keyword
https://read.qxmd.com/read/24012886/methamphetamine-inhibits-voltage-gated-potassium-currents-in-ng108-15-cells-possible-contribution-of-large-conductance-calcium-activated-potassium-channels
#21
JOURNAL ARTICLE
Ya-Jean Wang, Ming-Huan Chan, Hwei-Hisen Chen
Methamphetamine (MA), a highly abused amphetamine-like psychostimulant, has surged in popularity worldwide in the last decade. Repeated MA exposure has been shown to affect the alternative splice variant expression of large conductance Ca(2+)-activated K(+) (BK) channels. It remains unclear whether MA affects BK channel activity. The present study investigated the effects of MA on BK channels in NG108-15 mouse neuroblastoma×rat glioma hybrid cells using whole-cell and cell-attached patch clamp techniques. In whole-cell recordings, the macroscopic K(+) outward currents were inhibited by MA with an EC50 of 146μM, but not affected by dopamine (DA)...
November 25, 2013: Toxicology Letters
https://read.qxmd.com/read/23889535/pharmacological-characterization-of-a-novel-centrally-permeable-p2x7-receptor-antagonist-jnj-47965567
#22
JOURNAL ARTICLE
Anindya Bhattacharya, Qi Wang, Hong Ao, James R Shoblock, Brian Lord, Leah Aluisio, Ian Fraser, Diane Nepomuceno, Robert A Neff, Natalie Welty, Timothy W Lovenberg, Pascal Bonaventure, Alan D Wickenden, Michael A Letavic
BACKGROUND AND PURPOSE: An increasing body of evidence suggests that the purinergic receptor P2X, ligand-gated ion channel, 7 (P2X7) in the CNS may play a key role in neuropsychiatry, neurodegeneration and chronic pain. In this study, we characterized JNJ-47965567, a centrally permeable, high-affinity, selective P2X7 antagonist. EXPERIMENTAL APPROACH: We have used a combination of in vitro assays (calcium flux, radioligand binding, electrophysiology, IL-1β release) in both recombinant and native systems...
October 2013: British Journal of Pharmacology
https://read.qxmd.com/read/23843440/dopaminergic-modulation-of-gabaergic-transmission-in-the-entorhinal-cortex-concerted-roles-of-%C3%AE-1-adrenoreceptors-inward-rectifier-k%C3%A2-%C2%BA-and-t-type-ca%C3%A2-%C3%A2-%C2%BA-channels
#23
JOURNAL ARTICLE
Nicholas I Cilz, Lalitha Kurada, Binqi Hu, Saobo Lei
Whereas the entorhinal cortex (EC) receives profuse dopaminergic innervations from the midbrain, the effects of dopamine (DA) on γ-Aminobutyric acid (GABA)ergic interneurons in this brain region have not been determined. We probed the actions of DA on GABAA receptor-mediated synaptic transmission in the EC. Application of DA increased the frequency, not the amplitude, of spontaneous IPSCs (sIPSCs) and miniature IPSCs (mIPSCs) recorded from entorhinal principal neurons, but slightly reduced the amplitude of the evoked IPSCs...
December 2014: Cerebral Cortex
https://read.qxmd.com/read/23644142/effects-of-mk-801-and-amphetamine-treatments-on-allergic-lung-inflammatory-response-in-mice
#24
JOURNAL ARTICLE
Eduardo Kenji Hamasato, Ana Paula Ligeiro de Oliveira, Adriana Lino-dos-Santos-Franco, Alison Ribeiro, Viviane Ferraz de Paula, Jean Pierre Schatzmann Peron, Amílcar Sabino Damazo, Wothan Tavares-de-Lima, João Palermo-Neto
Glutamate acts as a neurotransmitter within the Central Nervous System (CNS) and modifies immune cell activity. In lymphocytes, NMDA glutamate receptors regulate intracellular calcium, the production of reactive oxygen species and cytokine synthesis. MK-801, a NMDA receptor open-channel blocker, inhibits calcium entry into mast cells, thereby preventing mast cell degranulation. Several lines of evidence have shown the involvement of NMDA glutamate receptors in amphetamine (AMPH)-induced effects. AMPH treatment has been reported to modify allergic lung inflammation...
August 2013: International Immunopharmacology
https://read.qxmd.com/read/22436698/serotonin-5-ht2c-receptor-mediated-inhibition-of-the-m-current-in-hypothalamic-pomc-neurons
#25
JOURNAL ARTICLE
T A Roepke, A W Smith, O K Rønnekleiv, M J Kelly
Hypothalamic proopiomelanocortin (POMC) neurons are controlled by many central signals, including serotonin. Serotonin increases POMC activity and reduces feeding behavior via serotonion [5-hydroxytryptamine (5-HT)] receptors by modulating K(+) currents. A potential K(+) current is the M-current, a noninactivating, subthreshold outward K(+) current. Previously, we found that M-current activity was highly reduced in fasted vs. fed states in neuropeptide Y neurons. Because POMC neurons also respond to energy states, we hypothesized that fasting may alter the M-current and/or its modulation by serotonergic input to POMC neurons...
June 1, 2012: American Journal of Physiology. Endocrinology and Metabolism
https://read.qxmd.com/read/22416645/anti-psychotic-and-sedative-effect-of-calcium-channel-blockers-in-mice
#26
JOURNAL ARTICLE
S Umukoro, T O Bakre, C Onwuchekwa
Calcium channel blockers (CCBs) are widely used as therapeutic agents, for the treatment of cardiovascular disorders. However, the discovery that CCBs bind to various regions of the brain suggest that they might also offer some beneficial effects in the treatment of neuropsychiatry disorders. This study was carried out to evaluate the anti-psychotic and sedative effects of two notable calcium channel blockers, verapamil and nifedipine in mice. The anti-psychotic effects of the CCBs were studied in the animal model of amphetamine-induced stereotyped behavioral disorders...
December 2010: African Journal of Medicine and Medical Sciences
https://read.qxmd.com/read/22077243/use-of-the-molecular-adsorbent-recirculating-system-mars%C3%A2-for-the-management-of-acute-poisoning-with-or-without-liver-failure
#27
REVIEW
Xavier Wittebole, Philippe Hantson
INTRODUCTION: There is an increasing interest in recent developments in bioartificial and non-bioartificial devices, so called extracorporeal liver assist devices, which are now used widely not only to increase drug elimination, but also to enhance the removal of endogenous substances in acute liver failure. Most of the non-bioartificial techniques are based on the principle of albumin dialysis. The objective is to remove albumin-bound substances that could play a role in the pathophysiology of acute liver failure by dialysing blood against an albumin-containing solution across a high flux permeable membrane...
November 2011: Clinical Toxicology
https://read.qxmd.com/read/21644994/dopamine-release-mediated-by-the-dopamine-transporter-facts-and-consequences
#28
REVIEW
Vincent Leviel
Spontaneous and/or stimulated neural activity of the nigrostriatal dopamine (DA) pathway makes amines run out from the neurons. This DA dynamic follows a rather complex path, running in or out the terminals, and flushing or diffusing into the extracellular space. The location of this leakage is not limited to the axon terminals; it also occurs from the cell bodies and dendrites. This molecular release mechanism was, for a long time, considered as being produced, in part, by the exocytosis of previously stored vesicles...
August 2011: Journal of Neurochemistry
https://read.qxmd.com/read/21159975/molecular-switch-from-l-type-ca-v-1-3-to-ca-v-1-2-ca2-channel-signaling-underlies-long-term-psychostimulant-induced-behavioral-and-molecular-plasticity
#29
JOURNAL ARTICLE
Thomas P Giordano, Thomas F Tropea, Shirish S Satpute, Martina J Sinnegger-Brauns, Joerg Striessnig, Barry E Kosofsky, Anjali M Rajadhyaksha
L-type Ca(2+) channel (LTCC)-activated signaling cascades contribute significantly to psychostimulant-induced locomotor sensitization; however, the precise contribution of the two brain-specific subunits Ca(v)1.2 and Ca(v)1.3 remains mostly unknown. In this study, by using amphetamine and cocaine locomotor sensitization in mutant mice expressing dihydropyridine (DHP)-insensitive Ca(v)1.2 LTCCs (Ca(v)1.2DHP(-/-)), we find that, as opposed to a previously identified role of the Ca(v)1.3 subunit of LTCCs in development of sensitization, the Ca(v)1...
December 15, 2010: Journal of Neuroscience
https://read.qxmd.com/read/21110986/t-type-calcium-channel-antagonism-produces-antipsychotic-like-effects-and-reduces-stimulant-induced-glutamate-release-in-the-nucleus-accumbens-of-rats
#30
JOURNAL ARTICLE
Jason M Uslaner, Sean M Smith, Sarah L Huszar, Rashida Pachmerhiwala, Richard M Hinchliffe, Joshua D Vardigan, Shannon J Nguyen, Nathan O Surles, Lihang Yao, James C Barrow, Victor N Uebele, John J Renger, Janet Clark, Pete H Hutson
T-type calcium channels are important in burst firing and expressed in brain regions implicated in schizophrenia. Therefore, we examined the effects of novel selective T-type calcium channel antagonists in preclinical assays predictive of antipsychotic-like activity. TTA-A2 blocked the psychostimulant effects of amphetamine and MK-801 and decreased conditioned avoidance responding. These effects appeared mechanism based, rather than compound specific, as two structurally dissimilar T-type antagonists also reduced amphetamine-induced psychomotor activity...
March 2012: Neuropharmacology
https://read.qxmd.com/read/20723887/mood-disorder-susceptibility-gene-cacna1c-modifies-mood-related-behaviors-in-mice-and-interacts-with-sex-to-influence-behavior-in-mice-and-diagnosis-in-humans
#31
JOURNAL ARTICLE
David T Dao, Pamela Belmonte Mahon, Xiang Cai, Colleen E Kovacsics, Robert A Blackwell, Michal Arad, Jianxin Shi, Peter P Zandi, Patricio O'Donnell, James A Knowles, Myrna M Weissman, William Coryell, William A Scheftner, William B Lawson, Douglas F Levinson, Scott M Thompson, James B Potash, Todd D Gould
BACKGROUND: Recent genome-wide association studies have associated polymorphisms in the gene CACNA1C, which codes for Ca(v)1.2, with a bipolar disorder and depression diagnosis. METHODS: The behaviors of wild-type and Cacna1c heterozygous mice of both sexes were evaluated in a number of tests. Based upon sex differences in our mouse data, we assessed a gene × sex interaction for diagnosis of mood disorders in human subjects. Data from the National Institute of Mental Health Genetics Initiative Bipolar Disorder Consortium and the Genetics of Recurrent Early-Onset Major Depression Consortium were examined using a combined dataset that included 2021 mood disorder cases (1223 female cases) and 1840 control subjects (837 female subjects)...
November 1, 2010: Biological Psychiatry
https://read.qxmd.com/read/20565449/pharmacological-approaches-to-methamphetamine-dependence-a-focused-review
#32
REVIEW
Laurent Karila, Aviv Weinstein, Henri-Jean Aubin, Amine Benyamina, Michel Reynaud, Steven L Batki
Methamphetamine dependence is a serious worldwide public health problem with major medical, psychiatric, socioeconomic and legal consequences. Various neuronal mechanisms implicated in methamphetamine dependence have suggested several pharmacological approaches. A literature search from a range of electronic databases (PubMed, EMBASE, PsycInfo, the NIDA research monograph index and the reference list of clinicaltrials.gov) was conducted for the period from January 1985 to October 2009. There were no restrictions on the identification or inclusion of studies in terms of publication status, language and design type...
June 2010: British Journal of Clinical Pharmacology
https://read.qxmd.com/read/20200117/nicotinic-receptor-mediated-reduction-in-l-dopa-induced-dyskinesias-may-occur-via-desensitization
#33
JOURNAL ARTICLE
Tanuja Bordia, Carla Campos, J Michael McIntosh, Maryka Quik
L-DOPA-induced dyskinesias in Parkinson's disease are a significant clinical problem for which few therapies are available. We recently showed that nicotine reduces L-DOPA-induced abnormal involuntary movements (AIMs) in parkinsonian animals, suggesting it may be useful for the treatment of L-DOPA-induced dyskinesias. The present experiments were performed to understand the mechanisms whereby nicotine reduces L-DOPA-induced AIMs. We used a well established model of dyskinesias, L-DOPA-treated unilateral 6-hydroxydopamine-lesioned rats...
June 2010: Journal of Pharmacology and Experimental Therapeutics
https://read.qxmd.com/read/20122967/participation-of-l-type-calcium-channels-in-ethanol-induced-behavioral-stimulation-and-motor-incoordination-effects-of-diltiazem-and-verapamil
#34
JOURNAL ARTICLE
Pablo Baliño, Raúl Pastor, Carlos M G Aragon
Calcium flux through voltage gate calcium channels (VGCC) is involved in many neuronal processes such as membrane depolarization, gene expression, hormone secretion, and neurotransmitter release. Several studies have shown that either acute or chronic exposure to ethanol modifies calcium influx through high voltage activated channels. Of special relevance is the L-type VGCC. Pharmacological manipulation of L-type calcium channels affects ethanol intake, ethanol discrimination and manifestations of withdrawal syndrome...
June 19, 2010: Behavioural Brain Research
https://read.qxmd.com/read/20053846/amphetamine-increases-persistent-inward-currents-in-human-motoneurons-estimated-from-paired-motor-unit-activity
#35
JOURNAL ARTICLE
Esther Udina, Jessica D'Amico, Austin J Bergquist, Monica A Gorassini
Recruitment and repetitive firing of spinal motoneurons depend on the activation of persistent inward calcium and sodium currents (PICs) that are in turn facilitated by serotonin and norepinephrine that arise primarily from the brain stem. Considering that in rats motoneuron PICs are greatly facilitated by increasing the presynaptic release of norepinephrine with amphetamine, we sought similar evidence for the modulation of PICs in human motoneurons. Pairs of motor units were recorded during a gradually increasing and then decreasing voluntary contraction...
March 2010: Journal of Neurophysiology
https://read.qxmd.com/read/19876061/azelnidipine-a-long-acting-calcium-channel-blocker-could-control-hypertension-without-decreasing-cerebral-blood-flow-in-post-ischemic-stroke-patients-a-123i-imp-spect-follow-up-study
#36
JOURNAL ARTICLE
Masaki Watanabe, Teruyuki Hirano, Sadahisa Okamoto, Shinya Shiraishi, Seiji Tomiguchi, Makoto Uchino
Azelnidipine, a long-acting calcium channel blocker, is highly lipid soluble and selective for the vascular wall, and is expected to have an increasing effect on cerebral blood flow (CBF). The aim of this study is to investigate its safety and efficacy in stroke patients in the chronic stage as far as CBF is concerned using N-isopropyl-p-(123)I-iodo amphetamine ((123)I-IMP) single-photon emission computed tomography (SPECT). The patients were orally administered 8 or 16 mg of azelnidipine. Regional CBF was evaluated by (123)I-IMP SPECT using three-dimensional stereotactic region-of-interest (ROI) template (3D-SRT), a technique using anatomical standardization and ROI template consisting of 636 ROIs for the whole brain...
January 2010: Hypertension Research: Official Journal of the Japanese Society of Hypertension
https://read.qxmd.com/read/19512965/cognitive-impairment-and-cerebral-hypoperfusion-in-a-cadasil-patient-improved-during-administration-of-lomerizine
#37
JOURNAL ARTICLE
Toshiki Mizuno, Masaki Kondo, Noriko Ishigami, Aiko Tamura, Masahiro Itsukage, Hideyuki Koizumi, Reina Isayama, Akiko Hosomi, Yoshinari Nagakane, Takahiko Tokuda, Eizo Sugimoto, Yo Ushijima, Masanori Nakagawa
A 64-year-old woman was admitted to our hospital for recurrent stroke and cognitive impairment and was diagnosed with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Iodine-123 iodoamphetamine single photon emission computed tomography showed hypoperfusion in the whole brain, but cerebral blood flow increased dramatically after the administration of acetazolamide in the cerebral cortex. Lomerizine, a diphenylmethylpiperazine Ca2+ channel blocker, can selectively increase cerebral blood flow...
March 2009: Clinical Neuropharmacology
https://read.qxmd.com/read/19508876/behavioural-and-dopaminergic-alterations-induced-by-a-low-dose-of-win-55-212-2-in-a-conditioned-place-preference-procedure
#38
JOURNAL ARTICLE
Alexia Polissidis, Olga Chouliara, Andreas Galanopoulos, Marios Marselos, Zeta Papadopoulou-Daifoti, Katerina Antoniou
AIMS: This study investigated the role of the cannabinoid CB1 receptor agonist, WIN 55,212-2, on motor activity. Subsequently, the effects of a low, stimulatory dose of WIN 55,212-2 and cocaine, as a positive control, were evaluated using a conditioned place preference (CPP) procedure. Upon completion of CPP, in rats that had been treated with WIN 55,212-2, dopaminergic status and spontaneous and d-amphetamine-induced motor activity were assessed. MAIN METHODS: Sprague-Dawley rats were evaluated for habituated motor activity following WIN 55,212-2 (0, 0...
July 31, 2009: Life Sciences
https://read.qxmd.com/read/19010365/neurochemical-changes-in-the-striatum-of-dyskinetic-rats-after-administration-of-the-cannabinoid-agonist-win55-212-2
#39
JOURNAL ARTICLE
M G Morgese, T Cassano, S Gaetani, T Macheda, L Laconca, P Dipasquale, L Ferraro, T Antonelli, V Cuomo, A Giuffrida
Chronic use of levodopa, the most effective treatment for Parkinson's disease, causes abnormal involuntary movements named dyskinesias, which are linked to maladaptive changes in plasticity and disturbances of dopamine and glutamate neurotransmission in the basal ganglia. Dyskinesias can be modeled in rats with unilateral 6-hydroxydopamine lesions by repeated administration of low doses of levodopa (6 mg/kg, s.c.). Previous studies from our lab showed that sub-chronic treatment with the cannabinoid agonist WIN55,212-2 attenuates levodopa-induced dyskinesias at doses that do not interfere with physiological motor function...
January 2009: Neurochemistry International
https://read.qxmd.com/read/18377968/in-vivo-pharmacological-effects-of-jzp-4-a-novel-anticonvulsant-in-models-for-anticonvulsant-antimania-and-antidepressant-activity
#40
JOURNAL ARTICLE
Mark M Foreman, Taleen Hanania, Sharon C Stratton, Karen S Wilcox, H Steve White, James P Stables, Mark Eller
JZP-4 is a potent calcium and sodium channel blocker, which is currently being evaluated in patients as an anticonvulsant and mood stabilizer. In the current studies, JZP-4 was evaluated in a variety of animal models for anticonvulsant, antimania and antidepressant activity. In the mouse and rat maximal electroshock models, JZP-4 was slightly more potent than LTG. In the mouse pentylenetetrazole induced seizures model, JZP-4 was approximately twice as potent as lamotrigine in prolonging the time to clonus. In the mouse 6-Hz model for drug resistant or refractory epilepsy, JZP-4 had potent anticonvulsant activity at all current intensities, whereas LTG was active at only the lowest current intensity...
June 2008: Pharmacology, Biochemistry, and Behavior
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