ライフサイエンスコーパス: adult rat

1 PNS (sensory) but not CNS (retinal) axons in adult rat.

2 rent aspects of executive functioning in the adult rat.

3 ut not LTD at MF synapses of freely behaving adult rats.

4 tate gyrus (mPP-DG) synapses in juvenile and adult rats.

5 tion learning in adolescent rats, but not in adult rats.

6 in the primary cultured cardiomyocytes from adult rats.

7 ollowing unilateral C4 spinal hemisection in adult rats.

8 an be rapidly modified by reward training in adult rats.

9 forms of BLA hyperactivity in adolescent and adult rats.

10 d in the articular cartilage chondrocytes of adult rats.

11 d environment (EE) promotes OD plasticity in adult rats.

12 al disturbances on indices of DA function in adult rats.

13 lity during the task than either juvenile or adult rats.

14 natal insult blocked the induction of GHS in adult rats.

15 es, including the gastro-intestinal tract of adult rats.

16 y injection of axonal anterograde tracers in adult rats.

17 d in neurons of dorsal root ganglia (DRG) of adult rats.

18 ritic morphology of dentate gyrus neurons in adult rats.

19 after a thoracic spinal cord hemisection in adult rats.

20 e thoracic transection of the spinal cord in adult rats.

21 e thoracic spinal cord transection lesion in adult rats.

22 rn neurons of spinal slices taken from young adult rats.

23 mized, anesthetized, spontaneously breathing adult rats.

24 ficantly more slowly than either juvenile or adult rats.

25 ein into the T4 complete transection site of adult rats.

26 ter synaptic transmission in the PFC of male adult rats.

27 e-cell patch-clamp recordings in slices from adult rats.

28 xtracellular stimulation method in young and adult rats.

29 or unilaterally into the substantia nigra in adult rats.

30 cortex, while exerting excitatory effects in adult rats.

31 impairment in both SND and NOR procedures in adult rats.

32 focused attention and arousal regulation in adult rats.

33 neuronal activity in the cochlear nucleus of adult rats.

34 dy (CB) chemosensory reflex were examined in adult rats.

35 1 splice variants in control and salt-loaded adult rats.

36 sAHP in hippocampal slice neurons from young-adult rats.

37 ical areas after bilateral deafness in young adult rats.

38 l cortices after auditory deprivation in the adult rats.

39 Experiments were conducted in adult rats.

40 propria containing the myenteric plexus from adult rats.

41 amatergic drive of LAT projection neurons in adult rats.

42 dy (CB) chemosensory reflex were examined in adult rats.

43 slice cultures and acute brainstem slices of adult rats.

44 a play a critical role in this incubation in adult rats.

45 from aged rats compared to those in younger adult rats.

46 tory exploration and same-sex recognition of adult rats.

47 lete low-thoracic spinal cord transection in adult rats.

48 We generated controlled cortical impacts in adult rats.

49 n vivo in a model of chemical denervation in adult rats.

50 d schizophrenia, and in chronically-stressed adult rats.

51 breathing vagotomized urethane-anesthetized adult rats.

52 rainstem after brachial dorsal root crush in adult rats.

53 lasticity in postweanling pups compared with adult rats.

54 ty of layer 5 mPFC-BLA projection neurons in adult rats.

55 in extinction could exist in adolescent and adult rats.

56 se to cocaine administration in anesthetized adult rats.

57 In adult rats, 3.6% +/- 0.9% of cells still proliferate, wh

58 In contrast, in the mPFC of adult rats 5 weeks after they received nicotine treatmen

59 In juvenile and adult rats, a single class of USV is observed with an ag

60 In conclusion, in adult rats, accumulation of synaptic CP-AMPARs in the NA

61 We conclude that in anesthetized adult rats active expiration is driven by the pFL but re

62 dide(DiR)-labeled liposomes was evaluated in adult rats after single intravenous injection at dose of

63 In adult rats, albumin leakage into injured regions was mar

64 piriform cortex were sparser than typical in adult rat and did not enlarge with learning.

65 gions, including sensory nuclei, in both the adult rat and human, where it may regulate neuronal func

66 h light (LM) and electron microscopy (EM) in adult rat and mouse brain.

67 ative data on the anatomy of the nLOT in the adult rat and on the effects of age on its structure and

68 bead formation in the dendrites and axons of adult rat and rabbit retinal ganglion cells, and that re

69 e the cardiac side effects of doxorubicin in adult rats and decipher whether signaling pathways invol

70 rich fraction was isolated from the blood of adult rats and human volunteers and was analyzed by prot

71 y means of the elevated plus maze in control adult rats and in adult rats subjected to early EE or to

72 Here we show in young adult rats and mice that learning the hippocampus-depend

73 Adult rats and mice were photocoagulated using diode las

74 CSD was elicited chemically in adult rats and occurrence, amplitude, duration and propa

75 e ethanol-induced anxiolysis was measured in adult rats, and amygdaloid tissues were used for miRNA p

76 growth plate (AG) cartilage chondrocytes in adult rats, and superficial layer (IS) versus deep layer

77 vade the CRF receptor system in juvenile and adult rats, and the mechanisms that control them are lik

78 /lower jaw border,(1) FP/LJ border) in SI of adult rats, and used a retrograde axonal tracer (cholera

79 t grafted into the transected spinal cord of adult rats as a supportive environment for regeneration

80 antly down-regulated after focal ischemia in adult rats as well as after oxygen-glucose deprivation i

81 ial cells of the ventral cochlear nucleus in adult rats at 1, 7, 15, and 30 days following bilateral

82 synapses in neocortex and hippocampus of the adult rat, based on aldehyde-fixed material stabilized w

83 klotho mRNA expression in the developing and adult rat brain and report moderate, widespread expressi

84 d a DPP10 antibody to label DPP10 protein in adult rat brain by immunohistochemistry.

85 re, we evaluated gamma-H2AX formation in the adult rat brain following neuronal excitation evoked by

86 Adult rat brain microglia (resting or activated with lip

87 Immunoelectron microscopy of the adult rat brain showed that GluN2D is predominantly expr

88 ghly expressed in O4(+) OL precursors of the adult rat brain than those of the neonatal brain.

89 Oligodendrocyte apoptosis was induced in the adult rat brain using a lentivirus to express experiment

90 I and -URP binding site distributions in the adult rat brain, and found that they fully overlapped at

91 here that NDCBE is expressed throughout the adult rat brain, and selectively concentrates in presyna

92 rate that IRSp53 is expressed throughout the adult rat brain.

93 both isoforms in PSD fractions isolated from adult rat brain.

94 Twenty-six healthy human adults rated brushing on the hand during fMRI.

95 lasmids into the tibialis anterior muscle of adult rats by in vivo electroporation.

96 ree questions: (1) whether PTEN knockdown in adult rats by nongenetic techniques enables CST regenera

97 BBB is disrupted differently in neonatal and adult rats by transient middle cerebral artery occlusion

98 r conditioning) or conditioned inhibition in adult rats by using serial section transmission electron

99 ssed in the somata and proximal dendrites of adult rat CA1 pyramidal cells.

100 Here we show that adult rats can learn to perceive otherwise invisible inf

101 sumption, showing that completely spinalized adult rats can recover unassisted hindlimb weight suppor

102 Adult rats can thus develop a novel cortical sensorimoto

103 Using membranes prepared from adult rat cardiac myocytes and fibroblasts, we found tha

104 cytes, human embryonic cardiac myocytes, and adult rat cardiac myocytes.

105 d by coexpression of CN-Aalpha/PKCepsilon in adult rat cardiac myofibroblasts (ARVFs) on a larger sca

106 4mtD3cpv, MitoCam) was expressed in cultured adult rat cardiomyocytes and the free mitochondrial calc

107 and insulin action were analyzed in primary adult rat cardiomyocytes incubated with conditioned medi

108 al expression of cMyBP-C(C10mut) in cultured adult rat cardiomyocytes was used to investigate protein

109 s motors selectively reduced IKur current in adult rat cardiomyocytes.

110 is channel complex in heterologous cells and adult rat cardiomyocytes.

111 lated transcript (CART) peptide depletion in adult rats, CART shRNAs or scrambled control shRNAs were

112 roligin 3 (NL3) or neuroligin 2 (NL2) in the adult rat cerebral cortex following in utero electropora

113 sion of CB2SH3- or CB2SH3+ in neurons of the adult rat cerebral cortex.

114 shing the set point for fibrotic activity in adult rat CFs and identify a key role for the modulation

115 We discovered that adult rat CFs express 190 GPCRs and that activation of p

116 lower and opioid effects are more evident in adult rats compared to early postnatal rats.

117 vivo recordings from the STN of anesthetized adult rats demonstrated that the spike firing rate was i

118 d that GABAergic responses in adolescent and adult rat DGCs are still depolarizing from rest.

119 vitro model of axonal dieback as well as an adult rat dorsal column crush model of spinal cord injur

120 f KChIP1, KChIP2, KChIP3, DPP6, and DPP10 in adult rat dorsal root ganglion (DRG) and spinal cord by

121 and beta1 integrin transport and traffic in adult rat dorsal root ganglion axons and PC12 cells.

122 and organs, enables siRNA to gain entry into adult rat dorsal root ganglion neurons in culture.

123 We now find that treatment of adult rat dorsal root ganglion neurons in vitro with LRP

124 In young adult rats, DPPIV inhibition resulted in an increase in

125 t depletion of amphoterin mRNA from cultured adult rat DRG neurons attenuates neurite outgrowth, poin

126 ood pressure and heart rate were obtained in adult rats during 4 weeks of CIHH exposure.

127 ) and dorsal striatum (DS) of adolescent and adult rats during a reward-motivated instrumental task.

128 ded daily from VTA neurons in adolescent and adult rats during learning and maintenance of a cued, re

129 e and Epac1 null E12.5 mouse heart explants, adult rat epicardial cells, and immortalized mouse embry

130 axonal translational machinery is present in adult rats, even when adult neurogenesis is blocked.

131 e demonstrate that VTA dopamine neurons from adult rats exhibit enhanced IPSCs after adolescent alcoh

132 ro brainstem slice preparation obtained from adult rats exposed either to air or CIHH for 4 weeks.

133 Experiments were performed on adult rats exposed to CIH for 10 days.

134 In contrast, LC neurons of adult rats exposed to repeated social stress were relati

135 Accordingly, in vitro recordings from adult rats exposed to WIN during adolescence demonstrate

136 t middle cerebral artery occlusion (MCAO) in adult rats, expression of FosDT and Fos was induced.

137 Older and younger adults rated faces high in trust cues similarly, but old

138 of nicotine to brain slices from drug-naive adult rats followed by a period of recovery resulted in

139 ynaptic plasticity in the accumbens shell of adult rats following cocaine self-administration.

140 cantly reduced secondary injury pathology in adult rats following spinal contusion injury and LV-ChAB

141 of a continuous growth-promoting pathway in adult rats, formed by grafted Schwann cells overexpressi

142 Compared to young rats, adult rats had delayed functional recovery, whereas the

143 lear export in ventricular myocytes from the adult rat heart.

144 isolated neonatal murine cardiomyocytes and adult rat hearts (Langendorff preparation) mitochondrial

145 perative in vivo in ventricular tissues from adult rat hearts overexpressing resistin.

146 ed the splicing patterns in the neonatal and adult rat hearts.

147 on, and gene expression differ from those of adult rat hepatocytes.

148 tended access cocaine self-administration in adult rats, high conductance Ca2+ -ermeable AMPA recepto

149 beta-amyloid peptide), and (ii) cultures of adult rat hippocampal astrocytes generated from control

150 ace with in vitro tissue simulant containing adult rat hippocampal NPCs (aNPCs) and their neuronal pr

151 roduction of long-term potentiation (LTP) in adult rat hippocampal slices that can account for one te

152 Here, we report that treatment of adult rat hippocampal slices with BDNF or with tetraethy

153 from dentate gyrus granule cells (DGGCs) in adult rat hippocampal slices.

154 citatory post-synaptic potentials (EPSPs) in adult rat hippocampal slices.

155 rt we show that alpha-synuclein-accumulating adult rat hippocampus neural progenitors present aberran

156 zed synapses from postnatal day 15 (P15) and adult rat hippocampus that had undergone theta-burst sti

157 ization of CaMKII in CA1 stratum radiatum of adult rat hippocampus, by using immuno-electron microsco

158 e systemic HDACi administration in the young adult rat hippocampus.

159 on of MMP-2 and MMP-9 in early postnatal and adult rat hippocampus.

160 y in principal cells and interneurons of the adult rat hippocampus.

161 highest EAAC1 levels were found in the young adult rat hippocampus.

162 luences plasticity in the brain of young and adult rats; however, the effects were dependent of age a

163 The neonatal PCP treatment induced in the adult rat hyperlocomotion in response to amphetamine (Am

164 ound that populations of interneurons in the adult rat hypothalamus switched between dopamine and som

165 ion of the GABA(A) receptor delta-subunit in adult rats in localized regions of the nucleus accumbens

166 Chronically epileptic male adult rats in the pilocarpine model of temporal lobe epi

167 ecordings in prefrontal cortical slices from adult rats in which DISC1 function was reduced in vivo b

168 Previous studies in adult rats indicate that the loss of dense contralateral

169 two different systems: zebrafish embryos and adult rats, indicating that this NKA-mediated regulatory

170 Angiotensin II was infused into healthy adult rats, inducing chronic hypertension, and microRNA

171 even in sterile rat embryo islets, germ-free adult rat islets, and neogenic tubular complexes.

172 erences in dendritic spine morphology in the adult rat LA after fear conditioning, conditioned inhibi

173 esence of progenitor cells in the uninjured, adult rat lacrimal gland (LG).

174 osomes accumulate in dendritic spines of the adult rat lateral amygdala (LA) during consolidation of

175 Adult rats learned a skilled forelimb grasping task and

176 ibrils and mitochondria, both collected from adult rat left ventricular myocytes.

177 In this study, we show that the adult rat liver harbors a small pool of endogenous mesen

178 al amygdala (MePD) are sexually dimorphic in adult rats: males have more astrocytes in the right MePD

179 endocannabinoid effects are more evident in adult rats (mature) compared to early postnatal (immatur

180 itical influence of the estrous cycle on the adult rat medial prefrontal cortex transcriptome resulti

181 Adult rat mesenteric tissues were harvested and cultured

182 nitric oxide synthase in the fat pad of the adult rat mesentery during inhibition of angiopoietin si

183 19) altered the size and organization of the adult rat midbrain dopaminergic (DA) populations.

184 cortex (OFC) and increase activity in NAC in adult rats, mimicking the imbalance during adolescence.

185 In dissociated adult rat mixed retinal cultures, dominant negative CASP

186 overy of diaphragm function after SCI in the adult rat model.

187 a drop in tobacco screen time for youth- and adult-rated movies (42.3% [95% CI, 24.1%-60.2%] and 85.4

188 positioned to measure local [Ca(2+)]Cleft in adult rat myocytes.

189 uneate nucleus (CN) of forelimb-intact young adult rats (n=38) as the first part in a series of studi

190 w representation in forelimb amputated young adult rats (n=5) at 7 to 24 weeks after amputation.

191 ophysiological recordings in forelimb intact adult rats (n=8) to map the body representation in VPL w

192 ssure injection in both free solution and in adult rat neocortex in vivo, revealing IgG diffusion in

193 wann cells in vitro from freshly dissociated adult rat nerve.

194 , 6 weeks after forelimb amputation in young adult rats, new input from the shoulder becomes expresse

195 ia immunoreactivity was found throughout the adult rat NTS.

196 as not toxic to highly purified perinatal or adult rat O-2A/OPCs.

197 es long-distance optic nerve regeneration in adult rats of both sexes.

198 Adult rat offspring that received low compared with high

199 s the HGF activation of cMet in neonatal and adult rat OL precursors.

200 Compared with those of young adult rats, old rats' V1 neurons exhibited significantly

201 Arc ensembles in adult rat olfactory bulb (OB) and anterior piriform cort

202 n in different brain areas of adolescent and adult rats on withdrawal days 1 and 14 showed time-depen

203 t of Set-beta to cellular membranes promoted adult rat optic nerve axon regeneration after injury in

204 ansplanted into either normal spinal cord of adult rats or the injury site in a dorsal column hemisec

205 After lateral fluid percussion injury in adult rats, oral treatment with EVT901 reduced neuronal

206 granule cells (GCs) generated in newborn and adult rats over extended periods of time.

207 The AE network location in adult rats overlaps with the perinatal pFRG and appears

208 cal properties of pyramidal neurons in young adult rats (P30-P60) exposed to ethanol inhalation durin

209 To control for age-dependent effects, adult rats (PD75-89) were exposed to identical experimen

210 icacy of DOR agonists in primary cultures of adult rat peripheral sensory neurons and in a rat behavi

211 r to intravenous nicotine-associated cues in adult rats progressively increases or incubates after wi

212 ents suggests that voluntary exercise in the adult rat rapidly and transiently induces apoptosis, fol

213 However, infusions of normal adult rat renal cells have been a successful therapy in

214 ic effector in situ We now show that EV from adult rat renal tubular cells significantly improved ren

215 Thy1 and HCN4, a cation channel subunit, in adult rat retina.

216 vascular complexes freshly isolated from the adult rat retina.

217 In adult rat retinal ganglion cells, based on patch-clamp r

218 lectrode array recordings from postnatal and adult rat retinas, we demonstrated that adenosine signif

219 nitored acidic organelles moving in axons of adult rat sensory neurons to determine whether Lis1 and

220 benefit the intrinsic ability of axotomized adult rat sensory neurons to undergo axonal regeneration

221 sponse (UPR) and cholesterol biosynthesis in adult rat sensory neurons.

222 nerve recordings of respiratory activity in adult rats show that bilateral injections of pyridoxal-p

223 However, adult rats showed sensitized fear learning, aberrant bas

224 Electrophysiological measurements in adult rat slices confirmed this prediction and displayed

225 ed an immunohistochemical approach in normal adult rat small intestinal and ascending colonic tissue.

226 nd kindlin-1 on sensory axon regeneration in adult rat spinal cord after dorsal root crush and adeno-

227 this, we microinjected ferritin into intact adult rat spinal cords.

228 non-noxious tactile activity in the healthy adult rat spinal dorsal horn via activation of spinal 5-

229 Adult rats spinal transected as neonates (NTX rats) at t

230 Trunk actions are important in adult rats spinalized as neonates (NTX rats) that walk a

231 In adult rat striatal neurons in vivo, native ERK from syna

232 es to the psychostimulant amphetamine in the adult rat striatum and medial prefrontal cortex (mPFC) i

233 vated plus maze in control adult rats and in adult rats subjected to early EE or to massage.

234 ches to investigate the mechanisms of GHS in adult rats subjected to neonatal colonic insult by intra

235 ression of endogenous alpha-synuclein in the adult rat substantia nigra by adeno-associated virus-med

236 at the ES in the seminiferous epithelium of adult rat testes, most notably at the apical ES at the S

237 components of the basement membrane (BM) in adult rat testes.

238 calization in the seminiferous epithelium of adult rat testes.

239 expression of sFRP1 is tightly regulated in adult rat testis to control spermatid adhesion and sperm

240 The steady-state protein level of Slc15a1 in adult rat testis was not affected by F5-peptide treatmen

241 ion, and synapse-related immunoreactivity of adult rat TH cells.

242 found a subpopulation of DCN neurons in the adult rat that express doublecortin, a plasticity-relate

243 Here, we show in young adult rats that 10 d of monaural conductive hearing loss

244 (both CA3 and CA1) and prefrontal cortex of adult rats that had experienced repeated seizures in the

245 vHipp and BLA high-frequency stimulation in adult rats that received repeated injections of saline o

246 Here, we demonstrate that adult rats that were exposed to intermittent hypoxia as

247 After CTX in adult rats, the chorda tympani nerve was labeled with bi

248 Compounds 2 and 5 were tested in adult rats to evaluate their long-term effects on dopami

249 lateral cochlear ablations were performed on adult rats to examine the short-term (16 and 24 hours an

250 or piriform cortex (aPC) must be engaged for adult rats to learn to discriminate highly similar odors

251 g mechanisms, we subjected 13 Sprague Dawley adult rats to unilateral 14 psi blast exposure to induce

252 Next, we conducted the same analysis in adult rats treated with eight daily noncontingent cocain

253 owth responses to regulated NT-3 expression, adult rats underwent a C3 dorsal funiculus lesion.

254 Adult rats underwent complete tibial nerve transection f

255 n vitro, using the following three groups of adult rats: unexposed control (Ctrl); sound exposed with

256 (TBI) induced by lateral fluid percussion in adult rats, using 2 new ligands for PET: (18)F-GE-179 fo

257 eptor subtypes modulate risk-taking in young adult rats, using a "Risky Decision-making Task" that in

258 2.22) are comparable with values for healthy adult rat ventricles (1.98 - 3.63).

259 nocolocalization experiments in neonatal and adult rat ventricular cardiomyocytes as well as murine h

260 In addition, cultured neonatal and adult rat ventricular cardiomyocytes were subjected to s

261 ected two ENTPD isoforms, ENTPD-1 and -2, in adult rat ventricular CFs.

262 In the adult rat ventricular myocyte model, both WT-Kv11.1 and

263 alyzed contractility in the whole rat heart, adult rat ventricular myocytes (ARVMs), and myofibrils f

264 tutively bis-phosphorylated form in isolated adult rat ventricular myocytes and in mouse and rat vent

265 Using adult rat ventricular myocytes and mouse-derived cardiac

266 y and immunofluorescence in freshly isolated adult rat ventricular myocytes and those in short-term p

267 We investigated subpopulations of PLM in adult rat ventricular myocytes based on phosphorylation

268 Isolated adult rat ventricular myocytes were infected with wild-t

269 e-induced hypertrophy in H9c2 cardiac cells, adult rat ventricular myocytes, and human induced plurip

270 Forster resonance energy transfer imaging of adult rat ventricular myocytes, surprisingly suggest tha

271 afficking, and pharmacological mechanisms in adult rat ventricular myocytes.

272 chondroitinase can restore plasticity in the adult rat visual cortex suggest a potential treatment fo

273 r anaesthesia, the middle cerebral artery of adult rats was occluded for 60 min using the filament mo

274 Using adult rats we determined that pharmacological depletion

275 behavioral pharmacology and biochemistry in adult rats, we determined that betaAR activity during, b

276 Using multiple kinetic models in free-living adult rats, we first demonstrate that DHA uptake from th

277 In anaesthetized adult rats, we have found that Purkinje cells recorded f

278 In adult rats, we have identified a pathway linking the vlP

279 g ionic current blockers into the preBotC of adult rats, we identify the hyperpolarization-activated

280 al analyses in hippocampal slices from young adult rats, we show that E2 acutely suppresses inhibitio

281 Adult rats were hemorrhaged to a pressure of 30 to 35 mm

282 The eyes of anesthetized adult rats were injured by either weight drop or low-vel

283 Specifically, infant, juvenile and adult rats were presented with mild foot-shocks and thei

284 Fifty adult rats were randomly assigned to either (1) a sham g

285 Adult rats were trained in a staircase-reaching task and

286 Adult rats were ventilated with high (18 ml/kg, positive

287 entations in the anterior piriform cortex of adult rats when odor was associated with water reward ov

288 vioral neuroscience experiments, at least in adult rats where SWDs are prevalent.

289 superior cervical ganglion-pineal circuit of adult rats, which can be noninvasively silenced by expos

290 days after permanent auditory deprivation in adult rats, which is partly reversed 90 days after deafn

291 dependent plasticity in the visual cortex of adult rats while recording single unit and population ac

292 In addition, animal studies have shown that adult rats who suffered febrile seizures during developm

293 Adult rats; wild-type/nicotinamide adenine dinucleotide

294 Pavlovian conditioned approach procedure in adult rats with a history of adolescent alcohol consumpt

295 g from individual thalamocortical neurons in adult rats with a recently developed automatic tracing t

296 but differentially, altered in neonatal and adult rats with BDV infection.

297 m awake unexposed controls and sound-exposed adult rats with behavioural evidence of tinnitus.

298 ral nervous system infection of neonatal and adult rats with Borna disease virus (BDV) results in neu

299 genesis, functional outcome, and survival in adult rats with brain lesions.

300 Adult rats with sciatic nerve crush were immediately and