コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
1 5-HTP also caused monkeys to perseverate on their gaze r
2 5-HTP increased central concentrations of serotonin and
3 5-HTP SR might be used to treat patients with intestinal
4 5-HTP SR might in particular be therapeutically relevant
5 5-HTP SR produced plasma 5-HTP levels well within the ra
6 5-HTP SR robustly increased brain 5-HT synthesis and lev
7 5-HTP SR's pro-serotonergic effects were stronger in mic
8 5-HTP treatment gradually reduced the rhythmicity of the
13 data, our mouse data suggest that an adjunct 5-HTP SR drug could safely and effectively elevate 5-HTE
20 study measured the activities of L-DOPA and 5-HTP decarboxylase (DDC and 5-HTPDC) in the substantia
21 These findings provide a causal link between 5-HTP and social gaze behaviors in nonhuman primates and
22 idence for a modulatory relationship between 5-HTP and social gaze behaviors in nonhuman primates and
23 the inhibition of N-methyltransferase blocks 5-HTP-induced head twitches in betaarr2-KO mice, indicat
29 yme dopa decarboxylase, which converts (11)C-5-HTP to (11)C-serotonin and increased after inhibition
34 ion (66%) in the pancreatic uptake of [(11)C]5-HTP in T1D subjects was observed, and this was most ev
38 n the beta-cell volume, implying that [(11)C]5-HTP retention is a useful noninvasive surrogate marker
39 oncept study, the ex vivo and in vivo [(11)C]5-HTP signal was compared with the number of islets tran
50 In contrast, the morphine treatment enhances 5-HTP accumulation in dorsal raphe nucleus, cortex and c
53 vivo of accumulation of 5-hydroxytryptophan (5-HTP) in tissue from the dorsal and median raphe nuclei
55 the serotonin precursor 5-hydroxytryptophan (5-HTP) increased the intensity of serotonin immunolabeli
56 th the direct precursor 5-hydroxytryptophan (5-HTP) would modulate the ability of rhesus macaques (bo
57 iate precursor of 5-HT, 5-hydroxytryptophan (5-HTP), in two model opisthobranch molluscs, the nudibra
60 that SR delivery will substantially improve 5-HTP's drug properties, by minimizing adverse effects a
65 s upregulated by all doses except TN-200 muM 5-HTP, and cell survival gene, FOXO3, was upregulated by
66 3, was upregulated by HS-50, 200 and 500 muM 5-HTP, suggesting 5-HTP involvement in cell turnover und
68 pletely blocked the enhanced accumulation of 5-HTP, but had no effect on basal accumulation of 5-HTP,
69 , but had no effect on basal accumulation of 5-HTP, except at the highest doses of 1.0 or 3.3 nmol, w
74 e, suggesting that the disruptive effects of 5-HTP on social gaze behaviors are likely driven by a do
77 onergic neurons also displayed low levels of 5-HTP immunolabeling that were above background levels.
78 ssed rats had significantly higher levels of 5-HTP in cortex and midbrain compared to sham-stressed c
79 esults support the notion that production of 5-HTP is a rate-limiting step in serotonin synthesis and
81 nin pathway, through oral supplementation of 5-HTP, influences signaling pathways and cellular proces
82 ined effects of sound stress and morphine on 5-HTP accumulation are identical to those obtained by ea
86 y of the components of this cascade prevents 5-HTP-induced, but not N-methyltryptamine-induced, head
87 ata, appreciated in the context of published 5-HTP clinical data, suggest that 5-HTP SR could represe
88 eding chow that contains 5-HTP slow release (5-HTP SR) to TPH2-R439H mice restores levels of 5-HT in
90 nistering the direct precursor of serotonin, 5-HTP, on orienting and inhibiting social gaze in nonhum
93 rapid absorption and elimination of standard 5-HTP immediate release (IR) likely curtail 5-HTP IR's a
98 published 5-HTP clinical data, suggest that 5-HTP SR could represent a new therapeutic approach to t
103 the effects of feeding chow, with or without 5-HTP SR, to mice with the TPH2-R439H mutation and witho