ライフサイエンスコーパス: Sprague-Dawley rat

1 odium azide, 37 degrees C) and in vivo (male Sprague-Dawley rats).

2 ive taste memory on taste preference in male Sprague Dawley rats.

3 endritic release of CCK in the brain in male Sprague Dawley rats.

4 e post-retrieval extinction paradigm in male Sprague Dawley rats.

5 al ischemia-reperfusion injury (IRI) in male Sprague Dawley rats.

6 tegmental area (VTA) of adolescent mice and Sprague Dawley rats.

7 enates and cultured hippocampal neurons from Sprague Dawley rats.

8 One hundred sixteen male Sprague Dawley rats.

9 Twenty-seven healthy Sprague Dawley rats.

10 learned helplessness (cNLH); and (3) control Sprague Dawley rats.

11 seeking, an animal model of relapse, in male Sprague Dawley rats.

12 into separate WAT depots in male and female Sprague Dawley rats.

13 rotid artery occlusion (BCCAO) in adult male Sprague Dawley rats.

14 capable, uncontrollable tail shocks (ISs) in Sprague Dawley rats.

15 uced seizures in urethane anesthetized, male Sprague Dawley rats.

16 ular, and imaging approaches in adult female Sprague Dawley rats.

17 vector and to knock down VAN GLP-1Rs in male Sprague Dawley rats.

18 growth, and phenotype of OMECs cultured from Sprague-Dawley rats.

19 d high CNS permeability in C57Bl/6s mice and Sprague-Dawley rats.

20 e superior colliculus and globus pallidus of Sprague-Dawley rats.

21 owing its intravenous administration to male Sprague-Dawley rats.

22 both autistic-like behavior and epilepsy in Sprague-Dawley rats.

23 nds were created on the palatal mucosa of 54 Sprague-Dawley rats.

24 entration and AQP2 protein in the kidneys of Sprague-Dawley rats.

25 y, with greater effects in BN versus control Sprague-Dawley rats.

26 T ) were recorded in 28 conscious adult male Sprague-Dawley rats.

27 signaling and hedonic expression in 21 male Sprague-Dawley rats.

28 in O/W emulsions after oral gastric feeding Sprague-Dawley rats.

29 AL did not affect CO2 sensitivity in control Sprague-Dawley rats.

30 of this study was to test this hypothesis in Sprague-Dawley rats.

31 enovirus-mediated overexpression of sFlt1 in Sprague-Dawley rats.

32 was induced by cortical contusion injury in Sprague-Dawley rats.

33 ar changes were seen after 6 weeks of VWR in Sprague-Dawley rats.

34 Lewis rats but were significantly altered in Sprague-Dawley rats.

35 lorinated, and provided as drinking water to Sprague-Dawley rats.

36 vivo in DMBA induced mammary tumor in female Sprague-Dawley rats.

37 Agents were administered in diets to female Sprague-Dawley rats.

38 GDER was induced in 6- to 8-week-old male Sprague-Dawley rats.

39 m DORA-22, an analog of the DORA MK-6096, in Sprague-Dawley rats.

40 Male Sprague-Dawley rats.

41 y sustained testosterone suppression in male Sprague-Dawley rats.

42 al day 5 (P5), 14 (P14), and adults (P72) in Sprague-Dawley rats.

43 atial memory for a well-learned task in male Sprague-Dawley rats.

44 behaviors and drug consumption compared with Sprague-Dawley rats.

45 Thirty-two adult male Sprague-Dawley rats.

46 r mandibular molar roots in 65 mature female Sprague-Dawley rats.

47 induced by cecal ligation and perforation in Sprague-Dawley rats.

48 ed liver samples was examined using eighteen Sprague-Dawley rats.

49 cardium 1 week after ischemia-reperfusion in Sprague-Dawley rats.

50 olliphor P 407 gels (KP 407) intranasally in Sprague-Dawley rats.

51 bicin were conducted in male BALB/c mice and Sprague-Dawley rats.

52 adult-born hippocampal neurons in adult male Sprague-Dawley rats.

53 cision in the anterior edentulous maxilla of Sprague-Dawley rats.

54 One dose of amphetamine was injected into Sprague-Dawley rats.

55 We tested male Sprague-Dawley rats (12 months old) with permanent middl

56 After gingival resection in 120 Sprague-Dawley rats, 2 microg rhTSG-6 in 5-microL phosph

57 tering HUP-A i.p. or intrathecally to female Sprague-Dawley rats (200-235 g body weight) after modera

58 Male Sprague-Dawley rats (200-250 g) and male C3H/HeN wild-ty

59 Sprague Dawley rats (24, female) were randomly assigned

60 xperiments were conducted using anesthetized Sprague-Dawley rats 3 weeks after treatment with either

61 cordings of phrenic nerve activity in female Sprague Dawley rats (3-4 months) revealed a direct corre

62 Sprague-Dawley rats (3 mo old) that received HNGF6A requ

63 Male Sprague-Dawley rats (3-6 months) were administered eithe

64 Nonheparinized male Sprague-Dawley rats (300-450 g, n=68) were randomly assi

65 Male Sprague Dawley rats (350-450 g) were chronically implant

66 ibrillary acidic protein promoter in 62 male Sprague Dawley rats, 4 dominant-negative soluble N-ethyl

67 Pregnant Sprague-Dawley rats (5-month-old) were exposed to high d

68 In male Sprague-Dawley rats 6-OHDA (n = 12) or vehicle (n = 10)

69 ted 4 different hemorrhage models using male Sprague-Dawley rats (6 rats/model), aged 10 to 14 weeks

70 Sprague-Dawley rats (6-8 weeks old) were injected with f

71 Tregs, we studied selected groups of newborn Sprague-Dawley rats according to feeding plan: dam+/-LR1

72 s were administered in an i.v. bolus to male Sprague Dawley rats after starting a s.c. infusion of ME

73 Delivery of NaF was compared in Sprague Dawley rats after suprachoroidal, posterior subc

74 ed Geniposide-induced hepatic injury in male Sprague-Dawley rats after 3-day intragastric administrat

75 We conducted a 9-month study in Sprague-Dawley rats after 45 minutes of bilateral renal

76 to a pharmacokinetic study performed on male Sprague-Dawley rats after administration of a single dos

77 d by anti-OPH IgG and cytokines formation in Sprague Dawley rats and Balb/c mice, respectively.

78 sensitization to cocaine was established in Sprague Dawley rats and was measured by locomotion and b

79 Thirty-two healthy male Sprague-Dawley rats and 47 human adults underwent threat

80 We also performed experiments with male Sprague-Dawley rats and CPEB-deficient mice (C57BL6 or m

81 ehaviorally sensitive, low alcohol-consuming Sprague-Dawley rats and DBA/2 mice and behaviorally inse

82 using microdosing of the unlabeled ligand in Sprague-Dawley rats and in wild-type and KOR knockout mi

83 is and/or beta-AR levels in diabetic hearts, Sprague-Dawley rats and miR-133a transgenic (miR-133aTg)

84 rom freshly excised lung, obtained from both Sprague-Dawley rats and New Zealand White rabbits.

85 Adult male Sprague-Dawley rats and pulmonary epithelial cells.

86 Sprague-Dawley rats, SU5416/hypoxia-treated Sprague-Dawley rats, and SU5416/hypoxia-treated C57BL/6

87 Normal Sprague-Dawley rats as well as RH or streptozotocin (STZ

88 g to AKAPs in the nucleus accumbens shell of Sprague-Dawley rats attenuates reinstatement induced by

89 Male Sprague-Dawley rats, Balb/c mice, and C57Bl6/J mice.

90 PH was induced in male Sprague Dawley rats by monocrotaline, hypoxia, or bleomy

91 Stroke was induced in adult Sprague Dawley rats by occluding the middle cerebral art

92 PAH was induced in male Sprague-Dawley rats by administering monocrotaline.

93 CP was induced in Sprague-Dawley rats by an intraductal injection of 2% tr

94 Hypertension was induced in male Sprague-Dawley rats by delivering AngiotensinII for 42 d

95 8)F- AMC20: was evaluated in brain slices of Sprague-Dawley rats by in vitro autoradiography and in l

96 TPase (RhoAV14) in the AH outflow pathway in Sprague-Dawley rats by using lentiviral vector-based gen

97 tic dysfunction and hypertension in pregnant Sprague-Dawley rats challenged with lipopolysaccharide (

98 Male Sprague-Dawley rats consumed caffeine (0.3 g/l) or water

99 ed behaviors occurred in both Long-Evans and Sprague-Dawley rats despite the fact that the 6-week HFD

100 onverges on the prosurvival role of MEF2D in Sprague Dawley rat embryonic (E18) hippocampal neurons.

101 The present study in Sprague Dawley rats examined the possibility that the or

102 Studies were performed on adult, male, Sprague-Dawley rats exposed to either short-term (ST; 10

103 iver, and fat were collected from adult male Sprague-Dawley rats exposed to increasing doses of the P

104 selectively bred Crl:OP[CD] rats and outbred Sprague-Dawley rats fed an HE diet showing high levels o

105 g a 34 G needle and Indian ink injections in Sprague Dawley rats, followed by histology.

106 ned reduction of CNS beta-amyloid (Abeta) in Sprague-Dawley rats following oral administration.

107 ingivalis lipopolysaccharide injection in 64 Sprague-Dawley rats for 7 to 21 days.

108 on the medial surface of the kidney in five Sprague-Dawley rats for MR imaging at 11.7 T.

109 tumor-bearing aged, female, retired breeder Sprague-Dawley rats for PET imaging.

110 Male Sprague-Dawley rats had an intracaudate injection of aut

111 oltage oscillations at 100 Hz in dissociated Sprague Dawley rat hippocampal neurons in single trial r

112 ding on receptor movement and positioning in Sprague Dawley rat hippocampal neurons.

113 t that acutely increasing O-GlcNAcylation in Sprague Dawley rat hippocampal slices induces an NMDA re

114 prelimbic region of the mPFC of adult, male, Sprague Dawley rats impaired the acquisition and reconso

115 Sprague-Dawley rats, implanted for EEG/EMG recording, we

116 Sprague-Dawley rats in four parallel groups (N=9 per gro

117 ion in awake and spontaneously behaving male Sprague Dawley rats interacting with a female, I tested

118 Adult male Sprague-Dawley rats INTERVENTIONS: Anesthetized rats wer

119 We isolated EGCs from male Sprague-Dawley rats, intestinal resections of 6 patients

120 We assigned 25 male Sprague-Dawley rats into four groups: intraosseous lipid

121 In the current study, changes in male Sprague Dawley rat liver caused by dietary treatment wit

122 For the in vivo effect, we employed a Sprague-Dawley rat mandible defect model utilizing 1 mic

123 Maxillary second molars were extracted in Sprague Dawley rats (n = 30), and either bisphosphonate

124 Male Sprague Dawley rats (n = 32) received a four-boost serie

125 Metabolic changes in fed and fasted Sprague Dawley rats (n = 36) were studied at 9.4 T after

126 Seven week old Sprague Dawley rats (n=18 male, n=18 female) received da

127 Two groups of Sprague-Dawley rats (n = 15 for group 1; n = 10 for grou

128 H/PeF region of isoflurane-anesthetized male Sprague-Dawley rats (n = 19).

129 Sprague-Dawley rats (n = 32) were subjected to sham or v

130 ut function from the (18)F-FDG PET images in Sprague-Dawley rats (n = 4) and C57BL/6 mice (n = 5), us

131 Male Sprague-Dawley rats (n = 45; age, 12 weeks) were inocula

132 Sprague-Dawley rats (n = 7) underwent ferric chloride ap

133 Male Sprague-Dawley rats (n = 9 for laser Doppler study and n

134 Male Sprague-Dawley rats (n=31) were anesthetized and treated

135 ction, and colon mucosal environment in male Sprague-Dawley rats (n=8/group).

136 neurons from the glabrous skin of adult male Sprague-Dawley rats, NCX activity, as assessed with fura

137 is issue, we transduced primary neurons from Sprague-Dawley rats or APP(-/-) mice (B6.129S7-App(tm1Db

138 analyzed hepatic transcriptional dynamics in Sprague-Dawley rats over a period of 24 hours to assess

139 Young Sprague Dawley rats (PND 21) were assigned to environmen

140 C57Bl/6J mice; juvenile Sprague-Dawley rats, primary human neutrophils.

141 ein 1) is administered at the spinal cord of Sprague Dawley rats, priming is detected at the peripher

142 Sprague Dawley rats received a spinal cord transection a

143 ion brain injury or sham surgery, adult male Sprague Dawley rats received vehicle or rolipram (0.03 m

144 To test this hypothesis, 6-week-old Sprague-Dawley rats received a neurotoxic dose of capsai

145 Male Sprague-Dawley rats received bilateral infusions of a Cr

146 Seventy-two Sprague-Dawley rats received daily 0, 10 (low-dose [LD])

147 Nine immunocompetent Sprague-Dawley rats received intravenous injection of fe

148 Male Sprague-Dawley rats received multiple intracutaneous inj

149 In two separate experiments, male Sprague-Dawley rats received nicotine injections (0.4 mg

150 To test this hypothesis, adult male Sprague-Dawley rats received sham surgery or moderate pa

151 ted and high-fat, high-carbohydrate diet-fed Sprague-Dawley rats, respectively, using intravenous adm

152 This study used male Sprague-Dawley rats responding under a progressive ratio

153 le burst of high-intensity exercise) in male Sprague-Dawley rats restores the defective hypoglycemia

154 that spinal nerve ligation (SNL, L5) in male Sprague Dawley rats resulted in behavioral allodynia, wh

155 Ten Sprague-Dawley rats served as normal controls.

156 paminergic neurons in the SNpc of Wistar vs. Sprague-Dawley rat strains.

157 d a multimodal approach, with five groups of Sprague-Dawley rats studied for 8 months: control rats,

158 PH was studied in monocrotaline-treated Sprague-Dawley rats, SU5416/hypoxia-treated Sprague-Dawl

159 Male Sprague-Dawley rats subjected to myocardial infarction (

160 nction compared with reconsolidation in male Sprague-Dawley rats that had been trained to self-admini

161 study in chronically catheterized awake male Sprague-Dawley rats that received an acute VMH microinje

162 A controlled laboratory study of 3y male Sprague-Dawley rats that were randomized to 4 groups of

163 we show that in conscious, unrestrained male Sprague Dawley rats the infusion of insulin into the thi

164 We report here that in Sprague Dawley rat, the MOP receptor-selective agonist D

165 We studied, in male Sprague Dawley rats, the role of the cognate hyaluronan

166 ressure and heart rate were recorded in male Sprague Dawley rats throughout this study.

167 ced by 2,4,6-trinitrobenzenesulfonic acid in Sprague Dawley rats to identify inflammation-induced cha

168 cordings in an in vitro slice preparation of Sprague Dawley rats to investigate the effects of physio

169 we used activity-guided optogenetics in male Sprague Dawley rats to silence IL pyramidal neurons opti

170 he pharmacokinetic studies were performed in Sprague-Dawley rats to assess the feasibility of transde

171 nerve as a model of neuropathic pain in male Sprague-Dawley rats to assess the time-dependent changes

172 ime course study was performed exposing male Sprague-Dawley rats to CB11 via nose-only inhalation wit

173 Esophagojejunostomy was performed on Sprague-Dawley rats to induce carcinogenesis, and LY3023

174 After exposing Sprague-Dawley rats to intra-aortic porcine pancreatic e

175 Preliminary in vivo recording in Sprague-Dawley rats to monitor GluA in the cortex during

176 We trained male Sprague-Dawley rats to self-administer methamphetamine (

177 ways and their postsynaptic targets in adult Sprague-Dawley rats to understand how these striatal cir

178 udal extent of the ventrolateral medulla, in Sprague Dawley rats treated with hydralazine or saline.

179 anastomosis rat and sham-operated, pair-fed Sprague-Dawley rats treated with ammonia-lowering therap

180 next generation sequencing of the livers of Sprague-Dawley rats treated with TAA at three doses (4.5

181 Sprague-Dawley rats under isoflurane anesthesia were exp

182 ng 40 seconds on the right cornea of 36 male Sprague Dawley rats, under general anesthesia.

183 Male Sprague-Dawley rats undergoing permanent middle cerebral

184 Fifteen Sprague-Dawley rats underwent 2D phase-contrast MR imagi

185 Separate groups of intact male Sprague-Dawley rats underwent a single episode of social

186 Sprague-Dawley rats underwent bilateral subdiaphragmatic

187 Pregnant Sprague-Dawley rats underwent bilateral uterine artery l

188 To address this issue, male Sprague-Dawley rats underwent cocaine self-administratio

189 Male Sprague-Dawley rats underwent complete spinal cord trans

190 Adult male Sprague-Dawley rats underwent diaphragm electromyography

191 Seven-day-old Sprague-Dawley rats underwent left carotid ligation foll

192 Therefore, to address this question, male Sprague-Dawley rats underwent surgeries for implantation

193 Adult male Sprague-Dawley rats underwent UNx (n = 6) or sham (n = 6

194 n, the extent of covalent protein binding in Sprague-Dawley rats upon exposure to 8:2 FTOH and the 6:

195 tears was characterized in otherwise normal Sprague-Dawley rats using Schirmer's test.

196 s after the initial ischemic injury, in male Sprague-Dawley rats via intraspinal injections of chondr

197 l function for both strains; however, in the Sprague-Dawley rats, VWR exacerbated falls in GFR and RP

198 In Sprague-Dawley rats, VWR reduced eNOS and EC SOD, but in

199 The BLA of male Sprague-Dawley rats was transduced to express either ChR

200 The common peroneal nerve of Sprague-Dawley rats was transected and repaired immediat

201 Using male Sprague Dawley rats, we examined if PACAP (.25-1.0 micro

202 Here, after research involving Sprague Dawley rats, we reported that spinal nerve ligat

203 Using female Sprague-Dawley rats, we carried out two rounds of experi

204 In male Sprague-Dawley rats, we performed bile diversions from t

205 In adult Sprague-Dawley rats, we used intracranial self-stimulati

206 Sprague-Dawley rats weighing approximately 400 g receive

207 illation was electrically induced in 30 male Sprague-Dawley rats weighing between 450 and 550 g.

208 Sprague Dawley rats were allowed free access to a palata

209 Seventy Sprague Dawley rats were divided into control, experimen

210 inistering and 36 cocaine-administering male Sprague Dawley rats were employed).

211 Male Sprague Dawley rats were exposed to repeated hypoxia or

212 For this, Sprague Dawley rats were given access either to 1 hour (

213 Following acquisition, male and female Sprague Dawley rats were given either short access (thre

214 Male Sprague Dawley rats were given GABAergic lesions of the

215 Male Sprague Dawley rats were implanted with a cannula in the

216 Young, adult male Sprague Dawley rats were implanted with bilateral dorsal

217 Male Sprague Dawley rats were infused with angiotensin II (An

218 Male Sprague Dawley rats were initially conditioned for morph

219 Male Sprague Dawley rats were subjected to a sciatic nerve cr

220 Forty mature female Sprague Dawley rats were subjected to ligature-induced e

221 RMTg in punished reward seeking, adult male Sprague Dawley rats were tested in several cost-benefit

222 Male adult Sprague Dawley rats were trained on a water maze spatial

223 lth in two generations of offspring, GC-eGFP Sprague Dawley rats were weaned onto HFD (45% fat) or Co

224 The alterations in Sprague-Dawley rats were accompanied by an increase in a

225 es of medial prefrontal cortex (mPFC) of six Sprague-Dawley rats were acquired with a transmission el

226 Sprague-Dawley rats were administered a combination of a

227 lt (4-6 months) and aged (20-24 months) male Sprague-Dawley rats were anesthetized with isoflurane, p

228 Forty 5-week-old male Sprague-Dawley rats were assigned to two study groups af

229 Male neonatal Sprague-Dawley rats were briefly exposed to 0.1 to 5,000

230 Female Sprague-Dawley rats were concurrently exposed to vapor-p

231 Sprague-Dawley rats were distributed into three groups,

232 Male Sprague-Dawley rats were divided into 3 groups, an ethan

233 Eighty-five adult Sprague-Dawley rats were divided into 3 groups: control,

234 Thirty-two Sprague-Dawley rats were divided into 4 groups based on

235 Sprague-Dawley rats were divided into experimental (E),

236 Using a validated ischemic wound model, Sprague-Dawley rats were divided into four groups for da

237 Twenty-four male Sprague-Dawley rats were divided into three groups (cont

238 Ten-week old female Sprague-Dawley rats were divided into three groups (n =

239 Male Sprague-Dawley rats were dosed orally with 3 mg/kg of on

240 Sprague-Dawley rats were exposed (parental, F1, and F2 g

241 Male Sprague-Dawley rats were exposed nose-only to citrate-bu

242 Male Sprague-Dawley rats were exposed to 10 Gy WBI using Cesi

243 Male Sprague-Dawley rats were exposed to CORT by their drinki

244 Sprague-Dawley rats were exposed to the CAM vapor for 1.

245 Sprague-Dawley rats were fed a HFD (45% fat) or a matche

246 Male Sprague-Dawley rats were fed either a HFD or low-fat die

247 institutional animal care committee, 60 male Sprague-Dawley rats were fed either a standard chow for

248 Male Sprague-Dawley rats were fed isocaloric amounts of an Et

249 Adult, male Sprague-Dawley rats were given either lipopolysaccharide

250 Sprague-Dawley rats were given feed containing dioxin-li

251 Adult male Sprague-Dawley rats were implanted with electrodes targe

252 Sprague-Dawley rats were intraperitoneally given dimethy

253 Male Wistar and Sprague-Dawley rats were monitored after subcutaneous ad

254 In vivo small-animal PET studies in Sprague-Dawley rats were performed at baseline and after

255 Sprague-Dawley rats were presented randomly with mild st

256 To test this hypothesis, male Sprague-Dawley rats were pretreated with a neurotoxic re

257 Male Sprague-Dawley rats were pretreated with octreotide or o

258 Twenty-four Sprague-Dawley rats were randomized into controls, mild,

259 Thus, adult Sprague-Dawley rats were randomized into four groups: 1)

260 Male Sprague-Dawley rats were randomized into two groups and

261 Forty Sprague-Dawley rats were randomized to cecal ligation an

262 One week after MI, adult male Sprague-Dawley rats were randomized to treatment for 4 w

263 Sprague-Dawley rats were randomly assigned to one of the

264 Fifty-six Sprague-Dawley rats were randomly assigned to two groups

265 One hundred and twelve male Sprague-Dawley rats were randomly divided into 4 groups:

266 Forty Sprague-Dawley rats were randomly divided into four grou

267 Male adult Sprague-Dawley rats were rendered insulin-resistant by f

268 BMSCs isolated from femur and tibia of Sprague-Dawley rats were seeded onto 3 types of titanium

269 Eight groups (n=6) of normal Sprague-Dawley rats were studied: four groups received t

270 Sprague-Dawley rats were subjected to cold-water swim st

271 Male Sprague-Dawley rats were subjected to middle cerebral ar

272 Seven-day-old Sprague-Dawley rats were subjected to TBI using the cont

273 Male Sprague-Dawley rats were trained on an auditory fear con

274 To study cognitive performance, male Sprague-Dawley rats were trained on an object-discrimina

275 Groups of male and female adult Sprague-Dawley rats were trained on either the standard

276 Eight male Sprague-Dawley rats were trained to discriminate 10.0 mg

277 Male Sprague-Dawley rats were treated with CsA (n = 8, 20 mg/

278 Sprague-Dawley rats were treated with four injections of

279 Sprague-Dawley rats were untreated (control), laparatomi

280 Thirty-six Sprague-Dawley rats were used (n = 6/group/time point).

281 Sprague-Dawley rats were used for cardiomyocyte isolatio

282 Male Sprague-Dawley rats were used to assess dosimetry, antag

283 Overnight-fasted, anaesthetized Sprague-Dawley rats were used to determine the effects o

284 BALB/cJ mice and Sprague-Dawley rats were used to evaluate the effects du

285 Thirty-six Sprague-Dawley rats were used.

286 learning and retention compared with outbred Sprague Dawley rats, whereas bLRs show reduced extinctio

287 C450Y CCT4 was identified in a stock of Sprague-Dawley rats, whereas H147R CCT5 was found in a h

288 frying under vacuum (9.9kPa), after feeding Sprague-Dawley rats, while also understanding its relati

289 vical ganglion (SCG) neurons from adult male Sprague Dawley rats with or without added NGF and compar

290 ds were generated on the dorsal skin of male Sprague-Dawley rats with a 10-mm sterile punch.

291 We treated pregnant Sprague-Dawley rats with BPA at 0, 0.25, 2.5, 25, or 250

292 ) into the dorsal medial NTS (dmNTS) of male Sprague-Dawley rats with coronary artery ligation-induce

293 Four male Sprague-Dawley rats with different blood glucose concent

294 ation in sympathetic neurons from adult male Sprague-Dawley rats with electrophysiological and optica

295 Adult male Sprague-Dawley rats with hyperglycemia were divided into

296 t maternal inflammation (modeled by pregnant Sprague-Dawley rats with lipopolysaccharides (LPS) chall

297 ry-olfactory artery (ACA/OA) bifurcations in Sprague-Dawley rats with or without ECFCs transfusion.

298 In this study, intrarectal inoculations of Sprague-Dawley rats with predatory bacteria were perform

299 IUGR (bilateral uterine artery ligation) in Sprague-Dawley rats with sham controls was used.

300 cemic (10-15 mg/dL) clamps were performed in Sprague-Dawley rats with simultaneous electrocardiogram