ライフサイエンスコーパス: conditioned taste aversion

1 ves intact the development of a LiCl-induced conditioned taste aversion.

2 itched from "good" to "bad" as occurs during conditioned taste aversion.

3 on corticosterone secretion, body weight, or conditioned taste aversion.

4 or memory, since they successfully expressed conditioned taste aversion.

5 rtical lesions had no impact on LiCl-induced conditioned taste aversion.

6 ecreases food intake in rats without causing conditioned taste aversion.

7 epting or avoiding taste stimuli following a conditioned taste aversion.

8 inducing agent used in laboratory studies of conditioned taste aversion.

9 sed with respect to the neural substrates of conditioned taste aversion.

10 e acquisition of latent inhibition (LI) of a conditioned taste aversion.

11 endocrine responses including development of conditioned taste aversion.

12 t due to sickness as icv TTR did not cause a conditioned taste aversion.

13 2, or 4 g/kg) aversive effects as indexed by conditioned taste aversion.

14 duce food intake, induce pica, and produce a conditioned taste aversion.

15 rs, increased feeding and the formation of 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 ion rate of conditioned fear responses and a conditioned taste aversion as well as enhanced performan

26 Data gathered using a conditioned taste aversion assay also suggest that, alth

27 levels and enhanced novel taste learning and conditioned taste aversion, but not memory retrieval.

28 ts show more locomotor circling and enhanced conditioned taste aversion compared to male rats.

29 A conditioned taste aversion could not be classically cond

30 After acquisition of a conditioned taste aversion (CTA) against sucrose, intrao

31 g and with reduced sensitivity to MA-induced conditioned taste aversion (CTA) and hypothermia.

32 4 T magnetic field is sufficient to induce a conditioned taste aversion (CTA) and induce brainstem ex

33 ite following sodium depletion, and a normal conditioned taste aversion (CTA) for alanine when paired

34 basolateral complex (BLA) of the amygdala on conditioned taste aversion (CTA) in a latent inhibition

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

36 Here, we use conditioned taste aversion (CTA) in rats, a cortically d

37 rsion-associated brain areas and to induce a conditioned taste aversion (CTA) in these strains is unk

38 rabrachial nucleus (PBN) failed to acquire a conditioned taste aversion (CTA) induced by lithium chlo

39 Conditioned taste aversion (CTA) is a phenomenon in whic

40 A conditioned taste aversion (CTA) is acquired when an ani

41 ctivity) when spontaneous recovery (SR) of a conditioned taste aversion (CTA) is reduced.

42 Conditioned taste aversion (CTA) learning is a robust fo

43 Conditioned taste aversion (CTA) learning occurs after t

44 Conditioned taste aversion (CTA) learning, in which anim

45 tein kinase A (PKA) activity interferes with conditioned taste aversion (CTA) memories.

46 olden hamsters (Mesocricetus auratus) with a conditioned taste aversion (CTA) paradigm.

47 ar cortex, is widely regarded as integral to conditioned taste aversion (CTA) retention, a link that

48 emory in choice-based versus no-choice-based conditioned taste aversion (CTA) tasks in rats.

49 PBN lesion efficacy was confirmed using conditioned taste aversion (CTA) tests.

50 srupt retention of a preoperatively acquired conditioned taste aversion (CTA) to 0.3 M alanine.

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

52 ecutive days prior to the establishment of a conditioned taste aversion (CTA) to saccharin.

53 perant task before and after ethanol-induced conditioned taste aversion (CTA) to saccharin.

54 linergic agonist, was infused into IC before conditioned taste aversion (CTA) training with a familia

55 tently as a correlate of the expression of a conditioned taste aversion (CTA) when conditioning occur

56 Paraquat is a herbicide capable of eliciting conditioned taste aversion (CTA), a behavioral response

57 both strains readily acquired a LiCl-induced conditioned taste aversion (CTA), the suppressive effect

58 correlate of the behavioral expression of a conditioned taste aversion (CTA).

59 ly reinforcing drugs of abuse also support a conditioned taste aversion (CTA).

60 cquisition and/or behavioral expression of a conditioned taste aversion (CTA).

61 insular cortical memory representations for conditioned taste aversion (CTA).

62 uring training in a one-trial learning task, conditioned taste aversion (CTA).

63 tion of a contextually reactivated memory of conditioned taste aversion (CTA).

64 ex (mPFC) is involved in the extinction of a conditioned taste aversion (CTA).

65 g acquisition and throughout extinction of a conditioned taste aversion (CTA).

66 uces symptoms of visceral illness, such as a conditioned taste aversion (CTA).

67 of EtOH- and lithium chloride (LiCl)-induced conditioned taste aversion (CTA).

68 of neurons activated following expression of conditioned taste aversion (CTA).

69 e correlated with behavioral expression of a conditioned taste aversion (CTA).

70 actors, and implicated in the development of conditioned taste aversion (CTA).

71 arned to dislike the taste of saccharin [via conditioned taste aversion (CTA)].

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

73 Conditioned taste aversions (CTA) based on lithium chlor

74 t such as lithium chloride (referred to as a conditioned taste aversion, CTA); (2) access to a very p

75 he effects of permanent forebrain lesions on conditioned taste aversions (CTAs) and conditioned odor

76 postrema (AP) lesions attenuate LiCl-induced conditioned taste aversions (CTAs) by disruption of info

77 ral role in the acquisition and retention of conditioned taste aversions (CTAs) in rodents, but large

78 Conditioned taste aversions (CTAs) may be acquired when

79 nsected chorda tympani nerves (CTX) received conditioned taste aversions (CTAs) to the free fatty aci

80 insular cortex (IC) attenuate acquisition of conditioned taste aversions (CTAs).

81 Behavioral experiments testing for conditioned taste aversion did not confirm that SEB chal

82 acterized the acquisition of ethanol-induced conditioned taste aversion, ethanol-induced conditioned

83 ehaviours, including active place avoidance, conditioned taste aversion, fear conditioning and spatia

84 e of the taste cue has been interpreted as a conditioned taste aversion for decades.

85 ve induces locomotor circling and leads to a conditioned taste aversion if paired with a novel taste.

86 ith a saccharin taste developed a persistent conditioned taste aversion in both preference and taste

87 ering food intake, body weight, or causing a conditioned taste aversion in mice lacking neuronal GLP1

88 The significance of these findings to conditioned taste aversion is discussed.

89 Here, we used conditioned taste aversion learning in the rat model, wh

90 NaB also enhanced conditioned taste aversion learning induced by pairing s

91 vidly were trained first to reject it (i.e., conditioned taste aversion learning) and then to enjoy i

92 high EtOH withdrawal with low drinking, high conditioned taste aversion, low tolerance to EtOH-induce

93 r potency and did not promote formation of a conditioned taste aversion (malaise-like behavior).

94 srupts spatial memory in the hippocampus and conditioned taste aversion memory in the insular cortex.

95 nsumption with LiCl injection, by making the conditioned taste aversion more resistant to extinction.

96 instrumental training procedures and either conditioned taste aversion or satiation devaluation proc

97 e neuronal substrates of LI as assessed in a conditioned taste aversion paradigm by comparing regiona

98 on latent inhibition (LI) were assessed in a conditioned taste aversion paradigm.

99 Experiment 2 used a conditioned taste-aversion procedure to establish that r

100 reas lithium chloride, at doses that produce conditioned taste aversion, reduced metabolic rate.

101 and show a delay in extinguishing an ethanol-conditioned taste aversion, suggesting that they drink l

102 nsitivity (experiment 4) or consumption on a conditioned taste aversion test that does not elicit ant

103 A conditioned taste aversion test was performed to assess

104 Ethanol produced dose-dependent conditioned taste aversion that was the same in both gen

105 pani nerve transection (CTX) acquired a LiCl-conditioned taste aversion to 0.1 M NaCl at the same rat

106 core administration of GLP-1 did not cause a conditioned taste aversion to saccharin, suggesting that

107 of an ingestate was confirmed in rats with a conditioned taste aversion to sucrose: after paired expo

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

109 ar cortex in acquisition and expression of a conditioned taste aversion was assessed using two differ

110 However, LiCl can induce memory given that a conditioned taste aversion was obtained for a novel tast

111 correlate of the behavioral expression of a conditioned taste aversion, was also assessed.

112 Conditioned taste aversion, which also depends on the am