コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 eled as well as the caudal, intermediate and rostral ventrolateral medulla.
2 -derived EVs were taken up by neurons in the rostral ventrolateral medulla.
3 mouse model by stimulating C1 neurons in the rostral ventrolateral medulla.
4 on in the nucleus tractus solitarius and the rostral ventrolateral medulla.
5 cerebral blood flow (CBF) by activating the rostral ventrolateral medulla.
6 e retrotrapezoid nucleus (RTN) reside in the rostral ventrolateral medulla.
7 tricular nucleus of the hypothalamus and the rostral ventrolateral medulla.
8 arious sites within the brain, including the rostral ventrolateral medulla.
9 subunits and NAD(P)H oxidase activity in the rostral ventrolateral medulla.
10 neurones that project to the spinal cord or rostral ventrolateral medulla.
11 paucisynaptic, converging on neurones in the rostral ventrolateral medulla.
12 lycolaldehyde onto adrenergic neurons in the rostral ventrolateral medulla.
13 infection in mice induces activation of the rostral ventrolateral medulla, a major sympathetic cente
14 eptors and its corresponding mRNA within the rostral ventrolateral medulla, a primary vasomotor regio
15 st growth rate, neurovascular contact at the rostral-ventrolateral medulla, altered baroreflex blood
16 we measured orexin-A mRNA expression in the rostral ventrolateral medulla and antagonized both orexi
17 -derived EVs circulate to the presympathetic rostral ventrolateral medulla and contribute to oxidativ
18 hboring neurons that send projections to the rostral ventrolateral medulla and express CRH type 1 rec
19 (i.e., hypothalamic paraventricular nucleus, rostral ventrolateral medulla and nucleus of the solitar
20 increased cell excitability in the midbrain (rostral ventrolateral medulla) and alleviated the develo
21 an increased orexin-A mRNA expression in the rostral ventrolateral medulla, and blocking orexin recep
22 g hypothalamus, dorsal pons, dorsal medulla, rostral ventrolateral medulla, and caudal ventrolateral
23 he PVN and circumventricular organs, but not rostral ventrolateral medulla, and increased the phospho
24 halamic region, A5 catecholamine cell group, rostral ventrolateral medulla, and lateral paragigantoce
25 s, locus coeruleus, spinal trigeminal tract, rostral ventrolateral medulla, and medullary reticular n
27 stress in the nucleus tractus solitarius and rostral ventrolateral medulla as well as in the adrenal
28 ventricular nucleus in the hypothalamus, the rostral ventrolateral medulla (C1 adrenergic cell group)
29 eled by 6 days post-injection, including the rostral ventrolateral medulla (C1 adrenergic neurons), r
31 ermine the contribution of catecholaminergic rostral ventrolateral medulla catecholaminergic neurones
32 us (middle, mNTS, and rostral, rNTS) and the rostral ventrolateral medulla (caudal, cRVLM, and rostra
33 m of the SND was previously claimed only for rostral ventrolateral medulla, caudal raphe, and rostral
34 se preinspiratory neurones were found in the rostral ventrolateral medulla close (200-350 microm) to
35 In conclusion, NK1R-expressing cells of the rostral ventrolateral medulla control both respiratory r
36 ntromedial prefrontal cortex synapses in the rostral ventrolateral medulla decreases stress-induced g
38 mpathetic premotor neurons were found in the rostral ventrolateral medulla (including to C1 adrenergi
39 porin prior to lentivirus injection into the rostral ventrolateral medulla, increasing the proportion
40 to microinjection of angiotensin II into the rostral ventrolateral medulla is dependent upon expressi
41 retrofacial nucleus (SRF) is a region of the rostral ventrolateral medulla known to play a crucial ro
46 d and circulating EVs from CHF rats into the rostral ventrolateral medulla of normal rats evoked an i
47 ctivated by designer drug) injected into the rostral ventrolateral medulla or treatment with a beta2A
48 rved in the A5 region, ventromedial medulla, rostral ventrolateral medulla, paraventricular hypothala
49 that an increase in oxidative stress in the rostral ventrolateral medulla plays a critical role in t
50 tromedial prefrontal cortex terminals in the rostral ventrolateral medulla preferentially activates n
52 l, intra-PVN release of CRH, which activates rostral ventrolateral medulla-projecting neurons via sti
53 ctions to the nucleus tractus solitarius and rostral ventrolateral medulla result in sympathoexcitati
54 T) projections from the DRN terminate in the rostral ventrolateral medulla (RVL) and if so, whether t
55 Reticulospinal sympathoexcitatory neurons of rostral ventrolateral medulla (RVL) are selectively exci
58 on reticulo-spinal vasomotor neurones of the rostral ventrolateral medulla (RVL) has been addressed i
60 us coeruleus, nucleus of the solitary tract, rostral ventrolateral medulla (RVL)) and in three region
61 citatory reticulospinal neurons found in the rostral ventrolateral medulla (RVL), including neurons o
62 te and inhibit reticulospinal neurons in the rostral ventrolateral medulla (RVL), possibly via influe
66 (PVN) neurones that project directly to the rostral ventrolateral medulla (RVLM) (PVN-RVLM neurones)
67 The mRNA level of preproenkephalin in the rostral ventrolateral medulla (rVLM) 72 hr after EA was
69 while recording sympathetic neurons from the rostral ventrolateral medulla (RVLM) and pontine noradre
70 s (ROb), the ventromedial medulla (VMM), the rostral ventrolateral medulla (rVLM) and the A5 cell gro
71 uding the C1 catecholamine cell group of the rostral ventrolateral medulla (RVLM) and the nucleus of
72 ological studies suggest that neurons in the rostral ventrolateral medulla (RVLM) are more responsive
73 athoexcitatory reticulospinal neurons of the rostral ventrolateral medulla (RVLM) are oxygen detector
77 rted that microinjection of ethanol into the rostral ventrolateral medulla (RVLM) elicits modest incr
79 pothesis is that SNA depends on input to the rostral ventrolateral medulla (RVLM) from neurons in the
80 icular, activation of AT(1) receptors in the rostral ventrolateral medulla (RVLM) has been suggested
82 gonists of the SST-2 receptor (sst2 ) in the rostral ventrolateral medulla (RVLM) lower sympathetic n
86 e-cell patch-clamp recordings were made from rostral ventrolateral medulla (RVLM) neurones of brainst
87 gnificant increase in the firing rate of PVN-rostral ventrolateral medulla (RVLM) neurons and sympath
88 fter tracer deposits in pressor sites of the rostral ventrolateral medulla (RVLM) occupied a zone ext
89 This study investigated the AT(1)R in the rostral ventrolateral medulla (RVLM) of rabbits with CHF
90 type 1 receptors (AT1R) was increased in the rostral ventrolateral medulla (RVLM) of rabbits with chr
91 aken to evaluate the effect of apelin in the rostral ventrolateral medulla (RVLM) on blood pressure,
92 cular nucleus (PVN) neurones innervating the rostral ventrolateral medulla (RVLM) play important role
93 d rats revealed that glycine released in the rostral ventrolateral medulla (RVLM) plays a critical ro
94 ts decreases with estrogen injections in the rostral ventrolateral medulla (RVLM) region that contain
96 in-1 receptor (NK1R)-expressing cells of the rostral ventrolateral medulla (RVLM) regulate respiratio
98 tent of spinal axon collateralization of rat rostral ventrolateral medulla (RVLM) sympathetic premoto
100 These cells are located in a portion of the rostral ventrolateral medulla (RVLM) that is difficult t
101 3-mediated cardiovascular control within the rostral ventrolateral medulla (RVLM) using selective rec
102 dependent superoxide anion production in the rostral ventrolateral medulla (RVLM) was increased by 2.
103 d, and the paraventricular nucleus (PVN) and rostral ventrolateral medulla (RVLM) were microdissected
104 sympathoexcitatory vasomotor neurons of the rostral ventrolateral medulla (RVLM) were recorded in an
105 I1-imidazoline receptor is expressed in the rostral ventrolateral medulla (RVLM) where it mediates v
106 vascular sympathetic premotor neurons in the rostral ventrolateral medulla (RVLM) with bilateral micr
108 icroinjection of [Pyr(1) ]apelin-13 into the rostral ventrolateral medulla (RVLM), a major source of
109 ry raphe nuclei, ventromedial medulla (VMM), rostral ventrolateral medulla (RVLM), A5 cell group and
110 mediated by glutamatergic activation of the rostral ventrolateral medulla (RVLM), and accordingly, m
111 he solitary tract (NTS), area postrema (AP), rostral ventrolateral medulla (RVLM), and lateral parabr
112 undance in nucleus tractus solitarius (NTS), rostral ventrolateral medulla (RVLM), and PVN, and augme
113 (PVN), the parabrachical nucleus (PBN), the rostral ventrolateral medulla (RVLM), and the nucleus of
116 tory-modulated presympathetic neurons in the rostral ventrolateral medulla (RVLM), but the underlinin
117 lera toxin b neuronal tract tracing from the rostral ventrolateral medulla (RVLM), express NPY Y1 rec
118 harge of sympathetic premotor neurons in the rostral ventrolateral medulla (RVLM), neurons in the cau
120 e present in ventral medullary nuclei [e.g., rostral ventrolateral medulla (RVLM), raphe pallidus (RP
121 e perifornical hypothalamus (PeH) and in the rostral ventrolateral medulla (RVLM), which results in t
122 tward potassium current (I(A)) in identified rostral ventrolateral medulla (RVLM)-projecting PVN neur
142 ontrol: nucleus tractus solitarius (NTS) and rostral ventrolateral medulla (RVLM)] cytokine surges we
143 o cardiovascular centers of the medulla, the rostral ventrolateral medulla (RVLM; a vasopressor regio
146 termined whether respiratory neurones in the rostral ventrolateral medulla (VLM) express P2X2 recepto
148 and protein levels of mGluR5 in the PVN and rostral ventrolateral medulla were significantly higher
149 Fos (marker of neuronal activity) within the rostral ventrolateral medulla, which suggests enhanced c