ライフサイエンスコーパス: vagotomy

1 brainstem slices 4 days following unilateral vagotomy.

2 which was not noted in the dogs with truncal vagotomy.

3 sulting response to treatment with drugs and vagotomy.

4 f the NOS inhibitor, L-NAME, or by bilateral vagotomy.

5 d following acute sinoaortic denervation and vagotomy.

6 dy markedly enhanced, even in the absence of vagotomy.

7 hat is markedly enhanced by subdiaphragmatic vagotomy.

8 oth paws was potentiated by subdiaphragmatic vagotomy.

9 en interrupted by bilateral subdiaphragmatic vagotomy.

10 ndergo dramatic afferent reinnervation after vagotomy.

11 s observed in these neurones before or after vagotomy.

12 eas cholangiocyte apoptosis was increased by vagotomy.

13 toms that can be blocked by subdiaphragmatic vagotomy.

14 revent or reverse the potentiating effect of vagotomy.

15 e anti-inflammatory efferent pathway by left vagotomy.

16 axis and is potentiated by subdiaphragmatic vagotomy.

17 ndoscopic Congo red testing assured complete vagotomy.

18 r hexamethonium but not with guanethidine or vagotomy.

19 to-spinal nerves was combined with bilateral vagotomy.

20 tractility was abolished by subdiaphragmatic vagotomy.

21 e MC4-R antagonist SHU9119 or by ipsilateral vagotomy.

22 l these beneficial effects were abrogated by vagotomy.

23 inine methyl ester (L-NAME), or by bilateral vagotomy.

24 carried out both before and after bilateral vagotomy.

25 ses in HR which were attenuated by bilateral vagotomy.

26 hese responses were not altered by bilateral vagotomy.

27 tests would be comparable to that following vagotomy.

28 5% CI: 0.28-1.20) compared to superselective vagotomy.

29 ile withholding lung inflation and following vagotomy.

30 These effects were abolished by vagotomy.

31 responses were not significantly altered by vagotomy.

32 combined with contralateral subdiaphragmatic vagotomy.

33 hizotomy plus contralateral subdiaphragmatic vagotomy.

34 h) airway occlusions, pre- and postbilateral vagotomy.

35 or by coeliac plus coeliac accessory branch vagotomy.

36 leostomy (9.0% MIS), enterectomy (5.2% MIS), vagotomy (1.8% MIS), and pediatric antireflux procedures

37 (4.4% vs. 2.1%, P < 0.001), and less use of vagotomy (5.7% vs. 1.7%, P < 0.001).

38 Vagotomy, a severing of the peripheral axons of the vagu

39 ed to the Sh group, and subsequent bilateral vagotomy abolished both responses.

40 After transection of SC, bilateral vagotomy abolished PD in response to VCMS, providing evi

41 Subsequent bilateral vagotomy abolished the VS-induced increase in PD in the

42 radykinin-induced hyperalgesia 2 weeks after vagotomy, additional denervation of the adrenal medulla

43 f NR1 short hairpin RNA (shRNA), and hepatic vagotomy also nullified glycine's effect.

44 Neither nodose ganglionectomy nor vagotomy altered the CB1 receptor terminal-like staining

45 In addition, hepatic branch vagotomies and pharmacologic inhibition studies were per

46 ley rats underwent complete subdiaphragmatic vagotomies and were injected 18 weeks later with 3 micro

47 perforation or penetration; 18 had undergone vagotomy and 11 gastrectomy.

48 Truncal vagotomy and administration of hexamethonium significant

49 The effects of vagotomy and adrenalectomy on the expression of Fos prot

50 ine flow was abolished by bilateral cervical vagotomy and by renal nerve sectioning.

51 Vagotomy and capsaicin treatment attenuate dorsal vagal

52 hearts were denervate by bilateral cervical vagotomy and cardiac sympathectomy.

53 Hepatic branch vagotomy and direct pharmacologic inhibition of FBPase i

54 Administration of atropine, acute vagotomy and duodenal mucosal application of capsaicin e

55 onal activity were obtained before and after vagotomy and during delayed-I tests in decerebrate, para

56 ted the risk of PD in patients who underwent vagotomy and hypothesized that truncal vagotomy is assoc

57 Open proximal gastric vagotomy and LPGV, but not ASPTV, decreased MAO (p < 0.0

58 Vagotomy and pretreatment with capsaicin but not splanch

59 Billroth-2 gastrectomy, and 33 patients with vagotomy and pyloroplasty for both short- and long-segme

60 were significantly reduced 10 days following vagotomy and were restored to control levels by 30 days

61 ey rats underwent bilateral subdiaphragmatic vagotomy and were sacrificed 10, 30, or 60 days later.

62 ays after section of their peripheral axons (vagotomy) and examined with the whole-cell patch-clamp t

63 Ns maintained in vivo for 5-6 days following vagotomy, and then in vitro for 2-9 h.

64 ecretion by i.p. IL-1 beta is not altered by vagotomy; and (3) the inhibitory effect of vagotomy on a

65 adykinin-induced hyperalgesic behavior after vagotomy are dependent on a hormonal signal released fro

66 Two patients underwent parietal cell vagotomy as well.

67 c anterior seromyotomy and posterior truncal vagotomy (ASPTV; n = 10), or laparoscopic proximal gastr

68 After bilateral vagotomy, atropine pretreatment and pre-contraction of t

69 ad this procedure, and surgical and chemical vagotomy attenuates tumour-induced anorexia and leads to

70 Vagotomy blocked all c-fos responses to acid perfusion o

71 Vagotomy blocked all physiological effects of ESOw perfu

72 Subdiaphragmatic vagotomy blocked the IL-1beta-induced increase in IL-1be

73 creases brain IL1beta mRNA; subdiaphragmatic vagotomy blocks this effect.

74 tion in the DMNV in adult rats with cervical vagotomy (BrdU positive cells; from 27 +/- 4 to 69 +/- 1

75 nly for enhanced respiratory modulation with vagotomy but also the varied activities observed with th

76 e known to regenerate after subdiaphragmatic vagotomy, but neither the question of whether the regene

77 However, vagotomy, but not sham vagotomy, prevented ghrelin's dow

78 Vagotomy, by removing such inhibition, allows greater de

79 Total subdiaphragmatic vagotomy can confound the interpretation of experimental

80 cal analyses demonstrated that, as following vagotomy, capsaicin induced dendritic degeneration, decr

81 However, vagotomy caused a dramatic up-regulation of p55-ir in va

82 ade of spinal iGLURs combined with bilateral vagotomy completely blocked PVN-induced tachycardia.

83 Vagotomy decreased ductal secretion.

84 Vagotomy decreased the expression of M3 acetylcholine re

85 Vagotomy did not affect IL-1beta-induced IL-1beta mRNA p

86 Vagotomy did not alter gastric clock gene expression com

87 In addition, vagotomy did not alter stimulation of plasma ACTH or cor

88 However, vagotomy did not alter stimulation of plasma corticoster

89 Bilateral cervical vagotomy did not significantly alter the effects of DD a

90 Vagotomy did not significantly influence the magnitude o

91 This study tested whether subdiaphragmatic vagotomy disrupts sickness responses by interrupting eff

92 It is concluded that subdiaphragmatic vagotomy does not change the rat's thermal responsivenes

93 he data suggested that common hepatic branch vagotomy does not interfere with hepatic energy status.

94 polysaccharide (LPS) fever, whereas surgical vagotomy does not, splanchnic mediation of the first pha

95 cy operation for intractable ulcer bleeding, vagotomy/drainage is associated with lower postoperative

96 For patients with perforated ulcers, vagotomy/drainage produced similar outcomes as local pro

97 Conversely, vagotomy/drainage was associated with a significantly lo

98 en surgical approach (local procedure alone, vagotomy/drainage, or vagotomy/gastric resection) and 30

99 rts of all patients in Denmark who underwent vagotomy during 1977-1995 and a matched general populati

100 owing bilateral barodenervation and cervical vagotomy, EA (1-4 mA, 2 Hz, 0.5 ms) was performed at the

101 owing bilateral barodenervation and cervical vagotomy, either EA for 30 min at P5-P6 acupoints or con

102 Vagotomy eliminated ghrelin's inhibition of HMGB1 and at

103 Unilateral supra-nodose vagotomy eliminated p55-ir from ipsilateral central vaga

104 We have recently shown that subdiaphragmatic vagotomy enhances bradykinin-induced hyperalgesic behavi

105 anch hepatic vagotomy (unlike gastroduodenal vagotomy) entirely blocked these fat-induced changes.

106 pared open and laparoscopic proximal gastric vagotomies for efficacy of acid reduction and preservati

107 Following vagotomy, frequency fell and peak phrenic activity and t

108 Subsequent bilateral vagotomy further reduced or abolished the residual respo

109 patients undergoing local procedures alone, vagotomy/gastric resection was associated with significa

110 local procedure alone, vagotomy/drainage, or vagotomy/gastric resection) and 30-day postoperative out

111 In rats with acute subdiaphragmatic vagotomy, ghrelin (12 nmol kg(-1) h(-1)) significantly i

112 Vagotomy had no apparent effect on the behavioral expres

113 Vagotomy had no effect on occlusion-accelerated clearanc

114 a protective effect, whereas superselective vagotomy has a minor effect.

115 Subdiaphragmatic vagotomy has been repeatedly shown to attenuate the febr

116 Laparoscopic proximal gastric vagotomy has the potential to become accepted therapy fo

117 Yet, patients with ulcers who have had a vagotomy have been shown to die from cancer more frequen

118 as significantly reduced by subdiaphragmatic vagotomy, hexamethonium (20 mg kg(-1)) and N (G)-nitro-L

119 Vagotomy impairs cholangiocyte proliferation and enhance

120 sed stomach obtained from rats 4 weeks after vagotomies in vitro.

121 owing bilateral barodenervation and cervical vagotomy in anesthetized cats, bradykinin (BK, 1-10 micr

122 esis of BDL rats was virtually eliminated by vagotomy in association with decreased cholangiocyte cAM

123 decreased cholangiocyte apoptosis caused by vagotomy in BDL rats.

124 paroscopic methods have been used to perform vagotomy in patients with duodenal ulcer; however, no di

125 imicked the effect of total subdiaphragmatic vagotomy in potentiating the depression of BK-induced PE

126 crose infusions after total subdiaphragmatic vagotomy in rats with a previously acquired CTA against

127 within the dorsal vagal complex, or hepatic vagotomy in rats.

128 l pressure and were abolished by ipsilateral vagotomy, indicating mediation via a vagal-dependent mec

129 Vagotomy induced a decrease in mechanical baseline paw w

130 n the present study, we investigated whether vagotomy-induced attenuation of febrile responsiveness r

131 gland by suprarenal ganglionectomy prevented vagotomy-induced decrease in baseline paw withdrawal thr

132 The observed vagotomy-induced plasticity within this key feeding cent

133 Blockade of this relay, including vagotomy, inhibits obesity-induced activation of the bet

134 Acute subdiaphragmatic vagotomy, intestinal mucosal application of the local an

135 Vagotomy is also an unavoidable component of some bariat

136 Full truncal vagotomy is associated with a decreased risk for subsequ

137 rwent vagotomy and hypothesized that truncal vagotomy is associated with a protective effect, whereas

138 relaxation of airway smooth muscle following vagotomy is mediated by sequential activation of tachyki

139 V; n = 10), or laparoscopic proximal gastric vagotomy (LPGV; n = 10).

140 ented the decrease in cAMP levels induced by vagotomy, maintained cholangiocyte proliferation, and de

141 Vagotomy markedly attenuated plasma ACTH secretion at 2

142 ts received either complete subdiaphragmatic vagotomies (n = 18) or sham surgeries (n = 12).

143 tropine sulfate (2 mg/kg, i.v.) or bilateral vagotomy nearly abolished the bradycardia and attenuated

144 mediating the accommodation reflex following vagotomy occurs in the gastric myenteric plexus.

145 y vagotomy; and (3) the inhibitory effect of vagotomy on activation of the HPA axis appears to be spe

146 ocyte functions, we evaluated the effects of vagotomy on cholangiocyte proliferation and secretion in

147 kolin administration prevents the effects of vagotomy on cholangiocyte proliferation, apoptosis, and

148 We studied the effect of subdiaphragmatic vagotomy on plasma ACTH stimulation in rats by intraperi

149 We investigated impact of bilateral vagotomy on respiratory and cardiovascular responses to

150 The effects of timed feeding and vagotomy on temporal clock gene expression (clock, bmal1

151 Due to low survival rate, the effect of vagotomy on Voc-T could not be determined.

152 ty in the cardiac ganglia, whereas bilateral vagotomies only partially reduced PACAP-labeling.

153 ogs were randomized to open proximal gastric vagotomy (OPGV; n = 11), laparoscopic anterior seromyoto

154 rations in blood gases and were abolished by vagotomy or atropine.

155 er bilateral sub-diaphragmatic total truncal vagotomy or brainstem-hypothalamic pathway transectionin

156 However, vagotomy or capsaicin treatment did not diminish CCK-ind

157 protection persisted after subdiaphragmatic vagotomy or corticosterone receptor blockade.

158 Sham vagotomy or cutting the vagi caudal to the lungs did not

159 erate large inspiratory volumes after either vagotomy or during augmented breaths was impaired if cro

160 This tone was essentially abolished by vagotomy or ganglionic blockade, suggesting that it was

161 t decrease in the use of definitive surgery (vagotomy or resection) for ulcer complications.

162 Vagotomy or selective nerve blockade with tetrodotoxin (

163 rague-Dawley rats underwent subdiaphragmatic vagotomy or sham surgery 1 week prior to study.

164 In additional animals, vagotomy or sham vagotomy was performed in sham and sept

165 hat had undergone bilateral subdiaphragmatic vagotomy or systemic treatment with capsaicin, a neuroto

166 Truncal vagotomy or treatment of the coeliac ganglia with capsai

167 Truncal vagotomy or treatment of the coeliac ganglia with capsai

168 n, rats underwent bilateral subdiaphragmatic vagotomy or were sham-vagotomized.

169 Male rats were subjected to subdiaphragmatic vagotomy (or sham surgery) on day 0 and had a cannula im

170 0.5 mg kg-1) and by chronic subdiaphragmatic vagotomy performed 10-14 days prior to experimentation,

171 Subdiaphragmatic vagotomy prevented the IL-1-induced increases in body te

172 However, vagotomy, but not sham vagotomy, prevented ghrelin's down-regulatory effect on

173 Vagotomy prolonged the increase of mean systolic blood p

174 molecule that activates resolution, and that vagotomy reduced local pro-resolving mediators, thereby

175 Subdiaphragmatic vagotomy reduced the density of CCK-A receptor fibers in

176 However, in a third series of experiments vagotomy reduced the number of Fos-staining cells in the

177 Surgical or chemical vagotomy rendered animals sensitive to TNF release and s

178 lymph node primary gastrinoma, parietal cell vagotomy, reoperation and surgery for metastatic tumor,

179 Bilateral adrenalectomy or a unilateral vagotomy resulted in a selective reduction of inflammati

180 Vagotomy resulted in an inflammatory peritoneal lipid me

181 We tested the hypothesis that vagotomy results in the transient withdrawal of central

182 Bilateral cervical vagotomy revealed that vagal afferents modulated but did

183 In patients who underwent superselective vagotomy, risk of PD was similar to the general populati

184 (RYGB; n = 7), RYGB + common hepatic branch vagotomy (RYGB + HV; n = 6), or sham procedure (sham; n

185 Blockade of the K(ATP) channel and hepatic vagotomy significantly attenuated the effect of central

186 Bilateral vagotomy significantly reduced the bradycardia and most

187 Unilateral vagotomy significantly reduced the percentage of SP-resp

188 ague-Dawley rats were given subdiaphragmatic vagotomies, sparing only the common hepatic branch, and

189 tragastrically in controls and animals after vagotomy, splanchnic nerve resection, or chemical denerv

190 responses can be blocked by subdiaphragmatic vagotomy, suggesting that vagal afferents signal periphe

191 This together with the effects of vagotomy suggests that the activation of NE in turn incr

192 Vagotomy, systemic haloperidol, or intracerebroventricul

193 -Dawley) received a partial subdiaphragmatic vagotomy that spared a single branch.

194 At 45 weeks after the vagotomies, the animals were randomly assigned to affere

195 erves had been eliminated by chronic truncal vagotomy, the 5-HT3-mediated response was absent in thir

196 Fever was unaffected by subdiaphragmatic vagotomy, thus these data provide support for the conclu

197 with bilateral barodenervation and cervical vagotomy, topical application of bradykinin (BK, 1-10 mi

198 ur results demonstrate that subdiaphragmatic vagotomy triggers transient withdrawal and remodeling of

199 lionectomy (CSMG), or total subdiaphragmatic vagotomy (TSV) were exposed to hyperinsulinemic-hypoglyc

200 nificantly enhanced in vivo by acute truncal vagotomy (TV), hexamethonium (C6), and NG-nitro-L-argini

201 Strikingly, common branch hepatic vagotomy (unlike gastroduodenal vagotomy) entirely block

202 hen regenerate to a limited extent following vagotomy, very little is known about the response of cen

203 Laparoscopic proximal gastric vagotomy was comparable to OPGV in decreasing stimulated

204 Anterior seromyotomy and posterior truncal vagotomy was less effective in decreasing MAO and requir

205 dditional groups of animals, bilateral trunk vagotomy was performed at 5 hrs after CLP before ghrelin

206 In additional animals, vagotomy or sham vagotomy was performed in sham and septic animals immedi

207 physiological variables, and the effects of vagotomy were examined in anesthetized cats.

208 Risk of PD was also decreased after truncal vagotomy when compared to the general population cohort

209 delayed-I tests were similar to those after vagotomy, with the exception of firing-rate differences

210 Furthermore, common branch hepatic vagotomy without diabetes induced indexes of obesity.