ライフサイエンスコーパス: periaqueductal gray

1 ygenase metabolites as has been shown in the periaqueductal gray ().

2 6) parabrachial/Kolliker-Fuse nuclei; and 7) periaqueductal gray.

3 found in the hypothalamus, dorsal raphe, and periaqueductal gray.

4 e in 9 regions, including lateral septum and periaqueductal gray.

5 om the ventromedial prefrontal cortex to the periaqueductal gray.

6 s of two general areas: the hypothalamus and periaqueductal gray.

7 r limitans nucleus, superior colliculus, and periaqueductal gray.

8 aining, as well as the cuneiform nucleus and periaqueductal gray.

9 he ventral secondary cortex targets midbrain periaqueductal gray.

10 l prefrontal cortex, insula, and dorsal pons/periaqueductal gray.

11 pontine reticular formation, and the lateral periaqueductal gray.

12 ing neurons of the substantia nigra, and the periaqueductal gray.

13 , pontine and caudal dorsal raphe nuclei and periaqueductal gray.

14 f the hypothalamus; and to the ventrolateral periaqueductal gray.

15 the stria terminals, subfornical organ, and periaqueductal gray.

16 ne analgesia elicited from the ventrolateral periaqueductal gray.

17 circuit comprising the nucleus accumbens and periaqueductal gray.

18 e midcingulate cortex, insula, amygdala, and periaqueductal gray.

19 it presynaptic GABA neurotransmission in the periaqueductal gray.

20 amygdala and globus pallidus, and bilateral periaqueductal gray.

21 this effect correlated with activity in the periaqueductal gray.

22 s known to have extensive projections to the periaqueductal gray.

23 matosensory cortex, anterior insula, and the periaqueductal gray.

24 periaqueductal gray (54%); and ventrolateral periaqueductal gray (52%) when compared with basal bindi

25 ); dorsal raphe nucleus (53%); dorsal medial periaqueductal gray (54%); and ventrolateral periaqueduc

26 m the medial prefrontal cortex to the dorsal periaqueductal gray, a brainstem area vital for defensiv

27 Moreover, imminence-driven periaqueductal gray activity correlated with increased s

28 differential cardiac timing responses within periaqueductal gray, amygdala and insula.

29 The midbrain periaqueductal gray, an essential link between forebrain

30 in structures involved in vocal production (periaqueductal gray and anterior hypothalamus) was signi

31 inhibition blocks ERK MAPK activation in the periaqueductal gray and caudal brain stem.

32 ially to the posterior hypothalamic area and periaqueductal gray and caudally along the brachium of t

33 Substantial labeling of the locus coeruleus, periaqueductal gray and forebrain regions occurred at la

34 as well as in discrete cells in the lateral periaqueductal gray and in the central gray nucleus.

35 y in the ventrolateral portion of the caudal periaqueductal gray and in the lateral septum in aggress

36 high levels of GFAP in medial regions of the periaqueductal gray and in the nucleus accumbens.

37 central roles in pain and affect, including periaqueductal gray and nearby dorsal raphe and nucleus

38 reticular formation, midbrain raphe nuclei, periaqueductal gray and parabrachial nucleus.

39 anterior hypothalamus) and of the midbrain (periaqueductal gray and paralemniscal tegmentum) reveal

40 ncreased functional connectivity between the periaqueductal gray and rostral anterior cingulate, as h

41 CB1R desensitization in the periaqueductal gray and spinal cord following 7 d of tre

42 m and also expressed at much lower levels in periaqueductal gray and spinal cord, structures known to

43 system (CNS) pain modulatory regions (i.e., periaqueductal gray and subarachnoid lumbar spinal cord)

44 rtions of the lateral septum), midbrain (the periaqueductal gray and the intermediate layers of super

45 ior paraventricular nucleus of the thalamus, periaqueductal gray and ventrolateral medulla.

46 s, anterior and posterior PVH, ventrolateral periaqueductal gray, and Barrington's nucleus.

47 tal cortex, ventral striatum, temporal lobe, periaqueductal gray, and cerebellum in eight inbred stra

48 cells, neurons in the lateral parabrachial, periaqueductal gray, and dorsal raphe containing fluorog

49 mRNA is also detected in mammillary nuclei, periaqueductal gray, and dorsal raphe.

50 medial parabrachial, solitary, ventrolateral periaqueductal gray, and interfascicular nuclei.

51 rway motor control (i.e., the Kolliker-Fuse, periaqueductal gray, and intermediate reticular nuclei).

52 nd medial and ventrolateral divisions of the periaqueductal gray, and it sends a light input to the a

53 luding the lateral parabrachial nucleus, the periaqueductal gray, and laminae I-II of the spinal trig

54 lis, perifornical and anterior hypothalamus, periaqueductal gray, and lateral parabrachial nucleus.

55 luding the tuberomammillary nucleus, ventral periaqueductal gray, and locus coeruleus.

56 f the lamina terminalis, supraoptic nucleus, periaqueductal gray, and medial nucleus of the solitary

57 ions, including the ventral tuberal nucleus, periaqueductal gray, and paraventricular regions of the

58 rorubral area, ventrolateral division of the periaqueductal gray, and pontine central gray.

59 stria terminalis, paraventricular thalamus, periaqueductal gray, and precoeruleus.

60 descending pain modulatory system (amygdala, periaqueductal gray, and rostral-ventromedial medulla),

61 BGluM increases in the ipsilateral striatum, periaqueductal gray, and somatosensory cortex, and in co

62 and/or downregulation in cerebellum, caudal periaqueductal gray, and spinal cord and attenuated tole

63 r nucleus, the medial and lateral lemniscus, periaqueductal gray, and the interpeduncular nucleus.

64 rom neurons in the lateral parabrachial, the periaqueductal gray, and/or the dorsal raphe nuclei.

65 portion); ventromedial hypothalamus; lateral periaqueductal gray; and medial, central, and basolatera

66 minalis, along with their projections to the periaqueductal gray, are strongly implicated in freezing

67 and kappa opioid receptor agonists into the periaqueductal gray area (PAG).

68 ucleus, Kolliker-Fuse nucleus, ventrolateral periaqueductal gray area, central nucleus of the amygdal

69 caudal A10 cell group (A10dc) located in the periaqueductal gray area.

70 nucleus, median eminence, infundibular stem, periaqueductal gray, area postrema, pontine raphe nucleu

71 g) analgesia elicited from the ventrolateral periaqueductal gray as measured by the tail-flick and ju

72 nucleus, retrochiasmatic area, ventrolateral periaqueductal gray, Barrington's nucleus), hypothalamic

73 tex, anterior cingulate, the cerebellum, and periaqueductal gray, brain areas that mediate task perfo

74 signaling is modulated in the ventrolateral periaqueductal gray by persistent inflammation different

75 vidence for substantial dual labeling in the periaqueductal gray, caudal portions of the zona incerta

76 the ventral tegmental area (VTA), habenula, periaqueductal gray, cerebellum, hypothalamus, and hippo

77 to predict arm and leg stimulation from the periaqueductal gray, control regions (e.g., white matter

78 tween the ventromedial prefrontal cortex and periaqueductal gray correlated with somatosensory decrea

79 partum lesions of the caudal intercollicular periaqueductal gray (cPAG-x) was confirmed and was exten

80 her OT receptor activity in the ventrocaudal periaqueductal gray (cPAGv) contributes to mothers' redu

81 nervation of the ventrolateral column of the periaqueductal gray distinguished the midbrain.

82 ductal gray (vl PAG) versus the dorsolateral periaqueductal gray (dl PAG), in the rabbit, elicits two

83 lating neuronal activity of the dorsolateral periaqueductal gray (dl-PAG) through excitatory and inhi

84 mate receptors (mGlu(5)) in the dorsolateral periaqueductal gray (dlPAG) and mobilizing 2-AG.

85 that VMHdm/c projection to the dorsolateral periaqueductal gray (dlPAG) induces inflexible immobilit

86 stral or caudal portions of the dorsolateral periaqueductal gray (dlPAG).

87 l motor nucleus of the vagus), ventrolateral periaqueductal gray, dorsal parabrachial nucleus, perive

88 amus (LH), mediolateral septum, dorsolateral periaqueductal gray, dorsal raphe, ventral tegmental are

89 hese subdivisions included the ventrolateral periaqueductal gray, dorsomedial hypothalamus, dorsolate

90 The dorsal and ventral periaqueductal gray (dPAG and vPAG, respectively) are em

91 al gray (VPAG), or sympathoexcitatory dorsal periaqueductal gray (DPAG), differentially modulates CBF

92 rojections from the ARC to the ventrolateral periaqueductal gray during EA at P5-P6 contribute to inh

93 (vmPFC), insula, amygdala, hypothalamus, and periaqueductal gray emerge as central brain structures u

94 wedge of labeled neurons in the dorsolateral periaqueductal gray extending into the deep layers of th

95 ygdala, bed nucleus of the stria terminalis, periaqueductal gray, hippocampus, and dorsal anterior ci

96 g paraventricular nucleus, and ventrolateral periaqueductal gray); hypothalamic visceromotor pattern

97 idus nucleus, nucleus of the solitary tract, periaqueductal gray, hypothalamic paraventricular nucleu

98 ephalic tegmentum, parabrachial nucleus, and periaqueductal gray), hypothalamus, limbic and paralimbi

99 ervation of the parabrachial nucleus and the periaqueductal gray, important nociceptive structures.

100 fralimbic prefrontal cortex, hippocampus and periaqueductal gray in extinction learning, while mainta

101 dies in the midbrain reticular formation and periaqueductal gray in four clinically documented and ge

102 ic motor nucleus, in a band just beneath the periaqueductal gray in the midbrain, in ventricular regi

103 ircuitry implicated in retaliation (amygdala/periaqueductal gray) in youths with DBD and low levels o

104 ar and posterior hypothalamus, zona incerta, periaqueductal gray, intermediate layers of the contrala

105 rect evidence supporting the notion that the periaqueductal gray is a site for higher cortical contro

106 ia elicited by morphine in the ventrolateral periaqueductal gray is mediated in part by NMDA and chol

107 f the projections from the ICx to the dorsal periaqueductal gray is sufficient for provoking flight b

108 ral mesencephalic reticular formation (MRF), periaqueductal gray, Kolliker-Fuse nucleus, and pontis c

109 sal lateral hypothalamic area, ventrolateral periaqueductal gray, lateral parabrachial nucleus and ca

110 terminalis, central nucleus of the amygdala, periaqueductal gray, lateral parabrachial nucleus, nucle

111 scle tone such as those in the ventrolateral periaqueductal gray, lateral pontine tegmentum, locus ce

112 ted [(35)S]GTPgammaS binding was observed in periaqueductal gray, locus coeruleus, lateral parabrachi

113 mic nucleus, posterior hypothalamic nucleus, periaqueductal gray, locus coeruleus, nucleus accumbens,

114 ulomotor nucleus, red nucleus, raphe nuclei, periaqueductal gray, locus coeruleus, trigeminal nucleus

115 ned the role of eNOS within the dorsolateral periaqueductal gray mater (dlPAG) on cardiovascular resp

116 bnormal in hippocampus ( approximately 10%), periaqueductal gray matter ( approximately 13%), fimbria

117 the olfactory bulb ( approximately 10%) and periaqueductal gray matter ( approximately 16%).

118 Nitric oxide (NO) within the dorsal periaqueductal gray matter (dPAG) attenuated cardiovascu

119 al cortex, the lateral hypothalamus, and the periaqueductal gray matter (PAG) are involved in these c

120 ase in the total phosphatase activity in the periaqueductal gray matter (PAG) from morphine-pelleted

121 roinjection of dipyrone (metamizol) into the periaqueductal gray matter (PAG) in rats causes antinoci

122 The periaqueductal gray matter (PAG) is a major neuroanatomi

123 orsal horn (DH) by brain regions such as the periaqueductal gray matter (PAG) plays a critical role i

124 The periaqueductal gray matter (PAG) projections to the intr

125 The periaqueductal gray matter (PAG), a known modulator of s

126 nervate various targets, including thalamus, periaqueductal gray matter (PAG), and lateral parabrachi

127 nd the dorsolateral quadrant of the midbrain periaqueductal gray matter (PAG).

128 r ibotenic acid lesions of the ventrolateral periaqueductal gray matter (vlPAG) attenuated antinocice

129 -immunoreactive (TH-ir) cells in the ventral periaqueductal gray matter (vPAG) expressed Fos protein

130 reased gray matter in the midbrain including periaqueductal gray matter and nucleus cuneiformis, wher

131 e right amygdala and decreased activation in periaqueductal gray matter and the rostral anterior cing

132 rodents, that deep brain stimulation in the periaqueductal gray matter can rapidly and reversibly ma

133 Because chemokine administration into the periaqueductal gray matter inhibits opioid-induced analg

134 , followed by opioid administration into the periaqueductal gray matter of the brain results in an in

135 mygdala, prefrontal cortex, hippocampus, and periaqueductal gray matter to the control of conditioned

136 y cortex, the anterior cingulate cortex, the periaqueductal gray matter, and other regions.

137 cingulate cortex, caudate nuclei, brain stem periaqueductal gray matter, cerebellum, and occipital co

138 sterior hypothalamic nuclei), and brainstem (periaqueductal gray matter, dorsal and central superior

139 more modest, but labeling was strong in the periaqueductal gray matter, dorsal raphe nucleus, and la

140 tions to lateral hypothalamus, dorsal raphe, periaqueductal gray matter, pericerulear region, rostrov

141 al scar, these fibers elongated in white and periaqueductal gray matter, reaching the farthest distan

142 rea, Edinger-Westphal nucleus, ventrolateral periaqueductal gray matter, reticular formation, peduncu

143 was mediated by projections to the midbrain periaqueductal gray matter.

144 r cortices, nucleus accumbens, amygdala, and periaqueductal gray matter.

145 nuclei, central nucleus of the amygdala, and periaqueductal gray matter.

146 he hypothalamus; and ventral tegmental area, periaqueductal gray, medial and posterior pretectal nucl

147 the wFMNs: superior colliculus, red nucleus, periaqueductal gray, mesencephalon, pons, and several nu

148 tive axons descended ventromedially into the periaqueductal gray, moving caudally and arborizing exte

149 from identified spino-parabrachial and spino-periaqueductal gray neurons indicated the presence of pa

150 ial longitudinal fasciculus, supraoculomotor periaqueductal gray, nucleus of the optic tract, the inf

151 mine the organization of the medial preoptic-periaqueductal gray-nucleus paragigantocellularis pathwa

152 al midbrain/pontine tegmentum, including the periaqueductal gray/nucleus cuneiformis.

153 oidance) dependent on the extended amygdala, periaqueductal gray, or septum, all regions that project

154 We demonstrate in rats that the periaqueductal gray (PAG) affects motor systems at the f

155 The periaqueductal gray (PAG) and amygdala are known to be i

156 The ventrolateral periaqueductal gray (PAG) and pontine reticular formatio

157 ceptors, acts by an unknown mechanism in the periaqueductal gray (PAG) and raphe magnus (RM) to stimu

158 could be mediated in part by actions in the periaqueductal gray (PAG) and the dorsal raphe nucleus (

159 To determine if the periaqueductal gray (PAG) and the dorsal raphe nucleus (

160 CeL neurons directly project to the midbrain periaqueductal gray (PAG) and the paraventricular nucleu

161 se VMH efferents travel caudally through the periaqueductal gray (PAG) and then ventrally through the

162 The midbrain periaqueductal gray (PAG) and ventromedial medulla (VMM)

163 The different subdivisions of the midbrain periaqueductal gray (PAG) are intricately (and different

164 attention or expectancy have identified the periaqueductal gray (PAG) as a key brainstem structure i

165 the endogenous cannabinoid anandamide in the periaqueductal gray (PAG) by in vivo microdialysis in th

166 he generation of DRRs and stimulation of the periaqueductal gray (PAG) can induce the release of GABA

167 binds to mu-opioid receptors (MORs), and the periaqueductal gray (PAG) contains a dense population of

168 The periaqueductal gray (PAG) coordinates behaviors essentia

169 r 4 (TLR4)-mediated neuroinflammation in the periaqueductal gray (PAG) drives tolerance.

170 onnectivity fluctuations between the DMN and periaqueductal gray (PAG) dynamically tracked spontaneou

171 Activation of the dorsal periaqueductal gray (PAG) evokes defense-like behavior i

172 pothalamic nucleus (VMH) that project to the periaqueductal gray (PAG) form a crucial segment of the

173 NK(1)-Substance P receptors in the midbrain periaqueductal gray (PAG) in defensive rage behavior in

174 imulation in different parts of the midbrain periaqueductal gray (PAG) in the cat generates four diff

175 l evidence that neurons in the ventrolateral periaqueductal gray (PAG) innervate the medial pericoeru

176 The periaqueductal gray (PAG) is a brain region involved in

177 The periaqueductal gray (PAG) is an important center that co

178 The ventrolateral periaqueductal gray (PAG) is an important neuronal netwo

179 The midbrain periaqueductal gray (PAG) is involved in many basic surv

180 Evidence suggests the periaqueductal gray (PAG) is involved in the integration

181 The periaqueductal gray (PAG) is known to be essential for v

182 The ventrolateral portion of the periaqueductal gray (PAG) is one brain region in which l

183 t.SIGNIFICANCE STATEMENT We demonstrate that periaqueductal gray (PAG) microglia contribute to the se

184 expression is increased in the ventrolateral periaqueductal gray (PAG) neurons following precipitated

185 and spontaneous firings of rat ventrolateral periaqueductal gray (PAG) neurons, either mechanically d

186 tracellular Ca(2+) levels in dissociated rat periaqueductal gray (PAG) neurons, which express GPR55 m

187 ral nucleus, deep mesencephalic nucleus, and periaqueductal gray (PAG) of both sexes.

188 ala by recording neurons in the amygdala and periaqueductal gray (PAG) of rats during fear conditioni

189 norecipient nuclei as well as in the DRN and periaqueductal gray (PAG) of the mesencephalon.

190 te nucleus (ARC) of the hypothalamus and the periaqueductal gray (PAG) of the midbrain.

191 M), but not following co-injections into the periaqueductal gray (PAG) or into the spinal subarachnoi

192 by lesions of brainstem regions such as the periaqueductal gray (PAG) or the rostral ventromedial me

193 The periaqueductal gray (PAG) orchestrates survival behavior

194 The midbrain periaqueductal gray (PAG) plays a central role in the de

195 nal motor system, in which the mesencephalic periaqueductal gray (PAG) plays a central role, as demon

196 The periaqueductal gray (PAG) plays an important role in mor

197 Stimulation of neurons in the periaqueductal gray (PAG) produces antinociception that

198 The midbrain periaqueductal gray (PAG) region is organized into disti

199 beta-endorphin in the rVLM as well as in the periaqueductal gray (PAG) that are involved in EA-mediat

200 ng emotions and projects to the amygdala and periaqueductal gray (PAG) to modulate emotional response

201 ng pain modulatory system that runs from the periaqueductal gray (PAG) to the spinal cord.

202 on of prefrontal cortical projections to the periaqueductal gray (PAG) were defined with retrograde a

203 lamus (CH) have been shown to project to the periaqueductal gray (PAG) which, in turn, sends descendi

204 ult of increased microglia activation in the periaqueductal gray (PAG), a central locus mediating the

205 state functional connectivity (rs-fc) of the periaqueductal gray (PAG), a key region in the descendin

206 yngeal nerve (ISLN) activates neurons of the periaqueductal gray (PAG), a midbrain region implicated

207 We found that pain PEs were encoded in the periaqueductal gray (PAG), a structure important for pai

208 havior in the cat elicited from the midbrain periaqueductal gray (PAG), and that such effects are blo

209 halamus, the amygdala, the hypothalamus, the periaqueductal gray (PAG), and the brainstem reticular f

210 ciation between the brainstem areas, such as periaqueductal gray (PAG), and the headache phase of mig

211 rticular, the medullary reticular formation, periaqueductal gray (PAG), and ventromedial nucleus of t

212 In the ventrolateral periaqueductal gray (PAG), endogenous pathways which dam

213 reas, the dorsal raphe nucleus (DRN) and the periaqueductal gray (PAG), in addition to EW.

214 d 81, 96, 106, and 82 tolerance genes in the periaqueductal gray (PAG), prefrontal cortex, temporal l

215 ministered systemically or directly into the periaqueductal gray (PAG), produces a significantly grea

216 stent with the location of areas such as the periaqueductal gray (PAG), rostral ventral medulla, and

217 We show that BDNF-containing neurons in the periaqueductal gray (PAG), the central structure for pai

218 ctions to the rostral midbrain including the periaqueductal gray (PAG), the deep layers of the superi

219 lowing administration into the ventrolateral periaqueductal gray (PAG), the dorsal PAG, and the rostr

220 or-expressing neurons (LepRb neurons) in the periaqueductal gray (PAG), the largest population of Lep

221 D), the lateral hypothalamic area (LHA), the periaqueductal gray (PAG), the parabrachial nucleus (Pb)

222 lateral and the upper lateral portion of the periaqueductal gray (PAG), the Su3 and PV2 nuclei of the

223 ds and to determine the role of the midbrain periaqueductal gray (PAG), which mediates stress-induced

224 ted to be present in regions of the midbrain periaqueductal gray (PAG).

225 ic neurons and CRF receptors is the midbrain periaqueductal gray (PAG).

226 hypothalamus and dorsolateral aspect of the periaqueductal gray (PAG).

227 baroreflex attenuation) evoked by the dorsal periaqueductal gray (PAG).

228 t exert its effect on these functions is the periaqueductal gray (PAG).

229 ulates nociception and blood pressure in the periaqueductal gray (PAG).

230 projections from the amygdala to the ventral periaqueductal gray (PAG).

231 east in part by morphine's action within the periaqueductal gray (PAG).

232 ation of the mPFC subdivisions, amygdala and periaqueductal gray (PAG).

233 tex, insula, nucleus accumbens, amygdala and periaqueductal gray (PAG).

234 r a network of forebrain structures plus the periaqueductal gray (PAG).

235 nucleus of the stria terminalis (BSTm), and periaqueductal gray (PAG).

236 ral striatum, amygdala, midline thalamus and periaqueductal gray (PAG).

237 procedures to affect c-Fos expression in the periaqueductal gray (PAG).

238 tic (MPO) produced dense labeling within the periaqueductal gray (PAG); anterogradely labeled fibers

239 tral tegmental area (VTA), and ventrolateral periaqueductal gray (PAGvl).

240 he substantia nigra, ventral tegmental area, periaqueductal gray, parabrachial nucleus, and dorsal va

241 were confined to the ventral tegmental area, periaqueductal gray, parabrachial nucleus, and locus coe

242 sal lateral hypothalamic area, ventrolateral periaqueductal gray, parabrachial nucleus, and nucleus o

243 ei, hippocampus, amygdala, substantia nigra, periaqueductal gray, paratrochlear nucleus, paralemnisca

244 the two fiber types was also observed in the periaqueductal gray, particularly in the vicinity of the

245 ypothalamic areas, Edinger-Westphal nucleus, periaqueductal gray, pedunculopontine tegmental nucleus,

246 d nucleus of the stria terminalis, amygdala, periaqueductal gray, raphe and parabrachial nuclei) and

247 gdala, hypothalamus, zona incerta, thalamus, periaqueductal gray, raphe nuclei, lateral parabrachial

248 These findings indicate that neurons in the periaqueductal gray region of the brain have an inherent

249 eritonally) or neurotensin directly into the periaqueductal gray region of the brain.

250 xide (NO) donating compounds into the dorsal periaqueductal gray region of the midbrain (PAG) decreas

251 potency of the opioid beta-endorphin in the periaqueductal gray region of the midbrain (PAG).

252 crease in the levels of mu receptor in their periaqueductal gray region, while AS-MOR MM rats showed

253 the hand of nine normal subjects within the periaqueductal gray region.

254 al cortex, lateral orbitofrontal cortex, and periaqueductal gray relative to controls but showed grea

255 The periaqueductal gray represents the final common pathway

256 pramammillary nuclei; ventrolateral midbrain periaqueductal gray; rostral and midlevel ventrolateral

257 sis that neurons in the rostral ventromedial periaqueductal gray (rvmPAG) are a source of inhibitory

258 olaminergic and cholinergic cell groups, the periaqueductal gray, several brainstem reticular nuclei,

259 formation, cerebellum, parabrachial nucleus, periaqueductal gray, thalamus, hypothalamus, amygdala, b

260 und no evidence that neurons of the midbrain periaqueductal gray that project to the RVM are postsyna

261 measured in the dorsal central gray matter (periaqueductal gray), the locus coeruleus, the ventromed

262 inalis, the medial and central amygdala, the periaqueductal gray, the dorsal raphe, and the locus coe

263 amic nuclei, the medial geniculate body, the periaqueductal gray, the ventral tegmental area, the sup

264 ual anterior cingulate cortex (sgACC) to the periaqueductal gray to the rostral ventromedial medulla

265 orphine microinjected into the ventrolateral periaqueductal gray using both the foot-withdrawal and t

266 and lateral nuclei of the hypothalamus; and periaqueductal gray, ventral tegmental area, substantia

267 In lateral periaqueductal gray, virgin mice showed a significant Eg

268 electrical stimulation of the ventrolateral periaqueductal gray (vl PAG) versus the dorsolateral per

269 resynaptic GABA release in the ventrolateral periaqueductal gray (vlPAG) activates the descending ant

270 ulatory regions, including the ventrolateral periaqueductal gray (vlPAG) and locus ceruleus (LC).

271 een shown that the ventrolateral part of the periaqueductal gray (VLPAG) and the adjacent dorsal deep

272 The ventrolateral periaqueductal gray (vlPAG) is a critical structure in t

273 The ventrolateral periaqueductal gray (vlPAG) is a key structure in the de

274 The ventrolateral periaqueductal gray (vlPAG) is an integral locus for mor

275 een central amygdala (CeA) and ventrolateral periaqueductal gray (vlPAG) is implicated in several dis

276 The midbrain ventrolateral periaqueductal gray (vlPAG) is known to be a crucial sup

277 n (PG) E2 signaling within the ventrolateral periaqueductal gray (vlPAG) is pronociceptive in naive a

278 antagonist pretreatment in the ventrolateral periaqueductal gray (vlPAG) of rats.

279 inociception elicited from the ventrolateral periaqueductal gray (vlPAG) on two nociceptive measures.

280 Given that the ventrolateral periaqueductal gray (vlPAG) plays a major role in morphi

281 hat the ventrolateral column of the midbrain periaqueductal gray (vlPAG) region mediates the hypotens

282 ed IS induces DeltaFosB in the ventrolateral periaqueductal gray (vlPAG), and levels of the protein a

283 the arcuate nucleus (ARC) and ventrolateral periaqueductal gray (vlPAG).

284 arily to axon terminals in the ventrolateral periaqueductal gray (vlPAG).

285 responses, from the brainstem ventrolateral periaqueductal gray (vlPAG).

286 la (17%), midline raphe (40%), ventrolateral periaqueductal gray (VLPAG, 15%), lateral hypothalamic a

287 croinjecting morphine into the ventrolateral periaqueductal gray (vPAG) develops with repeated admini

288 orphine microinjected into the ventrolateral periaqueductal gray (vPAG) was evaluated.

289 istration of morphine into the ventrolateral periaqueductal gray (vPAG), a key structure contributing

290 of neurons of the sympathoinhibitory ventral periaqueductal gray (VPAG), or sympathoexcitatory dorsal

291 the antinociceptive action of ventrolateral periaqueductal gray (vPAG)-administered morphine.

292 l forebrain (SLEA) and the ventral tegmentum/periaqueductal gray (VT/PAG), while foci of increased si

293 rgic locus ceruleus and dopaminergic ventral periaqueductal gray wake neurons.

294 eta-endorphin analgesia in the ventrolateral periaqueductal gray was confirmed by its sensitivity to

295 Activation in the periaqueductal gray was significantly increased during t

296 lus retroflexus, interpeduncular nuclei, and periaqueductal gray were also stained with this antibody

297 The PVH and ventrolateral periaqueductal gray were recipients of GABAergic outputs

298 etabolic decreases in insular cortex and the periaqueductal gray, were noted.

299 cerebellum, hippocampus, olfactory bulb, and periaqueductal gray, with in situ hybridization.

300 CG and OFC, mPFC, LHA, VMN, hippocampus, and periaqueductal gray, with largest effect sizes in mPFC a