ライフサイエンスコーパス: locomotor activity

1 rexia and body weight loss without affecting locomotor activity.

2 he Drosophila brain control daily rhythms in locomotor activity.

3 but emphasize their importance in promoting locomotor activity.

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

5 mbens triggered MAPK signaling and modulated locomotor activity.

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

7 d adiposity without affecting food intake or locomotor activity.

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

9 depression of spontaneous or cocaine-induced locomotor activity.

10 mice were normal in development and general locomotor activity.

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

12 spontaneous alternation, but did not affect locomotor activity.

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

14 aytime versus nighttime feeding behavior, or locomotor activity.

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

16 s would be sufficient to produce coordinated locomotor activity.

17 ircadian rhythmicity of body temperature and locomotor activity.

18 that is sufficient to initiate and maintain locomotor activity.

19 the spinal networks to generate coordinated locomotor activity.

20 nse characterized by a transient increase in locomotor activity.

21 otype in new directions by examining in-cage locomotor activity.

22 omotor activity and inhibits novelty induced locomotor activity.

23 e same drug concentrations that gave maximal locomotor activity.

24 ure interacts with thermoregulation, but not locomotor activity.

25 t mice does not develop because of increased locomotor activity.

26 o nausea/malaise or prolonged suppression of locomotor activity.

27 ithout affecting normal pain sensitivity and locomotor activity.

28 the generation of ultradian rhythms (URs) of locomotor activity.

29 rics, including hearing, vision, weight, and locomotor activity.

30 gnificant attenuation in amphetamine-induced locomotor activity.

31 ed within clock neurons for normal circadian locomotor activity.

32 , like BTR, is controlled independently from locomotor activity.

33 al adaptations and decreases the baseline of locomotor activity.

34 ts on water maze escape, place preference or locomotor activity.

35 ut affecting nicotine self-administration or locomotor activity.

36 food intake, fat uptake or absorption, or in locomotor activity.

37 xhibited by SHRs, while having no effects on locomotor activity.

38 inemia, and hepatic steatosis and normalized locomotor activity.

39 tor outputs to modulate circadian control of locomotor activity.

40 uced only a partial reduction on spontaneous locomotor activity.

41 ithout affecting baseline visual function or locomotor activity.

42 d circadian behavioral rhythms and decreased locomotor activity.

43 ty, but did not affect plus maze behavior or locomotor activity.

44 spension test but spared anpirtoline-induced locomotor activity.

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

46 reduces AMPH-stimulated dopamine efflux and locomotor activity.

47 lmitate, decreased food intake and increased locomotor activity.

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

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

50 chitecture that may account for the enhanced locomotor activity.

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

52 in mice, decreasing methamphetamine-induced locomotor activity.

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

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

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

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

57 erneurons is rhythmically modulated with the locomotor activity.

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

59 argets of maternal rest that modulate larval locomotor activity.

60 c Drosophila increased survival and improved locomotor activity.

61 INs, each likely playing different roles in locomotor activities.

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

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

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

65 icle improves significantly sensorimotor and locomotor activity 7 and 14 days after stroke, reduces i

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

67 ing neuronal damage and behavioral deficits (locomotor activity, 8-arm radial maze task).

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

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

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

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

72 Locomotor activity and anxiety-like behavior were increa

73 he treatment period, animals were tested for locomotor activity and anxiety-like behavior.

74 cy did not induce significant alterations of locomotor activity and anxiety-related indices in the no

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

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

77 wherein radiotelemetry determined home cage locomotor activity and body temperature at 23 degrees C

78 clozapine, and risperidone were assessed for locomotor activity and catalepsy.

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

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

81 vo, suppression of TSC1 expression increased locomotor activity and decreased habituation in a hippoc

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

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

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

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

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

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

88 10-30 mg/kg i.p.) dose-dependently increased locomotor activity and electrical brain-stimulation rewa

89 Locomotor activity and elevated plus maze test/forced sw

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

91 leads to increased food intake and decreased locomotor activity and energy expenditure, and ultimatel

92 rioration at >61 days and exhibited abnormal locomotor activity and enhanced tremor.

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

94 tat (5, 50, or 100 mg/kg) on novelty-induced locomotor activity and found that it blunted exploration

95 Therefore, we assayed locomotor activity and immobility-defined sleep in a new

96 exposed to E. coli as neonates had increased locomotor activity and impaired motor coordination as ju

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

98 d CNO dose-dependently decreases spontaneous locomotor activity and inhibits novelty induced locomoto

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

100 of the dorsal mPFC enhanced cocaine-induced locomotor activity and occluded behavioral sensitization

101 rain regions associated with impulsivity and locomotor activity and of alpha7-nAChRs in hypothalamic

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

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

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

105 T did not significantly reduce the increased locomotor activity and rearing behavior observed in the

106 w A53T mice develop age-dependent changes in locomotor activity and reduced anxiety-like behavior.

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

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

109 We quantified spontaneous locomotor activity and responsiveness to sensory stimuli

110 the excitability of SCN neurons, we examined locomotor activity and SCN firing in mice lacking Kv1.4

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

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

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

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

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

116 M peak is associated with courtship-related locomotor activity and the A peak is due to an artifact

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

118 ads to a lean phenotype, increased nocturnal locomotor activity, and activation of brown adipose tiss

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

120 Assessments of in vivo neurochemistry, locomotor activity, and cardiovascular parameters were c

121 rgy expenditure, respiratory exchange ratio, locomotor activity, and food intake.

122 d lead to decreased glucose levels, enhanced locomotor activity, and improved cognition.

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

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

125 7% decrease in lifespan, reduced spontaneous locomotor activity, and no lifespan increase when reared

126 test which provides a measure of anxiety and locomotor activity, and object placement, a measure of s

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

128 cortex, and a deficit in social interaction, locomotor activity, and prepulse inhibition.

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

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

131 ral health, olfactory abilities, exploratory locomotor activity, anxiety-like behaviors and pain resp

132 ct effects on thermoregulatory processes and locomotor activity are likely mediated by different mech

133 Pacemaker neurons critical for locomotor activity are not necessary for TPR; instead, t

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

135 xpenditure, such as feeding, metabolic rate, locomotor activity, arousal, growth and reproduction.

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

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

138 TH-induced decreases in body temperature and locomotor activity at 23 degrees C were also attenuated

139 effectively suppresses phencyclidine-evoked locomotor activity at doses that do not impair neuromusc

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

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

142 d that HCRT neuron-ablated larvae had normal locomotor activity, but demonstrated an increase in slee

143 Clozapine also dramatically reduced locomotor activity, but in the absence of catalepsy.

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

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

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

147 The present results indicate that increased locomotor activity can be correlated to TH protein expre

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

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

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

151 (5, 8, 10, and 15 mg/kg) every 12 hours in a locomotor activity chamber and a challenge dose of 5 mg/

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

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

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

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

156 The effects on locomotor activity could be reversed by direct delivery

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

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

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

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

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

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

163 WT mice showed a marked reduction in locomotor activity following acute administration of hal

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

165 null allele of Csnk1e showed an increase in locomotor activity following MA administration.

166 flick test for nociception, and a measure of locomotor activity for general arousal.

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

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

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

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

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

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

173 We also demonstrate that clozapine decreases locomotor activity in a 5-HT(2A)-dependent manner, in th

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

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

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

177 There were no group differences in locomotor activity in an open field on the copulation te

178 Locomotor activity in an open field was also elevated.

179 QTL) mapping of methamphetamine (MA)-induced locomotor activity in C57BL/6J (B6) x DBA/2J (D2)-F(2) m

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

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

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

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

184 oventricular application of insulin promoted locomotor activity in MUFA-fed mice, whereas SFA-mice we

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

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 (cAMP response element binding protein), and locomotor activity in rats raised in enriched (EC), impo

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

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

193 Chronic E2 decreased locomotor activity in the open field and enhanced perfor

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

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

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

197 energy expenditure as a result of increased locomotor activity, increased thermogenesis in brown adi

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

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

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

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

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

203 ptin and amino acid signaling, and increased locomotor activity, likely attributable to increased mel

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

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

206 es influence body weight and cocaine-induced locomotor activity (LMA).

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

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

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

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

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

212 firing rate with bioluminescence imaging and locomotor activity monitoring.

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

214 Analysis of locomotor activity of diquat dibromide and the neurotoxi

215 as first-generation medications suppress the locomotor activity of Egr3(-/-) and WT mice to a similar

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

217 n be conveniently estimated by measuring the locomotor activity of the flies using techniques and ins

218 These changes correlate with increased locomotor activity of the Mecp2-deficient animals, sugge

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

220 Sound stimulus during the day reduced the locomotor activity of wild-type sibling larvae, while HC

221 Exposure to light during the night decreased locomotor activity of wild-type siblings, but induced an

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

223 GluN3A KO mice showed impaired locomotor activity on a variety of motor function tests,

224 Locomotor activity or food reinforced operant responding

225 raperitoneally) had no significant effect on locomotor activity or intracranial self-stimulation.

226 e with CNO-mediated changes in ANS function, locomotor activity or motor coordination.

227 are observed at doses that do not influence locomotor activity or reinstatement responding following

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

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

230 penditure, with no change in caloric intake, locomotor activity, or thyroid hormone levels.

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

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

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

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

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

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

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

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

239 played enhanced spontaneous and drug-induced locomotor activity, relative to control transplanted Mit

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

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

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

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

244 Analysis of locomotor activity revealed no major differences in dail

245 ination (narrow bean traverse and gait), and locomotor activity revealed no significant differences b

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

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

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

249 ct of translation control genes on circadian locomotor activity rhythms in flies.

250 As in previous studies, locomotor activity rhythms in older mice required more d

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

252 in neuronal remodeling, which contributes to locomotor activity rhythms.

253 e start of foraging of 3.3 h, and whole-hive locomotor-activity rhythms were delayed by an average of

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

255 rmance, and between striatal 5-HT levels and locomotor activity strongly implicate regionally-specifi

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

257 Locomotor activity tests were performed once a week for

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

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

260 its have markedly shorter (0.5 h) periods of locomotor activity than wild-type (WT) mice.

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

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

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

264 locomotor output of animals from horizontal locomotor activity to vertical activity, further highlig

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

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

267 Locomotor activity was also affected in some cases.

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

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

270 ncillary effects on behavioral activation as locomotor activity was either unaffected, as in the case

271 Significantly reduced locomotor activity was exhibited in B6.TH-tabw2 congenic

272 ousing conditions when the nicotine-mediated locomotor activity was expressed as a percent change fro

273 was increased to near that of wild type, and locomotor activity was improved.

274 Interestingly, locomotor activity was increased in [dA(2)]GLP-1/GcG mic

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

276 nificantly increased during daytime, overall locomotor activity was not significantly different.

277 Increased locomotor activity was observed after 4-MMC administrati

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

279 Maximal locomotor activity was obtained after treatment with a h

280 Capsaicin's effect on S4-evoked locomotor activity was potent until the lumbar 5 (L5) se

281 Locomotor activity was unaltered by vector administratio

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

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

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

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

286 No associated changes in locomotor activity were observed.

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

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

289 owever, mGluR5(KD-D1) animals showed reduced locomotor activity when placed in a novel environment, a

290 intoxication, low doses of ethanol stimulate locomotor activity whereas high doses induce sedation.

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

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

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

297 AP-DNSynCAM1 mice) exhibit disrupted diurnal locomotor activity with enhanced and more frequent episo

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