ライフサイエンスコーパス: serotoninergic

1 rom this laboratory showed that sprouting of serotoninergic (5-HT) axons in the hamster's superior co

2 in a significant increase in the density of serotoninergic (5-HT) fibers in the superficial layers o

3 functions as a partial agonist of the human serotoninergic 5HT2B receptor.

4 ibited negligible off-target interactions at serotoninergic and adrenergic G-protein-coupled receptor

5 ctions (e.g., to the amygdala, the striatum, serotoninergic and dopaminergic nuclei), flexibly regula

6 of the dendrites that there is indeed both a serotoninergic and noradrenergic innervation of gamma-mo

7 Genes linked to dopaminergic, serotoninergic and noradrenergic signaling, metabolism (

8 eled fibers were unequivocally identified as serotoninergic and originating from one of the labeled n

9 We hypothesized that the serotoninergic antagonist [3H]ketanserin would label sim

10 crease was dose-dependent and was blocked by serotoninergic antagonists.

11 rom this laboratory showed that sprouting of serotoninergic axons in the hamster's superior colliculu

12 onger input from catecholaminergic than from serotoninergic axons.

13 to the lateral subdivision of the IPN, high serotoninergic binding was localized to the dorsal IPN,

14 abel serotoninergic fibers and boutons, 1048 serotoninergic boutons were observed in close contact wi

15 level of the orbitofrontal cortex (OFC) with serotoninergic, but not dopaminergic, integrity being im

16 ivity of anti-52-kD SSA/Ro antibodies with a serotoninergic cardiac receptor, 5-hydroxytryptamine (HT

17 active TH-ir cells but did not injure nearby serotoninergic cells, increased total daily sleep by app

18 These results suggest that a serotoninergic challenge activates basal ganglia circuit

19 neurons is sufficient to mediate effects of serotoninergic compounds on food intake.

20 em, where they provided terminals in the the serotoninergic dorsal and median raphe nuclei, and the c

21 Selected subsets of serotoninergic dorsal raphe neurons may influence discre

22 airway in waking, and that in sleep, reduced serotoninergic drive plays a significant role in upper a

23 stribution patterns of catecholaminergic and serotoninergic fibers also vary between species.

24 -hydroxytryptamine-immunoreactivity to label serotoninergic fibers and boutons, 1048 serotoninergic b

25 ed sprouting capacity of both CST and spinal serotoninergic fibers.

26 ergic-andrenergic, glutaminergic-GABAnergic, serotoninergic, histaminergic, and cholinergic systems.

27 We hypothesized that in OSAHS, excitatory serotoninergic influences are important for maintaining

28 Dopaminergic and serotoninergic innervation was normal.

29 Both peripheral and serotoninergic inputs control VGLUT3+ neurons firing.

30 tical layers are identified, consistent with serotoninergic layer 5a neuronal vulnerability previousl

31 rted small responses in humans with OSAHS to serotoninergics may relate, in part, to study design and

32 ovides a robust model for the examination of serotoninergic mechanisms in epilepsy.

33 e control monkeys and monkeys with selective serotoninergic medial caudate depletions, dopamine-deple

34 Overall, the cutaneous serotoninergic/melatoninergic system could counteract or

35 The cutaneous serotoninergic/melatoninergic system: securing a place u

36 nition task in rats to study the role of the serotoninergic modulation in the medial PFC (mPFC) in me

37 ors by reducing descending noradrenergic and serotoninergic modulation of spinal pain signals.

38 an be affected in psychiatric illness and by serotoninergic modulation.

39 nd patients with migraine, and reduced FC in serotoninergic networks localized in the insula, tempora

40 nsiderable body of literature indicates that serotoninergic neurons affect diaphragm activity both th

41 argeted the cell bodies and dendrites of DRN serotoninergic neurons and LC noradrenergic neurons but

42 Rather, distinct serotoninergic neurons can act as inhibitory modulators

43 This demonstrates that individual serotoninergic neurons can modulate distinct types of be

44 However, our results revealed that MnR serotoninergic neurons displayed little firing changes d

45 function of VGLUT3 in acetylcholinergic and serotoninergic neurons has been elucidated, the role of

46 protein, which controls apoptosis of the NSM serotoninergic neurons in Caenorhabditis elegans.

47 few subpopulations of catecholaminergic and serotoninergic neurons in the carp brain.

48 Many non-serotoninergic neurons in the raphe nuclei were also inf

49 Moreover, activation of DRN serotoninergic neurons reduces looming-evoked defensive

50 tem respiratory groups, the locations of the serotoninergic neurons that modulate breathing have not

51 These findings suggest that although serotoninergic neurons with direct influences on diaphra

52 1A autoreceptors reduces the excitability of serotoninergic neurons, which decreases serotonin releas

53 e DRN GABAergic neurons that in turn inhibit serotoninergic neurons.

54 rammed cell death in the sister cells of the serotoninergic neurosecretory motor (NSM) neurons, and f

55 erotonin (5-HT) transporter (SERT) regulates serotoninergic neurotransmission by clearing 5-HT releas

56 ministration in nonhuman primates influences serotoninergic neurotransmission via at least two ways:

57 dopaminergic, GABAergic, glutamatergic, and serotoninergic neurotransmitters in first-episode psycho

58 d with key neuromodulator systems, including serotoninergic, noradrenergic, dopaminergic, and opioid

59 toradiography for the muscarinic, nicotinic, serotoninergic, opioid, and kainate receptors.

60 any retrogradely labeled neurons were either serotoninergic or catecholaminergic.

61 cholinergic or monoaminergic (noradrenergic, serotoninergic or dopaminergic) nuclei in the brainstem

62 c denervation although not with differential serotoninergic or nigrostriatal dopaminergic denervation

63 this study compared the effects of selective serotoninergic or selective dopaminergic depletions of t

64 ortical terminal fields of noradrenergic and serotoninergic pathways were not affected by NGF.

65 to synapse, cell adhesion, glutamatergic and serotoninergic pathways, both confirming findings of pre

66 rsal cochlear nucleus, we concluded that the serotoninergic projection pattern to the cochlear nucleu

67 reference to the ascending dopaminergic and serotoninergic projections.

68 eurons in the NTS, A5 or Locus Coeruleus, no serotoninergic raphe neurons nor any cholinergic neurons

69 habenula (LHb) is bilaterally connected with serotoninergic raphe nuclei, and expresses high density

70 eus, histaminergic tuberomammillary nucleus, serotoninergic raphe nucleus, and dopaminergic ventral t

71 ogy of depression after DD, including NA-LC, serotoninergic-raphe nuclei and dopaminergic-ventral teg

72 Serotoninergic raphespinal fibres below the lesion showe

73 o explain the functional effects of specific serotoninergic receptor (5-HT(2A)R) stimulation with psi

74 (R)-PZQ modulation of serotoninergic signaling occurs over a concentration ran

75 ns induced by recreational drugs that act on serotoninergic synapses.

76 Although the serotoninergic system has been linked to PFC functionali

77 We hypothesized that the serotoninergic system in PFC, in particular the 5-HT2A r

78 hether genetic variation in genes across the serotoninergic system is associated with chronic widespr

79 which was previously believed not to have a serotoninergic system.

80 Specific relationships to cholinergic and serotoninergic systems localized to granular and infragr

81 ed with drugs targeting the dopaminergic and serotoninergic systems.

82 cits are not seen at either noradrenergic or serotoninergic terminals.

83 s indicate the causal involvement of reduced serotoninergic transmission in the emergence of compulsi

84 Serotoninergic transmission is implicated in the photic

85 esting the effectiveness of a combination of serotoninergics, trazodone, and L-tryptophan, in our ani