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1 l drug ecstasy, is a potent serotonin (5-HT) releaser.
2 ol sulfate despite the disadvantages for the releaser.
3 ive uptake inhibitors or as amphetamine-like releasers.
4 of the DAT to other uptake blockers, but not releasers.
5 logs did not act as substrate-type serotonin releasers.
6  in BAT had lower basophil count compared to releasers (249 vs 630 counts/min).
7 nd phentermine, as well as a non-amphetamine releaser, 4-benzylpiperidine, were all unaffected.
8 as a rich pharmacology including inhibitors, releasers (amphetamines, which promote the exchange mode
9 ur 4-year long study and cycling between the releaser and nonreleaser phenotypes occurred at least on
10                In addition, MDMA is a potent releaser and reuptake inhibitor of presynaptic serotonin
11         D-Fenfluramine, a putative serotonin releaser and reuptake inhibitor, is commonly prescribed
12 e is a serotonin (5-hydroxytryptamine, 5-HT) releaser and reuptake inhibitor.
13                    Fenfluramine, a serotonin releaser and uptake inhibitor, has been widely prescribe
14 brid' activity as a SERT substrate (ie, 5-HT releaser) and DAT blocker, whereas 4-MePPP is a blocker
15 trosoglutathione (GSNO, widely used as an NO releaser) and sodium nitroprusside (SNP, which is a NO+
16 ystem to serve as a FA/CO(2) battery, a H(2) releaser, and a hydrogenative CO(2) converter.
17 ethyl 4-MA was an efficacious substrate-type releaser at DAT that evoked an inward depolarizing curre
18 n uptake blocker at low concentrations and a releaser at high concentrations.
19 Methylone, MDC, and HHMC were substrate-type releasers at monoamine transporters as determined in vit
20 sion was generally lower in nonreleaser than releaser basophils.
21                  Pheromones can induce both "releaser" (behavioral) and "priming" (physiological) eff
22                                           In releaser cells, FcepsilonRI cross-linking up-regulated >
23  by prior literature, including formaldehyde releasers, cobalt-nickel-potassium dichromate, acrylates
24 tions of a newly identified water-soluble CO releaser (CORM-A1) that, unlike the first prototypic mol
25 pagation, can act as an autonomous intrinsic releaser for the occurrence of a motivated behavior.
26 Apis mellifera, possess unrelated primer and releaser functions for the workers and act as a sex attr
27 nd CSE(-/-) macrophages using the slow H(2)S releaser GYY3147 and the CSE inhibitor DL-propargylglyci
28 ine (MDMA) and fenfluramine, two potent 5-HT releasers, inhibit SOs within the entorhinal cortex (EC)
29 mine, an indirect presynaptic norepinephrine releaser, into dorsal hand veins of 49 normotensive men
30       Despite being nonselective transporter releasers like MDMA, the APBT compounds failed to produc
31      We report that exposure to the dopamine releaser methamphetamine for 10 days elicits a long-last
32 creased stereotypic response to the dopamine releaser, methamphetamine, and an insensitivity to the a
33                       Finally, although a DA releaser, muscimol was neither self-administered in drug
34 pase A2alpha (cPLA2alpha), the rate-limiting releaser of arachidonic acid used for pro-inflammatory e
35  (HYCOs) that combine an Nrf2 inducer with a releaser of carbon monoxide (CO), an anti-inflammatory p
36 LHRH and AA, whereas sodium nitroprusside, a releaser of NO, stimulated LH and FSH release.
37 ethamphetamine (MDMA, Ecstasy) is a powerful releaser of serotonin.
38 imarily act in early carcinogenesis as broad releasers of developmental plasticity rather than as sti
39         The toil of 3 billion years by these releasers of molecular oxygen finally triggered the Camb
40  These consumers of carbon dioxide were also releasers of molecular oxygen.
41 igated the effect of FK409, a spontaneous NO releaser, on the development of allograft vasculopathy,
42 inhibitor and as a prodrug for the monoamine-releaser phenmetrazine (PM), and it may serve as a clini
43         The main component, 9-ODA, acts as a releaser pheromone by attracting workers to the queen an
44 nteraction with the DAT as a pure blocker or releaser rather than their structural similarity to coca
45 given these compounds function as primer and releaser signals that regulate the social organization o
46  dilation in the piglet, responses to the NO releasers SNP and SNAP are unchanged by the Kca channel
47   The potencies of amphetamine-like dopamine releasers such as 3,4-methylenedioxymethamphetamine, met
48                                    Monoamine releasers such as d-amphetamine constitute one class of
49 nor by reverse SERT transport induced by 5HT releasers such as MDMA.
50 methamphetamine (MDMA) is a potent monoamine releaser that produces an acute euphoria in most individ
51 ty of different dopamine uptake blockers and releasers to inhibit dopamine uptake, measured using fas
52 ed c-fos induction by the specific serotonin releaser-uptake inhibitor dexfenfluramine and alteration
53 (via the parent drug PDM) and as a monoamine releaser (via the active metabolite PM).
54                         PCA is a potent 5-HT releaser which can induce gliosis in the rodent brain.
55  intrinsic biochemical behavior of a slow CO releaser, which may be advantageous in the treatment of
56                     MDMA, a potent monoamine-releaser with particularly pronounced serotonin- releasi