ライフサイエンスコーパス: chorda tympani

1 r chain, promontory, round window niche, and chorda tympani.

2 onses to sodium in the contralateral, intact chorda tympani.

3 hat all taste neurons projecting through the chorda tympani (27%) and greater superficial petrosal ne

4 Physiological studies suggest convergence of chorda tympani and glossopharyngeal afferent axons onto

5 ogical recordings from two taste nerves, the chorda tympani and glossopharyngeal, revealed depressed

6 Specifically, the chorda tympani and greater superficial petrosal nerve te

7 We found that the terminal fields of the chorda tympani and greater superficial petrosal nerves a

8 ncreased in comparison with controls in both chorda tympani and lingual nerves after both procedures,

9 rphological observations were made on feline chorda tympani and lingual nerves proximal and distal to

10 volumes of the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves at adulthood

11 The glossopharyngeal, chorda tympani, and greater superficial petrosal nerves

12 Chorda tympani (CT) and glossopharyngeal (IXth) nerves r

13 eness occurred after combined section of the chorda tympani (CT) and greater superficial petrosal ner

14 stry following electrical stimulation of the chorda tympani (CT) nerve in rats.

15 rogeneous taste mixtures on responses of the chorda tympani (CT) nerve in the hamster (Mesocricetus a

16 The chorda tympani (CT) nerve innervates lingual taste buds

17 Chorda tympani (CT) nerve responses of lean mice to swee

18 Lean mice exhibited significant increases in chorda tympani (CT) nerve responses to sweet compounds a

19 amiloride (100 muM) treatment and bilateral chorda tympani (CT) nerve transection.

20 was anastomosed to the distal portion of the chorda tympani (CT) nerve using fibrin glue (IX-CT rats)

21 e more responsive to bitter stimuli than the chorda tympani (CT) nerve, and this is particularly true

22 polarized taste receptor cells (TRCs) and by chorda tympani (CT) taste nerve recordings.

23 Chorda tympani (CT) transection reduced average discrimi

24 The greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves te

25 ion, the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves we

26 s of the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngeal (IX) nerves we

27 dramatically enlarged terminal fields of the chorda tympani (CT), greater superficial petrosal (GSP),

28 The central fibers of the chorda tympani (CT), greater superficial petrosal nerve

29 oxic lectin ricin was applied to the hamster chorda tympani (CT), producing anterograde degeneration

30 on (pain, temperature, touch, etc.), and the chorda tympani (CT), which conducts taste information.

31 In contrast, the chorda tympani (CT), which innervates anterior tongue ta

32 e greater superficial petrosal (GSP) and the chorda tympani (CT).

33 differed from cells with evoked responses to chorda tympani (CT; which innervates taste buds on the r

34 ry in rats with bilateral transection of the chorda tympani (CTX), bilateral transection of the gloss

35 red before and after glossopharyngeal (GLX), chorda tympani (CTX), or combined glossopharyngeal and c

36 staining was reduced in the dextran-labeled chorda tympani fibers and terminals as well as adjacent

37 lingual epithelium, beginning embryonically, chorda tympani fibers are misdirected and innervate inap

38 y functions as a chemoattractant that allows chorda tympani fibers to distinguish their fungiform pap

39 Responses of single chorda tympani fibers to mixtures of taste stimuli were

40 ors including (a) numbers and type of active chorda tympani fibers, (b) compensatory responses to NaC

41 the extracellular space by primary afferent chorda tympani fibers.

42 f the dietary manipulation on the developing chorda tympani field was evident when it occurred from E

43 pani (CTX), or combined glossopharyngeal and chorda tympani (GLX + CTX) transection, as well as after

44 The chorda tympani, greater superficial petrosal, and glosso

45 In the rat gustatory system, the chorda tympani, greater superficial petrosal, and glosso

46 Overexpression of either factor disrupted chorda tympani innervation patterns either before or dur

47 orded from rat glossopharyngeal (n = 30) and chorda tympani (n = 22) neurons.

48 eling revealed those NST subnuclei receiving chorda tympani nerve (CT) afferents, those connecting wi

49 timulation was examined in rats in which the chorda tympani nerve (CT) and/or glossopharyngeal nerve

50 Rats that had the chorda tympani nerve (CT) bilaterally transected showed

51 ogically confirmed cross-regeneration of the chorda tympani nerve (CT) into the posterior tongue in t

52 earch has focused on neural responses of the chorda tympani nerve (CT) to taste stimuli.

53 Chorda tympani nerve (CT) transection (CTX) raises sodiu

54 The chorda tympani nerve (CT), one of three nerves that conv

55 Electrical stimulation of the chorda tympani nerve (CT; innervating taste buds on the

56 ed in the glossopharyngeal nerve than in the chorda tympani nerve and involved all taste qualities; r

57 n adult rats after unilateral axotomy of the chorda tympani nerve and/or maintenance on a sodium-rest

58 In contrast, many chorda tympani nerve branches were observed near the epi

59 Chorda tympani nerve branching was reduced in NT4 overex

60 al level in combination with the labeling of chorda tympani nerve fibers with biotinylated dextran in

61 there were also group-related differences in chorda tympani nerve function, with OE mice showing a gr

62 ctional salt taste responses from the intact chorda tympani nerve in sodium-restricted rats in which

63 Fungiform taste bud degeneration after chorda tympani nerve injury has been well documented in

64 15), P25, or at adulthood, while leaving the chorda tympani nerve intact.

65 Neither the glossopharyngeal nor the chorda tympani nerve is necessary for normal sensitivity

66 FFAs stimulate afferent taste signals in the chorda tympani nerve of male and female rats and that th

67 During sonidegib treatment, chorda tympani nerve responses to lingual chemical stimu

68 sodium restriction combined with unilateral chorda tympani nerve section leads to a rapid and specif

69 ified pathogen-free rats received unilateral chorda tympani nerve section or sham section followed by

70 Thus, it appears that the chorda tympani nerve terminal field defaults to its earl

71 ess of the age when the nerves were cut, the chorda tympani nerve terminal field expanded to a volume

72 tenance of injured peripheral axons, and the chorda tympani nerve terminal field organization in the

73 cant and persistent reduction of the labeled chorda tympani nerve terminal field volume and density i

74 We measured the integrated responses of the chorda tympani nerve to 500 mM concentrations of NaCl, N

75 Electrophysiological responses of the chorda tympani nerve to NaCl were blunted by estrogen tr

76 In Experiment 1, rats with chorda tympani nerve transection (CTX) acquired a LiCl-c

77 In rats, chorda tympani nerve transection (CTX) greatly increases

78 Chorda tympani nerve transection (CTX) has been useful t

79 Chorda tympani nerve transection eliminated all labeled

80 The terminal field of the chorda tympani nerve was assessed 35 d following nerve s

81 After CTX in adult rats, the chorda tympani nerve was labeled with biotinylated dextr

82 evelopmental periods, terminal fields of the chorda tympani nerve within the nucleus of the solitary

83 te: warming the anterior edge of the tongue (chorda tympani nerve) from a cold temperature can evoke

84 ter compounds, was cross-reinnervated by the chorda tympani nerve.

85 ith intact (SHAM) and bilaterally transected chorda tympani nerves (CTX) received conditioned taste a

86 ividual neurons in both glossopharyngeal and chorda tympani nerves differed in their relative sensiti

87 terminal fields of the glossopharyngeal and chorda tympani nerves in the nucleus of the solitary tra

88 hysiological recordings from the lingual and chorda tympani nerves proximal to the repair allowed cha

89 conclusion that, for transected lingual and chorda tympani nerves, epineurial suturing is the prefer

90 nd only for nicotine and denatonium, and for chorda tympani neurons, some similarity to quinine was f

91 The chorda tympani responses to mineral salts were monitored

92 The chorda tympani responses to NaCl, KCl, NH4Cl and CaCl2 w

93 The order of effectiveness was: chorda tympani section > trigeminal section > thermal in

94 ed rat fungiform taste receptor cells and by chorda tympani taste nerve recordings.

95 ccounts for all of the amiloride-insensitive chorda tympani taste nerve response to Na+ salts and par

96 ta, and extracellularly, surrounding labeled chorda tympani terminal fibers and boutons in the NST.

97 ndent factors determine the formation of the chorda tympani terminal field during later development.

98 is required for a permanent expansion of the chorda tympani terminal field in the offspring.

99 al exhibited enlarged and irregularly shaped chorda tympani terminal fields.

100 ctioned that innervates the anterior tongue (chorda tympani), the posterior tongue (glossopharyngeal)

101 gery groups: bilateral GL transection (GLX), chorda tympani transection (CTX), SHAM surgery, and comb

102 The present studies examined the effect of chorda tympani transection (neoCTX) of neonates on adult

103 volved all taste qualities; responses in the chorda tympani were more depressed to sweet and umami st