Abstract:
:Tityustoxin (TsTx) inhibited high affinity choline uptake (HAChU) in cortical slices of the rat brain. The effect was dependent on the concentration of tityustoxin, energy source, incubation time, temperature, and the pH of the incubation medium. The inhibitory effect was dependent upon the presence of sodium and calcium ions in the incubation medium; barium ions could not replace calcium. Both tetrodotoxin and ethyleneglycol-tetra-acetic acid (EGTA) blocked the inhibitory effect of tityustoxin on high affinity choline uptake. On this evidence, it is suggested that the effect of tityustoxin might be related to its action on cell depolarization, causing an increase in the release of acetylcholine (ACh).
journal_name
Neuropharmacologyjournal_title
Neuropharmacologyauthors
Macedo TM,Gomez MVdoi
10.1016/0028-3908(83)90014-xsubject
Has Abstractpub_date
1983-02-01 00:00:00pages
233-7issue
2eissn
0028-3908issn
1873-7064journal_volume
22pub_type
杂志文章abstract::We have used a focal stimulation method to study neurotransmission at synapses onto hippocampal pyramidal neurons in cultures derived from neonatal rats. Single functional boutons were visualized by activity-dependent preloading with the fluorescent dye FM1-43, then focally stimulated by localized application of eleva...
journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(95)00143-t
更新日期:1995-11-01 00:00:00
abstract::A number of pre-clinical studies have shown that brain-generated acetaldehyde, the first metabolite of ethanol, exerts reinforcing effects that promote the acquisition of ethanol intake, while chronic intake maintenance appears to be mediated by alcohol-induced brain neuroinflammation/oxidative stress. Recently, it wa...
journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2018.12.001
更新日期:2019-03-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2018.08.014
更新日期:2018-10-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(82)90134-4
更新日期:1982-12-01 00:00:00
abstract::Activation of the kappa opioid receptor (KOR) system mediates negative emotional states and considerable evidence suggests that KOR and their natural ligand, dynorphin, are involved in ethanol dependence and reward. The central amygdala (CeA) plays a major role in alcohol dependence and reinforcement. Dynorphin peptid...
journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2013.10.005
更新日期:2014-02-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(82)90091-0
更新日期:1982-04-01 00:00:00
abstract::Chronic nicotine administration in animals, and smoking in humans, causes up-regulation of α4β2* neuronal nicotinic receptors (nAChRs), which has been hypothesized to contribute to the addictive actions of nicotine. We used a rat model to test whether such up-regulatory effects differ in adolescents versus adults, and...
journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2015.08.015
更新日期:2015-12-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2015.09.013
更新日期:2016-02-01 00:00:00
abstract::GABAA and glycine receptors are close relatives in the "gene superfamily" of ligand-gated ion channels, but have distinctly different pharmacology. For example, barbiturates have two effects on GABAA receptors (GABAA-R): at low micromolar concentrations (2-5 microM), the anesthetic barbiturate methohexital potentiates...
journal_title:Neuropharmacology
pub_type: 杂志文章
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2012-06-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(93)90184-5
更新日期:1993-08-01 00:00:00
abstract::24S-hydroxycholesterol (24S-HC) is a brain-derived product of lipid metabolism present in the systemic circulation, where its level can change significantly in response to physiological and pathophysiological conditions. Here, using electrophysiological and optical approaches, we have found a high sensitivity to 24S-H...
journal_title:Neuropharmacology
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更新日期:2017-05-01 00:00:00
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journal_title:Neuropharmacology
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doi:10.1016/j.neuropharm.2010.09.013
更新日期:2011-02-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(83)90206-x
更新日期:1983-11-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:1994-11-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(93)90127-o
更新日期:1993-01-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2007.04.016
更新日期:2007-07-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/s0028-3908(99)00126-4
更新日期:1999-11-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2012-02-01 00:00:00
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journal_title:Neuropharmacology
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更新日期:1997-02-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2007-03-01 00:00:00
abstract::To study individual differences in nicotine preference and intake, male and female rats were given free access to a choice of oral nicotine (10 or 20 mg/L) or water for 24 h/day for periods of at least six weeks, starting at adolescence or adulthood. A total of 341 rats, were used in four different experiments; weight...
journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2011-07-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2002-03-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2011-10-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:2000-09-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
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更新日期:1998-12-01 00:00:00
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journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/0028-3908(91)90203-n
更新日期:1991-02-01 00:00:00
abstract::Diazepam binding inhibitor (DBI) acts in brain by binding to GABAA/benzodiazepine receptors (GBR) and to mitochondrial benzodiazepine receptors (MBR). Because DBI acting at MBR, has been shown to be an effector of ACTH-induced steroidogenesis and stress is known to change the level of GBR and MBR, the model of acute n...
journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/s0028-3908(11)80015-8
更新日期:1991-12-01 00:00:00
abstract::Histamine H3 receptor (H3R) antagonists are currently being investigated for the possible therapeutic use in various cognitive deficits such as those in schizophrenia, attention deficit hyperactivity disorder and Alzheimer's disease. Our previous studies suggest a role for H3Rs in ethanol-related behaviors in rat and ...
journal_title:Neuropharmacology
pub_type: 杂志文章
doi:10.1016/j.neuropharm.2010.10.027
更新日期:2011-06-01 00:00:00