ライフサイエンスコーパス: anaesthetized

1 of whether the animal was awake, behaving or anaesthetized.

2 n the skin under the cathodal electrodes was anaesthetized.

3 In anaesthetized A-IV(+/+) mice, meal-stimulated gastric ac

4 as recorded simultaneously from both eyes of anaesthetized adult Brown-Norway rats (ketamine: xylazin

5 ined midbrain dopamine neurons in isoflurane-anaesthetized adult mice.

6 two age groups (8 and 12 weeks old) of young anaesthetized adult normal WKY and SHR were acquired in

7 Experiments were performed on anaesthetized adult rats and mice.

8 umbar dorsal root ganglion (DRG) neurones in anaesthetized adult rats, classified from dorsal root co

9 In anaesthetized adult rats, we have found that Purkinje ce

10 rve bundle supplying a segment of jejunum in anaesthetized adult rats.

11 Cats were anaesthetized (alpha-chloralose 60 mg/kg, intraperitonea

12 Adult male Wistar rats were anaesthetized and ABP was monitored via a femoral arteri

13 t activities of 88 C-fibres were recorded in anaesthetized and artificially ventilated rats when the

14 In anaesthetized and artificially ventilated rats, ATP- and

15 ity of over a hundred single neurons in both anaesthetized and awake animals.

16 to monocular orientation selectivity in both anaesthetized and awake conditions.

17 rons in the primary visual cortex of lightly anaesthetized and awake mice, during sensory processing.

18 naptic conductances--in the visual cortex of anaesthetized and awake mice.

19 local field potential (LFP) activity in both anaesthetized and awake mouse sensori-motor cortex.

20 At 22 months of age, animals were anaesthetized and catheter-based haemodynamics evaluated

21 In both anaesthetized and decerebrate rats, sectioning the spina

22 in the intrascapular subcutaneous region of anaesthetized and heparinized nondiabetic Sprague-Dawley

23 nnabinoid agonist HU 210 has been studied in anaesthetized and in decerebrated rabbits.

24 Animals were terminally anaesthetized and the extensor digitorum longus muscles

25 Compared to the anaesthetized animal, we show that magnocellular and par

26 and compare these responses to those in the anaesthetized animal.

27 of PFC inputs by the HC in the awake or the anaesthetized animal.

28 In intact halothane-anaesthetized animals (n = 10), static contraction and p

29 ented that neurons in the auditory cortex of anaesthetized animals generally display transient respon

30 ditions selected for his model (e.g. heavily anaesthetized animals, negligible intramyocyte O(2) part

31 In intact, pentobarbitone-anaesthetized animals, the jaw-depressor reflex (JDR) ev

32 In anaesthetized animals, there is wide variation in the du

33 ity of supporting studies being conducted on anaesthetized animals.

34 riments were carried out on alpha-chloralose-anaesthetized, artificially ventilated and atenolol (1 m

35 In six anaesthetized beagle dogs control contractions increased

36 ydrated (DH) (48 h water deprived) rats were anaesthetized, bilaterally vagotomized and underwent acu

37 ERGs were recorded from anaesthetized Brown Norway rats in response to brief ful

38 he anterior chamber and lateral ventricle of anaesthetized Brown-Norway rats were cannulated with fin

39 e situations where the patient prefers to be anaesthetized but intubation may be difficult following

40 al ganglionated plexus was recorded in eight anaesthetized canines using a 16-channel linear microele

41 stimulation, the present experiments in the anaesthetized cat provide a physiological confirmation o

42 -associated patterns in the visual cortex of anaesthetized cat.

43 riments were carried out in alpha-chloralose anaesthetized cats to determine if these cardiac vagal p

44 rmoregulation, experiments were performed on anaesthetized cats to determine the quantitative respons

45 he left thoracic sympathetic chain (T1-5) of anaesthetized cats to identify the afferents' responses

46 Experiments were performed on anaesthetized cats to investigate the receptive properti

47 Experiments were performed on anaesthetized cats to test the hypothesis that fluid flo

48 We show here, in primary visual cortex of anaesthetized cats under neuromuscular blockade, that co

49 mesenteric lymph and portal venous plasma in anaesthetized cats was measured with an enzyme-linked im

50 n lamina I of the lumbosacral spinal cord of anaesthetized cats were characterized by recording their

51 ygen concentrations in the striate cortex of anaesthetized cats while using visual stimuli to activat

52 In anaesthetized cats, the effects of stimulation of the re

53 isovolumetric conditions in alpha-chloralose anaesthetized cats.

54 ic chain or rami communicates (T(2)-T(5)) in anaesthetized cats.

55 c chain or rami communicantes (T(2)-T(5)) in anaesthetized cats.

56 ones in segments T5-T9 of the spinal cord of anaesthetized cats.

57 nts from the longissimus lumborum muscles of anaesthetized cats.

58 c chain or rami communicantes (T(2)-T(5)) in anaesthetized cats.

59 erents in the L6 dorsal roots of 30 Nembutal-anaesthetized cats.

60 ected from the inferior alveolar nerve in 17 anaesthetized cats.

61 d from the left sympathetic chain (T2-T5) in anaesthetized cats.

62 th KCL placed upon the suprasylvian gyrus of anaesthetized cats.

63 etal muscle receptors in thirteen chloralose-anaesthetized cats.

64 recorded from the left sympathetic chain in anaesthetized cats.

65 VSD) in an animal experimental setting using anaesthetized cats.

66 able in both groups of mice in the awake and anaesthetized conditions.

67 a were obtained in both in situ and in vivo (anaesthetized/conscious) rats and suggest that following

68 e conclude that MAP is largely maintained in anaesthetized DH rats by a PVN-driven component of sSNA

69 this study, we acquired diffusion data from anaesthetized dogs and created a DTI-based atlas for a c

70 In anaesthetized dogs connected to cardiopulmonary bypass,

71 ry intercostal muscles in all interspaces in anaesthetized dogs were severed so that the diaphragm wa

72 In chloralose-anaesthetized dogs, a cardiopulmonary bypass was establi

73 In anaesthetized dogs, multiunit and single motor unit (SMU

74 l muscles in all interspaces were severed in anaesthetized dogs, so that the diaphragm was the only m

75 reasing pulsatile perfusion were assessed in anaesthetized dogs, with the anterior descending coronar

76 control of LSNA and RSNA in alpha-chloralose anaesthetized female rats, but only during pro-oestrus.

77 In chloralose-anaesthetized female rats, nanoinjection of NPY into the

78 and primary fields of the auditory cortex of anaesthetized ferrets, and comparing these responses wit

79 of neurons in the primary auditory cortex of anaesthetized ferrets.

80 studied in spinal cord slices prepared from anaesthetized, free-ranging hamsters.

81 Mice were anaesthetized, gavaged with FITC-dextran for measures of

82 tracheal vagal afferent nerve stimulation in anaesthetized guinea pigs.

83 s from the ventral cochlear nucleus (VCN) of anaesthetized guinea-pigs in response to iterated ripple

84 ugh initiated from the trachea and larynx in anaesthetized guinea-pigs is mediated by capsaicin-insen

85 voked a cough when applied to the trachea of anaesthetized guinea-pigs, but they substantially reduce

86 aryngeal afferent nerves regulating cough in anaesthetized guinea-pigs.

87 The retractor muscle of anaesthetized hamsters was contracted (once per 2 s for

88 group of capillaries in cremaster muscles of anaesthetized hamsters were electrically stimulated to c

89 In anaesthetized hamsters, acetylcholine (ACh) microiontoph

90 In anaesthetized hamsters, we have investigated the spread

91 amputees; referral of touch to an absent or anaesthetized hand after stimulation of a foot [6, 7] or

92 sthesia in mice, 12 female C57Bl/6 mice were anaesthetized in a crossover protocol with the following

93 We conducted measurements in a urethane-anaesthetized in vivo rat preparation to characterize sy

94 d nucleus raphe obscurus of nine adult cats, anaesthetized, injected with a neuromuscular blocking ag

95 ted neurons were recorded extracellularly in anaesthetized intact or vagotomized rats.

96 mporal shifts of r and r are coordinated, 12 anaesthetized juvenile pigs had pairs of colours of aero

97 rhage in the gyrencephalic brain of propofol-anaesthetized juvenile swine using subdural electrode st

98 and leptin, we investigated alpha-chloralose anaesthetized late pregnant rats, which exhibited increa

99 ode recordings from primary visual cortex of anaesthetized macaque monkeys (Macaca mulatta).

100 le units in the reticular formation of three anaesthetized macaque monkeys whilst TMS was performed o

101 In the gluteus maximus muscle of anaesthetized male C57BL/6 mice (aged 3-4 months), brief

102 In anaesthetized male C57BL/6J mice (3 months old), concent

103 In anaesthetized male C57BL/6J mice (3-5 months old), the G

104 In anaesthetized male C57BL/6J mice (aged 4 months), the gl

105 tion of the pelvic nerve (PN) in 12 urethane-anaesthetized male rats were tested for responses to mec

106 eries and downstream epicardial vessels in 6 anaesthetized male sheep using balloon catheters.

107 f phenylephrine and sodium nitroprusside, in anaesthetized male Wistar rats at a core temperature (T(

108 Anaesthetized, male Sprague-Dawley rats were exposed to

109 s were performed on spontaneously breathing, anaesthetized, male Wistar rats undergoing short-term sy

110 LFP) in primary visual cortex, in sufentanil-anaesthetized marmoset monkeys.

111 In the V1 of anaesthetized marmosets, the EEG frequency spectrum unde

112 iking activity throughout the entire LGN, in anaesthetized marmosets.

113 tra-vascular sensor in the carotid artery of anaesthetized, mechanically ventilated pigs, without lun

114 e and changes in plasma volume in isoflurane-anaesthetized mice (C57BL/6J) pre-treated with rolipram

115 ular layer of the olfactory bulb (bottom) of anaesthetized mice (representative traces from n = 7 CA1

116 dilatation of skeletal muscle arterioles in anaesthetized mice in situ.

117 ation (a-tsDCS) for short periods of time to anaesthetized mice sustaining a spinal cord injury leads

118 We previously demonstrated in anaesthetized mice that a short period of trans-spinal s

119 By using an eight-beam probe, we show in anaesthetized mice that small groups of single neurons c

120 The gastric mucosal surface of anaesthetized mice was exposed and mucosal surface pH wa

121 ellular electrophysiological recordings from anaesthetized mice we first show that simple light steps

122 Intact stomachs of anaesthetized mice were perfused with a weakly buffered

123 The left anterior crural muscles of anaesthetized mice were stimulated to perform 150 eccent

124 proved ability to withstand heat exposure in anaesthetized mice, it protected the intestine from inju

125 In anaesthetized mice, second-order (2A) distributing arter

126 in vivo extracellular recordings in urethane-anaesthetized mice, we demonstrate that single units and

127 glomeruli by using two-photon microscopy in anaesthetized mice.

128 cted in CA1 stratum radiatum of rTMS-treated anaesthetized mice.

129 ry following severe hyperthermia exposure in anaesthetized mice.

130 cally exposed, intact femoral artery (FA) of anaesthetized mice.

131 ensembles with single-cell resolution in non-anaesthetized models show that, in contrast to the predo

132 show that the same phenomenon is present in anaesthetized monkeys even at anaesthetic levels known t

133 ed that ventral root stimulation (VRS) in an anaesthetized mouse causes a depressor response and a re

134 oinjected IL-1beta in the nTS bilaterally in anaesthetized naive adult rats, which increased fR and p

135 In urethane-anaesthetized, neuromuscularly blocked and vagotomized S

136 Seven days postsurgery, LTF was studied in anaesthetized, neuromuscularly blocked and ventilated ra

137 adectomized (GDX) male Fischer 344 rats were anaesthetized, neuromuscularly blocked and ventilated.

138 In urethane-chloralose anaesthetized, neuromuscularly blocked, artificially ven

139 In urethane-chloralose anaesthetized, neuromuscularly blocked, ventilated rats,

140 dly increases total peripheral resistance in anaesthetized non-human primates, a response associated

141 Experiments were performed on anaesthetized normoxic (N) and chronically hypoxic (CH)

142 Experiments were performed on anaesthetized normoxic (N) rats and chronically hypoxic

143 ic balloon catheters were passed through the anaesthetized nose, and an endotracheal tube occlusion d

144 ute burst pacing-induced AF were examined in anaesthetized open chest pigs.

145 le-unit pulmonary vagal C fibre afferents in anaesthetized, open-chest rats.

146 hing on venous return have been derived from anaesthetized or reduced animal preparations, making an

147 silenced primary visual cortex (V1), in nine anaesthetized owl monkeys injected with a neuromuscular

148 ed by I.V. phenylephrine or nitroprusside in anaesthetized, paralysed and artificially ventilated rat

149 periments were performed in alpha-chloralose-anaesthetized, paralysed and artificially ventilated rat

150 capnic hypoxia were investigated in urethane-anaesthetized, paralysed and ventilated rats.

151 red averaging in the thoracic spinal cord of anaesthetized, paralysed cats.

152 equivalent of human childhood) and were then anaesthetized, paralysed, ventilated and prepared with p

153 esistance arterioles in cremaster muscles of anaesthetized (pentobarbital sodium, 65 mg kg(-1)) mice.

154 ion by CA from nitrite with acetazolamide in anaesthetized pigs during alveolar hypoxia in vivo.

155 Measurements were made in anaesthetized pigs under control conditions and during 1

156 Anaesthetized pigs were subjected to either sham treatme

157 We found that acetazolamide prevents HPV in anaesthetized pigs, as in other mammalian species.

158 al potassium concentrations were measured in anaesthetized potassium-replete and potassium-depleted r

159 eadily detectable using electrophysiology in anaesthetized preparations and for which neural circuits

160 Decerebrate unanaesthetized or barbiturate-anaesthetized preparations were used.

161 In some anaesthetized preparations, eupnoea is eliminated follow

162 synovial lining of the knee joint cavity of anaesthetized rabbits at a constant rate, along with a f

163 on was infused into the knee joint cavity of anaesthetized rabbits for 30 min, with or without hyalur

164 In spinalized, anaesthetized rabbits morphine depressed the JDR to the

165 n 3.6 mg ml-1 were infused into the knees of anaesthetized rabbits, with Ringer solution as control i

166 hritis, and was tested in the knee joints of anaesthetized rabbits.

167 rolled joint fluid pressure (Pj) in knees of anaesthetized rabbits.

168 he release of beta-endorphin in the urethane anaesthetized rat following electrical stimulation of th

169 We have utilized an anaesthetized rat model of insulin-induced hypoglycaemia

170 In the present study we used an anaesthetized rat model to first confirm the presence of

171 ydrokainate (DHK) was microinjected into the anaesthetized rat nTS or applied to rat nTS slices.

172 An in vivo anaesthetized rat preparation was used to measure pancre

173 In an anaesthetized rat preparation, application of exendin-4

174 In the in vivo anaesthetized rat preparation, bilateral microinjections

175 In the in vivo anaesthetized rat preparation, unilateral microinjection

176 the posterior lobe of the ketamine/xylazine-anaesthetized rat to examine the relationship between co

177 air into the sealed pharyngeal airway of the anaesthetized rat while measuring nasal pressure under c

178 tion of afferents have been performed in the anaesthetized rat.

179 assess renal iron (Fe2+/3+) transport in the anaesthetized rat.

180 he medulla oblongata was investigated in the anaesthetized rat.

181 67156 altered reflex bladder activity in the anaesthetized rat.

182 (LC) noradrenergic neurons was determined in anaesthetized rats (n = 15) by in vivo extracellular ele

183 in 5 microl) into the lateral ventricles of anaesthetized rats also induces spontaneous epileptiform

184 sure applied to the isolated upper airway in anaesthetized rats before and after microinjection of mu

185 loop of Henle (TALH) in vivo was examined in anaesthetized rats by perfusing loops of Henle of superf

186 ) was studied in the submandibular glands of anaesthetized rats by stimulating the nerve supplies wit

187 nhibitor, neostigmine (NEOS), in the rRPa of anaesthetized rats decreased cold-evoked BAT sympathetic

188 y (RSNA) and blood pressure were recorded in anaesthetized rats during epicardial application of brad

189 ge 12-50 nm) could be detected in the NTS in anaesthetized rats in response to electrical stimulation

190 nhibitor of pancreatic exocrine secretion in anaesthetized rats in vivo and in pancreatic lobules in

191 We used anaesthetized rats in which pontine microinjections of a

192 The present experiments on anaesthetized rats investigated the role of 5-HT3 recept

193 enous administration of Hcrt-1 (orexin-A) to anaesthetized rats on glutamate and GABA release in the

194 Our data obtained in anaesthetized rats revealed that glycine released in the

195 Cystometry performed on control anaesthetized rats revealed that intravesical instillati

196 n in situ'isolated' spinal cord preparation (anaesthetized rats spinalized at T10-T11 and cauda equin

197 First, we established in anaesthetized rats that graded concentrations of hyperto

198 C and HC stimulation in awake and isoflurane-anaesthetized rats that were chronically implanted with

199 on on tongue movements and flow mechanics in anaesthetized rats that were prepared with an isolated u

200 In three groups of anaesthetized rats the effect of A(2A)-receptor inhibiti

201 ecordings using sharp electrodes in urethane-anaesthetized rats to elucidate the cellular dynamics of

202 r multi-electrode arrays (MEAs) in the DH of anaesthetized rats to simultaneously measure activity ac

203 Increased left ventricular contractility in anaesthetized rats was observed when DVMN neurones were

204 After surgical preparation, anaesthetized rats were administered 3 mg/kg Staphylococ

205 jection in the dorsal vagal complex (DVC) of anaesthetized rats while monitoring gastric tone.

206 from hippocampal CA1 neurons was examined in anaesthetized rats with a unilateral common carotid arte

207 to the NTS reduced phrenic nerve activity of anaesthetized rats with an elevated arterial P(CO(2)) .

208 ein secretion was investigated in vivo using anaesthetized rats with pancreatic ductal cannulas, and

209 In anaesthetized rats with unilateral lesions of around 70%

210 ronal cultures) or unconscious animals (e.g. anaesthetized rats).

211 cellular space of the brain, demonstrated in anaesthetized rats, and hold promise for future in vivo

212 In anaesthetized rats, arterial blood pressure (ABP) and fe

213 In four groups of anaesthetized rats, arterial blood pressure (ABP), femor

214 In urethane-chloralose-anaesthetized rats, bilateral inhibition of the RTN with

215 aintain SNA and arterial pressure at rest in anaesthetized rats, but this loss reduces the sympathoex

216 recorded from single SCN neurons in urethane-anaesthetized rats, categorized them by the statistical

217 In mesenteric small arteries of anaesthetized rats, EFS failed to stimulate major dilata

218 ns, identified by juxtacellular labelling in anaesthetized rats, had a slow regular discharge, were v

219 ight chain in astrocytes) reduced the HVR in anaesthetized rats, indicating that exocytotic release o

220 During continuous bladder cystometry in anaesthetized rats, inhibition of pannexin 1 channels us

221 acutely implanted onto the sciatic nerve of anaesthetized rats, the device conferred repeatable stim

222 n of tetanus-evoked oscillations in urethane-anaesthetized rats, validate our observations in vitro,

223 le unit recordings obtained from 32 urethane-anaesthetized rats, when analysed in groups based upon h

224 tral artery (CVA) in spontaneously breathing anaesthetized rats, whilst simultaneously recording tail

225 effect on vagal bronchopulmonary C-fibres in anaesthetized rats.

226 e concentrations in the prefrontal cortex of anaesthetized rats.

227 e firing rate of ccRTN neurons in isoflurane-anaesthetized rats.

228 pendent phrenic and hypoglossal (XII) LTF in anaesthetized rats.

229 ation of peripheral afferents in vivo, using anaesthetized rats.

230 P) were found in the spinal cord of urethane-anaesthetized rats.

231 orticogram (ECoG) to cortical stimulation in anaesthetized rats.

232 lateral frontal electrocorticogram (ECoG) of anaesthetized rats.

233 entially to theta and ripple oscillations in anaesthetized rats.

234 aline vehicle 100 nl into the RP in urethane-anaesthetized rats.

235 de synthase (NOS) biosynthesis inhibitor, in anaesthetized rats.

236 ympathetic postganglionic neurones (PGNs) in anaesthetized rats.

237 sitive to the pattern of hypoxic exposure in anaesthetized rats.

238 acilitation (LTF) of phrenic motor output in anaesthetized rats.

239 magnetic resonance imaging (7 Tesla-fMRI) in anaesthetized rats.

240 ed respiratory frequency and tidal volume in anaesthetized rats.

241 00-1500 p.p.m., 10 breaths) were measured in anaesthetized rats.

242 -locked to hippocampal theta oscillations in anaesthetized rats.

243 lity was measured manometrically in urethane-anaesthetized recipient rats in response to intra-arteri

244 entrolateral medulla (RVLM) were recorded in anaesthetized sino-aortic denervated and vagotomized rat

245 These events were measured in cats that were anaesthetized, so that recovery of spindle afferent func

246 In anaesthetized spinalized rats electrical stimulation of

247 In anaesthetized, spontaneously breathing mice, integrated

248 In anaesthetized, spontaneously breathing rats, intratrache

249 In anaesthetized, spontaneously breathing rats, intravenous

250 Experiments were performed on anaesthetized, spontaneously breathing, intubated neonat

251 In vivo experiments in anaesthetized Sprague-Dawley rats showed that pregnant a

252 Eleven anaesthetized Sprague-Dawley rats were surgically prepar

253 Overnight-fasted, anaesthetized Sprague-Dawley rats were used to determine

254 ences in VNS heart control between awake and anaesthetized states, the physiological expression of th

255 When the same animals were anaesthetized, the integration of local motion signals w

256 The animals were anaesthetized (thiobutabarbital 120 mg kg(-1) ) and surg

257 In anaesthetized, tracheotomized and spontaneously breathin

258 intercostal (IIC) muscles were studied in 11 anaesthetized, tracheotomized and spontaneously breathin

259 Saphenous nerves and spinal roots of anaesthetized transgenic mice expressing axoplasmic yell

260 We compared the cardiac performance of anaesthetized TRPV(1) knockout (TRPV(1)(-/-)) mice and t

261 In anaesthetized, vagi-intact rats, injection of opioid ago

262 Hg) were assessed in the following groups of anaesthetized, vagotomized adult Sprague-Dawley rats (ag

263 response to lung inflation, were recorded in anaesthetized, vagotomized and artificially ventilated r

264 at C4 (three injections, 5-min intervals) in anaesthetized, vagotomized and ventilated male rats.

265 gonist, AS-19 (10 muM, 5 mul; 3 x 5 min), in anaesthetized, vagotomized and ventilated male Sprague-D

266 crol) was administered intrathecally (C4) to anaesthetized, vagotomized and ventilated male Sprague-D

267 rated phrenic nerve activity was measured in anaesthetized, vagotomized, neuromuscularly blocked and

268 roximately 500 microA) stimulus intensity in anaesthetized, vagotomized, neuromuscularly blocked and

269 ue-Dawley rats (14-15 months old) which were anaesthetized, vagotomized, neuromuscularly blocked and

270 enic nerve activity was recorded in urethane-anaesthetized, vagotomized, paralysed and ventilated rat

271 of the descending aorta in 14 Dial-urethane anaesthetized, vagotomized, paralysed, artificially vent

272 After exposure to CIH, urethane-anaesthetized, vagotomized, ventilated, paralysed rats h

273 monary stretch receptors (SARs) in halothane-anaesthetized ventilated rats.

274 s muscle (GG(EMG)) activity were recorded in anaesthetized, ventilated and vagotomized rats.

275 MIGET-determined gas exchange shunt in nine anaesthetized, ventilated canines.

276 gas exchange in 27 paired samples from seven anaesthetized, ventilated canines.

277 Anaesthetized, ventilated rats were exposed to a 30 min

278 tion to phrenic nerve activity in chloralose-anaesthetized, ventilated, neuromuscularly blocked, vago

279 In chloralose-anaesthetized, ventilated, vagotomized rats, acute hypox

280 ver an area of forearm skin that was locally anaesthetized via application of EMLA (2.5 % lidocaine (

281 In anaesthetized wild-type mice, exercise increased phenyle

282 In Saffan-anaesthetized Wistar rats, we have studied the role of a

283 distension of the urinary bladder in the dog anaesthetized with a mixture of chloralose and urethane.

284 s by sodium cyanide, were studied in the cat anaesthetized with a mixture of chloralose and urethane.

285 Cats were anaesthetized with alpha-chloralose (60 mg/kg, intraperi

286 Dogs were anaesthetized with alpha-chloralose, a cardiopulmonary b

287 after spinal cord transection (SCT) in cats anaesthetized with alpha-chloralose.

288 In 14 adult male cats anaesthetized with chloralose, one cerebral hemisphere w

289 One month later mice were anaesthetized with isoflurane and isometric force-produc

290 e Wistar rats (10-12 weeks old; n = 72) were anaesthetized with ketamine (3 mg kg(-1) ) and xylazine

291 e recorded from adult wild-type C57/BL6 mice anaesthetized with ketamine (70 mg kg(-1)) and xylazine

292 Rats were anaesthetized with pentobarbital, paralysed and ventilat

293 esthetized with urethane, but not in animals anaesthetized with pentobarbital.

294 bradycardia, hypotension and apnoea in rats anaesthetized with pentobarbitone.

295 Increased LV contractility in rats anaesthetized with urethane was also observed when DVMN

296 atropine increases LV contractility in rats anaesthetized with urethane, but not in animals anaesthe

297 eased left ventricular contractility in rats anaesthetized with urethane, confirming the existence of

298 ged (13 month) male Sprague-Dawley rats were anaesthetized with urethane, vagotomized, paralysed and

299 A) and third-order (3A) MAs of pentobarbital-anaesthetized Young (3-6 months) and Old (24-26 months)

300 Studying the gluteus maximus muscle (GM) of anaesthetized young (4 months) and old (24 months) male