ライフサイエンスコーパス: locomotor activity

1 nergic relays to support morning and evening locomotor activity.

2 I) and enhanced sensitivity to MK801-induced locomotor activity.

3 ircadian rhythmicity of body temperature and locomotor activity.

4 tor outputs to modulate circadian control of locomotor activity.

5 d circadian behavioral rhythms and decreased locomotor activity.

6 s food intake and body weight and normalizes locomotor activity.

7 reduces AMPH-stimulated dopamine efflux and locomotor activity.

8 d intake, intestinal nutrient absorption and locomotor activity.

9 lmitate, decreased food intake and increased locomotor activity.

10 or does it translate to a non-weight-bearing locomotor activity.

11 progressive ratio test but had no effect on locomotor activity.

12 chitecture that may account for the enhanced locomotor activity.

13 a high-fat diet, while not altering general locomotor activity.

14 in mice, decreasing methamphetamine-induced locomotor activity.

15 ected 0.2% saccharin self-administration nor locomotor activity.

16 ress-induced potentiation of cocaine-induced locomotor activity.

17 the overall effect to a 19.2% improvement of locomotor activity.

18 V1 interneurons are essential for high-speed locomotor activity.

19 erneurons is rhythmically modulated with the locomotor activity.

20 ervous system (SNS) and increase CR-specific locomotor activity.

21 argets of maternal rest that modulate larval locomotor activity.

22 c Drosophila increased survival and improved locomotor activity.

23 rexia and body weight loss without affecting locomotor activity.

24 he Drosophila brain control daily rhythms in locomotor activity.

25 but emphasize their importance in promoting locomotor activity.

26 cts in the forced swim test without altering locomotor activity.

27 mbens triggered MAPK signaling and modulated locomotor activity.

28 A release in the dorsal striatum or baseline locomotor activity.

29 d adiposity without affecting food intake or locomotor activity.

30 play, but not social exploratory behavior or locomotor activity.

31 depression of spontaneous or cocaine-induced locomotor activity.

32 d acute inhibition of Mc4r signaling reduces locomotor activity.

33 mice were normal in development and general locomotor activity.

34 of L2 flexor-related and L5 extensor-related locomotor activity.

35 spontaneous alternation, but did not affect locomotor activity.

36 O) mice display a longer circadian period of locomotor activity.

37 aytime versus nighttime feeding behavior, or locomotor activity.

38 s that are a major source of rhythmicity and locomotor activity.

39 s would be sufficient to produce coordinated locomotor activity.

40 that is sufficient to initiate and maintain locomotor activity.

41 the spinal networks to generate coordinated locomotor activity.

42 ine synthesis capacity (Cohen's d = 2.5) and locomotor activity.

43 sufficient to cause a decrease in MA-induced locomotor activity.

44 s raised by dams exposed to LB showed higher locomotor activity.

45 udies in rodents where Mc4r agonists reduced locomotor activity.

46 im-short and cold is abrogated have abnormal locomotor activity.

47 d body neurons important for ethanol-induced locomotor activity.

48 any changes in response latencies or general locomotor activity.

49 thermal thresholds, motor coordination, nor locomotor activity.

50 tical to the circadian rhythms in Drosophila locomotor activity.

51 mice lacking the Dmrt3 gene display impaired locomotor activity.

52 eases striatal levels of dopamine and evokes locomotor activity.

53 had obvious metabolic disorders and loss of locomotor activity.

54 eeding, and drinking were validated, but not locomotor activities.

55 logical circadian rhythms and increase their locomotor activity 2-3h prior to the next scheduled feed

56 epressive-like behaviors and increased basal locomotor activity (41%).

57 microglia marker) positive cells and reduced locomotor activity 72 h after transient forebrain ischem

58 oned to regulate dopamine (DA) signaling and locomotor activity, a canonical measure of basal ganglia

59 as adjusted their energy expenditure, Tb and locomotor activity according to season and also time of

60 ns is required for the adaptive reduction of locomotor activity after feeding.

61 ncreased metabolism, energy expenditure, and locomotor activity, along with increased body temperatur

62 e phenotypes, including a reduction in adult locomotor activity, alterations in visceral adipose tiss

63 60 uM reduced fat accumulation and increased locomotor activity (an indicator of energy expenditure)

64 the LNvs influence: temporal organization of locomotor activity, analyzed in males, and sleep, analyz

65 r show bursts of morning (M) and evening (E) locomotor activity and a "siesta" in the middle of the d

66 et restfulness were characterised by minimal locomotor activity and a low theta/delta ratio in the lo

67 Furthermore, a decreased spontaneous locomotor activity and absent thermogenic reaction to th

68 Locomotor activity and anxiety-like behavior were increa

69 ating mice during maternal care and analysed locomotor activity and anxiety-like behaviour in the off

70 months, and were distinct from reductions in locomotor activity and anxiety.

71 tantly, we showed that wild-type S1R rescues locomotor activity and ATP levels of flies expressing th

72 s of Cdk5 in dorsolateral striatum increased locomotor activity and attenuated motor learning.

73 Locomotor activity and body temperature in combination p

74 g cis-element in daily maintenance of animal locomotor activity and body temperature rhythmicity.

75 lar clock oscillations and renders circadian locomotor activity and body temperature rhythms unstable

76 include disrupted circadian rhythms in both locomotor activity and body temperature.

77 2R knockout mice, this mutant restored basal locomotor activity and cocaine-induced locomotor activit

78 necessary and sufficient for normal evening locomotor activity and daytime sleep profiles, respectiv

79 lphaB-expressing mice also exhibit decreased locomotor activity and decreased dopamine-regulated CREB

80 f qrfp or its receptors results in increased locomotor activity and decreased sleep during the day.

81 h behavioral state, increasing robustly with locomotor activity and decreasing with rest.

82 en known to be involved in the regulation of locomotor activity and development of psychosis.

83 ceptor (Dh31r) expression resulted in normal locomotor activity and did not enhance the arrhythmic ph

84 g two distinct behavioral paradigms: general locomotor activity and directed, visually guided navigat

85 epileptogenesis were associated with altered locomotor activity and distorted circadian rhythm.

86 liver microsomes and compared to cocaine in locomotor activity and drug discrimination paradigms in

87 10-30 mg/kg i.p.) dose-dependently increased locomotor activity and electrical brain-stimulation rewa

88 Locomotor activity and elevated plus maze test/forced sw

89 in both HFD and/or OVX groups, and decreased locomotor activity and energy expenditure after OVX can

90 of LXRbeta function leads to abnormality in locomotor activity and exploratory behavior, signs of an

91 g in rodents which correlated with increased locomotor activity and HFO power in the OB.

92 of neural circuitry is reflected in enhanced locomotor activity and in the inability of the larvae to

93 uate the participation of D2R in spontaneous locomotor activity and motor learning.

94 ngth of the circadian free-running period of locomotor activity and normal sleep patterns in male mic

95 Viability and behavioral alteration in the locomotor activity and place preference, after IL treatm

96 VTA counteracted two drug-seeking behaviors, locomotor activity and place preference.

97 yond the dopaminergic system may also affect locomotor activity and psychosis.

98 w that 5-HT and octopamine jointly influence locomotor activity and quiescence in feeding and fasting

99 by a significant improvement in spontaneous locomotor activity and reduced anxiety-like behavior.

100 rosophila also resulted in severely impaired locomotor activity and reduced lifespan, mirroring patie

101 ian neurons (dTRAPPC9) resulted in increased locomotor activity and reduced sleep, concordant with th

102 ncreased spontaneous and amphetamine-induced locomotor activity and reduced spontaneous alternation,

103 We quantified spontaneous locomotor activity and responsiveness to sensory stimuli

104 vivo: these peaks coincide with the bouts of locomotor activity and result from independent activatio

105 (DN) subunits, leads to changes in circadian locomotor activity and shortens lifespan.

106 resetting, these mice exhibited consolidated locomotor activity and skipped the timed rest period (si

107 and characterized in Drosophila by assessing locomotor activity and sleep upon knockdown of those gen

108 cemaker neurons to brain areas that regulate locomotor activity and sleep.

109 nsequently, the mutant mice were impaired in locomotor activity and spatial memory and were resistant

110 supersensitive; adenylate cyclase activity, locomotor activity and stereotypy were exaggerated in DR

111 ly I:C and postnatal LPS produced changes in locomotor activity and temperature patterns, increases i

112 without corresponding changes in spontaneous locomotor activity and was transient, which has only bee

113 fixed-interval (FI) schedule of food reward, locomotor activity, and anxiety-like behavior], dopamine

114 n LNds, the clock neurons that drive evening locomotor activity, and AstC-R2 is required in these neu

115 r development, reduced weight loss, improved locomotor activity, and attenuated muscle wasting, with

116 record electroencephalogram, electromyogram, locomotor activity, and body temperature, and the effica

117 working memory, sensorimotor gating, native locomotor activity, and dopaminergic innervation.

118 d broadband gamma frequency power, increased locomotor activity, and impaired novel object recognitio

119 ing antinociception, hypothermia, catalepsy, locomotor activity, and in the drug discrimination parad

120 ed ventricles and impaired social behaviour, locomotor activity, and learning and memory.

121 7% decrease in lifespan, reduced spontaneous locomotor activity, and no lifespan increase when reared

122 further differed in body weight, spontaneous locomotor activity, and prepulse inhibition of startle.

123 cephalography (EEG), electromyography (EMG), locomotor activity, and subcutaneous temperature.

124 marker of psychotic-like behavior), memory, locomotor activity, and the density of cell-surface and

125 ctivity-promoting E cells paralleled evening locomotor activity, and the LUC profile from sleep-promo

126 in confer an approximately 24-hr rhythm onto locomotor activity are unclear, but involve the neuropep

127 Monitoring System (IRAMS) to measure murine locomotor activity as a surrogate measure of disease sev

128 own morphants showed a significantly reduced locomotor activity as well as distorted muscle integrity

129 ncing, and primary rewarding effects using a locomotor activity assay, an intracranial self-stimulati

130 Rats treated with Tamoxifen recovered some locomotor activity at 21 and 28 DPI, which could be rela

131 ur, and increased hedonic-like behaviour and locomotor activity at baseline, and resistance to develo

132 It had no effect on the locomotor activity at doses several fold higher than its

133 It does not affect the locomotor activity at doses several folds higher than it

134 and partial agonist RO5263397 on sleep/wake, locomotor activity, body temperature, and cataplexy were

135 L-Tsc1 KO mice displayed reduced locomotor activity, body temperature, and hepatic trigly

136 tal TLR7-activated mice have normal baseline locomotor activity, but are hyperresponsive to stimuli i

137 e did not affect general or morphine-induced locomotor activity, but markedly increased cocaine-induc

138 (GABA) neuronal activation similarly induced locomotor activity, but with striking differences in mod

139 s) altered clock gene expression and reduced locomotor activity by disrupting the central and periphe

140 ng or lengthening of the circadian period of locomotor activity can be obtained either by targeting d

141 The net effects of this modulatory system on locomotor activity can vary between different vertebrate

142 In contrast, locomotor activities, central box duration and sucrose p

143 cocaine injections (20 mg/kg) paired with a locomotor activity chamber (Paired) or home cage (Unpair

144 (5, 8, 10, and 15 mg/kg) every 12 hours in a locomotor activity chamber and a challenge dose of 5 mg/

145 mor (tremulous jaw movements), and decreased locomotor activity compared with administration of TBZ a

146 ant-induced behaviors relevant to addiction: locomotor activity, conditioned place preference, anxiet

147 sion of either protein caused an increase in locomotor activities consistent with enhanced synaptic r

148 nd SCN input and, when activated, suppresses locomotor activity, consistent with the behavioral hyper

149 x-, genotype-, and dose-dependent changes in locomotor activity, contextual fear conditioning, grip s

150 of oxytocin (0.03-0.3 mg/kg subcutaneous) on locomotor activity, core body temperature, and social be

151 LPS suppression of locomotor activity correlated with blood glucose concent

152 EEG, EMG, body temperature, and locomotor activity data were collected continuously duri

153 der, older age (> 7 postnatal weeks), higher locomotor activity, daytime recordings, and recent blood

154 both larvae and adult fruit flies, including locomotor activity, degeneration of dopaminergic neurons

155 ind that the overexpression of QRFP inhibits locomotor activity during the day, whereas mutation of q

156 phenotyping studies revealed alterations in locomotor activity, energy expenditure, and daily food i

157 ns and spiking activity coordinated with the locomotor activity expressed by the lumbar cord.

158 WD also decreased locomotor activity, expression of the D2 receptor and ty

159 ygen uptake, treadmill duration, spontaneous locomotor activity, fat oxidation, and fatty acid levels

160 Despite a large decrease in locomotor activity, FL-PGC-1alpha(-/-) mice exhibited th

161 ar (dHb-IPN) pathway expedites the return of locomotor activity following an unexpected negative stim

162 ly measures standing, feeding, drinking, and locomotor activities from 3D trajectories.

163 ional outcomes up to 3 weeks after stroke on locomotor activity, grip strength, sensory neglect, gait

164 inant human IGF1 (rhIGF1) improves lifespan, locomotor activity, heart rate, respiration patterns, an

165 aggressiveness (resident-intruder test), and locomotor activity (horizontal and vertical).

166 t of adult mice as well as increased general locomotor activity; however, reward behaviors were simil

167 ic neurons of Drosophila and observe reduced locomotor activity, impaired survival and an age-depende

168 PD altered several behavioural (reversal of locomotor activity impairment; cognitive impairment; del

169 jecting medium spiny neurons (iMSNs) impairs locomotor activities in a task-specific manner.

170 LG-IH also altered metabolic expenditure and locomotor activities in male offspring, and increased nu

171 DH44 PI-Hugin SEZ circuit controls circadian locomotor activity in a daily cycle but has minimal effe

172 s platform by characterizing ethanol-induced locomotor activity in a dose-dependent manner as well as

173 basal locomotor activity and cocaine-induced locomotor activity in a manner indistinguishable from wi

174 cond test 7 dpf fish revealed an increase in locomotor activity in all MeHg exposures tested.

175 ndent behavioral flexibility, and heightened locomotor activity in an open field arena.

176 Locomotor activity in an open field was also elevated.

177 ecessary for reduced methamphetamine-induced locomotor activity in C57BL/6J congenic mice harboring D

178 fluoxetine abolished methylphenidate-induced locomotor activity in DAT Val559 mice, mimicking the eff

179 tylcholine (ACh) activation markedly reduced locomotor activity in DD mice.

180 lized PER1 and PER2 expression and circadian locomotor activity in ENT1 KO mice.

181 We examined circadian locomotor activity in ENT1 KO vs WT littermates and foun

182 that electromyograms (EMGs) obtained during locomotor activity in mice were effective for identifica

183 underlying decreased methamphetamine-induced locomotor activity in mice.

184 od pressure without affecting SCN-controlled locomotor activity in murine models.

185 gamma power, and these rats showed enhanced locomotor activity in novel environment.

186 in real-time place preference and increased locomotor activity in open-field testing.

187 timing of clock gene expression and reduced locomotor activity in parallel with increased lung infla

188 ally, Gal-1 deficiency did not change normal locomotor activity in post-natal animals.

189 ly decreased spontaneous and cocaine-induced locomotor activity in rats expressing KORD to midbrain (

190 n of DeltaFosB-T149D in NAc leads to greater locomotor activity in response to an initial low dose of

191 Compound (-)-34 was also able to elevate locomotor activity in the above PD animal model signific

192 ator alone is sufficient to rescue circadian locomotor activity in the absence of the other.

193 th sexes exposed to + Nic exhibited elevated locomotor activity in the elevated plus maze and altered

194 , colonized E2-exposed larvae showed reduced locomotor activity in the light, in contrast to axenic E

195 ot alter baseline body weight, but increased locomotor activity in the open field across both sexes.

196 gy expenditure (EE) and a 3-fold decrease in locomotor activity in the unfed state.

197 lead to manganese dyshomeostasis and altered locomotor activity in zebrafish with CRISPR-induced slc3

198 place within the neural network controlling locomotor activity, including spinal interneurons.

199 more severe impairments, including decreased locomotor activity, inferior cued water maze performance

200 rats displayed blunted d-Amphetamine-induced locomotor activity, insensitivity to d-Amphetamine poten

201 admill, we show that vestibular influence on locomotor activity is modulated independently in each li

202 During walking, the vestibular influence on locomotor activity is phase-dependent and modulated in b

203 , we find that QRFP overexpression decreases locomotor activity largely in a light-specific manner.

204 h, and animals were assessed for changes in locomotor activity, learning, and memory 6 weeks later.

205 nduced behaviour in C. elegans and increased locomotor activity levels when injected into the central

206 ffort exertion through regulation of general locomotor activity levels.

207 tic Mecp2 mutant mice significantly improved locomotor activity, lifespan and gene expression normali

208 ctroencephalogram (EEG), electromyogram, and locomotor activity (LMA) and the efficacy of the TAAR1 p

209 molecular clock, in generating the mammalian locomotor activity (LMA) circadian rhythm.

210 regions of rat mPFC, in appetitive trace and locomotor activity (LMA) procedures.

211 EEG, EMG, body temperature (Tb), and locomotor activity (LMA) were recorded in Taar1 KO, OE,

212 lness and produces sustained arousal, higher locomotor activity (LMA), and hyperthermia, which are co

213 I3 interneurons are not necessary for normal locomotor activity, locomotor circuits rhythmically inhi

214 fects of PF-5190457 combined with alcohol on locomotor activity, loss-of-righting reflex (a measure o

215 KO) male mice show increased novelty-induced locomotor activity, lower baseline anxiety, and motivati

216 (vSPZ) is critical for rhythms of sleep and locomotor activity (Lu et al. [] J Neurosci 21:4864-4874

217 ression of clock genes, circadian rhythms of locomotor activity, lung function, and inflammatory and

218 ensure that their sensory responsiveness and locomotor activity match environmental demands.

219 Rats exhibited increases in spontaneous locomotor activity, measured by implanted radiotelemetry

220 xplained by differences in feeding behavior, locomotor activity, metabolic energy expenditure, or adi

221 firing rate with bioluminescence imaging and locomotor activity monitoring.

222 were associated with the morning or evening locomotor activities occurred ~4 hours before their resp

223 Analysis of locomotor activity of diquat dibromide and the neurotoxi

224 the use of the probes for the control of the locomotor activity of mice for over four weeks via progr

225 The BP, heart rate and locomotor activity of rats was analyzed and urinary sodi

226 Here we evoke fictive locomotor activity of various frequencies in upright spi

227 (VS) are sufficient to synchronize the daily locomotor activity of wild-type Drosophila melanogaster.

228 g RNA knockdown, serum parameters, circadian locomotor activity, Oil Red O staining, transient transf

229 Locomotor activity or food reinforced operant responding

230 not interact with the effects of alcohol on locomotor activity or loss-of-righting reflex.

231 reinstatement to cocaine, but did not affect locomotor activity or reinstatement to sucrose seeking.

232 n mice without affecting total fluid intake, locomotor activity or saccharin preference.

233 cits, but they did not have abnormalities of locomotor activity or social interaction.

234 any difference in basal motor coordination, locomotor activity, or conditioned place preference comp

235 mPFC-AcbSh pathway had no effect on running, locomotor activity, or feeding under ad libitum conditio

236 seeking without affecting operant learning, locomotor activity, or reinstatement of natural reward s

237 We reveal that circadian rhythms in host locomotor activity patterns and body temperature become

238 anges (PS bouts, SWS time, body temperature, locomotor activity) persisted after the CSDS regimen had

239 piny neurons (iMSNs) is sufficient to impair locomotor activity, phenocopying DA depletion models of

240 Memory, behavioral tasks, locomotor activity, presence of human antibodies specifi

241 mir-124 mutants exhibit profoundly abnormal locomotor activity profiles, including loss of anticipat

242 e report the use of animal models, including locomotor activity, protection, and rescue experiments i

243 hythms of clock gene expression in the lung, locomotor activity, pulmonary function, inflammatory, pr

244 activity of TRPA1 antagonists, bidirectional locomotor activity, receptor desensitization, and off-ta

245 neurons had increased energy expenditure and locomotor activity; reduced body weight, fat mass, and f

246 re includes the de facto assumption that any locomotor activity reflects an absence of fear.

247 While 14a increased locomotor activity relative to vehicle, it was significa

248 tive sensory feedback to the coordination of locomotor activity remains less clear.

249 y disrupted or restored dopamine content and locomotor activity, respectively.

250 Kiss1r KO females displayed markedly reduced locomotor activity, respiratory rate, and energy expendi

251 During ad libitum feeding, locomotor activity resumed its arrhythmic state, but per

252 Analysis of locomotor activity revealed no major differences in dail

253 Light pulses delay locomotor activity rhythm during the early night and adv

254 est period induces phase delays of circadian locomotor activity rhythm.

255 mple tracking system for assaying Drosophila locomotor activity rhythms and thought that it might als

256 eactivity and injections of SIFamide delayed locomotor activity rhythms circadian time-dependently, S

257 tion of the Drosophila homolog HDAC4 impairs locomotor activity rhythms of flies and decreases period

258 re sufficient to drive motivated feeding and locomotor activity similar to LHA (GABA) neurons, but wi

259 take, along with the circadian regulation of locomotor activity, sleep, and core body temperature.

260 lateral brain ventricle results in increased locomotor activity, stereotypical behavior, and decrease

261 mutant adults are viable but display reduced locomotor activity, susceptibility to starvation, elevat

262 Locomotor activity, Tb (measured in the rumen) and the l

263 According to our more extensive locomotor activity testing data, cebranopadol itself als

264 ng self-administration of 0.2% saccharin and locomotor activity tests.

265 ie prion inocula showed a faster decrease in locomotor activity than similar flies exposed to scrapie

266 Ultradian (~4 hr) rhythms in locomotor activity that do not depend on the master circ

267 and evening oscillators eliminates circadian locomotor activity, the molecular clock in either oscill

268 Through non-linear conversion of locomotor activity to "Locomotor Inactivity During Sleep

269 We further mapped discrete parameters of locomotor activity to epilepsy-like and anxiety-like beh

270 rotonin in inhibiting endogenously generated locomotor activity to neurons located in the posterior m

271 neous Kcnn2 mutations show abnormal gait and locomotor activity, tremor and memory deficits, but huma

272 -derived AstC is required to mediate evening locomotor activity under short (winter-like) and long (s

273 Comparative analysis of cocaine induced locomotor activity using PANs and thick acupuncture need

274 LS3 suppresses locomotor activity via a BK channel-specific mechanism i

275 A decrease in locomotor activity was also observed in mice treated sys

276 Locomotor activity was assessed in colonized and axenic

277 Interestingly, locomotor activity was decreased in the hybrid peptide g

278 stent wakefulness with mania-like qualities: locomotor activity was increased; sensitivity to D-amphe

279 Locomotor activity was measured using the open-field tes

280 aperitoneal) every other day for 14 days and locomotor activity was measured.

281 owever, after amphetamine injection, greater locomotor activity was observed in Het mice compared wit

282 ved neurologic deficit score and spontaneous locomotor activity was observed, and the stroke infarct

283 Locomotor activity was unaltered by vector administratio

284 In addition, cocaine-induced locomotor activity was used as a general 'read out' of m

285 imulant-induced increases in accumbal DA and locomotor activity, we theorized that performing this cu

286 Phase shifts of locomotor activity were analyzed in grass rats transferr

287 microstructural analysis of food intake, and locomotor activity were assessed.

288 ained improvements in motor coordination and locomotor activity were observed, even after onset of ne

289 dystonic movements or postures or change in locomotor activity were observed.

290 Several parameters of locomotor activity were shifted early in the disease tim

291 muscimol dose dependently reduced open-field locomotor activity, whereas 300 ng of picrotoxin caused

292 e also show that QRFP overexpression reduces locomotor activity, whereas animals that lack QRFP signa

293 : hypocretin and cgrp stimulated spontaneous locomotor activity, whereas galanin and nociceptin atten

294 dent signaling and increased cocaine-induced locomotor activity, whereas overexpression of GIRK2 incr

295 hat Nematostella exhibits rhythmic circadian locomotor activity, which is persistent in constant dark

296 irect comparison of luciferase activity with locomotor activity, which was assayed in the same flies

297 This effect was not explained by a change in locomotor activity, which was unaffected by STN-HFS.

298 or behavior; while LHA (Gal) neurons induced locomotor activity without compulsivity.

299 tudies, GluN2B inhibitors reduce MA-mediated locomotor activity, without affecting basal activity.

300 ts of imidacloprid on queens (egg-laying and locomotor activity), worker bees (foraging and hygienic