ライフサイエンスコーパス: interpeduncular

1 primarily localized in the visual, habenula-interpeduncular, and nigrostriatal-mesolimbic pathways.

2 the identification of the midbrain habenula-interpeduncular axis as a critical relay circuit in the

3 anges in gene expression within the habenulo-interpeduncular circuit during nicotine withdrawal.

4 rformed using RNA isolated from the habenulo-interpeduncular circuit of male mice withdrawn from chro

5 y at larval stages, that the dorsal habenulo-interpeduncular (dHb-IPN) pathway expedites the return o

6 t, suggesting that the development of a deep interpeduncular fossa was not as advanced as in living o

7 ulates downstream components of the habenulo-interpeduncular (Hb-IP) circuit is unknown.

8 c receptors (nAChRs) present in the habenulo-interpeduncular (Hb-IPn) system can modulate the reinfor

9 anxiety increases activity of neurons in the interpeduncular intermediate (IPI), a subregion of the i

10 press CRF-R2, including the dorsal raphe and interpeduncular nuclei and the nucleus of the solitary t

11 with the superior central (median raphe) and interpeduncular nuclei the NI appears to form a midline

12 The BBB in the cerebellum and pons/interpeduncular nuclei was highly sensitive to decrement

13 Fibers in the fasciculus retroflexus, interpeduncular nuclei, and periaqueductal gray were als

14 al amygdaloid nuclei, anterior pretectal and interpeduncular nuclei, as well as select laminae of the

15 lls in the following areas: habenula nuclei, interpeduncular nuclei, hippocampus, mammillary bodies,

16 nd the lateral septal, medial habenular, and interpeduncular nuclei.

17 rsal tegmental, posterodorsal tegmental, and interpeduncular nuclei; substantia nigra, central gray;

18 ily conserved forebrain to midbrain habenulo-interpeduncular nucleus (Hb-IPN) pathway consists of cho

19 The expression of Gscl is restricted to the interpeduncular nucleus (IP) in the ventral region of th

20 The interpeduncular nucleus (IP) is a key limbic structure,

21 teral habenula (LHb), medial habenula (MHb), interpeduncular nucleus (IP), and median raphe nucleus (

22 y, MHb together with its primary target, the interpeduncular nucleus (IP), have been identified as ma

23 ngly expressed in a subset of neurons in the interpeduncular nucleus (IP), median raphe/paramedian ra

24 s retroflexus, and its principal target, the interpeduncular nucleus (IP).

25 ons, which project almost exclusively to the interpeduncular nucleus (IPn) and are known to regulate

26 ons, which project almost exclusively to the interpeduncular nucleus (IPn) and are known to regulate

27 The interpeduncular nucleus (IPN) and its presynaptic inputs

28 We further show that the habenula (Hb)-interpeduncular nucleus (IPN) circuit retains a short-te

29 The medial habenula (mHb)/interpeduncular nucleus (IPN) circuitry is resident to d

30 The interpeduncular nucleus (IPN) exhibits many complex feat

31 In contrast, interpeduncular nucleus (IPN) GABAergic neurons that pro

32 s were designed to determine the role of the interpeduncular nucleus (IPN) in 3 forms of navigation:

33 f Chrna3 gene transcripts in the habenula or interpeduncular nucleus (IPn) increases nicotine intake

34 tic connection from medial habenula (MHb) to interpeduncular nucleus (IPN) is critical for emotion-re

35 rea implicated in nicotine dependence is the interpeduncular nucleus (IPN) located in the ventral mid

36 ACh at synapses of medial habenula (MHN) and interpeduncular nucleus (IPN) neurons in vitro elicited

37 cal substrate for familiarity signaling, the interpeduncular nucleus (IPN) of the midbrain, which is

38 l nAChRs in the medial habenula (MHb) to the interpeduncular nucleus (IPN) pathway are key mediators

39 eptors (nAChRs) in the medial habenula (MHb)-interpeduncular nucleus (IPN) pathway play critical role

40 ated in beta2(-/-) sections, although dorsal interpeduncular nucleus (IPN) retained a faint signal.

41 ors (nAChRs) in the medial habenula (MHb) or interpeduncular nucleus (IPN) triggers withdrawal-like b

42 show that the brainstem circuit linking the interpeduncular nucleus (IPN) with the nucleus incertus

43 conveys motor information may stem from the interpeduncular nucleus (IPN), a brain region that has r

44 related with nicotine-evoked currents in the interpeduncular nucleus (IPN), and that prolonged exposu

45 of beta4 subunits in medial habenula (MHb), interpeduncular nucleus (IPN), and VTA of beta4KO mice r

46 al habenula (MHb) and its unique output, the interpeduncular nucleus (IPN), in mice independently of

47 pha2 and beta4 are transcribed in the target interpeduncular nucleus (IPN), suggesting that the asymm

48 sors activate mouse GABAergic neurons in the interpeduncular nucleus (IPN).

49 nnervate distinct subregions of the midbrain interpeduncular nucleus (IPN).

50 s, the axons of which innervate the midbrain interpeduncular nucleus (IPN).

51 es medial habenular (MHb) projections to the interpeduncular nucleus (IPN).

52 cular intermediate (IPI), a subregion of the interpeduncular nucleus (IPN).

53 ptoms activates GABAergic neurons within the interpeduncular nucleus (IPN).

54 xtends projections almost exclusively to the interpeduncular nucleus (IPN).

55 ections to the unpaired midbrain target--the interpeduncular nucleus (IPN).

56 ar projections onto the midbrain target, the interpeduncular nucleus (IPN).

57 ease of glutamate and glycine in the lateral interpeduncular nucleus (LIPN).

58 The medial habenula-interpeduncular nucleus (MHb-IPN) pathway has recently b

59 connections with a subregion of the ventral interpeduncular nucleus (vIPN).

60 ese stimuli are represented in the habenula, interpeduncular nucleus and anterior hindbrain.

61 (B)R1 labeling was observed in the thalamus, interpeduncular nucleus and medial habenula.

62 Our findings suggest the interpeduncular nucleus as a site for integration of the

63 he subthalamic nucleus, substantia nigra and interpeduncular nucleus as well as in the hippocampus, d

64 l changes thought to occur in the MHb to the interpeduncular nucleus circuit in human smokers.

65 c dopamine circuitry and the medial habenula-interpeduncular nucleus complex, which are critical medi

66 c receptors expressed in medial habenula and interpeduncular nucleus during withdrawal.

67 habenular neurons project exclusively to the interpeduncular nucleus in the ventral midbrain.

68 taset by demonstrating that knockdown in the interpeduncular nucleus of a differentially expressed mR

69 l plexiform layer of the olfactory bulb, the interpeduncular nucleus of the midbrain, the ventral and

70 osterior mamilliary nucleus, and dorsomedial interpeduncular nucleus of the rabbit that were not dete

71 Optostimulation of Hb-MOR/interpeduncular nucleus terminals triggered avoidance an

72 on in neurons clustered above and behind the interpeduncular nucleus that project strongly to the ven

73 ontributing to despair-like behavior (Hb-MOR/interpeduncular nucleus) and anxiety (Hb-MOR/dorsal raph

74 depression (e.g., habenula, dorsal raphe and interpeduncular nucleus).

75 Because the MHb extensively innervates the interpeduncular nucleus, an area critical for both affec

76 gic-rich areas such as basolateral amygdala, interpeduncular nucleus, and facial nuclei.

77 monstrated PP receptors in the brainstem and interpeduncular nucleus, and the PP receptors in the bra

78 a, pineal body, preoptic area, hypothalamus, interpeduncular nucleus, area acusticolateralis, cerebel

79 he subthalamic nucleus, substantia nigra and interpeduncular nucleus, as well as other areas of the b

80 In the dorsal interpeduncular nucleus, both stimuli are topographicall

81 when microinjected into the habenula or the interpeduncular nucleus, but not into the cortex, ventra

82 rade tracing showed that, in addition to the interpeduncular nucleus, Hb-MOR neurons project to the d

83 splenial cortex, subiculum, medial habenula, interpeduncular nucleus, locus coeruleus, and brainstem

84 sal tegmental nucleus, dorsal raphe nucleus, interpeduncular nucleus, medial mammillary body, suprama

85 4 also was present in certain neurons of the interpeduncular nucleus, median raphe, superior collicul

86 IRP-LI was most heavily concentrated in the interpeduncular nucleus, nuclei interfascicularis and ro

87 the region just dorsal to the posterior VTA, interpeduncular nucleus, or medial mammillary nucleus.

88 ficial layer), arcuate hypothalamic nucleus, interpeduncular nucleus, paratrigeminal nucleus, and lam

89 subnuclei also differentially innervate the interpeduncular nucleus, raphe nuclei, substantia nigra

90 e more active in fish that are not courting: interpeduncular nucleus, red nucleus, and ventrolateral

91 dial amygdala, central gray, pontine nuclei, interpeduncular nucleus, substantia nigra, raphe complex

92 rus semicircularis, mesencephalic tegmentum, interpeduncular nucleus, superior and middle reticular n

93 s of Darkschewitsch, peripeduncular nucleus, interpeduncular nucleus, tegmental nuclei, locus coerule

94 m, torus semicircularis, cerebellar nucleus, interpeduncular nucleus, the medial octavolateral nucleu

95 ct projections to midbrain areas such as the interpeduncular nucleus, the median/paramedian nuclei, a

96 antia nigra, the ventral tegmental area, the interpeduncular nucleus, the raphe nuclei, the dorsal te

97 efferent habenular fibers projecting to the interpeduncular nucleus, the rostromedial tegmental area

98 s, the midbrain lateral tegmental field, the interpeduncular nucleus, the ventral pontine reticular f

99 ic input, the habenular nucleus inhibits the interpeduncular nucleus, thereby dis-inhibiting forebrai

100 which project IL-18-containing axons to the interpeduncular nucleus.

101 ts of the MHb homolog selectively target the interpeduncular nucleus.

102 medial habenula and its primary target, the interpeduncular nucleus.

103 subunits, which are highly expressed in the interpeduncular nucleus.

104 uctures such as the substantia nigra and the interpeduncular nucleus.

105 N to the adjacent fasciculus retroflexus and interpeduncular nucleus.

106 habenula and a 25% elevation in the related interpeduncular nucleus.

107 nly weakly into the adjacent anterior VTA or interpeduncular nucleus.

108 eral lemniscus, periaqueductal gray, and the interpeduncular nucleus.

109 subiculum, several thalamic regions, and the interpeduncular nucleus.

110 omposing the fasciculus retroflexus, and the interpeduncular nucleus; 2) nuclei and ascending tracts

111 and the thalamic posterior paraventricular, interpeduncular, oculomotor, and anterior olfactory nucl

112 we propose that the telencephalic-habenular-interpeduncular pathway plays an important role in contr

113 ndicate that nicotine activates the habenulo-interpeduncular pathway through alpha5-containing nAChRs

114 The habenulo-interpeduncular pathway, a highly conserved cholinergic

115 ular subpopulations and segregation of their interpeduncular projections.

116 ns thal. n; and paraventricular thal n), the interpeduncular red nucleus, substantia nigra, parabrach

117 The habenulo-interpeduncular system (HIPS) is now recognized as a cri

118 s required for the formation of the habenulo-interpeduncular system (HIPS), an important component of

119 ts demonstrate a major role for the habenulo-interpeduncular system and the nicotinic receptor subuni

120 est that the habenula-fasciculus retroflexus-interpeduncular system may be pan of the electroreceptiv

121 eral and the habenula-fasciculus retroflexus-interpeduncular systems.

122 ns, and in the anterior commissure, habenulo-interpeduncular tract, and the projections of hippocampa