taste aversion, an established consequence o
20 conditioning, nociception, and extinction of conditioned taste aversion and an appetitive instrumenta
21 e is a correlate or cause of meal satiation, conditioned taste aversion and aversive brain stimulatio
22 C75 administration in two models of illness, conditioned taste aversion and need-induced sodium appet
23                   IC lesions disrupted TPOA, conditioned taste aversion and taste neophobia.
24 ar cortex blocked behavioral expression of a conditioned taste aversion and this was evident not only
25  known to be important in feeding behaviors, conditioned taste aversion, and alarm.
26 ion rate of conditioned fear responses and a conditioned taste aversion as well as enhanced performan
27                        Data gathered using a conditioned taste aversion assay also suggest that, alth
28 levels and enhanced novel taste learning and conditioned taste aversion, but not memory retrieval.
29 ts show more locomotor circling and enhanced conditioned taste aversion compared to male rats.
30                                            A conditioned taste aversion could not be classically cond
31                       After acquisition of a conditioned taste aversion (CTA) against sucrose, intrao
32 g and with reduced sensitivity to MA-induced conditioned taste aversion (CTA) and hypothermia.
33 4 T magnetic field is sufficient to induce a conditioned taste aversion (CTA) and induce brainstem ex
34 ite following sodium depletion, and a normal conditioned taste aversion (CTA) for alanine when paired
35 basolateral complex (BLA) of the amygdala on conditioned taste aversion (CTA) in a latent inhibition
36 arabrachial nuclei (PBN) failed to acquire a conditioned taste aversion (CTA) in Experiment 1.
37                                 Here, we use conditioned taste aversion (CTA) in rats, a cortically d
38 rsion-associated brain areas and to induce a conditioned taste aversion (CTA) in these strains is unk
39 rabrachial nucleus (PBN) failed to acquire a conditioned taste aversion (CTA) induced by lithium chlo
40                                              Conditioned taste aversion (CTA) is a form of one-trial
41                                              Conditioned taste aversion (CTA) is a phenomenon in whic
42                                            A conditioned taste aversion (CTA) is acquired when an ani
43                                              Conditioned taste aversion (CTA) is an associative learn
44 ctivity) when spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced.
45                                              Conditioned taste aversion (CTA) learning is a robust fo
46                                              Conditioned taste aversion (CTA) learning occurs after t
47                                      We used conditioned taste aversion (CTA) learning, a form of ass
48                                              Conditioned taste aversion (CTA) learning, in which anim
49 tein kinase A (PKA) activity interferes with conditioned taste aversion (CTA) memories.
50 olden hamsters (Mesocricetus auratus) with a conditioned taste aversion (CTA) paradigm.
51 ar cortex, is widely regarded as integral to conditioned taste aversion (CTA) retention, a link that
52 emory in choice-based versus no-choice-based conditioned taste aversion (CTA) tasks in rats.
53      PBN lesion efficacy was confirmed using conditioned taste aversion (CTA) tests.
54 srupt retention of a preoperatively acquired conditioned taste aversion (CTA) to 0.3 M alanine.
55 nol-induced (1.5 g kg(-1) 20% ethanol, i.p.) conditioned taste aversion (CTA) to saccharin taste.
56 ecutive days prior to the establishment of a conditioned taste aversion (CTA) to saccharin.
57 perant task before and after ethanol-induced conditioned taste aversion (CTA) to saccharin.
58 linergic agonist, was infused into IC before conditioned taste aversion (CTA) training with a familia
59 tently as a correlate of the expression of a conditioned taste aversion (CTA) when conditioning occur
60 Paraquat is a herbicide capable of eliciting conditioned taste aversion (CTA), a behavioral response
61 both strains readily acquired a LiCl-induced conditioned taste aversion (CTA), the suppressive effect
62  chloride (LiCl) caused the development of a conditioned taste aversion (CTA), which rendered the typ
63 gastric malaise, a form of learning known as conditioned taste aversion (CTA).
64  correlate of the behavioral expression of a conditioned taste aversion (CTA).
65 ly reinforcing drugs of abuse also support a conditioned taste aversion (CTA).
66 cquisition and/or behavioral expression of a conditioned taste aversion (CTA).
67  as a consequence of retrieval of an ethanol-conditioned taste aversion (CTA).
68 ow IL neurons process devalued sucrose using conditioned taste aversion (CTA).
69  insular cortical memory representations for conditioned taste aversion (CTA).
70 uring training in a one-trial learning task, conditioned taste aversion (CTA).
71 tion of a contextually reactivated memory of conditioned taste aversion (CTA).
72 ex (mPFC) is involved in the extinction of a conditioned taste aversion (CTA).
73 g acquisition and throughout extinction of a conditioned taste aversion (CTA).
74 uces symptoms of visceral illness, such as a conditioned taste aversion (CTA).
75 of EtOH- and lithium chloride (LiCl)-induced conditioned taste aversion (CTA).
76 of neurons activated following expression of conditioned taste aversion (CTA).
77 e correlated with behavioral expression of a conditioned taste aversion (CTA).
78 actors, and implicated in the development of conditioned taste aversion (CTA).
79 arned to dislike the taste of saccharin [via conditioned taste aversion (CTA)].
80 ], low drinking [STDRLO]) or ethanol-induced conditioned taste aversion (CTA; high [HTA], low [LTA]).
81                                              Conditioned taste aversions (CTA) based on lithium chlor
82 t such as lithium chloride (referred to as a conditioned taste aversion, CTA); (2) access to a very p
83 he effects of permanent forebrain lesions on conditioned taste aversions (CTAs) and conditioned odor
84 postrema (AP) lesions attenuate LiCl-induced conditioned taste aversions (CTAs) by disruption of info
85 ral role in the acquisition and retention of conditioned taste aversions (CTAs) in rodents, but large
86                                              Conditioned taste aversions (CTAs) may be acquired when
87 nsected chorda tympani nerves (CTX) received conditioned taste aversions (CTAs) to the free fatty aci
88 insular cortex (IC) attenuate acquisition of conditioned taste aversions (CTAs).
89           Behavioral experiments testing for conditioned taste aversion did not confirm that SEB chal
90 acterized the acquisition of ethanol-induced conditioned taste aversion, ethanol-induced conditioned
91 ehaviours, including active place avoidance, conditioned taste aversion, fear conditioning and spatia
92 e of the taste cue has been interpreted as a conditioned taste aversion for decades.
93 ediating associative taste learning, such as conditioned taste aversion, has been well studied.
94 ve induces locomotor circling and leads to a conditioned taste aversion if paired with a novel taste.
95 ith a saccharin taste developed a persistent conditioned taste aversion in both preference and taste
96 ering food intake, body weight, or causing a conditioned taste aversion in mice lacking neuronal GLP1
97        The significance of these findings to conditioned taste aversion is discussed.
98 driven by release of cholecystokinin whereas conditioned taste aversion is mediated by serotonin and
99 he basolateral amygdala (BLA) in response to conditioned taste aversion is necessary to form a memory
100 Here we address this issue in the context of conditioned taste aversion learning by continuously trac
101                                Here, we used conditioned taste aversion learning in the rat model, wh
102                            NaB also enhanced conditioned taste aversion learning induced by pairing s
103 vidly were trained first to reject it (i.e., conditioned taste aversion learning) and then to enjoy i
104 high EtOH withdrawal with low drinking, high conditioned taste aversion, low tolerance to EtOH-induce
105 r potency and did not promote formation of a conditioned taste aversion (malaise-like behavior).
106 srupts spatial memory in the hippocampus and conditioned taste aversion memory in the insular cortex.
107 nsumption with LiCl injection, by making the conditioned taste aversion more resistant to extinction.
108  instrumental training procedures and either conditioned taste aversion or satiation devaluation proc
109 e neuronal substrates of LI as assessed in a conditioned taste aversion paradigm by comparing regiona
110 versive impact of sucrose devalued using the conditioned taste aversion paradigm in males and female
111 n the present study we subjected mice to the conditioned taste aversion paradigm, where animals learn
112 on latent inhibition (LI) were assessed in a conditioned taste aversion paradigm.
113                          Experiment 2 used a conditioned taste-aversion procedure to establish that r
114 reas lithium chloride, at doses that produce conditioned taste aversion, reduced metabolic rate.
115 and show a delay in extinguishing an ethanol-conditioned taste aversion, suggesting that they drink l
116 nsitivity (experiment 4) or consumption on a conditioned taste aversion test that does not elicit ant
117                                            A conditioned taste aversion test was performed to assess
118              Ethanol produced dose-dependent conditioned taste aversion that was the same in both gen
119 pani nerve transection (CTX) acquired a LiCl-conditioned taste aversion to 0.1 M NaCl at the same rat
120 core administration of GLP-1 did not cause a conditioned taste aversion to saccharin, suggesting that
121 of an ingestate was confirmed in rats with a conditioned taste aversion to sucrose: after paired expo
122                       The ability to acquire conditioned taste aversion was also assessed.
123 ar cortex in acquisition and expression of a conditioned taste aversion was assessed using two differ
124 However, LiCl can induce memory given that a conditioned taste aversion was obtained for a novel tast
125  correlate of the behavioral expression of a conditioned taste aversion, was also assessed.
126                                              Conditioned taste aversion, which also depends on the am

 
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