ライフサイエンスコーパス: anaesthetized

1 n the skin under the cathodal electrodes was anaesthetized.

2 of whether the animal was awake, behaving or 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 two age groups (8 and 12 weeks old) of young anaesthetized adult normal WKY and SHR were acquired in

6 Experiments were performed on anaesthetized adult rats and mice.

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

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

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

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

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

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

13 In anaesthetized and artificially ventilated rats, ATP- and

14 on single pulmonary C fibres was studied in anaesthetized and artificially ventilated rats.

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 In both anaesthetized and decerebrate rats, sectioning the spina

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

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

23 Animals were terminally anaesthetized and the extensor digitorum longus muscles

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

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

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

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

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

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

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

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

32 In chloralose-anaesthetized, artificially ventilated dogs, the splenic

33 ium and potassium excretion were examined on anaesthetized, artificially ventilated New Zealand White

34 In six anaesthetized beagle dogs control contractions increased

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

53 nts from the longissimus lumborum muscles of anaesthetized cats.

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

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

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

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

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

59 etal muscle receptors in thirteen chloralose-anaesthetized cats.

60 recorded from the left sympathetic chain in anaesthetized cats.

61 e left thoracic sympathetic chain (T1-T4) of anaesthetized cats.

62 viour of single motoneurones was assessed in anaesthetized cats.

63 from the right thoracic sympathetic chain of anaesthetized cats.

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

65 isovolumetric conditions in alpha-chloralose anaesthetized cats.

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

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

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

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

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

71 In anaesthetized dogs connected to cardiopulmonary bypass,

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

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

74 In chloralose anaesthetized dogs, a perfusion circuit allowed independ

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

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

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

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

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

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

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

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

83 tracheal vagal afferent nerve stimulation in anaesthetized guinea pigs.

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

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

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

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

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

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

90 In anaesthetized hamsters, acetylcholine (ACh) microiontoph

91 In anaesthetized hamsters, we have investigated the spread

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

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

100 06 upper limb motoneurones in ten chloralose-anaesthetized macaque monkeys.

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

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

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

107 Anaesthetized, male Sprague-Dawley rats were exposed to

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 ry following severe hyperthermia exposure in anaesthetized mice.

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

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

127 Experiments were performed on awake and anaesthetized mutant and wild-type control mice.

128 esponses during hypoxia was also observed in anaesthetized mutant mice.

129 In urethane-anaesthetized, neuromuscularly blocked and vagotomized S

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

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

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

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

134 oth superficial and deep laminae in urethane-anaesthetized newborn rats aged 3, 6, 10 and 21 days, an

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

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

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

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

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

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

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

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

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

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

145 ntophoresis were performed in pentobarbitone-anaesthetized, paralysed and artificially ventilated rat

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

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

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

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

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

151 Anaesthetized pigs were subjected to either sham treatme

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

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

154 Decerebrate unanaesthetized or barbiturate-anaesthetized preparations were used.

155 In some anaesthetized preparations, eupnoea is eliminated follow

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

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

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

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

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

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

162 cted into the synovial cavity of the knee in anaesthetized rabbits.

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

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

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

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

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

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

169 In the in vivo anaesthetized rat preparation, bilateral microinjections

170 In the in vivo anaesthetized rat preparation, unilateral microinjection

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

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

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

174 he medulla oblongata was investigated in the anaesthetized rat.

175 67156 altered reflex bladder activity in the anaesthetized rat.

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

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

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

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

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

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

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

183 These studies in anaesthetized rats demonstrate that tracheal occlusion a

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

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

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

187 We used anaesthetized rats in which pontine microinjections of a

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

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

190 Cystometry performed on control anaesthetized rats revealed that intravesical instillati

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

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

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

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

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

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

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

198 ents innervating the mid-jejunum of urethane-anaesthetized rats was recorded with extracellular micro

199 In anaesthetized rats we tested responses evoked by systemi

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

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

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

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

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

205 In anaesthetized rats with unilateral lesions of around 70%

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

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

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

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

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

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

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

213 In anaesthetized rats, hindlimb contraction alone significa

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

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

216 In anaesthetized rats, using a focal recording technique, a

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

218 In anaesthetized rats, we have examined the role of adenosi

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

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

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

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

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

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

225 lateral frontal electrocorticogram (ECoG) of anaesthetized rats.

226 entially to theta and ripple oscillations in anaesthetized rats.

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

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

229 ympathetic postganglionic neurones (PGNs) in anaesthetized rats.

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

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

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

233 e a Bezold-Jarisch (B-J) depressor reflex in anaesthetized rats.

234 nd after cocaine administration in halothane anaesthetized rats.

235 otor nucleus (DVMN) of pentobarbitone sodium anaesthetized rats.

236 (RVL) has been addressed in this study using anaesthetized rats.

237 e determined on C1-C3 dorsal horn neurons in anaesthetized rats.

238 ed respiratory frequency and tidal volume in anaesthetized rats.

239 -locked to hippocampal theta oscillations in anaesthetized rats.

240 e concentrations in the prefrontal cortex of anaesthetized rats.

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

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

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

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

245 In anaesthetized spinalized rats electrical stimulation of

246 In anaesthetized, spontaneously breathing mice, integrated

247 In anaesthetized, spontaneously breathing rats, intratrache

248 In anaesthetized, spontaneously breathing rats, intravenous

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

250 Eleven anaesthetized Sprague-Dawley rats were surgically prepar

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

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

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

254 In anaesthetized, tracheotomized and spontaneously breathin

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

256 ng two series of experiments using a supine, anaesthetized, tracheotomized rat in which tongue muscle

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

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

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

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

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

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

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

264 We recorded phrenic activity in seven anaesthetized, vagotomized, glomectomized, paralysed and

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

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

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

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

269 tly controlled isocapnic hypoxia in urethane-anaesthetized, vagotomized, paralysed and ventilated rat

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

271 descending aorta in thirty-six 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 Anaesthetized, ventilated rats were exposed to a 30 min

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

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

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

279 In anaesthetized wild-type mice, exercise increased phenyle

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

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

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

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

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

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

286 Male cats were anaesthetized with alphaxalone-alphadolone and breathed

287 Male cats were anaesthetized with alphaxalone-alphadolone and breathed

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

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

290 Rats were anaesthetized with pentobarbital, paralysed and ventilat

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

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

293 t 28.5-31 C in young guinea-pigs (150-300 g) anaesthetized with sodium pentobarbitone.

294 On the sixth day, the rats were anaesthetized with urethane or pentobarbitone and prepar

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