ライフサイエンスコーパス: splanchnic

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

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

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

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

5 tracer enrichments from which whole-body and splanchnic amino acid and protein kinetics were calculat

6 absorption, whole-body protein turnover, and splanchnic amino acid metabolism.

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

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

9 4 signaling molecule is expressed in ventral splanchnic and branchial-arch mesoderm and outflow-tract

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

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

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

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

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

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

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

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

18 rculatory complications (including systemic, splanchnic and pulmonary complications), which can event

19 of leptin with respect to increasing lumbar, splanchnic and renal SNA, as well as baroreflex control

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

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

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

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

24 Vasodilatation (splanchnic and systemic) and hyperdynamic circulation ar

25 Vasodilatation (splanchnic and systemic) and the hyperdynamic circulatio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 The splanchnic bed produces cortisol at rates approximating

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 rotein dynamics or leucine transamination in splanchnic bed.

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

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

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

53 rge volume of distribution in the prehepatic splanchnic bed.

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

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

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

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

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

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

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

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

62 Heart failure is associated with splanchnic circulation congestion, leading to bowel wall

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 nvasive approach to follow the status of the splanchnic circulation.

66 aim was to explore the possible link between splanchnic circulatory changes and exhaled CH4 in an att

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

68 .9 +/- 0.4 microg/min) and accounted for all splanchnic cortisol and D3 cortisol production.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 The median splanchnic extraction fraction of hourly dietary Phe int

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

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

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

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

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

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

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

96 Leg and splanchnic glucose metabolism were assessed using a comb

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 keletal muscle and consequent restriction of splanchnic glutamine supply.

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

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

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

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

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

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

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

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

136 Splanchnic insulin extraction, directly measured using t

137 /- 15% (P < 0.05) increase of peripheral and splanchnic interstitial distribution volumes for [(14)C]

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

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

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

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

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

143 We show that downstream of Gli the Foxf1+ splanchnic mesenchyme promotes medial constriction of th

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 definitive endoderm (DE) and the surrounding splanchnic mesoderm (SM).

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

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

150 We show that SHF population in the mouse splanchnic mesoderm (SpM-SHF) undergoes polarized morpho

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

170 elium and mesenchymal cells derived from the splanchnic mesoderm.

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

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

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

174 ermal epithelium and mesenchyme derived from 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 mpathetic nervous system through the greater splanchnic nerve (GSN), and elevation of pro-inflammator

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

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

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

183 res by increasing venous capacitance through splanchnic nerve modulation.

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

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

197 reased the efferent discharge in the greater splanchnic nerve.

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

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

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

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

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

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

204 ment strategy was guided by clinical status, splanchnic organ functions, anatomy of residual gut, and

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

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

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

208 d lactate concentration gradients across the splanchnic organs.

209 increasing the gut oxygen consumption beyond splanchnic oxygen delivery.

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

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

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

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

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

215 tor is multifaceted and may adversely affect splanchnic perfusion.

216 Improved splanchnic/peripheral glucose uptake and enhanced suppre

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

218 Thus, splanchnic production of cortisol occurs in nondiabetic

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

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

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

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

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

224 es and then consider regional changes in the splanchnic, renal, cerebral, and uterine circulations in

225 PJ34 significantly protected against splanchnic reperfusion-induced intestinal hyperpermeabil

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

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

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

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

230 ch exhibited increases in lumbar SNA (LSNA), splanchnic SNA and heart rate (HR) compared to non-pregn

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

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

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

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

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

236 Splanchnic spillover was higher than nonsplanchnic syste

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

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

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

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

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

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

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

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

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

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

247 Leg and splanchnic tissues contributed a greater portion of syst

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

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

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

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

252 ly occurs at unusual sites such as cerebral, splanchnic, upper-extremity, renal, ovarian, or retinal

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

254 Splanchnic uptake of glucose precursors could account fo

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

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

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

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

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

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

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

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

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

264 Splanchnic vascular hypocontractility with subsequent in

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

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

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

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

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

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

271 Hemorrhage-induced splanchnic vasoconstriction causing pressure wave reflec

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

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

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

275 (1-7), which leads to activation of MasR and splanchnic vasodilatation in rats.

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

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

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

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

280 Splanchnic vasodilatators improved hepatocyte engraftmen

281 Subsequently, increased inflow from splanchnic vasodilation and increased cardiac output lea

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

283 ammation, vasoconstriction, and extrahepatic splanchnic vasodilation.

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 rotizing pancreatitis and is associated with splanchnic vein thrombosis and pancreatic head necrosis.

289 Risk factors for stricture development were splanchnic vein thrombosis and pancreatic head parenchym

290 stroke, major adverse cardiovascular events, splanchnic vein thrombosis, and bleeding in a cohort wit

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

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

293 hy malformation is a rare condition in which splanchnic venous blood bypasses the liver draining dire

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

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

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

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

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

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,