ライフサイエンスコーパス: tyramine

1 ditions, the most concentrated BA was always tyramine.

2 makes it a promising tool for quantifying of tyramine.

3 process is not facilitated by the substrate tyramine.

4 m the electrooxidation and polymerization of tyramine.

5 es and ratiometric response was obtained for tyramine.

6 nylalanine to phenethylamine and tyrosine to tyramine.

7 rine DHPG/NE ratio and the pressor effect of tyramine.

8 e were achieved with these concentrations of tyramine.

9 phenylethylamine, benzylamine, dopamine, and tyramine.

10 arboxylase (TDC), which converts tyrosine to tyramine.

11 s the plant PPO's acceptance or rejection of tyramine.

12 be reduced and legal limits established for tyramine.

13 anisation specifically through the action of tyramine.

14 sed to 47% with increasing concentrations of tyramine (0.129 to 25.8 mmol/L; P<0.001).

15 along with two natural monomers N-E-caffeoyl tyramine (1) and N-E-feruloyl tyramine (2), using centri

16 ne concentration after the administration of tyramine (12 vs. 56+/-63 pg per milliliter [0.07 vs. 0.3

17 in which the intermediate 4-[(18)F]fluoro-m-tyramine ([(18)F]16) was prepared using a diaryliodonium

18 s N-E-caffeoyl tyramine (1) and N-E-feruloyl tyramine (2), using centrifugal partition chromatography

19 percentage reductions in FVC in response to tyramine (-24 +/- 7 vs. -55 +/- 6 %), phenylephrine (-12

20 young men, the vasoconstrictor responses to tyramine (-25 +/- 1 versus -56 +/- 6%), phenylephrine (-

21 did not significantly blunt the response to tyramine (-30 +/- 2 versus -36 +/- 7%; P = 0.4) or pheny

22 Maximal vasoconstrictor responses to tyramine (-30 +/- 3 versus -41 +/- 3%), phenylephrine (-

23 Tyramine (4-hydroxyphenethylamine), which is a monoamine

24 r compared with young men in the presence of tyramine (-6 +/- 7 versus -31 +/- 6%), phenylephrine (-3

25 differentially blunt the pressor response to tyramine, a marker for NE uptake.

26 mpact courtship drive and were controlled by tyramine-a biogenic amine related to dopamine, whose rol

27 How tyramine acts on neuronal, cellular and circuit levels i

28 atients supine and standing before and after tyramine administration.

29 artery for intra-arterial administration of tyramine, an agent which displaces noradrenaline from th

30 ulation, we infused graded concentrations of tyramine, an indirect presynaptic norepinephrine release

31 -trans-feruloyl tyramine, and N-cis-feruloyl tyramine, an unreported N-feruloyl tyramine dimer was ch

32 In bovine adrenal chromaffin vesicles, tyramine and (-)erythro-hydroxyephedrine have apparent p

33 rong inducers of bfeA transcription, whereas tyramine and 3,4-dihydroxymandelic acid demonstrated low

34 Use of leaves of some species with prunasin, tyramine and beta-p-arbutin, may be limited in food appl

35 rations of bark lignans, coumarins, proline, tyramine and defensive proteins, and was characterized b

36 oriented approximately perpendicular to the tyramine and directed toward the extracellular surface.

37 used as a carbon and nitrogen source, while tyramine and dopamine can be used only as sources of nit

38 amine (PEA) and its hydroxylated derivatives tyramine and dopamine.

39 Tyramine and histamine are the biogenic amines (BA) most

40 Extremely high tyramine and histamine contents, 1700 and 700 mg/kg, res

41 The synergistic cytotoxicity of tyramine and histamine should be taken into account when

42 Co-treatment with tyramine and histamine was associated with a stronger cy

43 of dietary BA, the in vitro cytotoxicity of tyramine and histamine was investigated.

44 erivatization with benzoyl chloride, whereas tyramine and histamine were analysed by fluorescence det

45 Tyramine and histamine were toxic for HT29 intestinal ce

46 logically active biogenic amines, especially tyramine and histamine, in fermented beverages.

47 Tyramine and histamine, the most toxic biogenic amines (

48 When used to analyze transport of tyramine and hydroxyephedrine by the vesicular amine tra

49 To further clarify the roles of tyramine and its metabolite octopamine, we have cloned t

50 Results showed that N-E-feruloyl tyramine and N-E-caffeoyl tyramine exhibited the highest

51 We conclude that tyramine and octopamine act as neurotransmitters/modulat

52 Flies with a mutation in dTdc2 lack neural tyramine and octopamine and are female sterile due to eg

53 Tyramine and octopamine released from neurons expressing

54 ions (CFSs) of lactic acid bacteria (LAB) on tyramine and other biogenic amine production by differen

55 tyrosine and phenylalanine were converted to tyramine and phenethylamine by tyrosine and phenylalanin

56 The reproducibility of delta15N of tyramine and phenethylamine measured by GCC-IRMS average

57 opposite trend was observed, with histamine, tyramine and putrescine being the most abundant in Pigno

58 ere was prevalence of cadaverine followed by tyramine and putrescine; and total amine levels were low

59 re-activity analyses of APP derivatives with tyramine and the neurotoxin 1-methyl-4-phenylpyridinium

60 ctivities elicited by trace amines such as p-tyramine and the psychostimulant amphetamines are manife

61 Dietary amines such as tyramine and tryptamine also inhibited G34 cleavage.

62 Tyramine and tryptamine were found in cheese from high S

63 l SCC categories contained spermine; whereas tyramine and tryptamine were only detected in cheese fro

64 thylamine, putrescine, spermine, spermidine, tyramine and tryptamine) in fish tissues.

65 cadaverine, spermidine, spermine, histamine, tyramine and tryptamine) were determined.

66 osine decarboxylase to convert tyrosine into tyramine and tyramine beta-hydroxylase to convert tyrami

67 Only two biogenic amines (tryptamine and tyramine) and two polyamines (spermidine and spermine) w

68 own serotonin, norepinephrine, dopamine, and tyramine, and because the lung is a major metabolic orga

69 Phenylethylamine, tyramine, and dopamine are oxidized by TynA to the corre

70 ng, resistance to the NE-releasing effect of tyramine, and increased sensitivity to adrenergic agonis

71 e outward transport or external binding of m-tyramine, and it was prevented by cocaine.

72 ic acid, rutin, scopoletin, N-trans-feruloyl tyramine, and N-cis-feruloyl tyramine, an unreported N-f

73 ve and dietary monoamines such as serotonin, tyramine, and phenylethylamine.

74 mine, naTA, N-acetylserotonin, OA, dopamine, tyramine, and serotonin also have been consistently iden

75 ding L-3,4-dihydroxyphenylalanine, dopamine, tyramine, and serotonin were identified and their relati

76 We conclude that TyrR is a receptor for tyramine, and suggest that it serves to curb high levels

77 noreactive with antisera against octopamine, tyramine, and the enzymes required for their synthesis,

78 yramine, combined the patterns seen with the tyramine- and octopamine antisera.

79 nity to tyramine releasing sites, a specific tyramine antibody was applied.

80 fandel red wines revealed that histamine and tyramine are produced during yeast and malolactic fermen

81 t of the mammalian DATs in that dopamine and tyramine are the preferred substrates, whereas octopamin

82 Our findings establish tyramine as a neurotransmitter in C. elegans, and we sug

83 sized a series of (p-O-sulfamoyl)-N-alkanoyl tyramines as nonsteroidal estrone sulfatase inhibitors.

84 e legal limit, increases the cytotoxicity of tyramine at concentrations frequently reached in some fo

85 t from one isolate, S. thermophilus produced tyramine at low (47 isolates) and medium (10 isolates) l

86 rovides direct evidence that octopamine- and tyramine-based neuromodulation can be mediated by astroc

87 opic correlations that demonstrated feruloyl tyramines being incorporated into the lignin biopolymers

88 We found that levels of tyramine beta-hydroxylase (TbetaH), an essential enzyme

89 synthesis, tyrosine decarboxylase (TDC) and tyramine beta-hydroxylase (TBH).

90 ns tyrosine decarboxylase gene, tdc-1, and a tyramine beta-hydroxylase gene, tbh-1.

91 xylase to convert tyrosine into tyramine and tyramine beta-hydroxylase to convert tyramine into octop

92 Tyramine beta-monooxygenase (TbetaM) belongs to a family

93 The enzyme tyramine beta-monooxygenase (TbetaM) belongs to a small

94 Tyramine beta-monooxygenase (TbetaM) catalyzes the synth

95 Tyramine beta-monooxygenase (TbetaM), the insect homolog

96 idue, Met471, coordinating the Cu(M) site of tyramine beta-monooxygenase (TbetaM).

97 n of cAMP when exposed to the trace amines p-tyramine, beta-phenethylamine, tryptamine, and octopamin

98 Tyramine, beta-phenylethylamine, tryptamine, and octopam

99 with the closely related invertebrate enzyme tyramine-beta-hydroxylase, which converts tyramine to OA

100 pine-induced increase in egg laying requires tyramine biosynthesis.

101 Therefore, tyramine can act as a classical inhibitory neurotransmit

102 This has led to a model in which tyramine can bind to either the Cu(I) or Cu(II) forms of

103 Tyramine can bind to two characterized receptors in hone

104 Owing to its chemical properties, tyramine can react with nitrite, a common food additive,

105 eir mode of action was also different, while tyramine caused cell necrosis, histamine induced apoptos

106 conformation) with either Na(125)I or (125)I-tyramine cellobiose, also known as the cell-trapping lig

107 Injection of (125)I-tyramine-cellobiose-HDL demonstrated significantly great

108 g for TDC, the enzyme converting tyrosine to tyramine, combined the patterns seen with the tyramine-

109 synthesis of antimicrobial hydroxycinnamoyl-tyramine conjugates, and prevention of the hypersensitiv

110 increased synthesis of the hydroxycinnamoyl-tyramine conjugates, feruloyl-tyramine (FT) and coumaroy

111 will not cause a rise in blood pressure when tyramine-containing foods are ingested.

112 samples ranged from 3.3 to 30 mg/L, and the tyramine content ranged from 1.0 to 3.0 mg/L.

113 Increased cadaverine and tyramine contents were found in samples with good sensor

114 Activation of LGC-55 by tyramine coordinates the output of two distinct motor pr

115 ugates, feruloyl-tyramine (FT) and coumaroyl-tyramine (CT).

116 previously reported to incorporate feruloyl tyramine derivatives.

117 Tyramine detection was linearly proportional in response

118 ontrast, two substrates of DAT, dopamine and tyramine, did not significantly impact cross-linking.

119 The pressor response to tyramine differentially distinguished maprotiline from s

120 -feruloyl tyramine, an unreported N-feruloyl tyramine dimer was characterized as the most abundant po

121 se inhibitor (p-O-sulfamoyl)-N-tetradecanoyl tyramine (DU-14) could reverse scopolamine induced amnes

122 that the vasoconstrictor responses evoked by tyramine during exercise or adenosine were repeatable in

123 ith their sum were putrescine, histamine and tyramine, even if reached levels were below toxicity thr

124 The low and high doses of tyramine evoked significant reductions in FVC (vasoconst

125 to brachial artery infusions of two doses of tyramine (evokes endogenous noradrenaline release) in 10

126 FVC responses to intra-arterial tyramine (evokes endogenous noradrenaline release), phen

127 es to local intrafemoral artery infusions of tyramine (evokes noradrenaline (NA) release), phenylephr

128 that N-E-feruloyl tyramine and N-E-caffeoyl tyramine exhibited the highest DPPH scavenging activity

129 at the lower end of NET inhibition, whereas tyramine exhibits a linear relation, with NET inhibition

130 Tyramine ferulate is a sink for the anticipated build-up

131 ohol-derived units and significant levels of tyramine ferulate.

132 ntained four amines; there was prevalence of tyramine followed by histamine, phenylethylamine and put

133 f 350 nM for (p-O-sulfamoyl)-N-tetradecanoyl tyramine for the inhibition of MDA-MB-231 estrone sulfat

134 te the utility of (p-O-sulfamoyl)-N-alkanoyl tyramines for the inhibition of breast cancer cell estro

135 droxycinnamoyl-tyramine conjugates, feruloyl-tyramine (FT) and coumaroyl-tyramine (CT).

136 The inhibitory tyramine-gated chloride channel, LGC-55, induces head re

137 rward locomotion through the activation of a tyramine-gated chloride channel, LGC-55.

138 f LGC-55 in C. elegans, the first identified tyramine-gated chloride channel.

139 o inhibit egg laying, in part via the LGC-55 tyramine-gated Cl(-) channel on the HSNs.

140 Surprisingly, tyramine had a stronger and more rapid cytotoxic effect

141 ontribute to a model in which octopamine and tyramine have distinct and separable neural activities.

142 The two biogenic amines octopamine and tyramine have recently been shown to modulate various pa

143 tants, with altered levels of octopamine and tyramine, have a locomotion deficit.

144 hand, the bacterial-related biogenic amines, tyramine, histamine, tryptamine and beta-phenylethylamin

145 Octopamine- and tyramine immunostaining in the central complex differed

146 In each brain hemisphere tyramine immunostaining was found in four neurons innerv

147 These results indicate an essential role for tyramine in cocaine sensitization in Drosophila.

148 not restore the vasoconstrictor responses to tyramine in contracting muscle during heavy rhythmic han

149 HILIC-UPLC-MS approach was elevated urinary tyramine in galN-treated rats, reflecting disturbed amin

150 our technique was demonstrated by analyzing tyramine in spiked serum and milk.

151 flies had reduced amounts of the trace amine tyramine in the brain because of reduced activity of the

152 The amount of tyramine in the cheeses with the addition of the strain

153 en various potential roles of octopamine and tyramine in the larval brain, such as locomotion, learni

154 nses to endogenous noradrenaline release via tyramine in the skeletal muscle circulation, similar to

155 s, particularly of cadaverine, histamine and tyramine, in low-salt products.

156 a representative of a family of hydrophobic tyramines, in addition to being a potent bactericidal Gr

157 m-Tyramine increased the rate of reaction of (2-aminoethyl

158 This m-tyramine-induced increase in reactivity appeared to requ

159 In both protocols, the tyramine-induced increases in deep venous noradrenaline

160 However, tyramine-induced mobilization of norepinephrine stores p

161 Endotoxemia lessened the tyramine-induced reduction in leg vascular conductance (

162 emia + hypoxia (-17% +/- 21%) attenuated the tyramine-induced reduction in leg vascular conductance c

163 al BH(4) supplementation augments reflex and tyramine-induced VC in aged skin, suggesting that reduce

164 O: -17 +/- 2% DeltaCVC(base); P < 0.001) and tyramine infusion (Y: - 33 +/- 4% DeltaCVC(base), O: -15

165 er: 17 +/- 3% Delta CVC(base); P < 0.01) and tyramine infusion (young: 41 +/- 3, older: 21 +/- 4% Del

166 in temperature (T(sk)) = 30.5 degrees C) and tyramine infusion, respectively.

167 conductance) was evaluated by femoral artery tyramine infusion.

168 Here, we show that tyramine inhibits head movements and forward locomotion

169 s determined by heart rate (HR) change after tyramine injection into the artery that perfused the sin

170 ine and tyramine beta-hydroxylase to convert tyramine into octopamine.

171 Tyramine is a biogenic compound derived from the decarbo

172 ansmitter in C. elegans, and we suggest that tyramine is a genuine neurotransmitter in other inverteb

173 Tyramine is an important neurotransmitter, neuromodulato

174 been reported; therefore, the measurement of tyramine is an urgent concern.

175 stomach lumen, the most favoured reaction in tyramine is C-nitrosation, which generates mutagenic pro

176 e shown that the product of C-nitrosation of tyramine is mutagenic, in the present article tyramine n

177 The trace biogenic amine tyramine is present in the nervous systems of animals ra

178 PSS/AuNP/1-m-4-MP) for the quantification of tyramine is presented.

179 The trace amine para-tyramine is structurally and functionally related to the

180 Tyramine is synthesized from tyrosine by the enzyme tyro

181 u(II) form of TbetaM is also reduced at high tyramine, leading us to propose the existence of a bindi

182 using mutants having altered octopamine and tyramine levels and by genetic interference with both sy

183 Moreover, tyramine-like immunoreactivity was also found in brain r

184 Tyramine-like labeling was observed in AmTAR1-IR positiv

185 nd urocortins, together with the trace amine tyramine, may have a role in the human cardiovascular sy

186 describe the use of MIP-1 alpha in a biotin tyramine-mediated proximity selection to guide the selec

187 atial arrangement in the receptors, with the tyramine moiety of alkaloids or Tyr1 of opioid peptides

188 However, instead of the tyramine moiety that is present in methanofuran cofactor

189 residues in the bottom of the pocket and the tyramine N+ and OH groups forming ionic interactions or

190 After tyramine, NE spillover did not change significantly in p

191 n of Fru(M) by transformer expression in OCT/tyramine neurons changes the aggression versus courtship

192 The regulation of this tyramine neurotransmitter was found to be linked to pati

193 yramine is mutagenic, in the present article tyramine nitrosation mechanisms have been characterized

194 structurally similar to the bVMAT substrate tyramine, none of them were measurably transported into

195 enzyme capable of synthesizing morphine from tyramine, norlaudanosoline, and codeine.

196 Furthermore, tyramine normalized the doubled leg vascular conductance

197 dopamine transport activity; norepinephrine, tyramine, octopamine, and histamine also have high affin

198 Application of tyramine or octopamine to live preparations silenced dop

199 There was no evidence for feruloyl tyramines, or homologues thereof, accumulating as a chem

200 s could be rescued by feeding the flies with tyramine; other biogenic amines or amine precursors did

201 roup were structural features that increased tyramine oxidase inhibition.

202 Characterization of tyramine oxidase, carried out prior to the inhibition ex

203 induces transcription of genes encoding the tyramine oxidase, TynA, and the aromatic aldehyde dehydr

204 sayed using commercially available microbial tyramine oxidase.

205 und to be a weak noncompetitive inhibitor of tyramine oxidase.

206 ethyl ester in dry THF with phenethylamine, tyramine, p-methoxyphenethylamine, 2-(p-tolyl)ethylamine

207 d metabolites, such as tyrosine, tryptamine, tyramine, phenethylamine, dopamine, 3-methoxytyramine, s

208 was impaired using iontophoretic delivery of tyramine, phentolamine, and bretylium followed by a nore

209 cadaverine, spermine, spermidine), aromatic (tyramine, phenylethylamine) or heterocyclic (histamine,

210 spermine, spermidine, putrescine, histamine, tyramine, phenylethylamine, cadaverine and serotonin) we

211 onitoring of six biogenic amines (histamine, tyramine, phenylethylamine, tryptamine, putrescine, and

212 We show that tyramine plays a specific role in the inhibition of egg

213 The binding of heparin-tyramine polymer (HT) onto the polycarprolactone (PCL) s

214 Phenethylamine and tyramine prepared from a mixture of 18 amino acids were

215 Locally infused tyramine produced dose-dependent pressor responses, pred

216 50% CFS of P. acidophilus was the highest on tyramine production (55%) by Listeria monocytogenes, fol

217 Tyramine production by Escherichia coli was also inhibit

218 50% CFS of Pediococcus acidophilus inhibited tyramine production up to 98% by Salmonella paratyphi A.

219 Significant amounts of tyramine, putrescine, and cadaverine occurred especially

220 Of the BA examined, tyramine, putrescine, histamine and cadaverine showed hi

221 late Ca(2+) increases through the octopamine/tyramine receptor (Oct-TyrR) and the transient receptor

222 o serotonin receptors (ser-1 and ser-4), one tyramine receptor (ser-2), and two dopamine receptors (d

223 traction-response, whereas in solitary ones, tyramine receptor (TAR) signaling mediated repulsion-res

224 ccurring non-coding polymorphisms in tyra-3 (tyramine receptor 3), which encodes a G-protein-coupled

225 stigated the spatial brain expression of the tyramine receptor AmTAR1 using a specific antibody.

226 ramine, which indicates that this ionotropic tyramine receptor functions in tyramine signaling in viv

227 terns of different splice forms of the ser-2 tyramine receptor locus.

228 We show that the tyramine receptor SER-2 acts through a Galphao pathway t

229 tly, we analyze a mutant allele of the ser-2 tyramine receptor, a target of the ttx-3 Lhx gene in the

230 dopamine receptor, LGC-55 is a high-affinity tyramine receptor, and LGC-40 is a low-affinity serotoni

231 aviors, we have cloned a putative octopamine/tyramine receptor.

232 obe and in the gnathal ganglion suggest that tyramine receptors are involved in modulating gustatory

233 pressing brain structures are in vicinity to tyramine releasing sites, a specific tyramine antibody w

234 The dose of intravenous tyramine required to raise systolic blood pressure by 30

235 1 and TYRA-3, for NPY-like neuropeptides and tyramine respectively, do not appear to be involved in o

236 1) and female sex (P=0.02) predicted blunted tyramine responses.

237 The patients followed a tyramine-restricted diet during the medication trial and

238 al-time cell analysis, whether histamine and tyramine show synergistic toxicity towards intestinal ce

239 Finally, the N-E-caffeoyl tyramine showed the highest reducing power (EC50=26mug/m

240 Putrescine, cadaverine and tyramine showed very good correspondence with the irradi

241 Putrescine, cadaverine and tyramine showed very good correspondence with the level

242 is ionotropic tyramine receptor functions in tyramine signaling in vivo.

243 isolation, the activities of octopamine and tyramine signalings were respectively correlated with at

244 droxylation was observed for the reaction of tyramine solely with Met471Cys TbetaM.

245 We knocked out a tyramine-specific receptor, TyrR, which was expressed in

246 obes, antennal lobes), indicating that other tyramine-specific receptors may be expressed there.

247 trescine, cadaverine, histamine, serotonine, tyramine, spermidine and spermine), as well as microbiol

248 Here, we report that the biogenic amines tyramine (TA) and octopamine (OA) in Drosophila melanoga

249 In Caenorhabditis elegans, tyramine (TA) and octopamine (OA) inhibit aversive respo

250 The biogenic amine tyramine (TA) regulates many aspects of invertebrate phy

251 s ample evidence linking octopamine (OA) and tyramine (TA) to several neurophysiological functions in

252 opamine (OA), L-3, 4-dihydroxyphenylalanine, tyramine (TA), and serotonin as well as metabolites 5-hy

253 e interactions, we have defined the roles of tyramine (TA), octopamine, and neuropeptides in the inhi

254 nvertebrate-specific octopamine-OARalpha and tyramine-TAR signalings respectively mediate attractive

255 Tyramine temporally coordinates the different phases of

256 in and liver MAO A and then followed by oral tyramine than was found on administration of tyramine to

257 t common tyrosinase substrates (tyrosine and tyramine), the enzyme is classified as a catechol oxidas

258 In the case of tyramine, the product release from the oxidized enzyme-i

259 red to FD (from 1mgkg(-1) for putrescine and tyramine to 4mgkg(-1) for histamine); MS/MS method showe

260 tyramine than was found on administration of tyramine to controls.

261 assage of eggs through the vulva and release tyramine to inhibit egg laying, in part via the LGC-55 t

262 me tyramine-beta-hydroxylase, which converts tyramine to OA, suggesting that the OA-ir cells are inde

263 mmunostaining for TBH, the enzyme converting tyramine to octopamine, in contrast, was strikingly simi

264 yme that catalyzes the beta-hydroxylation of tyramine to yield octopamine.

265 reagent for the derivatization of histamine, tyramine, tryptamine and 2-phenylethylamine, which elimi

266 cadaverine, spermidine, spermine, histamine, tyramine, tryptamine and phenylethylamine) were determin

267 cadaverine, spermidine, spermine, histamine, tyramine, tryptamine and phenylethylamine) were determin

268 wine samples analysed had histamine (HIM) or Tyramine (TYM) levels above the limits considered as a p

269 vascular responses to noradrenaline (NA) and tyramine (TYR) are related to SNA such that individuals

270 BAs concentrations increased with time, tyramine (TYR), putrescine (PUT) and cadaverine (CAD) we

271 Cross-linking of DAT did not affect tyramine uptake.

272 ablished that the major product, MftA*, is a tyramine-valine-cross-linked peptide formed by MftC thro

273 AIY memory retrieval neurons sense tyramine via the SER-2 receptor, which is essential for

274 on in FBF in response to the highest dose of tyramine was blunted in older men compared with young me

275 osation of ethylbenzene, phenethylamine, and tyramine was carried out, using UV-visible absorption sp

276 Tyramine was found mainly in red wines at <1-3.4 mg/L, w

277 vasoconstriction caused by administration of tyramine was inversely related to workload.

278 Tyramine was isolated selectively and pre-concentrated b

279 was not influenced by ageing conditions, and tyramine was only detected in some samples after 43days

280 Overall, tyramine was the prevalent amine, followed by putrescine

281 polamine, scopoline, tropine, tropinone, and tyramine, was accomplished by comparison of the in-sourc

282 take and the pressor response to intravenous tyramine were assessed following the initial dose and af

283 asoconstrictor responses to the high dose of tyramine were determined in eight young adults during no

284 genous noradrenaline release (intra-arterial tyramine) were significantly blunted during moderate exe

285 sponses to local intra-arterial infusions of tyramine (which evokes endogenous NE release), phenyleph

286 C) responses to brachial artery infusions of tyramine (which evokes endogenous noradrenaline release)

287 he simulation analysis of phenethylamine and tyramine, which are major monoamine constituents of toba

288 (whole-body cooling) and pharmacologically (tyramine, which displaces noradrenaline from axon termin

289 ues range from 5 to 10 with the exception of tyramine, which exhibited smaller steady-state isotope e

290 enylacetic acid (DOPAC), methyldopamine, and tyramine, which gave negligible signals under conditions

291 ctive in a behavior that requires endogenous tyramine, which indicates that this ionotropic tyramine

292 m biogenic amines, especially histamine, and tyramine, which is an important consideration when selec

293 RIM synthesizes the neuromodulator tyramine, which is required in the L1 stage for learning

294 is associated with a large dietary intake of tyramine while taking MAO inhibitors has been reported;

295 increases in the tyrosine-derived metabolite tyramine, whose exogenous application elicits cell death

296 bly bound to this enzyme and displaceable by tyramine, will be an antidepressant which will not cause

297 In addition to this, co-injection of tyramine with DOPA, the precursor of melanin, had a stro

298 O: -34 +/- 2% DeltaCVC(base); P < 0.001) and tyramine (Y: -38 +/- 4% DeltaCVC(base), O: -35 +/- 3% De

299 ion (cold, young: 38 +/- 4, older: 31 +/- 3; tyramine, young: 36 +/- 3, older: 36 +/- 5 Delta %CVC(ba

300 ine (cold, young: 37 +/- 4, older: 34 +/- 4; tyramine, young: 40 +/- 4, older: 45 +/- 4% Delta CVC(ba

301 (4) (cold, young: 37 +/- 3, older: 36 +/- 3; tyramine, young: 41 +/- 2, older: 36 +/- 3% Delta CVC(ba