ライフサイエンスコーパス: male rat

1 amic neurons about paired whisker stimuli in male rat.

2 ntioxidant function and semen quality in old male rats.

3 n the prelimbic PFC (prPFC) and BLA of adult male rats.

4 EA signaling on stress, fear, and anxiety in male rats.

5 creased the motivation to consume cocaine in male rats.

6 bit PFC CRF neurons in working memory-tested male rats.

7 s of PPC in anesthetized and awake, behaving male rats.

8 disease, both groups were mated with healthy male rats.

9 CLA to the PFC in regulating impulsivity in male rats.

10 ne seeking was higher in female rats than in male rats.

11 l (30 mug/kg, s.c.) was performed in vivo in male rats.

12 mine release to self-administered cocaine in male rats.

13 onditions of hunger and food palatability in male rats.

14 ependent late LTP in hippocampal slices from male rats.

15 enhances vulnerability for drug addiction in male rats.

16 ut not maintenance, of morphine tolerance in male rats.

17 e effects in lung tissue of brain death (BD) male rats.

18 costerone levels even in previously stressed male rats.

19 d the antinociceptive effects of morphine in male rats.

20 cells were implanted in both hemispheres in male rats.

21 okinetics and tissue distribution of PFOA in male rats.

22 tenuates cardiomyopathy compared to diabetic male rats.

23 g in the trigeminal ganglion of anesthetized male rats.

24 ed by chronic cocaine self-administration in male rats.

25 One hundred ninety-eight adult male rats.

26 d by a homogenate of reproductive tissues of male rats.

27 icits in cognitive flexibility compared with male rats.

28 motivation for cocaine in self-administering male rats.

29 against renal ischemia-reperfusion injury in male rats.

30 olating distinct aspects of fear learning in male rats.

31 GLP-1R increased food motivation but only in male rats.

32 easing factor (CRF) in the NAc of female and male rats.

33 of scopolamine (0.1 and 0.5 mg/kg, i.p.) in male rats.

34 nd (i.e., motivation) for meth compared with male rats.

35 n in the amygdala were observed in female vs male rats.

36 g after choice-based voluntary abstinence in male rats.

37 n were observed in female rats compared with male rats.

38 y was injected into the VTA of TH::Cre adult male rats.

39 stent inflammation differently in female and male rats.

40 , causes increased reward for amphetamine in male rats.

41 ffect of resistance training on AHN in adult male rats.

42 ased ACh release in the prefrontal cortex of male rats.

43 hine antinociception in naive or CFA-treated male rats.

44 MPK- and nitric oxide-dependent mechanism in male rats.

45 these responses did not differ from those in male rats.

46 n depressive-like behavior in gonadectomized male rats.

47 in synaptic plasticity and spatial memory in male rats.

48 re-hanging test, and righting-reflex test in male rats.

49 g the single-prolonged stress (SPS) model in male rats.

50 L neurons using patch recordings in vitro in male rats.

51 ontrolling the neuroendocrine stress axis in male rats.

52 erm experience-dependent plasticity in adult male rats.

53 al inhibitions induced by DNQX in female and male rats.

54 roestrous phase and after ovariectomy and in male rats.

55 nto the DVC decreased food intake in healthy male rats.

56 rio-venous fistula model (AV-Shunt) in adult male rats.

57 f CA1 pyramidal neurons in slices from adult male rats.

58 alled the rostromedial tegmental nucleus) in male rats.

59 s of 2- to 24-week-old adult-born neurons in male rats.

60 perinatal, prepubertal, and adult female and male rats.

61 ticity in the basolateral amygdala (BLA), in male rats.

62 as a shortened anogenital distance (AGD) in male rats.

63 hase impact DA terminal neurotransmission in male rats.

64 modified, real-world TRAP in both female and male rats.

65 scaling (within 2 s of cue presentation) in male rats.

66 eases CP-AMPAR levels in males in the NAc of male rats.

67 etry-induced micturition in awake female and male rats.

68 istant Lewis or LID-prone Fischer-344 (F344) male rats.

69 the early postnatal amygdala of LR versus HR male rats.

70 in an altered aging profile in the thymus of male rats.

71 in anaesthetized, vagotomized and ventilated male rats.

72 ted in pavlovian cued-fear conditioned adult male rats.

73 PVN prevents the anxiolytic effect of OXT in male rats.

74 ced reinstatement of remifentanil seeking in male rats.

75 Adult male rats (10/group) received a single dose of 0, 11, 14

76 Here we show that, in male rats, 65% of somatostatin-expressing (SST) NTS neur

77 Brown Norway male rats (9 months of age) were randomly assigned to re

78 aversive to some rodent species, produced in male rats a long-lasting anxiety-like state that was mea

79 al cortex (PRC) and in AC of freely behaving male rats across wakefulness and sleep.

80 We demonstrate that STN DBS in male rats activates signaling downstream of tropomyosin

81 Using two-photon Ca(2+) imaging in male rat acute brain slices of the somatosensory neocort

82 32 weanling male rats (aged 21-28 days) were assigned into four grou

83 The metabolites formed were distinct in male rats: alpha-HBCD did not debrominate or stereoisome

84 ecorded in anesthetized and ventilated adult male rats and a multielectrode array was used to record

85 approach based on the movement statistics of male rats and a simple model for the neural responses wi

86 rease mediodorsal thalamic activity in adult male rats and evaluated the consequences for E/I balance

87 sity protein 95, and glutamate receptor 1 in male rats and female rats in diestrus.

88 al cortex spine density was also examined in male rats and female rats that received ketamine during

89 t circuits following motor training in adult male rats and find robust synaptic reorganization among

90 sence of neuropathic pain response in infant male rats and mice following nerve injury is due to an a

91 g granule cell layer synaptic integration in male rats and mice of both sexes.

92 role in exercise-induced PGC-1a expression, male rats and mice with SKM-specific Dio2 inactivation (

93 e, using hippocampal slices from young adult male rats and mice, we report that epileptiform activity

94 data obtained from open-field recordings in male rats and mice.

95 assessment of ocular histopathology in naive male rats and naive male rabbits receiving twice daily t

96 Remarkably, THC consumption by adolescent male rats and not female rats led to impaired Pavlovian

97 rim, 2014) and pCA3 (Lee et al., 2015) of 16 male rats and separately examined the responses of granu

98 ated during inhibition of sexual behavior in male rats and the effects of concurrent Meth and sexual

99 ed the metabolic responses to insulin in HFD male rats and these actions were abolished by inhibition

100 ned place avoidance (CPA) in otherwise naive male rats, and that avoidance behavior is associated wit

101 ressant-like effects of ketamine compared to male rats, and that ovarian-derived estradiol (E2) and p

102 MMP-2 and active MMP-2 from elastase-treated male rat aortic smooth muscle cells.

103 erent forms of relapse to alcohol-seeking in male rats are assembled from activity across the VTA and

104 high-responder (bHR) and low-responder (bLR) male rats are known to differ in their emotional reactiv

105 methamphetamine self-administration (SA) in male rats as compared with handled controls.

106 Here, using female and male rats as subjects, we examined the involvement of th

107 e activity and field potentials were made in male rats as they performed an incentive contrast lickin

108 ections of FKBP1b-expressing viral vector to male rats at either 13 months of age (long-term, LT) or

109 transection on gene expression in the adult male rat barrel cortex were investigated using RNA seque

110 vel organotypic slice culture (OTC) model of male rat BLA, and examined the contributions of specific

111 Using ex vivo male rat brain slice electrophysiology, we show that the

112 ndlimb transplantations were performed using male rats (Brown Norway to Lewis).

113 In male rats, buprenorphine and TRV130 decreased extinction

114 kine secretion was higher in both female and male rats, but inflammatory macrophages were higher only

115 A stressed phenotype was induced in male rats by administering a 7-d heterotypical stress pa

116 PH was induced in male rats by SU5416 (25 mg/kg subcutaneously) injection

117 s induced in 20 five-week-old Sprague-Dawley male rats by weekly rectal injections of increasing dose

118 olarizing stimulus in both tsA-201 cells and male rat CA1 pyramidal cells.

119 at investigates if mutual reward delivery in male rats can drive associative learning.

120 e individual neuron level in freely behaving male rats change as a function of vigilance state and ti

121 istic discounting task in which well trained male rats chose between small/certain or large/risky rew

122 By feeding male rats DEHP for 2 weeks, rat spermatogenesis became d

123 Last, feeding studies using male rats demonstrate that intra-NTS injections of DCPP-

124 nd cardiovascular disease show that diabetic male rats develop increased cardiac fibrosis and suppres

125 xpression with antisense oligonucleotides in male rats diminished motor deficits and nigral DA cell l

126 For 16 consecutive days during adolescence, male rats drank saccharin or alcohol after receiving sub

127 s in CSF and gray matter volumes observed in male rats due to superior metabolic homeostasis mechanis

128 d DMS neural activity in cocaine-experienced male rats during a decision-making task where blocks of

129 ly activate mesoaccumbal GABA projections in male rats during a novel cue-dependent operant value-shi

130 potentials in the dorsomedial PFC (dmPFC) of male rats during a set-shifting task that required them

131 ng behavior, HF and LF phenotypes emerged in male rats during extinction and in female rats during fe

132 and unit recordings in NR, HPC, and mPFC in male rats during slow oscillations under anesthesia, we

133 ypothalamo-pituitary-adrenal (HPA) output in male rats during tail suspension, whereas photostimulati

134 K(Ca)-sAHP component is markedly reduced in male rat epileptic neurons, whereas the NKA-sAHP compone

135 Stressed male rats, especially drinking-vulnerable individuals (>

136 These data show that male rats exhibit less impulsive choice than females and

137 The HF and LF male rats exhibited neuroanatomical distinctions that we

138 ity of dorsal hippocampal CA1 place cells as male rats explored a familiar or a novel environment.

139 Here we show that alcohol-dependent male rats fail to perform an emotional-learning task dur

140 uld improve metabolic insulin sensitivity in male rats fed a high-fat diet (HFD) via the modulation o

141 methylone administration (3, 6, 12 mg/kg) to male rats fitted with intravenous (iv) catheters for rep

142 ificant, enduring spatial memory problems in male rats following experimental prolonged FS (febrile s

143 o examine whether exposure of Sprague-Dawley male rats for two weeks to different shapes of AgNPs, cu

144 most optimal choice from session 1, whereas male rats from session 5.

145 either eGFP or mRFP), injected pairwise into male rat gastrocnemius, subcutaneous WAT and interscapul

146 y retrieval, in a within-subjects design, of male rats given systemic administration of saline or lip

147 Recuperated male rats had reduced aortic CoQ [22 d (35+/-8.4%; P<0.0

148 hythmic effects of BPS were female specific; male rat hearts were not affected by BPS at the organ, m

149 pproach to monitor NKA transport activity in male rat hippocampal neurons in situ We report that this

150 Here, we show that, in male rats, hippocampal GluT4 translocates to the plasma

151 In male rats, HMWH also signals via Toll-like receptor 4 (T

152 amp recordings were performed on prepubertal male rat hypothalamic slices, where TIDA neurons can be

153 y and makes different errors than a group of male rats, illustrating that memory alone may not be suf

154 ase in sucrose preference of female, but not male, rats in an E2P4-dependent manner.

155 NA and heart rate more dramatically in obese male rats; in obese females, the responses were abolishe

156 hyl-d-aspartate receptor (NMDAR) currents in male rat infralimbic prefrontal pyramidal neurons.

157 We randomly divided 24 adult male rats into 4 groups (n = 6 per group).

158 We first identified the region of the (male) rat IRt that contains the highest density of light

159 s to social affect are evident when an adult male rat is presented with a pair of unfamiliar male con

160 rotransmission exclusively on NAc D1-MSNs in male rats, it remains unknown how NAc MSNs control alcoh

161 Male rats lacking MeCP2 (Mecp2(ZFN/y)) were noticeably s

162 Water-restricted male rats learned to associate a light-tone cue (CS) wit

163 Male rats learned to associate one context with sucrose

164 recorded across behavior and sleep stages in male rats learning a spatial alternation task.

165 ulation activity in the medial PFC (mPFC) of male rats learning rules on a Y-maze.

166 ctor robustly reduced seizure frequency in a male rat model of focal neocortical epilepsy characteriz

167 also effective at suppressing seizures in a male rat model of temporal lobe epilepsy.

168 rm and long-term SRM in adult Sprague-Dawley male rats (n = 38).

169 x of chronically instrumented, freely moving male rats (n = 7) during stepwise reduction of the anest

170 Adult, male rats (n=10) underwent unilateral intrastriatal infu

171 F0 male rats (n=11-13) and female rats (n=6-12) were, respe

172 Our study shows that, in male rats, NAcC perturbation with glutamate or dopamine

173 lume were developed and tested in Long Evans male rats, namely: VSG, Fundal (F)-Resection, Gastric Sl

174 a continuous place navigation task in which male rats navigate to one of two (freely chosen) unmarke

175 In male rats, Nmb is also a marker of the RTN but, unlike i

176 Male rats of 3-4 weeks old were exposed to a hindpaw bur

177 interlobar arteries (RIA) in the 5-month-old male rat offspring.

178 We trained adult male rats on a multistage decision-making task to quanti

179 le postsynaptic hippocampal CA1 neurons from male rat or mouse brain slices causes intermittent, seco

180 Adolescent Sprague-Dawley male rats (PD30-43) were given 10 intermittent, intragas

181 nsembles and population decoding analyses in male rats performing a continuous spatial working memory

182 valuate, dopamine neurons were recorded from male rats performing a Pavlovian approach task containin

183 chronic unilateral 6-hydroxydopamine lesion male rats performing a skilled reach-to-grasp task the.

184 Here we find that in adult male rats, presentation of a social stimulus (novel or f

185 s after streptozotocin premedication, Wistar male rats presenting blood sugar levels >20 mmol/L were

186 Male rats pretreated with both deoxycorticosterone (DOC;

187 102), respectively, by liver microsomes from male rats pretreated with different inducers; untreated

188 course of a CRHR1 antagonist in 2-month-old male rats prevented early-life adversity-induced deficit

189 Chronic unpredictable stress (CUS) to adult male rats produced depression-like changes with cognitiv

190 newborn astrocytes in the medial amygdala of male rats, promoting sex differences in social play beha

191 nt, demand, and relapse-related behaviors in male rats, querying the roles of DA neuron inhibitory an

192 Thirty-five Wistar Han male rats randomly underwent sham or ascending (supraval

193 Retrograde tracing in adult male rats (Rattus norvegicus) revealed that the inferior

194 Adolescent male rats readily self-administered WIN in 2-h or 6-h se

195 Forty male rats received 100 mg/kg body weight of cimetidine (

196 Adult male rats received a 90-min right distal middle cerebral

197 nits in the dorsal CA1 hippocampal region as male rats received a battery of taste stimuli differing

198 Long Evans male rats received a controlled cortical impact (CCI) ov

199 s in the prelimbic region of the mPFC, while male rats received a sequence of stimulus presentations

200 Two weeks after GI, adult male rats received high-frequency EC DBS for 1 h, and an

201 ession in nucleus accumbens shell (NAcSh) of male rats reduces both addictive-related and anxiety-rel

202 eonatal ventral hippocampus lesion (NVHL) in male rats reproduces these neuronal characteristics and

203 nsitivity to low-dose ketamine in female and male rats, respectively.

204 ) grid spanned by 64 recording electrodes as male rats rested and foraged for rewards, revealing a hi

205 analysis from the prefrontal cortex (PFC) of male rats revealed changes in several genes associated w

206 maging and cluster analysis, we show that in male rats SCI decreases opioid responsiveness in vitro w

207 s was tightly linked to the caloric state of male rats, seesawing between long-term potentiation (iLT

208 Male rats self-administered cocaine intermittently (5 mi

209 dition, adolescent hypophysectomized (hypox) male rats served as controls in which GH was eliminated

210 Male rats showed anhedonia and depression-like behavior

211 s, all results are expected to generalize to male rats.SIGNIFICANCE STATEMENT The rodent vibrissal (w

212 We provide the first direct evidence that male rats, similar to humans, use both model-free and mo

213 responses within subcellular compartments of male rat spinal cord lamina I neurons.

214 Male rats (Sprague-Dawley) with histologically confirmed

215 msec for human stem cells and 11.55 msec for male rat stem cells vs 15.45 msec for sex-matched rat st

216 in the antidepressant effects of ketamine in male rats subjected to IS but not in female rats subject

217 r baseline glutathione levels in female than male rats suggest that female rats are perhaps protected

218 se preference and social play, in adolescent male rats that experienced chronic early-life adversity/

219 tress-induced anxiety using chemogenetics in male rats that express Cre recombinase from a Crh promot

220 0 min following intra-BNST PACAP infusion in male rats that had been previously exposed to CVS.

221 It was previously demonstrated in male rats that methamphetamine (Meth), when administered

222 eceptor-selective agonist VU0364572 in adult male rats that self-administer cocaine in a cocaine vs.

223 halamus (LH) are preferentially activated in male rats that show avoidance of a predator odor-paired

224 Here we found in male rats that TNFalpha and associated signal transducti

225 b (OB) in regards to S/N in vivo We show, in male rats, that locus ceruleus stimulation and pharmacol

226 acterized, in freely behaving Sprague Dawley male rats, the MD neural activity around hippocampal rip

227 fractions from the NAc of self-administering male rats, the phosphorylation of SRC at an activating s

228 We aimed at comparing, in male rats, the underlying neuronal determinants of incen

229 17alpha-E2 improves metabolic parameters in male rats, thereby proving that the beneficial effects o

230 ed mRNA (mtRNA) expression, we exposed adult male rats to both acute and chronic immobilization stres

231 hypothesis, we used operant conditioning in male rats to determine whether outbred strains, Sprague

232 across all vigilance states in freely moving male rats to determine whether the RSC and the ACA are e

233 We used Pavlovian counterconditioning in male rats to establish a conditioned stimulus (CS) as a

234 behavioral task that assesses the ability of male rats to exert behavioral restraint at the mere sigh

235 We trained adolescent and adult male rats to self-administer nicotine (2 h/d for 12 d) a

236 (LRT) and high-response trainer (HRT) adult male rats to various forms of physical exercise for 6-8

237 ioid-induced hyperalgesic priming (OIHP), in male rats, to identify nociceptor populations involved a

238 We investigated the adult male rat transcriptome using RNA-sequencing (RNA-seq) fo

239 action mediates sexual reward and memory in male rats treated with naloxone during mating experience

240 her exposure to MK-801 during adolescence in male rats triggers a state of excitatory-inhibitory imba

241 ations in the spiking activity of the SNr of male rats under CP55940.

242 effect of MDMA on temperature homeostasis in male rats under standard laboratory conditions and under

243 80 male rats underwent 90-min middle cerebral artery occlus

244 Male rats underwent an episode of restraint prior to the

245 Male rats underwent intravenous cocaine self-administrat

246 Adult male rats underwent oral gavage with THC or vehicle cont

247 Male rats underwent pilocarpine-induced status epileptic

248 Obese male rats underwent RYGB, VSG, or sham (control) operati

249 evidence exists for vagal innervation of the male rat urinary bladder and to assess whether those vag

250 inetic evidence supports the hypothesis that male rat urinary bladder tumors arise through urinary bl

251 in humans, based on increased incidences of male rat urinary bladder tumors at high exposure levels

252 We assessed decision making in adult male rats using a probabilistic reversal learning task a

253 ress-induced anhedonia was assessed in adult male rats using social defeat and intracranial self-stim

254 of the nLOT were estimated in adult and old male rats using stereological techniques.

255 footshock) can potentiate cocaine seeking in male rats via glucocorticoid-dependent cannabinoid type-

256 However, inhibition in male rats was not detected by EGR-1 activity mapping, wh

257 encoding FKBP1b into the hippocampus of aged male rats, we assessed the critical prediction that over

258 activation and in vivo electrophysiology in male rats, we demonstrated that the rostral entopeduncul

259 Using slices from visual cortex of young male rats, we describe a novel form of plasticity of exc

260 In male rats, we employed the action potential-clamp techni

261 In male rats, we first evaluated the role of nociceptor Tol

262 cing and single-unit recording techniques in male rats, we found that neurons in C2-C3 DRGs innervate

263 clinical model of adolescent THC exposure in male rats, we report that l-theanine pretreatment before

264 Using male rats, we show how different forms of relapse to alc

265 stration and fast-scan cyclic voltammetry in male rats, we show that low-dose, continuous amphetamine

266 ng juxtacellular recordings in freely moving male rats, we studied the bursting behavior of 102 subic

267 In unanesthetized male rats, we tested whether ablation of the RTN, CBs, o

268 In male rats, we used chemogenetics with intra-VTA microinf

269 Across four cohorts of male rats, we used discrete lesions of the mammillothala

270 In the present study male rats were chronically exposed to vaporized ethanol

271 Male rats were distributed in groups 1) control, 2) lipo

272 Forty-six male rats were distributed into the cimetidine group (Ci

273 Seventy-five male rats were divided into five groups: DM+PLAC: Diabet

274 Long-Evans male rats were exclusively used in all experiments.

275 12-13 week and 19-month-old male rats were exposed by inhalation to 10 mg/m(3) of Ti

276 Male rats were fed semi-synthetic diets for 1 wk that di

277 Old male rats were grouped into old control group (OCG), old

278 Young male rats were grouped into young control group (YCG) an

279 Male rats were imaged following administration of a sing

280 Gonadectomized male rats were implanted with a placebo, testosterone, o

281 on the reproductive system of young and old male rats were investigated.

282 ischer 344 (F344), and Brown-Norway (BN)] of male rats were maintained on a high-fat (HF) or regular

283 Finally, THC-exposed and control adult male rats were mated with THC-naive females.

284 Male rats were microinfused with PACAP (0-1 mug per rat)

285 Young male rats were provided PB, PM and DEET at equivalent hu

286 Male rats were subjected to 1 hour of water avoidance st

287 Adult male rats were subjected to 60 min of bilateral renal pe

288 Male rats were subjected to a two-hour middle cerebral a

289 Old male rats were submitted to RT (ladder climbing, progres

290 Long-Evans male rats were trained that presses on a lever under an

291 Here, male rats were trained to exert effort for a high-value

292 Forty-one, eight month old Fischer 344 male rats were treated with either the AIN (American Ins

293 nactivation, on regional hippocampal maps in male rats, when LC activity was manipulated just before

294 We tested in male rats whether catecholaminergic neurons that project

295 rphological changes of VTA dopamine cells in male rats, which in-turn regulate the long-term expressi

296 ntidepressant-like effects in gonadectomized male rats, while similarly regulating critical mediators

297 We treated newborn male rats with monosodium glutamate (MSG), a total growt

298 igh-resolution phase-contrast MRI in 9 adult male rats with myocardial infarction (MI) and in 5 sham-

299 and function of Nav1.7 protein in DRGs from male rats with paclitaxel-related CIPN and from male and

300 r fear output - signal threat probability in male rats (Wright et al., 2019).