ライフサイエンスコーパス: biogenic amine

1 cument the potent antioxidant action of this biogenic amine.

2 amine, but not to acetylcholine or any other biogenic amine.

3 hest concentrations of the amino acids and a biogenic amine.

4 dependence on the levels of several primary biogenic amines.

5 des, proteins, but also small molecules like biogenic amines.

6 en used extensively for the investigation of biogenic amines.

7 ecificity when urine samples are spiked with biogenic amines.

8 are modulated by multiple neuropeptides and biogenic amines.

9 e compound eye masks much of the signal from biogenic amines.

10 0-60 nM) whereas the C-terminal domain binds biogenic amines.

11 ve been used extensively for the analysis of biogenic amines.

12 es in cognitive states that are regulated by biogenic amines.

13 y has shown that fSR/BA is also modulated by biogenic amines.

14 e presence of many of the common interfering biogenic amines.

15 , each of them as interesting as traditional biogenic amines.

16 oxidases (MAO) A and B deaminate a number of biogenic amines.

17 siderable selectivity for dopamine and other biogenic amines.

18 serotonin, norepinephrine, dopamine or other biogenic amines.

19 which also have the capacity to concentrate biogenic amines.

20 increase and the formation of the undesired biogenic amines.

21 ors namely total volatile basic nitrogen and biogenic amines.

22 embled and used as a separation platform for biogenic amines.

23 outer mitochondrial membrane that metabolize biogenic amines.

24 from bobcat urine and identified it to be a biogenic amine, 2-phenylethylamine.

25 C method for simultaneously quantifying nine biogenic amines, 21 amino acids, and ammonium ions, in b

26 ant changes in plasma levels of amino acids, biogenic amines, acylcarnitines, and lipids.

27 ode of storage as well as granular uptake of biogenic amines affects the stoichiometry of their relea

28 eins regulate the clearance of extracellular biogenic amines after release and are important targets

29 tified metabolites, including sphingolipids, biogenic amines, amino acids and urea.

30 Various metabolites including biogenic amines, amino acids, lipids, were significantly

31 Biogenic amine amounts were higher in red than in white

32 thophysiology, we have begun to characterize biogenic amine and BH4 metabolism in the GTP cyclohydrol

33 During ripening, biogenic amine and free amino acid content, microbiologi

34 In contrast, all of the effects of the biogenic amine and peptide neurotransmitters, as well as

35 d agonist-induced internalization of several biogenic amine and peptide receptors.

36 nning confocal microscopy confirmed that the biogenic amine and the vital dye occurred in the same ce

37 orebrain to increased concentrations of this biogenic amine and to specific alterations of crucially

38 18 features from the homogenate profiles as biogenic amines and amino acids.

39 ltaneous quantification of 22 amino acids, 7 biogenic amines and ammonium ions in cheese samples in u

40 (MAO-A) is a key enzyme in the catabolism of biogenic amines and is expressed in brain noradrenergic

41 ue homogenizer has enabled the separation of biogenic amines and metabolites from these severely volu

42 Electrophoretic resolution of 14 biogenic amines and metabolites with similar mobilities

43 ession confers the linked abilities to store biogenic amines and modulate secretory vesicle pH over a

44 I then discuss the influence of several biogenic amines and neuropeptides on aggressive behavior

45 atalyzes the transfer of sulfonate groups to biogenic amines and other substrates, was foremost among

46 of larval Drosophila is modulated by various biogenic amines and peptides.

47 e compounds, such as phenolics, carotenoids, biogenic amines and phytosterols, which are highly desir

48 he optimal process parameters, regarding low biogenic amines and polyamines content, for "Futoski" ca

49 the total concentration of all the monitored biogenic amines and polyamines exceeded the level of 200

50 sed sensor was further tested with different biogenic amines and ratiometric response was obtained fo

51 of Glu146 in the selectivity of SULT1A3 for biogenic amines and suggest that this region is a key de

52 pacity; ii) high contents of spermine, total biogenic amines and total polyamines; and iii) the highe

53 In this study, the amino acid, biogenic amine, and trans- and cis-urocanic acid (UCA) c

54 ranged between 0.03mg/L and 0.63mg/L for the biogenic amines, and 0.05mg/L and 5.19mg/L for other com

55 pocalins that act as efficient scavengers of biogenic amines, and a similar function was postulated f

56 These ligands are peptides, lipids or biogenic amines, and act as transmitter molecules.

57 othesized, contributes to its preference for biogenic amines, and mutated two amino acids within this

58 The levels of biogenic amines, anthocyanins, polyphenols and antioxida

59 Biogenic amines are conserved signaling molecules that l

60 Biogenic amines are implicated in several mental disorde

61 Biogenic amines are important for neurotransmission and

62 Biogenic amines are important signaling molecules, and t

63 Proteins and biogenic amines are labeled with the fluorogenic reagent

64 Biogenic amines are typically regarded as neuromodulator

65 ic and oenological factors on the content of biogenic amines as quality index of sixty-five Abruzzo w

66 Principal component analysis using the biogenic amines as variables, allowed to separate the di

67 e amino acids, dipeptides, sugars, vitamins, biogenic amines, as well as different products of the AT

68 is study aimed to assess lipid oxidation and biogenic amine (BA) development in "muxama", a dry-cured

69 The qualitative and quantitative profile of biogenic amines (BA) in 50 samples of dry fermented saus

70 Tyramine and histamine are the biogenic amines (BA) most commonly found at high concent

71 Free amino acids (AA) and biogenic amines (BA) were quantified for the first time

72 Tyramine and histamine, the most toxic biogenic amines (BA), are often found in high concentrat

73 Biogenic amines (BAs) are biologically active molecules

74 for the extraction and determination of six biogenic amines (BAs) by NMR is presented.

75 The study evaluated the fatty acids and the biogenic amines (BAs) in 'Nduja of Spilinga stored in di

76 mph potentiates the effects generated by the biogenic amine betaPEA.

77 allowed us to identify critical residues for biogenic amine binding and to predict which members of t

78 if could be derived that was used to predict biogenic amine-binding function in other tick lipocalins

79 le evolutionary pathway for the evolution of biogenic amine-binding in tick lipocalins.

80 features of these proteins, a tick lipocalin biogenic amine-binding motif could be derived that was u

81 One such protein is a biogenic amine-binding protein (ABP) that binds serotoni

82 vary gland libraries led to the discovery of biogenic amine-binding proteins in soft (Ornithodoros) a

83 eeding nematocerous Diptera will function as biogenic amine-binding proteins.

84 are not required for steady-state levels of biogenic amines, but become rate limiting in conditions

85 gs link luminal conversion of amino acids to biogenic amines by gut microbes and probiotic-mediated s

86 This paper reports the determination of biogenic amines by high-performance liquid chromatograph

87 The detection and monitoring of biogenic amines by NMR, upon fish storage, is informatio

88 yser was developed for the analysis of eight biogenic amines (cadaverine, histamine, phenylethylamine

89 A further 33 biogenic amines can be monitored in samples for relative

90 a wide variety of organic cations including biogenic amines, cationic drugs, and neurotoxins.

91 otal volatile base nitrogen (TVBN), K-value, biogenic amines, color, and texture.

92 i-parameter approach: the trimethylamine and biogenic amines concentration changes were compared with

93 e principal mechanism by which extracellular biogenic amine concentrations are regulated.

94 Total biogenic amines content ranged from 88.86 to 796.68mgkg(

95 udy, a model to assess fish quality based on biogenic amine contents using fuzzy logic model (FLM) is

96 In addition, release of biogenic amines, cytokines, and leukotrienes was observe

97 , the intestinal concentrations of SCFAs and biogenic amines decreased with the dietary protein reduc

98 3-Iodothyronamine (T(1)AM) is a biogenic amine derivative of thyroid hormone present in

99 Transporters for the biogenic amines dopamine, norepinephrine, epinephrine an

100 DD2R-461, revealed that among the endogenous biogenic amines, dopamine is most potent at each recepto

101 segregation needed for advanced theories of biogenic amine dysfunction and pharmacogenetics.

102 endogenous sigma receptor ligands, including biogenic amines (e.g dopamine and serotonin), steroids (

103 E), lipids (e.g. arachidonic acid, PAF), and biogenic amines (e.g. ADP, serotonin, epinephrine, norep

104 asitic mother sporocyst depends on uptake of biogenic amines, e.g. serotonin, from the snail host.

105 activity or synaptic transmitter release by biogenic amines, e.g., octopamine, dopamine, or serotoni

106 ermophilus isolates have the ability to form biogenic amines, especially histamine, and tyramine, whi

107 r the determination of neurologically active biogenic amines, especially tyramine and histamine, in f

108 sicochemical and microbiological parameters, biogenic amines, fatty acids and texture profiles and se

109 bolites (208 in total) included amino acids, biogenic amines, fatty acids, bile acids, sugars, and li

110 les (e.g. prostanoids, leukotrienes, lipids, biogenic amines) followed by chromatography, mass spectr

111 ed from the retardation of microbial growth, biogenic amine formation and lipid oxidation during the

112 Twelve different biogenic amines formation in 58 isolates of Streptococcu

113 The release of biogenic amines from large dense core vesicles (LDCVs) d

114 h systemic symptoms due to hypersecretion of biogenic amines from metastatic lesions.

115 tanding the molecular pathways through which biogenic amines function in model organisms may improve

116 ed similar functional profiles for mammalian biogenic amine G protein-coupled receptor agonists and a

117 The ligand binding pocket of biogenic amine G protein-coupled receptors is embedded i

118 ocortical neurotransmitter systems utilizing biogenic amines, GABA, and glutamate.

119 zed TiO2 thin film was used to determine the biogenic amines generated by pork during storage.

120 ites, including acylcarnitines, amino acids, biogenic amines, glycerophospholipids, hexose, and sphin

121 e o2 loop in agonist-dependent activation of biogenic amine GPCRs has not been studied systematically

122 ve", while drugs targeting cytochrome P450s, biogenic amine GPCRs, and transporters have significantl

123 egree of structural homology found among all biogenic amine GPCRs, our findings should be of consider

124 Although various cellular responses of biogenic amines have been characterized in crustaceans,

125 Biogenic amines have been determined to be causal factor

126 The neuromodulatory transmitters, biogenic amines, have profound effects on multiple neuro

127 solely responsible for the production of the biogenic amine histamine.

128 e aim of the study was the monitoring of six biogenic amines (histamine, tyramine, phenylethylamine,

129 e chemiresistors in the detection of various biogenic amines (i.e. putrescine, cadaverine) and in the

130 s determination of 17 free amino acids and 8 biogenic amines in Alicante Monastrell wines was investi

131 ggests that the roles of classical and trace biogenic amines in all organisms may need to be reconsid

132 ol tool for routine quantitative analysis of biogenic amines in beverages for the average laboratory.

133 able HPLC method for the determination of 11 biogenic amines in beverages has been performed.

134 ied for determination of the above mentioned biogenic amines in beverages, and permitted an undemandi

135 to evaluate concentrations and evolution of biogenic amines in Canadian pork destined for the Japane

136 Biogenic amines in Canadian pork for the chilled export

137 as led to a new approach in the detection of biogenic amines in complex matrices.

138 nd underlying mechanisms mediated by various biogenic amines in Drosophila and other animals.

139 void the formation of high concentrations of biogenic amines in fermented food by bacteria, it is adv

140 e method was demonstrated by the analysis of biogenic amines in fish obtained from commercials of Val

141 chemical detection has been used to quantify biogenic amines in freeze-dried brains of Drosophila mel

142 s had an ability to produce twelve different biogenic amines in HDB and LDB.

143 chemical detection has been used to quantify biogenic amines in microdissected Drosophila melanogaste

144 vely quantify histamine in presence of other biogenic amines in real wine and fish matrices.

145 To understand the significance of biogenic amines in taste, we evaluated the ability of ta

146 These observations suggest a role of the biogenic amines in the initiation and modulation of moto

147 ctances is a general mechanism of action for biogenic amines in the modulation of C. elegans behavior

148 fast and accurate assay for the screening of biogenic amines in urine is required, without preclearan

149 The total content of biogenic amines in vinegars ranged from 23.35 to 1445.2

150 Biogenic amines in well defined subtypes of human tempor

151 re no significant differences in most of the biogenic amines including histamine, while there are sig

152 (MAO-B) is a key enzyme in the catabolism of biogenic amines, including dopamine, and alterations in

153 tral G cells can express VMAT1; transport of biogenic amines into secretory vesicles by VMAT1 is asso

154 understanding of the role of this important biogenic amine is better characterized.

155 nce one-shot biosensors for determination of biogenic amines is described and compared with high-perf

156 e (TH-GFP), for which the overall profile of biogenic amines is not found to be significantly differe

157 It appears that counteracting biogenic amines is of strong adaptive value in the conve

158 ing pocket of family A GPCRs that bind small biogenic amines is well characterized.

159 ted chloride channels that are receptors for biogenic amines: LGC-53 is a high-affinity dopamine rece

160 rotein-coupled receptors (GPCRs) targeted by biogenic amine ligands folds deeply into the transmembra

161 or core where the binding of cis-retinal and biogenic amine ligands is known to occur.

162 thought to sensitize central endothelium to biogenic amines like histamine, thereby leading to incre

163 ase of three important classes of mediators: biogenic amines, lipid mediators, and cytokines.

164 logues bound with muM affinity at off-target biogenic amine (M2, 5HT2A, beta3, 5HT2B, 5HT2C, and alph

165 witching in C. elegans and its dependence on biogenic amines may provide insight into how gait transi

166 resents a previously unrecognized pathway of biogenic amine metabolism.

167 Biogenic amines modulate key behaviors in both vertebrat

168 The biogenic amine The biogenic amine N1-acetyl-N2-formyl-5-methoxykynuramine (

169 Neuromodulators, including biogenic amines, neuropeptides, and hormones, are releas

170 A candidate gene screen of biogenic amine neurotransmitter systems identified signa

171 ptophan transporter related to the family of biogenic amine neurotransmitter transporters was functio

172 transporters are responsible for removal of biogenic amine neurotransmitters after release into the

173 Following vesicular release, the biogenic amine neurotransmitters dopamine, norepinephrin

174 d RNAi assays indicate that males likely use biogenic amine neurotransmitters through the nervous sys

175 tionally related to the amphetamines and the biogenic amine neurotransmitters.

176 ate, malonate, methylmalonate, and maleate), biogenic amines, nucleotide derivatives, phenols, and sp

177 However, biogenic amines observed in the other soybean products s

178 In fermented dairy products, the tested biogenic amines occurred in relatively low amounts (gene

179 The biogenic amine octopamine did not elicit pheromone produ

180 The role of the biogenic amine octopamine in modulating cholinergic syna

181 nt of male fly aggression has shown that the biogenic amine octopamine plays a role in the modulation

182 The biogenic amine octopamine regulates critical physiologic

183 ndent in that focal axon modulation with the biogenic amine octopamine, abolished signal integration

184 ogaster females before and after mating: the biogenic amine octopamine, which regulates ovulation rat

185 The two biogenic amines octopamine and tyramine have recently be

186 Here we show that a Drosophila biogenic amine, octopamine, is a potent wake-promoting s

187 ylamine (beta-PEA) and taurine are important biogenic amines of the sympathetic and parasympathetic n

188 Biogenic amines on fish tissue are formed as a result of

189 ed by feeding the flies with tyramine; other biogenic amines or amine precursors did not have the sam

190 analysis, such as concentration of glycerol, biogenic amines, organic acids, and aroma compounds were

191 binders of prohemostatic and proinflammatory biogenic amines, particularly serotonin, catecholamines,

192 ecules that modulate migration include small biogenic amines, peptide growth factors, cytokines, extr

193 d receptors (GPCRs), including receptors for biogenic amines, peptides, a nucleoside, and a sphingoli

194 tion of extrasynaptic concentrations of many biogenic amines, permitting direct access to many of the

195 idating the critical role that electroactive biogenic amines play in complex physiological processes

196 amidated gastrin G34 to G17 was inhibited by biogenic amine precursors (L-DOPA and 5-hydroxytryptopha

197 sis of metabolites in conjunction with their biogenic amine precursors in a single separation offers

198 tion of several metabolites along with their biogenic amine precursors in biological samples, specifi

199 ylethylamine, tryptamine, and octopamine are biogenic amines present in trace levels in mammalian ner

200 The amount of each specific biogenic amine produced by S. thermophilus was generally

201 ent in both samples with the addition of the biogenic amine producing strain almost evened out and th

202 ic acid bacteria (LAB) on tyramine and other biogenic amine production by different food borne-pathog

203 The aim of this study was to compare the biogenic amine production of two starter strains of Lact

204 e afferent nerves leading to itch, including biogenic amines, proteases, cytokines, and peptides.

205 cts storage: formation of trimethylamine and biogenic amines, proteolysis and different types of ferm

206 The content of eight biogenic amines (putrescine, cadaverine, spermidine, spe

207 The content of eight biogenic amines (putrescine, cadaverine, spermidine, spe

208 The content of seven biogenic amines (putrescine, cadaverine, spermidine, spe

209 of the previous studies have involved three biogenic amines: putrescine (Put), spermidine (Spd) and

210 e receptors (e.g., thyrotropin receptor) and biogenic amine receptors (e.g., dopamine receptor).

211 binding pocket is distinct from that of the biogenic amine receptors and rhodopsin where the native

212 The results of this study demonstrate that biogenic amine receptors freely diffusing within the pla

213 nal region of rhodopsin-like 7 transmembrane biogenic amine receptors in agonist-induced signaling ha

214 strate that the expression of several of the biogenic amine receptors is abrogated in specific cell t

215 and fighting have led to the suggestion that biogenic amine receptors may play a role in modulating i

216 iating this function in Drosophila, putative biogenic amine receptors were cloned by a novel procedur

217 residue contributed from transmembrane-3 of biogenic amine receptors, which may account for the shar

218 eak affinity for the CRF-binding protein and biogenic amine receptors.

219 eak affinity for the CRF-binding protein and biogenic amine receptors.

220 distinct from, but related to the classical biogenic amine receptors.

221 peridine compounds have affinity for several biogenic amine receptors.

222 eptors and overall low homology to all other biogenic amine receptors.

223 ne (GPCR97) that had significant homology to biogenic amine receptors.

224 Biogenic amines regulate a variety of behaviors.

225 ship drive and were controlled by tyramine-a biogenic amine related to dopamine, whose roles in most

226 compounds structurally related to classical biogenic amines, represent endogenous ligands of the tra

227 In the nematode Caenorhabditis elegans, the biogenic amines serotonin (5-HT) and octopamine regulate

228 The symporters for the biogenic amines serotonin (SERT), dopamine (DAT), and no

229 this study, we investigated the roles of the biogenic amines serotonin and octopamine in regulating l

230 nopheles gambiae have been shown to bind the biogenic amines serotonin, norepinephrine, and histamine

231 Disruptions of biogenic amine signaling contribute to human neurologica

232 r and neural pathways through which parallel biogenic amine signaling tunes behavior appropriately to

233 Ultimately, biogenic amines significant to the fly including L-3,4-d

234 Octopamine (OA), a biogenic amine similar to norepinephrine, has profound a

235 Eight biogenic amines (spermine, spermidine, putrescine, hista

236 sts were observed, including that vertebrate biogenic amines structurally related to octopamine acted

237 Biogenic amines such as serotonin and dopamine are inter

238 ns of the distributions of some of the major biogenic amines, such as dopamine (DA) and octopamine (O

239 Biogenic amines, such as like serotonin, are conserved n

240 Biogenic amines, such as serotonin and dopamine, can be

241 glial expression of ebony, an N-beta-alanyl-biogenic amine synthase, and show that Ebony activity in

242 an rhythm in Drosophila Ebony (N-beta-alanyl-biogenic amine synthetase) abundance can be visualized i

243 or D4 against not only D1-3,5 but also other biogenic amine targets have emerged, and D4 is once agai

244 Histamine (HA) is a biogenic amine that can accumulate to high concentration

245 Histamine is a biogenic amine that forms in a variety of foods and can

246 Histamine is a biogenic amine that is indispensable in the efficient fu

247 Histamine is a biogenic amine that is widely distributed and has multip

248 Histamine is a biogenic amine that mediates multiple physiological proc

249 Histamine is a potent biogenic amine that mediates numerous physiological proc

250 olyamines (PAs) are ubiquitous, polycationic biogenic amines that are implicated in many biological p

251 The biogenic amine The biogenic amine N1-acetyl-N2-formyl-5-

252 therapeutic utility of these agents supports biogenic amine theories of affective disorders and raise

253 teroendocrine cells that secrete peptides or biogenic amines to regulate digestion, insulin secretion

254 We demonstrate that C. elegans uses biogenic amines to switch between distinct crawling and

255 coupling of receptors ranging from those for biogenic amines to the phospholipid mediator PAF.

256 events, both with the potential to modulate biogenic amine tone in the CNS.

257 inct regulatory features on neuropeptide and biogenic amine transmitter secretion.

258 shed pharmacologically by many, but not all, biogenic amine transporter antagonists.

259 amine uptake inhibition assays based on the biogenic amine transporter binding results.

260 The biogenic amine transporters (BATs) regulate endogenous n

261 f regulated heteromeric assemblies involving biogenic amine transporters and PP2A and suggest that th

262 Na(+)/Cl(-)-coupled biogenic amine transporters are the primary targets of t

263 and potent inhibition of uptake at all three biogenic amine transporters.

264 l role in defining the permeation pathway of biogenic amine transporters.

265 at distinguish substrates from inhibitors in biogenic amine transporters.

266 Only two biogenic amines (tryptamine and tyramine) and two polyam

267 The quantity of biogenic amines (tryptamine, phenylethylamine, putrescin

268 The biogenic amine tyramine (TA) regulates many aspects of i

269 The trace biogenic amine tyramine is present in the nervous system

270 Here, we report that the biogenic amines tyramine (TA) and octopamine (OA) in Dro

271 On the other hand, the bacterial-related biogenic amines, tyramine, histamine, tryptamine and bet

272 e effects of haloperidol (HP) metabolites on biogenic amine uptake and release, and compared them to

273 ratios were selected for additional study in biogenic amine uptake inhibition assays based on the bio

274 Chemically, bimodal deactivation of biogenic amines via acetylation and succinylation parall

275 The effect of other potentially interfering biogenic amines was also evaluated.

276 In the control samples, the amount of biogenic amines was insignificant.

277 ardinella sp.) where the production of eight biogenic amines was monitored over fifteen days of stora

278 ation of Drosophila melanogaster behavior by biogenic amines, we have exploited the broad requirement

279 No biogenic amines were detected in any of the analyzed soy

280 No biogenic amines were detected in the 300MPa treatments,

281 None of the 8 biogenic amines were detected in the final products, whi

282 The concentrations of ochratoxin A and biogenic amines were far below the health-hazardous thre

283 Glycoalkaloids, thiols and biogenic amines were generally stable, while 5-hydroxy-m

284 mum particle size) has been employed and the biogenic amines were identified and quantified in a tota

285 Dissociation constants for biogenic amines were measured using isothermal titration

286 Individual biogenic amines were not correlated with their precursor

287 These biogenic amines were not detected in non-fermented soybe

288 Biogenic amines were then quantified in three brain regi

289 n, all the allergens, as well as most of the biogenic amines, were cleared at the 24-hour time point.

290 Gastrointestinal endocrine cells produce biogenic amines which are transported into secretory ves

291 ned by food depletion nor is it modulated by biogenic amines, which suggest it is not an aversive beh

292 may be a novel low affinity transporter for biogenic amines, which, under certain conditions, might

293 ne oxidases utilize O2 for the metabolism of biogenic amines while concomitantly generating H2O2 for

294 erry vinegars reached the highest amounts of biogenic amines, while apple, white and Sherry wine vine

295 istent with the binding pocket described for biogenic amines, while Lys3.26(130) and Asn7.32(305), ar

296 Histamine (HA), a biogenic amine with a broad spectrum of activities in bo

297 Histamine, a biogenic amine with both neurotransmitter and vasoactive

298 Histamine is a biogenic amine with extensive effects on many cell types

299 pti (AeD7), respectively, were shown to bind biogenic amines with high affinity and with a stoichiome

300 inks, and by discriminating between multiple biogenic amines with remote structural differences six c