ライフサイエンスコーパス: Long-Evans rat

1 rus in the visual cortex and pulvinar of the Long-Evans rat.

2 rebellar nuclei and vestibular nuclei of the Long-Evans rat.

3 subretinal space (SRS) of Sprague-Dawley or Long Evans rats.

4 how AW enables upward FRH in V1 of juvenile Long Evans rats.

5 zone on gestation days 5 and 6 (4 hr/day) in Long Evans rats.

6 g a specific gRNA in female transgenic Cas9+ Long Evans rats.

7 larger in area than the binocular region in Long Evans rats.

8 g a rat model of high ethanol consumption in Long Evans rats.

9 covery from chronic monocular deprivation in Long Evans rats.

10 l solution was injected into the vitreous of Long-Evans rats.

11 d anxiolytic effects in both male and female Long-Evans rats.

12 ic nucleus of the preoptic area (SDN-POA) in Long-Evans rats.

13 ale (experiment 1) and female (experiment 2) Long-Evans rats.

14 GF was injected into the subretinal space of Long-Evans rats.

15 erior colliculi of postnatal day 2 through 4 Long-Evans rats.

16 ily to gonadectomized, adrenalectomized male Long-Evans rats.

17 the voluntary consumption of ethanol in male Long-Evans rats.

18 al circuits in young, mature adult, and aged Long-Evans rats.

19 to assess spatial pattern separation in male Long-Evans rats.

20 6-month-old) and aged (24-26-month-old) male Long-Evans rats.

21 f young (6-8 months) and aged (25-28 months) Long-Evans rats.

22 and prefrontal cortex of freely-moving male Long-Evans rats.

23 ed leptin intracerebroventricularly (icv) to Long-Evans rats.

24 to the spatial code in pCA1 and dCA1 in male Long-Evans rats.

25 d calcium imaging methods in male and female Long-Evans rats.

26 o GABAergic neurons in LH of male and female Long-Evans rats.

27 her reinstatement responses to nicotine than Long-Evans rats.

28 attenuating nicotine self-administration in Long-Evans rats.

29 instatement of alcohol or cocaine seeking in Long-Evans rats.

30 ntion accuracy compared to heterozygotic and Long-Evans rats.

31 agenase were performed in Sprague-Dawley and Long-Evans rats.

32 toxic insult in adult multiparous and virgin Long-Evans rats.

33 ing the NYU impactor device in female, adult Long-Evans rats.

34 ) at spinal cord segment T10 of adult female Long-Evans rats.

35 imulation were evaluated for female and male Long-Evans rats.

36 stradiol-induced changes in spine density in Long-Evans rats.

37 o female and male, intact and gonadectomized Long-Evans rats.

38 P and recorded HD cells in the ADN of female Long-Evans rats.

39 tized albino (Sprague-Dawley) and pigmented (Long Evans) rats.

40 Adult, male Long-Evans rats (180-200 g, n = 7-9/group) were subjecte

41 Adult, male Long-Evans rats (180-200 g, n=7-9/group) were subjected

42 Adult, male Long-Evans rats (180-200 g, n=9-10/group) were subjected

43 ic artery (10 ng min(-1) for 60 min) of male Long-Evans rats (220-250 g, n = 24) induced constriction

44 lowered O2 consumption in all regions of the Long Evans rats (-41%).

45 es of CA3 neurons from young and aged, male, Long-Evans rats along the CA3 transverse axis.

46 model to characterize feeding in adult male Long Evans rats and aligned this behavioral response wit

47 RGCs were purified from 7- or 8-day-old Long Evans rats and cultured on polylysine/laminin-coate

48 ong-term food intake and body weight of lean Long Evans rats and of fatty Zucker (fa/fa) rats.

49 proves during adolescence in male and female Long-Evans rats and demonstrate that the increase in rev

50 e was harvested from 4-month-old (400-450 g) Long-Evans rats and grafted heterotopically into the abd

51 ve injury (SNI) model of neuropathic pain in Long-Evans rats and patch-clamp recordings in layer II/I

52 sed into the left cerebral ventricle of male Long-Evans rats and the effect of this s-ODN on subseque

53 om wild type mice, genetically altered mice, Long Evans rats, and cultured differentiated rat pheochr

54 ng ability was quantitated in young and aged Long-Evans rats, and molecular markers were assessed in

55 rsal-learning performance in male and female Long-Evans rats are linked to specific reinforcement-lea

56 ow that neurons in the POR and RSC of female Long-Evans rats are tuned to distinct but complementary

57 pared to alcohol naive counterparts, in male Long-Evans rats at 24-hours withdrawal from alcohol admi

58 tive microelectrodes in control and diabetic Long-Evans rats at 4 and 12 weeks after induction of dia

59 This study was performed in adult male Long-Evans rats at 48-h withdrawal from chronic alcohol

60 ecorded from the anterior dorsal thalamus of Long-Evans rats before and after administration of the s

61 ences in impulsive action in male and female Long Evans rats both before and after short (4-6 days) o

62 Compared to Long-Evans rats, Brattleboro rats exhibit diminished fea

63 nduced robust freezing in Sprague-Dawley and Long-Evans rats but not in Wistar rats.

64 reperfusion (FCIR) model was induced in male Long-Evans rats by a bilateral occlusion of both common

65 Experimental diabetes was induced in male Long-Evans rats by a single intraperitoneal injection of

66 - 0.9 to 4.5 +/- 0.8 (density units) in male Long-Evans rats by daily giving two intraperiotoneal inj

67 detachments were experimentally produced in Long-Evans rats by injecting modified phosphate-buffered

68 Focal cerebral ischemia was induced in Long-Evans rats by occlusion of the right middle cerebra

69 cal VVRs were induced in anesthetized, male, Long-Evans rats by sinusoidal galvanic vestibular stimul

70 l learning were documented in young and aged Long-Evans rats by using a hippocampal-dependent version

71 We measured Long-Evans rats' capacity for visual form discrimination

72 To do so, male Long-Evans rats chronically implanted with tetrodes in t

73 Male and female Long-Evans rats consumed either water and ground chow, o

74 Here, we gave female and male Long Evans rats cue light illumination paired or unpaire

75 RF), and neuropeptide Y levels in adult male Long-Evans rats defeated in a resident-intruder social a

76 Previous studies in Long-Evans rats demonstrated a significant relationship

77 cal age in Sprague Dawley rats compared with Long Evans rats, despite overall similar temporal sequen

78 ats were used since prior work showed female Long Evans rats did not acquire the safety discriminatio

79 As Long-Evans rats did not show a robust reinstatement resp

80 In Long Evans rats during the first postnatal week, GluR2-l

81 2-CH) local field potential activity of male Long-Evans rats during a PRL task wherein a target respo

82 gral) neurons of the dorsomedial striatum in Long-Evans rats during discrete periods of training of a

83 Female Long-Evans rats either received bilateral SynAb surgery

84 acterized model in which outbred, aged, male Long-Evans rats exhibit a spectrum of individual differe

85 Accordingly, Long-Evans rats exhibit differences in the expression of

86 f cocaine seeking by L822429, and found that Long-Evans rats exhibit greater sensitivity to NK1R anta

87 Female, Long Evans rats experienced a battery of adverse adolesc

88 depressant and pro-cognitive effects in male Long-Evans rats exposed to the chronic mild stress (CMS)

89 Adult Long-Evans rats, exposed prenatally to 1 of 4 doses of c

90 In Long-Evans rats, focal cerebral ischemia was produced by

91 e acute effect of 17alpha-Estradiol in adult Long Evans rats following chronic monocular deprivation,

92 Y stimulate food intake dose-responsively in Long-Evans rats for at least 4 h after intracerebroventr

93 sing spatial information and memory, in male Long-Evans rats foraging for food under risky situations

94 and their underlying molecular mechanisms in Long-Evans rat heart and in HL-1 cardiomyocyte cell line

95 On alternating days, adult male Long-Evans rats implanted with bilateral cannulas in the

96 The study was conducted in Long-Evans rats implanted with jugular catheters.

97 CA3 subregions during free foraging of male Long-Evans rats in a 2D environment, we found that rate

98 Here, using male Long-Evans rats in response-based and cue-based maze-run

99 demonstrated that optic nerve transection in Long-Evans rats increased superoxide levels in RGCs.

100 relay ipsilateral eye input to lateral V1 in Long Evans rats is a consequence of the existence of ocu

101 Using male tyrosine hydroxylase (TH)-Cre Long Evans rats, it was found that, under baseline condi

102 Thirty-two male Long Evans rats learned the rSMT.

103 Male Long-Evans rats learned to lever-press on a VR5 schedule

104 mponent of marijuana (Cannabis sativa), in a Long-Evans rat model affects reward-related behavior and

105 Male and female Long-Evans rats (N = 48) underwent a battery of assays i

106 Male, Long-Evans rats (n=72) underwent either sham or OBX surg

107 l (Sprague-Dawley rats [N=16]) or clozapine (Long-Evans rats [N=20]).

108 n behavior and neural activity in adolescent Long Evans rats of both sexes.

109 metabolic response to ozone was examined in Long-Evans rat offspring.

110 Thus, we evaluated male and female Long Evans rats on acquisition, dose-responsiveness, and

111 dult (5 months) and older (10 months) female Long-Evans rats on a win-shift (delay) 12-arm radial maz

112 We recorded from hippocampal neurons as male Long-Evans rats performed 6 blocks of an object discrimi

113 rawn (Post-EtOH) rats, we trained adult male Long-Evans rats, randomly assigned into the ethanol and

114 nfection than females, adult male and female Long Evans rats (Rattus norvegicus) were inoculated with

115 Long-Evans rats received 99 electrical stimulations of t

116 Halothane-NO(2)-O(2)-anesthetized Long-Evans rats received a 5-microl intracerebroventricu

117 Male Long-Evans rats received an 8-trial training session in

118 In experiment 1, male Long-Evans rats received bilateral sham or neurotoxic NA

119 Male Long-Evans rats received daily intraperitoneal injection

120 Male Long-Evans rats received either sham, ipsilaterally, or

121 Over 24 training days, male Long-Evans rats received ethanol injection (2.5 g/kg) in

122 Male Long-Evans rats received four trials per day for 7 days,

123 Male Long-Evans rats received ibotenic acid-induced lesions o

124 In experiment 1, Long-Evans rats received intra-BLA injections of halorho

125 Male Long-Evans rats received intra-BLA microinjections of vi

126 Adult male albino rabbits and Long-Evans rats received iontophoretic injections of bio

127 In experiment 2, male Long-Evans rats received NAcc transduction with halorhod

128 Male, Long-Evans rats received Pavlovian conditioning sessions

129 64 Male Long-Evans rats received unilateral cortical contusion a

130 Long-Evans rats received unilateral naris closure on pos

131 Diabetes was induced in Long Evans rats, resulting in a two- to threefold increa

132 iments were performed using needle-punctured Long Evans rat retinas.

133 Using a conflict model in which male Long-Evans rats retrieve memories of shock- and food-pai

134 ampal (VH) terminals in the PL of adult male Long-Evans rats selectively during paired trials reveale

135 We also compared the mycobiomes of Long-Evans rats separated from their mothers (hypersensi

136 Specifically, virgin Long-Evans rats showing vaginal estrus were handled brie

137 have been the focus of experimental study in Long-Evans rats, since they engender divergent changes i

138 Specifically, C3 opsonization in sera of Long Evans rat strain, and mouse strains widely used in

139 ed astrocytes in the MePD of male and female Long Evans rats that were gonadectomized as adults and t

140 ctions into the NAc shell of male and female Long-Evans rats that drank under the intermittent-access

141 In adult male Long-Evans rats that had undergone maternal separation,

142 e immunoreactivity in brain slices from male Long-Evans rats that received a 2-h exposure of 0, 20, 4

143 drenal transplants were evaluated in 14 male Long-Evans rats that received intraspinal injections of

144 xamined in the hippocampus of young and aged Long-Evans rats that were behaviorally characterized for

145 ings, the current work revealed that in male Long-Evans rats, the hippocampus and dorsolateral striat

146 In contrast, in Long Evans rats, this region is nearly exclusively domin

147 an established model of asymmetrical FGR in Long-Evans rats, this study investigated sex differences

148 We trained male Long Evans rats to associate a 10 s auditory conditioned

149 est this hypothesis, we exposed adult female Long-Evans rats to 2 weeks of moderate-intensity broadba

150 experiments in brain slice preparations from Long-Evans rats to investigate the ability of O-LM cells

151 task involving a gustometer, we trained male Long-Evans rats to report the degree to which a test sti

152 We trained male Long-Evans rats to self-administer alcohol (12% w/v) for

153 in vivo fixed potential amperometry in male Long-Evans rats to test if phasic nucleus accumbens shel

154 -old (n = 13) and 24-month-old (n = 27) male Long-Evans rats trained in the water maze on a standard

155 DS regulates ethanol self-administration in Long-Evans rats trained to self-administer a 10% ethanol

156 M/T cells and presumed granule cells in male Long-Evans rats under urethane anesthesia while testing

157 recorded vlPAG single-unit activity in male, Long Evans rats undergoing fear discrimination.

158 n postnatal days (PND) 3-15, male and female Long-Evans rats underwent 3 h daily MS.

159 e (NaIO(3))-induced model of GA in pigmented Long Evans rats using a comprehensive set of in vivo and

160 ial learning was evaluated in young and aged Long-Evans rats using the Morris water maze, and the tot

161 neurons from acute olfactory bulb slices of Long Evans rats, various capabilities of this technique

162 Retinal gene expression in diabetic Long Evans rats was measured by whole genome microarray

163 sembles of hippocampal neurons in adult male Long-Evans rats was monitored across a period of rapid s

164 In Long Evans rats, we measured dynamic and static properti

165 In male and female Long Evans rats, we used viral-mediated expression of HD

166 In this study, performed in female Long-Evans rats, we show that the NAc core directly cont

167 Male Long-Evans rats, weighing 300 to 400 g, fasted overnight

168 Male Long Evans rats were assessed for high versus low levels

169 Fifty-eight adult male Long Evans rats were assigned to either: EC, socially pa

170 Adult Long Evans rats were maintained on ethanol-containing or

171 Pigmented Long Evans rats were rendered diabetic with streptozotoc

172 Male long evans rats were trained in a delay discounting task

173 At 5 weeks of age, Long Evans rats were treated with weekly intraperitoneal

174 Male Long Evans rats were used since prior work showed female

175 Four groups of male Long Evans rats were used: Control, Control + green tea

176 Pregnant Long-Evans rats were administered either corn oil (contr

177 Male Long-Evans rats were administered nicotine bitartrate or

178 Twenty seven adult male Long-Evans rats were administered one of three treatment

179 Male, Long-Evans rats were allowed to drink 15% ethanol (v/v)

180 Male and female Long-Evans rats were assigned to one of three treatments

181 In 3 experiments, adult male Long-Evans rats were castrated and treated daily with an

182 In a series of 3 experiments, adult male Long-Evans rats were castrated and treated with 1 of 3 d

183 Adult male Long-Evans rats were confined to treatment- or nontreatm

184 Thirty-eight Long-Evans rats were divided into five groups: ovariecto

185 Long-Evans rats were divided into four treatment groups:

186 Female Long-Evans rats were divided into three groups (n = 10-1

187 Brown Norway/Long-Evans rats were divided into three groups with simi

188 Male Long-Evans rats were divided into three weight-matched g

189 Pregnant Long-Evans rats were dosed perinatally with 0 or 30.6 mg

190 Pregnant Long-Evans rats were exposed to filtered air, 0.4 ppm oz

191 Herein, 12-week-old Long-Evans rats were exposed to smoldering eucalyptus sm

192 Long-Evans rats were fed a basal diet or a similar diet

193 Pregnant Long-Evans rats were fed ad libitum with a diet containi

194 Virgin female Long-Evans rats were given one intra-VTA injection of mo

195 Male Long-Evans rats were implanted with a microdialysis prob

196 Male Long-Evans rats were implanted with intravenous catheter

197 Male Long-Evans rats were injected subcutaneously with citalo

198 Long-Evans rats were made diabetic with streptozotocin.

199 Pregnant Long-Evans rats were maintained on three diets throughou

200 al blood flow in young adult and middle-aged Long-Evans rats were measured.

201 inety-seven high-fat diet-induced obese male Long-Evans rats were monitored for BW loss during exendi

202 Long-Evans rats were pretrained on the pasta-matrix retr

203 Female Long-Evans rats were randomly assigned to one of two gro

204 In a final experiment, Long-Evans rats were restricted to two 2 h periods of ac

205 RGCs of postnatal day 4 to 5 Long-Evans rats were retrogradely labeled with the fluor

206 Male Long-Evans rats were rewarded with food pellets after th

207 In Experiment 1, ovariectomized, Long-Evans rats were subcutaneously (SC) administered se

208 Young and aged Long-Evans rats were tested in a Morris water maze task

209 Thirty-two male Long-Evans rats were tested on either the cued or uncued

210 To test this hypothesis, male and female Long-Evans rats were trained in a decision-making task i

211 Male and female Long-Evans rats were trained in a seek-take behavioral p

212 Male Long-Evans rats were trained in an unsignaled contextual

213 ng (3-6 months) and aged (22-26 months) male Long-Evans rats were trained on a discounting task used

214 Adult male Long-Evans rats were trained to consume either alcohol o

215 Long-Evans rats were trained to dig in cups that contain

216 Male, Long-Evans rats were trained to self-administer either e

217 Male Long-Evans rats were trained to self-administer heroin f

218 Long-Evans rats were used; modulation of copulatory beha

219 episode of reduced-intensity stimulation in Long-Evans rats, which are relatively resistant to devel

220 l alterations compared with normal wild-type Long-Evans rats, which provide evidence for a CNS functi

221 direction (HD) cells were recorded in female Long-Evans rats while they foraged in an environment sub

222 Diabetes mellitus was induced in Long Evans rats with streptozotocin, and an anti-alpha 4

223 Diabetes was induced in Long Evans rats with streptozotocin.

224 Adult male Long-Evans rats with bilateral stimulating electrodes ac

225 Two experiments were conducted using male Long-Evans rats with chronically implanted electrodes to

226 Male Long-Evans rats with chronically-implanted stimulating a

227 Male Long-Evans rats with diet-induced obesity received AGB i

228 VSG was performed on Long-Evans rats with diet-induced obesity.

229 VSG was performed in Long-Evans rats with diet-induced obesity.

230 ing with automated touchscreen tasks in male Long-Evans rats with selective lesions of medial septal/

231 Diabetes was induced in Long-Evans rats with streptozotocin, resulting in a two-

232 at basal plasma concentrations for 7 days in Long-Evans rats with uncontrolled diabetes induced by st

233 Ovariectomized, Long-Evans rats with unilateral implants into the NRM of

234 Ovx, Long-Evans rats with unilateral microinjections into the

235 Drd1-Cre(+) and Drd2-Cre(+) transgenic male Long-Evans rats with virally labeled PL->NAc neurons wer