ライフサイエンスコーパス: taste aversion

1 take, induce pica, and produce a conditioned taste aversion.

2 d feeding and the formation of a conditioned taste aversion.

3 he development of a LiCl-induced conditioned taste aversion.

4 erone secretion, body weight, or conditioned taste aversion.

5 "good" to "bad" as occurs during conditioned taste aversion.

6 ince they successfully expressed conditioned taste aversion.

7 ns had no impact on LiCl-induced conditioned taste aversion.

8 d intake in rats without causing conditioned taste aversion.

9 oiding taste stimuli following a conditioned taste aversion.

10 nt used in laboratory studies of conditioned taste aversion.

11 pect to the neural substrates of conditioned taste aversion.

12 n of latent inhibition (LI) of a conditioned taste aversion.

13 kness as icv TTR did not cause a conditioned taste aversion.

14 choice behavior when it was guided by innate taste aversion.

15 sponses including development of conditioned taste aversion.

16 ) aversive effects as indexed by conditioned taste aversion.

17 nduces pica, and produces robust conditioned taste aversions.

18 dence that drugs of abuse induce conditioned taste aversions.

19 sses are absolutely required for conditioned taste aversion, a learned behavior.

20 The impairment of a conditioned taste aversion, an established consequence of PBN damage

21 , nociception, and extinction of conditioned taste aversion and an appetitive instrumental response.

22 late or cause of meal satiation, conditioned taste aversion and aversive brain stimulation.

23 t genetic correlations were observed between taste aversion and ethanol-related behaviors measured in

24 Substantial strain differences in taste aversion and hypothermia were observed, but the ge

25 ration in two models of illness, conditioned taste aversion and need-induced sodium appetite.

26 IC lesions disrupted TPOA, conditioned taste aversion and taste neophobia.

27 ocked behavioral expression of a conditioned taste aversion and this was evident not only when lesion

28 conditioned fear responses and a conditioned taste aversion as well as enhanced performance in an att

29 Data gathered using a conditioned taste aversion assay also suggest that, although qualita

30 of GLP-1 receptors mediate the anorexia and taste aversion associated with GLP-1 administration.

31 atability, the current results indicate that taste aversions based on either lithium or activity redu

32 nhanced novel taste learning and conditioned taste aversion, but not memory retrieval.

33 f paraquat at a dose sufficient to condition taste aversion, but produce no other signs of overt toxi

34 locomotor circling and enhanced conditioned taste aversion compared to male rats.

35 d that amygdala was absolutely necessary for taste aversions conditioned with the intraoral method bu

36 ted aversions and the role of the context in taste aversion conditioning are discussed.

37 Following taste aversion conditioning to NaCl, neoCTX rats clearly

38 strongly modulates the speed and strength of taste aversion conditioning.

39 was then accomplished in 1 group by inducing taste aversion; controls received either saline or unpai

40 A conditioned taste aversion could not be classically conditioned to s

41 After acquisition of a conditioned taste aversion (CTA) against sucrose, intraoral infusion

42 educed sensitivity to MA-induced conditioned taste aversion (CTA) and hypothermia.

43 field is sufficient to induce a conditioned taste aversion (CTA) and induce brainstem expression of

44 g sodium depletion, and a normal conditioned taste aversion (CTA) for alanine when paired with lithiu

45 complex (BLA) of the amygdala on conditioned taste aversion (CTA) in a latent inhibition design.

46 nuclei (PBN) failed to acquire a conditioned taste aversion (CTA) in Experiment 1.

47 Here, we use conditioned taste aversion (CTA) in rats, a cortically dependent lea

48 ated brain areas and to induce a conditioned taste aversion (CTA) in these strains is unknown.

49 ucleus (PBN) failed to acquire a conditioned taste aversion (CTA) induced by lithium chloride (LiCl)

50 Conditioned taste aversion (CTA) is a phenomenon in which an individ

51 A conditioned taste aversion (CTA) is acquired when an animal consumes

52 n spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced.

53 Conditioned taste aversion (CTA) learning is a robust form of classi

54 Conditioned taste aversion (CTA) learning occurs after the pairing o

55 Conditioned taste aversion (CTA) learning, in which animals associat

56 A (PKA) activity interferes with conditioned taste aversion (CTA) memories.

57 rs (Mesocricetus auratus) with a conditioned taste aversion (CTA) paradigm.

58 s widely regarded as integral to conditioned taste aversion (CTA) retention, a link that has been pri

59 ice-based versus no-choice-based conditioned taste aversion (CTA) tasks in rats.

60 ion efficacy was confirmed using conditioned taste aversion (CTA) tests.

61 ion of a preoperatively acquired conditioned taste aversion (CTA) to 0.3 M alanine.

62 (1.5 g kg(-1) 20% ethanol, i.p.) conditioned taste aversion (CTA) to saccharin taste.

63 prior to the establishment of a conditioned taste aversion (CTA) to saccharin.

64 before and after ethanol-induced conditioned taste aversion (CTA) to saccharin.

65 nist, was infused into IC before conditioned taste aversion (CTA) training with a familiar taste.

66 correlate of the expression of a conditioned taste aversion (CTA) when conditioning occurs using tast

67 a herbicide capable of eliciting conditioned taste aversion (CTA), a behavioral response characterist

68 readily acquired a LiCl-induced conditioned taste aversion (CTA), the suppressive effects of sucrose

69 lithium chloride (LiCl)-induced conditioned taste aversion (CTA).

70 ctivated following expression of conditioned taste aversion (CTA).

71 with behavioral expression of a conditioned taste aversion (CTA).

72 implicated in the development of conditioned taste aversion (CTA).

73 f the behavioral expression of a conditioned taste aversion (CTA).

74 ng drugs of abuse also support a conditioned taste aversion (CTA).

75 nd/or behavioral expression of a conditioned taste aversion (CTA).

76 tical memory representations for conditioned taste aversion (CTA).

77 ng in a one-trial learning task, conditioned taste aversion (CTA).

78 ntextually reactivated memory of conditioned taste aversion (CTA).

79 involved in the extinction of a conditioned taste aversion (CTA).

80 n and throughout extinction of a conditioned taste aversion (CTA).

81 s of visceral illness, such as a conditioned taste aversion (CTA).

82 like the taste of saccharin [via conditioned taste aversion (CTA)].

83 ing [STDRLO]) or ethanol-induced conditioned taste aversion (CTA; high [HTA], low [LTA]).

84 Conditioned taste aversions (CTA) based on lithium chloride (Experim

85 thium chloride (referred to as a conditioned taste aversion, CTA); (2) access to a very palatable con

86 f permanent forebrain lesions on conditioned taste aversions (CTAs) and conditioned odor aversions (C

87 ) lesions attenuate LiCl-induced conditioned taste aversions (CTAs) by disruption of information abou

88 the acquisition and retention of conditioned taste aversions (CTAs) in rodents, but large lesions in

89 Conditioned taste aversions (CTAs) may be acquired when an animal co

90 da tympani nerves (CTX) received conditioned taste aversions (CTAs) to the free fatty acids (FFAs), l

91 ex (IC) attenuate acquisition of conditioned taste aversions (CTAs).

92 havioral experiments testing for conditioned taste aversion did not confirm that SEB challenge promot

93 e acquisition of ethanol-induced conditioned taste aversion, ethanol-induced conditioned place prefer

94 ncluding active place avoidance, conditioned taste aversion, fear conditioning and spatial learning.

95 te cue has been interpreted as a conditioned taste aversion for decades.

96 ocomotor circling and leads to a conditioned taste aversion if paired with a novel taste.

97 rin taste developed a persistent conditioned taste aversion in both preference and taste reactivity t

98 ntake, body weight, or causing a conditioned taste aversion in mice lacking neuronal GLP1R.

99 tinction tests revealed rapid attenuation of taste aversions in all of the LiCl-injected groups.

100 parabrachial nucleus (PBN) failed to learn a taste aversion induced by lithium chloride (LiCl) toxico

101 ignificance of these findings to conditioned taste aversion is discussed.

102 support the hypothesis that ethanol-induced taste aversion is mediated by the drug's rewarding prope

103 e GI tract suggests a new account of delayed taste aversion learning as well as learning about the po

104 Here, we used conditioned taste aversion learning in the rat model, wherein animal

105 the light CS in the first training phase or taste aversion learning in the second training phase.

106 hat have been shown to generate differential taste aversion learning in these strains.

107 NaB also enhanced conditioned taste aversion learning induced by pairing saccharin con

108 H3, c-Fos induction, and amygdalar-dependent taste aversion learning is constrained by endogenous his

109 r cortex, but also failed to induce stronger taste aversion learning than familiar Polycose.

110 Taste aversion learning thus may more properly be termed

111 rained first to reject it (i.e., conditioned taste aversion learning) and then to enjoy it again (i.e

112 itioning represents a molecular correlate of taste aversion learning, i.e. the formerly neutral CS no

113 details of the neural circuitry involved in taste aversion learning, including its anatomical distri

114 la (CNA), regions thought to be important in taste aversion learning.

115 l structure in transduction of the US during taste aversion learning.

116 strongly modulate the speed and efficacy of taste aversion learning.

117 iliar tastes as conditioned stimuli (CSs) in taste aversion learning.

118 thdrawal with low drinking, high conditioned taste aversion, low tolerance to EtOH-induced hypothermi

119 d did not promote formation of a conditioned taste aversion (malaise-like behavior).

120 egulates ingestive behavior without inducing taste aversion may open the possibility of a therapeutic

121 al memory in the hippocampus and conditioned taste aversion memory in the insular cortex.

122 lso attenuated the extinction of established taste aversion memory without altering the initial assoc

123 e from the adjacent insular cortex-dependent taste aversion memory.

124 that this is dissociable from AIC-dependent taste aversion memory.

125 th LiCl injection, by making the conditioned taste aversion more resistant to extinction.

126 l training procedures and either conditioned taste aversion or satiation devaluation procedures.

127 ubstrates of LI as assessed in a conditioned taste aversion paradigm by comparing regional c-Fos acti

128 The intestinal taste aversion paradigm has previously demonstrated that

129 hibition (LI) were assessed in a conditioned taste aversion paradigm.

130 Experiment 2 used a conditioned taste-aversion procedure to establish that rats with IBO

131 chloride, at doses that produce conditioned taste aversion, reduced metabolic rate.

132 elay in extinguishing an ethanol-conditioned taste aversion, suggesting that they drink less ethanol

133 Strains showing stronger taste aversion tended to show lower ethanol preference a

134 xperiment 4) or consumption on a conditioned taste aversion test that does not elicit antipredator re

135 A conditioned taste aversion test was performed to assess whether proa

136 Ethanol produced dose-dependent conditioned taste aversion that was the same in both genotypes.

137 ransection (CTX) acquired a LiCl-conditioned taste aversion to 0.1 M NaCl at the same rate as control

138 hila and report that the fly displays strong taste aversion to common carboxylic acids.

139 lued the food unconditioned stimulus (US) by taste aversion to differentiate stimulus-stimulus(CS-US)

140 tration of GLP-1 did not cause a conditioned taste aversion to saccharin, suggesting that the anorexi

141 ate was confirmed in rats with a conditioned taste aversion to sucrose: after paired exposure to sucr

142 the reinforcer after training by inducing a taste aversion to the food.

143 The ability to acquire conditioned taste aversion was also assessed.

144 acquisition and expression of a conditioned taste aversion was assessed using two different conditio

145 In contrast, after a taste aversion was conditioned to 150-mM NaCl, estrogen-

146 l can induce memory given that a conditioned taste aversion was obtained for a novel taste, presented

147 f the behavioral expression of a conditioned taste aversion, was also assessed.

148 Conditioned taste aversion, which also depends on the amygdala, is n

149 y pairing it with lithium chloride (acquired taste aversion), while the other distinctive flavor was