ライフサイエンスコーパス: Sprague-Dawley rat

1 al preoptic nucleus (VLPO) is lesioned (male Sprague-Dawley rats).

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

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

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

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

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

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

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

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

10 pmental age and exposure to NEC stressors in Sprague Dawley rats.

11 gy in the basolateral amygdala (BLA) in male Sprague Dawley rats.

12 ion of OVLT neurons, was used in adult, male Sprague Dawley rats.

13 he nucleus accumbens shell (AcbSh) in female Sprague Dawley rats.

14 6 intracranial glioma tumor model in 37 male Sprague Dawley rats.

15 ting to create a conditional GR knockdown in Sprague Dawley rats.

16 and stress-response signaling genes in male Sprague Dawley rats.

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

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

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

20 Male Sprague-Dawley rats.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 es and brought forward for testing in female Sprague-Dawley rats.

41 % in both humans without diabetes and normal Sprague-Dawley rats.

42 -maze spatial reversal learning task in male Sprague-Dawley rats.

43 low-twitch soleus (SOL) muscles derived from Sprague-Dawley rats?

44 Primary tenocytes from Achilles tendon of Sprague-Dawley rats 1 week after collagenase injection w

45 ns, 12 rhesus monkeys, 20 Yorkshire pigs, 20 Sprague-Dawley rats, 10 New Zealand White rabbits and 14

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

47 Sprague Dawley rats (2 months old) were commercially acq

48 Male Sprague Dawley rats (2-mo-old) were untreated (Con) or g

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

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

51 Anesthetized, ventilated Sprague-Dawley rats (280 +/- 30 g) and Vietnamese minipi

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

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

54 Using Sprague-Dawley rats (350-450 g; n = 61) and the recently

55 Materials and Methods Seventy male Sprague-Dawley rats (4 weeks old) received intraperitone

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

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

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

59 We fed male Sprague-Dawley rats a control diet, MCD diet, or betaine

60 heart compared to a control group (pregnant Sprague-Dawley rats administered vehicle).

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

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

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

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

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

66 s cocaine self-administration in 10-week-old Sprague Dawley rats and C57BL/6 mice.

67 We injected streptozotocin in male Sprague Dawley rats and treated them with a neutralizing

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

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

70 Blood-brain-barrier studies in Sprague-Dawley rats and CD-1 mice indicated that the maj

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

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

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

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

75 avioral sex differences had been reported in Sprague-Dawley rats and repeated some of the above measu

76 cardial left ventricular free walls of adult Sprague-Dawley rats and then treated with collagenase to

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

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

79 omics data were collected from the livers of Sprague Dawley rats at 4 or 14 days of being subjected t

80 In Sprague-Dawley rats at 10 mg/kg, compared to o(LA)(8)-PT

81 A patients post-resuscitation, and from male Sprague-Dawley rats at baseline and after 20 min CA foll

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

83 Female Sprague-Dawley rat bladders were partially obstructed (P

84 Diabetes was surgically induced in male Sprague Dawley rats by 90% pancreatectomy (Px).

85 Renal failure was induced in Sprague-Dawley rats by a high adenine diet supplemented

86 AAAs were generated in Sprague-Dawley rats by exposing the infrarenal, intralum

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

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

89 The RHV Sprague-Dawley rat challenge model enables comparative t

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

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

92 ution data and blood clearance kinetics from Sprague-Dawley rat data.

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

94 cephalographic data gathered from adult male Sprague Dawley rats during the aforementioned experiment

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

96 /-), and Tlr2(-/-)/Tlr4(-/-) mice as well as Sprague Dawley rats for all in vitro studies.

97 B) and examined the pharmacokinetics (PK) in Sprague-Dawley rats for 3 months in comparison to CAB.

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

99 Forty-eight male and female Sprague-Dawley rats had lumbar IVD puncture or sham surg

100 apping was performed in Langendorff-perfused Sprague-Dawley rat hearts (n=18), where novel algorithms

101 Langendorff-perfused adult Sprague-Dawley rat hearts were subjected to acute region

102 Pharmacokinetic studies in male Sprague Dawley rats highlighted a good exposure after or

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

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

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

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

107 To examine this, we profiled cohorts of Sprague-Dawley rats in a test of motivation to consume s

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

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

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

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

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

113 Using a male Sprague Dawley rat model of PNS-CNS injury, we show that

114 Male Sprague Dawley rats (N = 125) were trained to self-admin

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

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

117 Male Sprague Dawley rats (n = 62) were trained to self-admini

118 Female Sprague Dawley rats (N = 64) were evaluated for skilled

119 rtery ligation surgery was performed in male Sprague-Dawley rats (n = 13) followed by dual MEMRI and

120 For four weeks, healthy Sprague-Dawley rats (n = 30) were fed one of three diets

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

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

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

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

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

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

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

128 We provided Sprague Dawley rats of renal calcium oxalate stones with

129 ic reduced uterine perfusion pressure (RUPP) Sprague Dawley rats on gestational days (GD) 14, 16, and

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

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

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

133 Sprague Dawley rat pups underwent 14 days of postnatal m

134 Sprague Dawley rats received a lethal dose of AFB(1) (0.

135 Sprague Dawley rats received a spinal cord transection a

136 GLP1R signaling within the alBST, adult male Sprague Dawley rats received bilateral alBST-targeted in

137 n maxillary molars was examined in 40 female Sprague Dawley rats received zoledronic acid (7.5 ug/kg)

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

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

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

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

142 Male Sprague-Dawley rats received monocrotaline (MCT; 60 mg/k

143 Male Sprague-Dawley rats received multiple intracutaneous inj

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

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

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

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

148 S5B from RHV (ChAd-NS) was used to vaccinate Sprague-Dawley rats, resulting in high levels of cluster

149 Male Sprague Dawley rats self-administered cocaine during dai

150 In vivo experiments in anaesthetized Sprague-Dawley rats showed that pregnant animals (gestat

151 aintained intravenous self-administration in Sprague-Dawley rats similar to cocaine.

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

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

154 Male Sprague-Dawley rats subjected to myocardial infarction (

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

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

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

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

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

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

161 this, we used fasted or 4 hour postprandial Sprague Dawley rats to analyze ENaC expression and activ

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

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

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

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

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

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

168 ype 1 diabetes (T1D) was established in male Sprague-Dawley rats to study the efficacy and safety of

169 ntal protocols were performed in nondiabetic Sprague-Dawley rats to test the SNS with 1) adrenal deme

170 Using adult male Sprague-Dawley rats trained to self-administer intraveno

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

172 In Sprague-Dawley rats treated orally with DEP from birth t

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

174 Materials and Methods The cerebral cortex in Sprague-Dawley rats treated with gadopentetate dimeglumi

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

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

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

178 Pregnant Sprague-Dawley rats underwent bilateral uterine artery l

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

180 Male Sprague-Dawley rats underwent complete spinal cord trans

181 Adult male Sprague-Dawley rats underwent diaphragm electromyography

182 To investigate this issue, male Sprague-Dawley rats underwent inhibitory avoidance train

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

184 To address this, male and female Sprague-Dawley rats underwent spatial or cued-response B

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

186 Sprague-Dawley rats underwent surgery to induce volume o

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

188 tations of CeA 5-HT signaling in adult, male Sprague Dawley rats using an established model of alcoho

189 sk/reward decision-making in male and female Sprague-Dawley rats using a probabilistic discounting ta

190 chotic drug administration on SV2A levels in Sprague-Dawley rats using western blotting, [(3)H]UCB-J

191 Induction of diabetes in Sprague-Dawley rats via a single dose of STZ (70 mg/kg)

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

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

194 Using in vivo electrophysiology in male Sprague Dawley rats, we demonstrate that intra-vHipp THC

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

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

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

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

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

200 Sprague-Dawley rats weighing approximately 400 g receive

201 Sprague Dawley rats were allowed free access to a palata

202 Seventy Sprague Dawley rats were divided into control, experimen

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

204 Male Sprague Dawley rats were exposed to BOP frontally and la

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

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

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

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

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

210 Male Sprague Dawley rats were initially conditioned for morph

211 Male Sprague Dawley rats were injected with PBS or G-CSF duri

212 Thoracic aorta rings from Sprague Dawley rats were mounted in isolated tissue bath

213 Male Sprague Dawley rats were socially housed and underwent l

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

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

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

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

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

219 Sprague-Dawley rats were administered a combination of a

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

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

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

223 Sprague-Dawley rats were distributed into three groups,

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

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

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

227 Here, adult Sprague-Dawley rats were divided into acute and chronic

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

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

230 Twenty-three Sprague-Dawley rats were divided into three experimental

231 Eighteen male Sprague-Dawley rats were divided into three groups (6 ra

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

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

234 Sprague-Dawley rats were divided into three treatment gr

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

236 Male, Sprague-Dawley rats were employed in this study.

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

238 Female Sprague-Dawley rats were exposed either to SAM or filter

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

240 Sprague-Dawley rats were exposed to 5 doses of BPA [0, 2

241 Sprague-Dawley rats were exposed to BPA, vehicle, or pos

242 Adult, male Sprague-Dawley rats were exposed to nicotine (0.2 or 0.4

243 The maxillary first molars of 30 male Sprague-Dawley rats were extracted, and after healing, b

244 The maxillary right first molars of Sprague-Dawley rats were extracted, and gelatin scaffold

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 Male Sprague-Dawley rats were fed standard rat chow containin

250 ugh) were created in mandibular angles of 24 Sprague-Dawley rats were filled with DBBM Control, DBBM

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

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

253 Male Sprague-Dawley rats were injected with streptozotocin (3

254 Papillary muscles from male Sprague-Dawley rats were mounted onto an organ bath perf

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

256 Sprague-Dawley rats were presented randomly with mild st

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

258 teen days prior to treatment with MDMA, male Sprague-Dawley rats were provided water or water treated

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

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

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

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

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

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

265 Here, 24 male Sprague-Dawley rats were randomly divided into four grou

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

267 Twenty-four male Sprague-Dawley rats were randomly divided into three gro

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

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

270 155 male Sprague-Dawley rats were subjected to a combination of f

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

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

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

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

275 Male Sprague-Dawley rats were trained to nose-poke for discre

276 Male, Sprague-Dawley rats were trained to self-administer coca

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

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

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

280 Sprague-Dawley rats were used for cardiomyocyte isolatio

281 Sprague-Dawley rats were used in asphyxial cardiac arres

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

283 uite of in vitro transactivation assays, and Sprague-Dawley rats were used to assess maternal, fetal,

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 We investigated, in male Sprague-Dawley rats, whether BLA activity enables prelim

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

290 In Sprague Dawley rats with Cre-mediated expression of the

291 nt improvement in the cardiac output in male Sprague Dawley rats with no significant changes in eithe

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

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

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

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

296 Male Sprague-Dawley rats with jugular-vein catheterization we

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

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

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

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