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

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

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

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

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

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

10 onger input from catecholaminergic than from serotoninergic axons.

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

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

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

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

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

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

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

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

19 Selected subsets of serotoninergic dorsal raphe neurons may influence discre

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

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

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

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

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

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

26 Dopaminergic and serotoninergic innervation was normal.

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

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

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

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

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

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

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

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

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

36 Rather, distinct serotoninergic neurons can act as inhibitory modulators

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

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

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

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

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

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

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

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

45 1A autoreceptors reduces the excitability of serotoninergic neurons, which decreases serotonin releas

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

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

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

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

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

51 any retrogradely labeled neurons were either serotoninergic or catecholaminergic.

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

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

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

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

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

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

58 reference to the ascending dopaminergic and serotoninergic projections.

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

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

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

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

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

64 Although the serotoninergic system has been linked to PFC functionali

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

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

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

68 ed with drugs targeting the dopaminergic and serotoninergic systems.

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

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

71 Serotoninergic transmission is implicated in the photic

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