ライフサイエンスコーパス: petrosal

1 nerves by sectioning the greater superficial petrosal and glossopharyngeal nerves at postnatal day 15

2 while the epibranchial placodes (geniculate, petrosal and nodose) form visceral sensory neurons that

3 tem, the chorda tympani, greater superficial petrosal, and glossopharyngeal nerves have distinct but

4 The chorda tympani, greater superficial petrosal, and glossopharyngeal nerves were labeled in ad

5 odes generate the neurons of the geniculate, petrosal, and nodose cranial sensory ganglia.

6 buds and gustatory papillae (geniculate and petrosal) are reduced in volume by about 40% in mice wit

7 restricted to the dentition and an isolated petrosal bone, and this limited anatomical information h

8 sping (including a nail on the hallux) and a petrosal bulla likely evolved in the common ancestor of

9 nal field volumes of the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves at

10 eurons comprising the placode-derived nodose-petrosal complex occurred.

11 om BDNF-containing neurons in the nodose and petrosal cranial sensory ganglia.

12 d the number of VIP-ir neurons in the nodose/petrosal ganglia cultures and did not alter the numbers

13 abeled for specific neurochemicals in nodose/petrosal ganglia cultures.

14 Addition of NGF to nodose/petrosal ganglia neuron-enriched cultures significantly

15 Mature nodose and petrosal ganglia neurons (placodally derived afferent ne

16 ociated, enriched, cultures of mature nodose/petrosal ganglia neurons, and the neurons processed for

17 Although the geniculate and petrosal ganglia sustain at least half of their normal c

18 in CB (A(2B)) was down-regulated and that in petrosal ganglion (A(2A)) was up-regulated in caffeine-t

19 rker for dopaminergic neurons, in developing petrosal ganglion (PG), nodose ganglion, and dorsal root

20 Dissociate cultures of nodose-petrosal ganglion cells from newborn rats were grown in

21 larly striking in the cranial sensory nodose-petrosal ganglion complex (NPG), in which loss of either

22 ajor visceral sensory population, the nodose-petrosal ganglion complex (NPG), requires BDNF and NT4 f

23 Moreover, petrosal ganglion neurones were sensitive to hyperoxic e

24 rve fibers and tyrosine hydroxylase-positive petrosal ganglion neurons also expressed alpha7 subunits

25 enosine receptor mRNAs in cell bodies of the petrosal ganglion suggests that adenosine might also hav

26 A subpopulation of sensory neurons in the petrosal ganglion transmits information between peripher

27 of TRPC proteins in the rat carotid body and petrosal ganglion was examined using immunohistochemical

28 In the petrosal ganglion, A(1)-adenosine receptor mRNA was abun

29 nt neurones, located in the glossopharyngeal petrosal ganglion, already exhibited degenerative change

30 to hypoxia), consisting of the carotid body, petrosal ganglion, and nucleus of the solitary tract (NT

31 eripheral sensory neurons located within the petrosal ganglion, innervate the CB.

32 sinus nerve to the brain via neurons in the petrosal ganglion.

33 ine receptor protein in the carotid body and petrosal ganglion.

34 mRNA was seen in a few cells in the rostral petrosal ganglion.

35 d to the trunk of IXN in the vicinity of the petrosal ganglion.

36 two of these nerves, the greater superficial petrosal (GSP) and the chorda tympani (CT).

37 the chorda tympani (CT), greater superficial petrosal (GSP), and glossopharyngeal (IX) nerves in the

38 nal field expansion, the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngea

39 The greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngea

40 , terminal fields of the greater superficial petrosal (GSP), chorda tympani (CT), and glossopharyngea

41 th cranial nerve [CT and greater superficial petrosal (GSP)] nearly eliminated the discrimination of

42 ng the more proximal portions of the greater petrosal nerve (GPN).

43 sugar sensitivity of the greater superficial petrosal nerve (GSP) and the effect of amiloride on thes

44 the chorda tympani (CT), greater superficial petrosal nerve (GSP), and glossopharyngeal nerve (IX), t

45 , the chorda tympani and greater superficial petrosal nerve terminal fields were 1.4x and 1.6x larger

46 Thus, the greater superficial petrosal nerve was defasciculated, formed ectopic projec

47 PPG and its preganglionic root, the greater petrosal nerve.

48 chorda tympani (27%) and greater superficial petrosal nerves (15%) expressed Phox2b during developmen

49 f the chorda tympani and greater superficial petrosal nerves and overlapping fields that included the

50 eal, chorda tympani, and greater superficial petrosal nerves were labeled to examine their terminal f

51 chorda tympani (CT) and greater superficial petrosal nerves.

52 defined survival requirements of nodose and petrosal neurons for GDNF in vitro and in bdnf, gdnf, an

53 vated) family members were localized both in petrosal neurons that expressed tyrosine hydroxylase and

54 TRPC1 was expressed in only 28% of petrosal neurons, and of this population, 45% were tyros

55 palatal taste receptors (greater superficial petrosal) or in which a nongustatory nerve was sectioned

56 ivo, we analyzed development of nodose (NG), petrosal (PG), and vestibular (VG) ganglion cells in gen

57 uitary MR imaging, adrenal scintigraphy, and petrosal sampling were available in nine, five, and six

58 ossopharyngeal section > greater superficial petrosal section.

59 % of visceral afferent neurons in the nodose/petrosal sensory ganglion complex, including arterial ch

60 upregulated substantially in chemoreceptive petrosal sensory neurons in rats with hypertension.

61 ous study of bilateral simultaneous inferior petrosal sinus (IPS) sampling in healthy human subjects,

62 se findings suggest that there is a dominant petrosal sinus in healthy volunteers that appears to ref

63 Ratios of central ACTH to peripheral ACTH in petrosal sinus samples and jugular vein samples were cal

64 TH were negative in jugular vein samples and petrosal sinus samples before and after CRH (< 2 and < 3

65 entral to peripheral ACTH were diagnostic in petrosal sinus samples from 19 of 20 patients with surgi

66 erage ratio of central to peripheral ACTH in petrosal sinus samples was 17.7 before CRH and 90.0 afte

67 All patients underwent petrosal sinus sampling and jugular vein sampling before

68 ortisol level is the best screening test but petrosal sinus sampling for ACTH may be necessary to dis

69 Petrosal sinus sampling revealed no petrosal-to-peripher

70 Jugular vein sampling is less invasive than petrosal sinus sampling.

71 jugular vein sampling should be confirmed by petrosal sinus sampling.

72 adial artery of patients undergoing inferior petrosal sinus sampling.

73 vein (including the sigmoid sinus, inferior petrosal sinus, and the internal jugular vein), femoral

74 ISG), indicating the existence of a dominant petrosal sinus.

75 Bilateral sampling of the petrosal sinuses to distinguish Cushing disease from the

76 espite similar exogenous oCRH levels in both petrosal sinuses, oCRH caused a significant increase (P

77 urs in other autonomic ganglia including the petrosal, superior cervical and nodose ganglia.

78 neurons in autonomic ganglia, including the petrosal, superior cervical, and nodose ganglia, as well

79 Petrosal sinus sampling revealed no petrosal-to-peripheral ACTH gradients before corticotrop