ライフサイエンスコーパス: chorda

1 th intact taste systems and after unilateral chorda-lingual nerve transection.

2 ional PM-MA dynamics with various methods of chorda preservation during MVR to assess their impact on

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

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

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

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

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

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

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

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

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

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

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

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

15 Chorda tympani (CT) transection reduced average discrimi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 Chorda tympani nerve branching was reduced in NT4 overex

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 Chorda tympani nerve transection eliminated all labeled

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

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

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

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

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

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

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

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

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

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

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

87 The chorda tympani responses to mineral salts were monitored

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

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

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

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

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

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

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

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

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

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

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

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

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

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

102 The chorda tympani, greater superficial petrosal, and glosso

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

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

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