ライフサイエンスコーパス: splanchnic

1 by only approximately 65% (P < 0.05 leg vs. splanchnic).

2 l or, therefore by implication, flux via the splanchnic 11beta-HSD type 1 pathway.

3 More than one-half of splanchnic [3H]triglyceride uptake occurred in the liver

4 (35 +/- 2 vs. 29 +/- 1 nmol/min, P < 0.05), splanchnic 9,12,12-[(2)H](3)cortisol production was not

5 s that bladder pelvic and hypogastric/lumbar splanchnic afferents are functionally distinct and likel

6 ients with acute liver failure by decreasing splanchnic ammonia production, restoring normal regulati

7 d in left aortic sac mesothelium and in left splanchnic and branchial arch mesoderm near the junction

8 4 signaling molecule is expressed in ventral splanchnic and branchial-arch mesoderm and outflow-tract

9 aks in coherence in spectra of preganglionic splanchnic and cervical sympathetic nerves were dependen

10 glucose uptake (LGU) were measured using the splanchnic and leg catheterization methods, combined wit

11 lonic and jejunal preparations with attached splanchnic and mesenteric nerves were used to study mech

12 also enhanced leucine transamination in both splanchnic and muscle beds.

13 ted plasma free fatty acids (FFAs) alter the splanchnic and muscle glucose metabolism in women.

14 AAs) alone or in combination with insulin on splanchnic and muscle protein dynamics, we infused stabl

15 -mediated suppression of EGP and 2) augments splanchnic and peripheral tissue glucose uptake.

16 between, several cell populations, including splanchnic and pharyngeal mesoderm, postotic neural cres

17 ortal anastomosis (RPA) directly diverts the splanchnic and renal venous blood assuring a good portal

18 es have shown that haploinsufficiency of the splanchnic and septum transversum mesoderm Forkhead Box

19 in vasodilatation in the coronary, cerebral, splanchnic and skeletal muscle vascular beds.

20 tial for maintaining the distinction between splanchnic and somatic mesoderm and for differentiation

21 Vasodilatation (splanchnic and systemic) and hyperdynamic circulation ar

22 Vasodilatation (splanchnic and systemic) and the hyperdynamic circulatio

23 Vasodilatation (splanchnic and systemic) and the hyperdynamic circulatio

24 Enteric ganglia and components of splanchnic and vagus nerve circuitry were examined along

25 rointestinal tract and neuroinvasion via the splanchnic and vagus nerves.

26 ion of the lateral mesoderm into a visceral (splanchnic) and a somatic layer is a crucial event durin

27 ntravenous saline infusion while total-body, splanchnic, and D3 cortisol production (an index of 11be

28 mine this, we quantified in vivo whole-body, splanchnic, and hepatic 11beta-HSD1 activity in obese ty

29 Systemic, splanchnic, and leg FFA kinetics were measured.

30 Total body glucose disappearance, splanchnic, and leg glucose extractions were markedly lo

31 tive hydrolysis of arginine into urea in the splanchnic area and systemic circulation.

32 s are irreversibly trapped in the prehepatic splanchnic area within the acquisition period.

33 ional change, +4% versus -32%; P=0.004), and splanchnic arterial resistance did not increase as expec

34 rphyrinato iron (III) (FeTMPS) in a model of splanchnic artery occlusion shock (SAO).

35 nd during ischemia of the small intestine by splanchnic artery occlusion.

36 e ability of insulin and glucose to regulate splanchnic as well as muscle glucose metabolism.

37 net release (P < 0.05) of cortisol from the splanchnic bed (6.1 +/- 2.6 microg/min) and net uptake (

38 AAs largely determined protein anabolism in splanchnic bed by stimulating PS and decreasing protein

39 ectin concentrations and, if so, whether the splanchnic bed contributes to this phenomenon.

40 protein breakdown and increased synthesis in splanchnic bed in a dose-dependent manner.

41 ine if cortisol production occurs within the splanchnic bed in humans, 11 nondiabetic subjects were s

42 us parameters of lipid metabolism across the splanchnic bed in severely burned patients.

43 distribution of (18)F-FDG in the prehepatic splanchnic bed may complicate the analysis of dynamic PE

44 to determine whether spillover occurs in the splanchnic bed of humans.

45 The splanchnic bed produces cortisol at rates approximating

46 of Tyr to the systemic circulation where the splanchnic bed was a net remover of Tyr.

47 CO2 production by the splanchnic bed was not affected by the diet.

48 crog/min of cortisol was produced within the splanchnic bed, all of which occurred within the liver (

49 ng and exiting the renal bed, pulmonary bed, splanchnic bed, and leg in 4 groups of subjects.

50 rotein dynamics or leucine transamination in splanchnic bed.

51 e, whereas AAs acted on muscle as well as on splanchnic bed.

52 ) and Tyr (14.3 +/- 1.3 micromol/min) by the splanchnic bed.

53 n kidney and 3.0 +/- 0.7 micromol/min in the splanchnic bed.

54 rge volume of distribution in the prehepatic splanchnic bed.

55 actions and fluid redistribution from venous splanchnic beds to central pulmonary circulation need to

56 se findings imply substantive alterations in splanchnic blood flow control with ageing.

57 ric emptying, small bowel water content, and splanchnic blood flow measured by magnetic resonance ima

58 greatest in the splanchnic vasculature, and splanchnic blood flow was unaffected by PE.

59 Cardiac output and splanchnic blood flow were reduced by L-NMMA for control

60 ificant decreases in portocollateralization, splanchnic blood flow, portohepatic resistance, and port

61 rom increased venous stiffness and decreased splanchnic capacitance and may also be an adaptive mecha

62 For example, heart failure-associated splanchnic circulation congestion, bowel wall edema, and

63 Identical effects were observed in the splanchnic circulation in vivo.

64 , LPS and cytokine concentrations within the splanchnic circulation of alcoholic cirrhotic patients u

65 ng an increased uptake of amino acids in the splanchnic compartment.

66 .9 +/- 0.4 microg/min) and accounted for all splanchnic cortisol and D3 cortisol production.

67 originated in extrasplanchnic tissues since splanchnic cortisol production (mean 0-360 min: 254 +/-

68 ake 14.8 +/- 2.0 microg/min (P < 0.001), and splanchnic cortisol production 22.2 +/- 3.3 microg/min (

69 support the possibility that alterations in splanchnic cortisol production contribute to visceral fa

70 The liver accounts for all splanchnic cortisol production in obese nondiabetic huma

71 It is not known whether splanchnic cortisol production is regulated by nutrient

72 We conclude that most, if not all, of splanchnic cortisol production occurs within the liver.

73 estion of a mixed meal does not alter either splanchnic cortisol production or the conversion of D4 c

74 ve contributions of the viscera and liver to splanchnic cortisol production.

75 traction averaged 12.9 +/- 1.3% (P < 0.001), splanchnic cortisol uptake 14.8 +/- 2.0 microg/min (P <

76 cortisone 15.2 +/- 5.8 pmol/100 mL/min) and splanchnic (cortisol 64.0 +/- 11.4 nmol/min, d3-cortisol

77 min: 254 +/- 83 vs. 262 +/- 36 nmol/min) and splanchnic D3 cortisol production (mean 0-360 min: 72 +/

78 ortisol release (3.9 +/- 0.4 microg/min) and splanchnic D3-cortisol production (7.1 +/- 0.7 microg/mi

79 ), resulting in a strong correlation between splanchnic D3-cortisol production and total-body 3D-cort

80 Net splanchnic D3-cortisol release (3.9 +/- 0.4 microg/min)

81 Fractional splanchnic D4-cortisol extraction averaged 12.9 +/- 1.3%

82 In addition, the splanchnic effects of MasR required nitric oxide.

83 EA at P5-P6 decreased splanchnic evoked activity of cardiovascular barosensiti

84 Arterial concentrations and splanchnic exchange of glucose, lactate, pyruvate, glyce

85 s are rich in cysteine, we hypothesized that splanchnic extraction and the efficiency of cysteine uti

86 The median splanchnic extraction fraction of hourly dietary Phe int

87 Splanchnic extraction fractions of (18)F-FDG (E*) and (3

88 Splanchnic F-EPSPs but not colonic F-EPSPs were reduced

89 unted for by an additional contribution from splanchnic fat (means +/- SE; 331 +/- 76 micromol/l vs.

90 mU x kg(-1) x min(-1) insulin infusion rate, splanchnic FFA release decreased by only approximately 6

91 alterations in LTRvc was determined from the splanchnic first-pass clearance of [14C]lactate infused

92 PE dose-response for splanchnic flow and resistance were blunted for VVS comp

93 elevated; and (4) with head-up tilt testing, splanchnic flow was not reduced in Fontan patients versu

94 uptake was due in part, to a 50% increase in splanchnic fractional extraction.

95 Leg and splanchnic glucose metabolism were assessed using a comb

96 se at rates causing comparable inhibition in splanchnic glucose output is accompanied by a disproport

97 rial insulin induces a smaller inhibition in splanchnic glucose output than in controls; (c) infusion

98 in the obese resulted in a 75% reduction in splanchnic glucose output which was equivalent to that o

99 g/kg/min; 144 +/- 4 mg/min) known to inhibit splanchnic glucose output without influencing peripheral

100 accompanied by a less than 40% inhibition in splanchnic glucose output.

101 t in arterial insulin and a 75% reduction in splanchnic glucose output.

102 min(-1); P < 0.02) were also lower, whereas splanchnic glucose production (8.2 +/- 0.8 vs. 4.3 +/- 0

103 In the basal state splanchnic glucose production did not differ significant

104 her the rise in insulin or the inhibition in splanchnic glucose production observed in the controls.

105 Splanchnic glucose production was higher (P < 0.05) in t

106 n contrast, only IL/Hep increased (P < 0.05) splanchnic glucose production, indicating that elevated

107 of muscle glucose uptake and suppression of splanchnic glucose production.

108 l, muscle glucose uptake, and suppression of splanchnic glucose production.

109 Neither endogenous and splanchnic glucose productions nor rates of appearance o

110 ndicating a lower (P < 0.05) rate of initial splanchnic glucose uptake (1.4 +/- 1.5 vs. 4.8 +/- 0.8 m

111 glucose production (EGP) and stimulation of splanchnic glucose uptake (SGU) differ in nondiabetic hu

112 rmine whether insulin-induced stimulation of splanchnic glucose uptake (SGU) is also impaired, we sim

113 Splanchnic glucose uptake (SGU) plays a major role in th

114 The effect of pioglitazone on splanchnic glucose uptake (SGU), endogenous glucose prod

115 sly produced glucose and a higher first-pass splanchnic glucose uptake (SGU).

116 The defect in splanchnic glucose uptake appears to be due to decreased

117 In summary, both muscle and splanchnic glucose uptake are impaired in type 2 diabete

118 glucose, GLP-1 increases total body but not splanchnic glucose uptake in humans with type 1 diabetes

119 To determine whether GLP-1 increases splanchnic glucose uptake in humans, we studied seven su

120 On the other hand, they do not alter either splanchnic glucose uptake or splanchnic insulin extracti

121 IL/Hep did not alter splanchnic glucose uptake or the contribution of the ext

122 We have previously reported that splanchnic glucose uptake, hepatic glycogen synthesis, a

123 keletal muscle and consequent restriction of splanchnic glutamine supply.

124 Glycine flux and splanchnic glycine extraction were measured in 2 groups

125 Total and endogenous glycine flux and splanchnic glycine uptake did not differ significantly b

126 Intestinal bacterial flora may induce splanchnic hemodynamic and histological alterations that

127 Systemic and splanchnic hemodynamics were measured and blood samples

128 Systemic and splanchnic hemodynamics were measured and blood samples

129 s is characterized by disturbed systemic and splanchnic hemodynamics.

130 ify vascular response to vasoconstrictors in splanchnic, hepatic, and collateral vascular beds.

131 To examine if postprandial splanchnic/hepatic free fatty acid (FFA) delivery is inc

132 Angiogenesis in liver cirrhosis leads to splanchnic hyperemia, increased portal inflow, and porto

133 Enhanced postural thoracic hypovolemia and splanchnic hypervolemia are associated with postural sim

134 elated to excessive thoracic hypovolemia and splanchnic hypervolemia during orthostasis compared with

135 specific subtypes of ASICs in the vagal and splanchnic innervation of the stomach.

136 ot alter either splanchnic glucose uptake or splanchnic insulin extraction in nondiabetic humans.

137 Splanchnic insulin extraction, directly measured using t

138 /- 15% (P < 0.05) increase of peripheral and splanchnic interstitial distribution volumes for [(14)C]

139 addition of PR to a CR protocol prevents the splanchnic ischemia that initiates systemic inflammation

140 Total splanchnic lactate gradient (HV-RA) is positive in ALF.

141 side of the currently proposed domain in the splanchnic layer of the lateral plate mesoderm.

142 The contribution of splanchnic lipolysis to hepatic FFA delivery ranged from

143 ) fever, whereas surgical vagotomy does not, splanchnic mediation of the first phase was proposed.

144 Tbx1 is expressed in the splanchnic mesenchyme, the pharyngeal endoderm (PE) and

145 field (SHF), located in the ventral midline splanchnic mesenchyme, which provides additional myocard

146 VEGF-A signals endothelial cells within the splanchnic mesenchyme.

147 ield (SHF) progenitors in the pharyngeal and splanchnic mesoderm (SpM), but how these progenitors are

148 tion specifically in SHF cells in the caudal splanchnic mesoderm (SpM), where Wnt5a and Dvl2 are co-e

149 ria and OFT and are found also in the dorsal splanchnic mesoderm accompanied by the expression of the

150 ely, involved in the development of visceral/splanchnic mesoderm and non-visceral mesoderm in coeloma

151 ion of Bmp4 in the caudal branchial arch and splanchnic mesoderm and OFT myocardium by using a condit

152 ated from a midline secondary heart field of splanchnic mesoderm beneath the floor of the foregut.

153 in anterior and posterior second heart field splanchnic mesoderm between E8 and E10.

154 ents, showing that both cranial paraxial and splanchnic mesoderm contribute to branchiomeric muscle a

155 atic mesoderm and for differentiation of the splanchnic mesoderm into midgut musculature.

156 sphorylated-Erk and Pea3, identifies the AHF splanchnic mesoderm itself as a target for Fgf8 signalin

157 on these and other data, we propose that the splanchnic mesoderm layers in Drosophila and vertebrate

158 in the pharyngeal endoderm and/or overlying splanchnic mesoderm of the AHF at a stage prior to heart

159 d with these great arteries are derived from splanchnic mesoderm of the second heart field (SHF), an

160 ed together, these findings suggest that the splanchnic mesoderm responds to endodermal Hedgehog sign

161 Misexpression of DN-Tcf4 in the splanchnic mesoderm resulted in the failure of the gizza

162 urs while extensive morphogenesis, including splanchnic mesoderm sliding over the endoderm, results i

163 ry heart field within the branchial arch and splanchnic mesoderm that contributes to the aortic sac a

164 express Islet and Tbx1/10, evocative of the splanchnic mesoderm that produces the lower jaw muscles

165 ial mesoderm, to regulate eye muscle, and in splanchnic mesoderm to regulate OFT development.

166 s have MF20-expressing cardiomyocytes in the splanchnic mesoderm within the second heart field (SHF).

167 , Bapx1 is an early developmental marker for splanchnic mesoderm, consistent with a role in visceral

168 e early splenic primordium, derived from the splanchnic mesoderm, of homozygous mutant embryos.

169 heart field, derived from branchial arch and splanchnic mesoderm, patterns the forming outflow tract

170 ll death in both the pharyngeal endoderm and splanchnic mesoderm.

171 nd a loss of Id2 expression in the heart and splanchnic mesoderm.

172 es, cardiac outflow tract, inflow tract, and splanchnic mesoderm.

173 ermal epithelium and mesenchyme derived from splanchnic mesoderm.

174 elium and mesenchymal cells derived from the splanchnic mesoderm.

175 ription factor is expressed in the visceral (splanchnic) mesoderm, which is involved in mesenchymal-e

176 In the mouse embryo, the splanchnic mesodermal cells of the anterior heart field

177 that capsulin acts within a subpopulation of splanchnic mesodermal cells to control an essential earl

178 l-derived cell layer referred to here as the splanchnic mesodermal plate (SMP).

179 rolling and adherent leukocytes in the mouse splanchnic microcirculation.

180 mpathetic nervous system through the greater splanchnic nerve (GSN), and elevation of pro-inflammator

181 ffin cells are innervated by the sympathetic splanchnic nerve and translate graded sympathetic firing

182 inferior mesenteric ganglion and the lumbar splanchnic nerve bundle (LSN) were placed in a specializ

183 Hence, the splanchnic nerve is likely uninvolved in LPS fever.

184 undergone either transection of the thoracic splanchnic nerve or sham transection to the remaining ad

185 tomy and pretreatment with capsaicin but not splanchnic nerve resection abolished this response.

186 ally in controls and animals after vagotomy, splanchnic nerve resection, or chemical denervation with

187 ch point behavioral, visceromotor, and great splanchnic nerve responses to graded gastric balloon dis

188 tentiated the amplitude of F-EPSPs evoked by splanchnic nerve stimulation but not F-EPSPs evoked by c

189 y reduced the amplitude of F-EPSPs evoked by splanchnic nerve stimulation but not F-EPSPs evoked by c

190 d cholinergic fast EPSPs (F-EPSPs) evoked by splanchnic nerve stimulation but not F-EPSPs evoked by c

191 oring of adrenal catecholamine secretion and splanchnic nerve stimulation in anaesthetised mice.

192 that NaHS enhanced the inhibitory effect of splanchnic nerve stimulation on colonic motility.

193 ascular barosensitive rVLM neurons evoked by splanchnic nerve stimulation were reduced by EA and then

194 roactive peptide transmitter released by the splanchnic nerve under elevated sympathetic activity to

195 ent with anti-DH-SAP the sympathoexcitatory (splanchnic nerve) and pressor responses to electrical st

196 etabolic stress: hypoglycemia stimulates the splanchnic nerve, epinephrine is released from adrenomed

197 l chromaffin cells (ACCs), stimulated by the splanchnic nerve, generate action potentials (APs) at a

198 reased the efferent discharge in the greater splanchnic nerve.

199 ganglia and efferent fibers of the vagus and splanchnic nerves to invade initial target sites in the

200 cted selectively on presynaptic terminals of splanchnic nerves to modulate fast cholinergic synaptic

201 ordinary spectra of cervical sympathetic and splanchnic nerves was removed by partialization using th

202 y fibers traveling within both the vagus and splanchnic nerves.

203 Balb/c mice were subjected to splanchnic occlusion and reperfusion and were pretreated

204 in enteric ganglia and autonomic ganglia of splanchnic or vagus circuitry prior to sensory ganglia.

205 at hindlimb locomotor muscle(s), kidneys and splanchnic organs at rest and during dynamic treadmill e

206 expression of HO isoforms in liver cells and splanchnic organs from portal hypertensive (PH) and sham

207 The role of the splanchnic organs in lipopolysaccharide-induced alterati

208 ion, HO-1 is up-regulated in hepatocytes and splanchnic organs of PH rats, compared with SO animals,

209 l and nonparenchymal liver cells, as well as splanchnic organs, of both PH and SO rats.

210 first-pass clearance of [14C]lactate by the splanchnic organs.

211 d lactate concentration gradients across the splanchnic organs.

212 increasing the gut oxygen consumption beyond splanchnic oxygen delivery.

213 ecreased thoracic blood volume and increased splanchnic, pelvic, and leg blood volumes for all subjec

214 retation of Pico2 - Paco2 as an indicator of splanchnic perfusion during systemic hypocapnia.

215 ingly advocated as a more specific marker of splanchnic perfusion than Pico2 alone.

216 lly, improvements in hemodynamic parameters, splanchnic perfusion, and reduced sedation/neuromuscular

217 tor is multifaceted and may adversely affect splanchnic perfusion.

218 icrocirculatory blood flow, urine output, or splanchnic perfusion.

219 Improved splanchnic/peripheral glucose uptake and enhanced suppre

220 ea, with kinetics indicative of a first-pass splanchnic phenomenon.

221 Thus, splanchnic production of cortisol occurs in nondiabetic

222 ALF before liver transplantation, suggesting splanchnic production of lactate.

223 n deficiency was recently shown to stimulate splanchnic protein synthesis in vivo, whereas insulin en

224 dent insulinotropic polypeptide (GIP) in the splanchnic region in 10 obese patients with T2D before a

225 stress shifts blood volume from thoracic and splanchnic regions presumably to aid in heat dissipation

226 Splanchnic release of cortisol and 9,12,12-[(2)H](3)-cor

227 PJ34 significantly protected against splanchnic reperfusion-induced intestinal hyperpermeabil

228 umol/kg/6 h; P = 0.04), suggesting increased splanchnic sequestration of meal-derived glucose.

229 in increased basal and baroreflex control of splanchnic SNA (SSNA) and heart rate (HR) in rats in bot

230 his neuronal population tonically suppresses splanchnic SNA (SSNA), arterial pressure, and heart rate

231 uced mean AP (MAP; P < 0.001) and integrated splanchnic SNA (sSNA; P < 0.001) in DH rats (n = 6).

232 ateral microinjection of muscimol eliminated splanchnic SNA and produced the same degree of hypotensi

233 ralysed rats had significantly elevated MAP, splanchnic SNA, and rate of phrenic nerve discharge (PND

234 insulin-sensitive men are those derived from splanchnic sources.

235 ificant correlation between "true" and "net" splanchnic spillover (R = 0.84, P < 0.005), the latter r

236 are partitioned in tissues and indicate that splanchnic spillover from triglyceride-rich lipoproteins

237 s developed and demonstrated that nonhepatic splanchnic spillover rates in study A and study B of 69

238 Splanchnic spillover was higher than nonsplanchnic syste

239 The OZRs had elevated baseline splanchnic sympathetic nerve activity (SNA) and mean AP

240 Hypoxia elevates splanchnic sympathetic nerve activity (SNA) with differe

241 Kainic acid (KA)-induced seizures increased splanchnic sympathetic nerve activity by 97%, accompanie

242 reased vascular extraction of lactate by the splanchnic system (0.07 +/- 0.07 micromol/mL vs. -0.34 +

243 he fact that the clearance of lactate by the splanchnic system remains intact.

244 In contrast, lactate clearance by the splanchnic system was increased.

245 ranges for blood flow volume (BFV) in major splanchnic, thoracoabdominal, and neck vessels by using

246 anges in BFVs in response to a meal in major splanchnic, thoracoabdominal, and neck vessels were esti

247 eal bleeding as a result of diffuse visceral splanchnic thrombosis and portal hypertension.

248 rcentage of enteral leucine extracted by the splanchnic tissues among the 3 studies.

249 Leg and splanchnic tissues contributed a greater portion of syst

250 ir nonedematous counterparts and because the splanchnic tissues of all children with SAM have a relat

251 covered state, enteral leucine extraction by splanchnic tissues trended higher in the group that prev

252 A slight increase in all splanchnic tissues was also noticed.

253 ons regarding actual spillover in nonhepatic splanchnic tissues were required for the spillover calcu

254 ot, however, apply to incorporation rates in splanchnic tissues, which were instead dependent on the

255 Cysteine flux, oxidation, balance, and splanchnic uptake (SPU) were measured in 2 groups of chi

256 Splanchnic uptake of glucose precursors could account fo

257 obesity (a) despite basal hyperinsulinemia, splanchnic uptake of glucose precursors is increased, th

258 However splanchnic uptake of lactate, glycerol, alanine, free fa

259 The rate of splanchnic uptake of palmitate was 1.68 +/- 1.3 micromol

260 There was preferential splanchnic uptake of triglyceride fatty acids compared w

261 yporesponsiveness to vasoconstrictors in the splanchnic vascular bed, with several vasoactive molecul

262 tabolic flux data, measured across the human splanchnic vascular bed, within a genome-scale model of

263 traction of small resistance arteries in the splanchnic vascular beds.

264 re blocked in rats with cirrhosis to examine splanchnic vascular hemodynamics and portal pressure res

265 Ang-(1-7) mediated splanchnic vascular hypocontractility in ex vivo splanch

266 Splanchnic vascular hypocontractility with subsequent in

267 Production of Ang-(1-7) and splanchnic vascular reactivity to Ang-(1-7) was measured

268 ate that bariatric surgery leads to enhanced splanchnic vascular responses as a likely consequence of

269 Compromised capacitance function of the splanchnic vasculature and deficient abdominal lymph flo

270 dicating that activation of this receptor in splanchnic vasculature promotes portal inflow to contrib

271 oconstrictive impairment was greatest in the splanchnic vasculature, and splanchnic blood flow was un

272 is, little is known about its effects in the splanchnic vasculature, particularly those of the altern

273 Hemorrhage-induced splanchnic vasoconstriction causing pressure wave reflec

274 ity, especially for the intestinal donor, as splanchnic vasoconstriction that is intended to preserve

275 receptor partial agonist with a preferential splanchnic vasoconstrictor effect (FE 204038) in rats wi

276 estigated whether this system contributes to splanchnic vasodilatation and portal hypertension in cir

277 (1-7), which leads to activation of MasR and splanchnic vasodilatation in rats.

278 garding intrahepatic vascular resistance and splanchnic vasodilatation) and experimental methods used

279 creased intrahepatic vascular resistance and splanchnic vasodilatation) and recent advances in the di

280 creased intrahepatic vascular resistance and splanchnic vasodilatation) and recent advances in the di

281 enous inflow, which in turn is the result of splanchnic vasodilatation.

282 Splanchnic vasodilatators improved hepatocyte engraftmen

283 ent literature supports not only the role of splanchnic vasodilation and systemic vasoconstriction bu

284 a calcium channel blocker (nifedipine), and splanchnic vasodilators (nitroglycerine, calcitonin gene

285 rd and colleagues report on the relevance of splanchnic vein thrombosis (SVT) as a marker of occult m

286 Antithrombotic treatment of splanchnic vein thrombosis (SVT) is a clinical challenge

287 JAK2V617F screening in splanchnic vein thrombosis (SVT) patients without typica

288 on and may experience recurrence in both the splanchnic veins and other vein segments.

289 Abdominal congestion (i.e., splanchnic venous and interstitial congestion) manifests

290 It is unknown if splanchnic venous thrombosis (SVT) is a marker of occult

291 varies with vessel bed (alpha(1a) higher in splanchnic versus central arteries, P<0.05); competition

292 Levels of ACE2 and MasR were increased in splanchnic vessels from cirrhotic patients and rats comp

293 otensin system messenger RNA and proteins in splanchnic vessels from patients and rats with cirrhosis

294 nchnic vascular hypocontractility in ex vivo splanchnic vessels from rats with cirrhosis (but not con

295 In the splanchnic vessels of patients and rats with cirrhosis,

296 We conclude that the splanchnic viscera can contribute to liver ischemic repe

297 Activation of abdominal splanchnic visceral afferents during mesenteric ischaemi

298 sized that IL-1beta stimulates or sensitizes splanchnic visceral afferents to ischaemia and to the ac

299 ) is expressed in the septum transversum and splanchnic (visceral) mesoderm and is required for prope

300 Splanchnic volume was decreased in the S+ and S- groups,