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1 sponses including development of conditioned taste aversion.
2 ) aversive effects as indexed by conditioned taste aversion.
3 take, induce pica, and produce a conditioned taste aversion.
4 d feeding and the formation of a conditioned taste aversion.
5 erone secretion, body weight, or conditioned taste aversion.
6 kness as icv TTR did not cause a conditioned taste aversion.
7 choice behavior when it was guided by innate taste aversion.
8 he development of a LiCl-induced conditioned taste aversion.
9 "good" to "bad" as occurs during conditioned taste aversion.
10 ince they successfully expressed conditioned taste aversion.
11 ns had no impact on LiCl-induced conditioned taste aversion.
12 d intake in rats without causing conditioned taste aversion.
13 oiding taste stimuli following a conditioned taste aversion.
14 nt used in laboratory studies of conditioned taste aversion.
15 pect to the neural substrates of conditioned taste aversion.
16 n of latent inhibition (LI) of a conditioned taste aversion.
17 tive to each monotherapy, without inducing a taste aversion.
18 nduces pica, and produces robust conditioned taste aversions.
19 dence that drugs of abuse induce conditioned taste aversions.
20 sses are absolutely required for conditioned taste aversion, a learned behavior.
21              The impairment of a conditioned taste aversion, an established consequence of PBN damage
22 , nociception, and extinction of conditioned taste aversion and an appetitive instrumental response.
23 late or cause of meal satiation, conditioned taste aversion and aversive brain stimulation.
24 t genetic correlations were observed between taste aversion and ethanol-related behaviors measured in
25            Substantial strain differences in taste aversion and hypothermia were observed, but the ge
26 ration in two models of illness, conditioned taste aversion and need-induced sodium appetite.
27       IC lesions disrupted TPOA, conditioned taste aversion and taste neophobia.
28 ocked behavioral expression of a conditioned taste aversion and this was evident not only when lesion
29              Careful scrutiny of research on taste-aversion and fear learning, language, and imitatio
30  important in feeding behaviors, conditioned taste aversion, and alarm.
31 conditioned fear responses and a conditioned taste aversion as well as enhanced performance in an att
32            Data gathered using a conditioned taste aversion assay also suggest that, although qualita
33  of GLP-1 receptors mediate the anorexia and taste aversion associated with GLP-1 administration.
34 atability, the current results indicate that taste aversions based on either lithium or activity redu
35 nhanced novel taste learning and conditioned taste aversion, but not memory retrieval.
36 f paraquat at a dose sufficient to condition taste aversion, but produce no other signs of overt toxi
37  locomotor circling and enhanced conditioned taste aversion compared to male rats.
38 d that amygdala was absolutely necessary for taste aversions conditioned with the intraoral method bu
39 ted aversions and the role of the context in taste aversion conditioning are discussed.
40                                    Following taste aversion conditioning to NaCl, neoCTX rats clearly
41 strongly modulates the speed and strength of taste aversion conditioning.
42 was then accomplished in 1 group by inducing taste aversion; controls received either saline or unpai
43                                A conditioned taste aversion could not be classically conditioned to s
44           After acquisition of a conditioned taste aversion (CTA) against sucrose, intraoral infusion
45 educed sensitivity to MA-induced conditioned taste aversion (CTA) and hypothermia.
46  field is sufficient to induce a conditioned taste aversion (CTA) and induce brainstem expression of
47 g sodium depletion, and a normal conditioned taste aversion (CTA) for alanine when paired with lithiu
48 complex (BLA) of the amygdala on conditioned taste aversion (CTA) in a latent inhibition design.
49 nuclei (PBN) failed to acquire a conditioned taste aversion (CTA) in Experiment 1.
50                     Here, we use conditioned taste aversion (CTA) in rats, a cortically dependent lea
51 ated brain areas and to induce a conditioned taste aversion (CTA) in these strains is unknown.
52 ucleus (PBN) failed to acquire a conditioned taste aversion (CTA) induced by lithium chloride (LiCl)
53                                  Conditioned taste aversion (CTA) is a form of one-trial learning dep
54                                  Conditioned taste aversion (CTA) is a phenomenon in which an individ
55                                A conditioned taste aversion (CTA) is acquired when an animal consumes
56                                  Conditioned taste aversion (CTA) is an associative learning paradigm
57 n spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced.
58                                  Conditioned taste aversion (CTA) learning is a robust form of classi
59                                  Conditioned taste aversion (CTA) learning occurs after the pairing o
60                          We used conditioned taste aversion (CTA) learning, a form of associative lea
61                                  Conditioned taste aversion (CTA) learning, in which animals associat
62 A (PKA) activity interferes with conditioned taste aversion (CTA) memories.
63 rs (Mesocricetus auratus) with a conditioned taste aversion (CTA) paradigm.
64 s widely regarded as integral to conditioned taste aversion (CTA) retention, a link that has been pri
65 ice-based versus no-choice-based conditioned taste aversion (CTA) tasks in rats.
66 ion efficacy was confirmed using conditioned taste aversion (CTA) tests.
67 ion of a preoperatively acquired conditioned taste aversion (CTA) to 0.3 M alanine.
68 (1.5 g kg(-1) 20% ethanol, i.p.) conditioned taste aversion (CTA) to saccharin taste.
69 before and after ethanol-induced conditioned taste aversion (CTA) to saccharin.
70  prior to the establishment of a conditioned taste aversion (CTA) to saccharin.
71 nist, was infused into IC before conditioned taste aversion (CTA) training with a familiar taste.
72 correlate of the expression of a conditioned taste aversion (CTA) when conditioning occurs using tast
73 a herbicide capable of eliciting conditioned taste aversion (CTA), a behavioral response characterist
74  readily acquired a LiCl-induced conditioned taste aversion (CTA), the suppressive effects of sucrose
75 iCl) caused the development of a conditioned taste aversion (CTA), which rendered the typically rewar
76 s of visceral illness, such as a conditioned taste aversion (CTA).
77  lithium chloride (LiCl)-induced conditioned taste aversion (CTA).
78 ctivated following expression of conditioned taste aversion (CTA).
79  with behavioral expression of a conditioned taste aversion (CTA).
80 implicated in the development of conditioned taste aversion (CTA).
81 f the behavioral expression of a conditioned taste aversion (CTA).
82 ng drugs of abuse also support a conditioned taste aversion (CTA).
83 nd/or behavioral expression of a conditioned taste aversion (CTA).
84 uence of retrieval of an ethanol-conditioned taste aversion (CTA).
85 s process devalued sucrose using conditioned taste aversion (CTA).
86 tical memory representations for conditioned taste aversion (CTA).
87 ise, a form of learning known as conditioned taste aversion (CTA).
88 ng in a one-trial learning task, conditioned taste aversion (CTA).
89 ntextually reactivated memory of conditioned taste aversion (CTA).
90  involved in the extinction of a conditioned taste aversion (CTA).
91 n and throughout extinction of a conditioned taste aversion (CTA).
92 like the taste of saccharin [via conditioned taste aversion (CTA)].
93 ing [STDRLO]) or ethanol-induced conditioned taste aversion (CTA; high [HTA], low [LTA]).
94                                  Conditioned taste aversions (CTA) based on lithium chloride (Experim
95 thium chloride (referred to as a conditioned taste aversion, CTA); (2) access to a very palatable con
96 f permanent forebrain lesions on conditioned taste aversions (CTAs) and conditioned odor aversions (C
97 ) lesions attenuate LiCl-induced conditioned taste aversions (CTAs) by disruption of information abou
98 the acquisition and retention of conditioned taste aversions (CTAs) in rodents, but large lesions in
99                                  Conditioned taste aversions (CTAs) may be acquired when an animal co
100 da tympani nerves (CTX) received conditioned taste aversions (CTAs) to the free fatty acids (FFAs), l
101 ex (IC) attenuate acquisition of conditioned taste aversions (CTAs).
102       A new study finds that, in Drosophila, taste aversion depends on the immune system and the mush
103 havioral experiments testing for conditioned taste aversion did not confirm that SEB challenge promot
104 e acquisition of ethanol-induced conditioned taste aversion, ethanol-induced conditioned place prefer
105 ncluding active place avoidance, conditioned taste aversion, fear conditioning and spatial learning.
106 te cue has been interpreted as a conditioned taste aversion for decades.
107 ociative taste learning, such as conditioned taste aversion, has been well studied.
108 ocomotor circling and leads to a conditioned taste aversion if paired with a novel taste.
109 rin taste developed a persistent conditioned taste aversion in both preference and taste reactivity t
110 ntake, body weight, or causing a conditioned taste aversion in mice lacking neuronal GLP1R.
111 tinction tests revealed rapid attenuation of taste aversions in all of the LiCl-injected groups.
112 parabrachial nucleus (PBN) failed to learn a taste aversion induced by lithium chloride (LiCl) toxico
113 ignificance of these findings to conditioned taste aversion is discussed.
114 lease of cholecystokinin whereas conditioned taste aversion is mediated by serotonin and substance P.
115  support the hypothesis that ethanol-induced taste aversion is mediated by the drug's rewarding prope
116 al amygdala (BLA) in response to conditioned taste aversion is necessary to form a memory for a taste
117 e basolateral amygdala (BLA) is critical for taste aversion learning and retrieval, suggesting this c
118 e GI tract suggests a new account of delayed taste aversion learning as well as learning about the po
119 ess this issue in the context of conditioned taste aversion learning by continuously tracking gustato
120                    Here, we used conditioned taste aversion learning in the rat model, wherein animal
121  the light CS in the first training phase or taste aversion learning in the second training phase.
122 hat have been shown to generate differential taste aversion learning in these strains.
123                NaB also enhanced conditioned taste aversion learning induced by pairing saccharin con
124 H3, c-Fos induction, and amygdalar-dependent taste aversion learning is constrained by endogenous his
125 r cortex, but also failed to induce stronger taste aversion learning than familiar Polycose.
126                                              Taste aversion learning thus may more properly be termed
127 rained first to reject it (i.e., conditioned taste aversion learning) and then to enjoy it again (i.e
128 itioning represents a molecular correlate of taste aversion learning, i.e. the formerly neutral CS no
129  details of the neural circuitry involved in taste aversion learning, including its anatomical distri
130 te a direct role for amygdalocortical LTD in taste aversion learning.
131 la (CNA), regions thought to be important in taste aversion learning.
132 l structure in transduction of the US during taste aversion learning.
133  strongly modulate the speed and efficacy of taste aversion learning.
134 iliar tastes as conditioned stimuli (CSs) in taste aversion learning.
135 thdrawal with low drinking, high conditioned taste aversion, low tolerance to EtOH-induced hypothermi
136 d did not promote formation of a conditioned taste aversion (malaise-like behavior).
137 abe and rural Latino Panamanians to study if taste aversion may be a limiting factor in chlorination
138 egulates ingestive behavior without inducing taste aversion may open the possibility of a therapeutic
139 al memory in the hippocampus and conditioned taste aversion memory in the insular cortex.
140 lso attenuated the extinction of established taste aversion memory without altering the initial assoc
141  that this is dissociable from AIC-dependent taste aversion memory.
142 e from the adjacent insular cortex-dependent taste aversion memory.
143 th LiCl injection, by making the conditioned taste aversion more resistant to extinction.
144  geosmin in sucrose solution does not elicit taste aversion or reduce consumption.
145 l training procedures and either conditioned taste aversion or satiation devaluation procedures.
146 ubstrates of LI as assessed in a conditioned taste aversion paradigm by comparing regional c-Fos acti
147                               The intestinal taste aversion paradigm has previously demonstrated that
148 ct of sucrose devalued using the conditioned taste aversion paradigm in males and female rats.
149 t study we subjected mice to the conditioned taste aversion paradigm, where animals learn to associat
150 hibition (LI) were assessed in a conditioned taste aversion paradigm.
151              Experiment 2 used a conditioned taste-aversion procedure to establish that rats with IBO
152  chloride, at doses that produce conditioned taste aversion, reduced metabolic rate.
153 elay in extinguishing an ethanol-conditioned taste aversion, suggesting that they drink less ethanol
154                     Strains showing stronger taste aversion tended to show lower ethanol preference a
155 xperiment 4) or consumption on a conditioned taste aversion test that does not elicit antipredator re
156                                A conditioned taste aversion test was performed to assess whether proa
157  Ethanol produced dose-dependent conditioned taste aversion that was the same in both genotypes.
158 ransection (CTX) acquired a LiCl-conditioned taste aversion to 0.1 M NaCl at the same rate as control
159                               Fed flies show taste aversion to acetic acid, whereas starved flies sho
160 hila and report that the fly displays strong taste aversion to common carboxylic acids.
161 lued the food unconditioned stimulus (US) by taste aversion to differentiate stimulus-stimulus(CS-US)
162 tration of GLP-1 did not cause a conditioned taste aversion to saccharin, suggesting that the anorexi
163 ate was confirmed in rats with a conditioned taste aversion to sucrose: after paired exposure to sucr
164  the reinforcer after training by inducing a taste aversion to the food.
165           The ability to acquire conditioned taste aversion was also assessed.
166  acquisition and expression of a conditioned taste aversion was assessed using two different conditio
167                         In contrast, after a taste aversion was conditioned to 150-mM NaCl, estrogen-
168 l can induce memory given that a conditioned taste aversion was obtained for a novel taste, presented
169 f the behavioral expression of a conditioned taste aversion, was also assessed.
170                                  Conditioned taste aversion, which also depends on the amygdala, is n
171 y pairing it with lithium chloride (acquired taste aversion), while the other distinctive flavor was

 
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