Pharmacological properties of homomeric and heteromeric GluR1o and GluR3o receptors.

Abstract:

:Homomeric and heteromeric alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptor subunits GluR1o and GluR3o were expressed in Spodoptera frugiperda (Sf9) insect cells. Membranes containing the recombinant receptors showed a doublet of bands of the expected size (99-109 kDa) after western immunoblotting which was shifted to a single band upon deglycosylation. In (R,S)-[3H]AMPA binding experiments, high expression was seen (Bmax = 0.8-3.8 pmol/mg protein) along with high affinity binding to a single site (Kd, nM+/-S.D.): GluR1o, 32.5+/-2.7; GluR3o, 23.7+/-2.4; GluR1o + GluR3o, 18.1+/-2.9. The pharmacological profiles of these receptors resembled that of native rat brain AMPA receptors: AMPA analogues > L-glutamate > quinoxaline-2,3-diones > kainate. In the Xenopus oocyte expression system we had previously shown that the agonist (R,S)-2-amino-3-(3-carboxy-5-methyl-4-isoxazolyl)propionate (ACPA) exhibited an 11-fold selectivity for GluR3o vs. GluR1o. In this study, it was found that ACPA has 3-fold higher affinity at homomeric GluR3o and heteromeric receptors than at homomeric GluR1o, suggesting that its efficacy and/or desensitisation properties are different at GluR1o vs. GluR3o.

journal_name

Eur J Pharmacol

authors

Nielsen BS,Banke TG,Schousboe A,Pickering DS

doi

10.1016/s0014-2999(98)00668-2

subject

Has Abstract

pub_date

1998-11-06 00:00:00

pages

227-38

issue

2-3

eissn

0014-2999

issn

1879-0712

pii

S0014-2999(98)00668-2

journal_volume

360

pub_type

杂志文章
  • miR-671 promotes prostate cancer cell proliferation by targeting tumor suppressor SOX6.

    abstract::Prostate cancer is one of the most severe malignancies in men, and many genes and non-coding RNAs, included microRNAs (miRs), have been demonstrated to regulate prostate cancer progression. In the present study, we investigated the role of miR-671 in prostate cancer cell proliferation. We found that miR-671 was signif...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2018.01.016

    authors: Yu Y,Wang Z,Sun D,Zhou X,Wei X,Hou W,Ding Y,Ma Y,Hou Y

    更新日期:2018-03-15 00:00:00

  • Rationally designed chimeric peptide of met-enkephalin and FMRFa-[D-Ala2,p-Cl-Phe4]YFa induce multiple opioid receptors mediated antinociception and up-regulate their expression.

    abstract::The physiological role of NPFF/FMRFa family of peptides appears to be complex and exact mechanism of action of these peptides is not yet completely understood. In same line of scrutiny, another analog of YGGFMKKKFMRFamide (YFa), a chimeric peptide of met-enkephalin and FMRFamide, was rationally designed and synthesize...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2010.02.060

    authors: Vats ID,Chaudhary S,Sharma A,Nath M,Pasha S

    更新日期:2010-07-25 00:00:00

  • 20(S)-Protopanaxadiol, a metabolite of ginsenosides, induced cell apoptosis through endoplasmic reticulum stress in human hepatocarcinoma HepG2 cells.

    abstract::20(S)-Protopanaxadiol (PPD), a metabolite of ginsenosides, has been demonstrated to possess cytotoxic effects on several cancer cell lines. The molecular mechanism is, however, not well understood. In this study, we have shown that PPD inhibits cell growth and induces apoptosis in human hepatocarcinoma HepG2 cells. PP...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2011.06.008

    authors: Zhu GY,Li YW,Tse AK,Hau DK,Leung CH,Yu ZL,Fong WF

    更新日期:2011-10-01 00:00:00

  • Calcitonin gene-related peptide inhibits the cardiac fibroblasts senescence in cardiac fibrosis via up-regulating klotho expression.

    abstract::It has been documented cardiac fibroblasts as the predominant cell population undergoing senescence in heart. Calcitonin gene-related peptide (CGRP) exhibits a wide range of cardiovascular protective effects. Whether CGRP protects against cardiac fibroblasts senescence in cardiac fibrosis remains unknown. Here, we det...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2018.10.023

    authors: Li WQ,Tan SL,Li XH,Sun TL,Li D,Du J,Wei SS,Li YJ,Zhang BK

    更新日期:2019-01-15 00:00:00

  • Antidepressant effects of TBE-31 and MCE-1, the novel Nrf2 activators, in an inflammation model of depression.

    abstract::The Nuclear factor (erythroid 2-derived)-like 2 (Nrf2) plays a key role in inflammation which is implicated in the pathophysiology of depression. The Nrf2 activators have antidepressant effects in animal models of depression. The present study was undertaken to examine whether TBE-31 [(±)-(4bS,8aR,10aS)-10a-ethynyl-4b...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2016.10.037

    authors: Yao W,Zhang JC,Ishima T,Ren Q,Yang C,Dong C,Ma M,Saito A,Honda T,Hashimoto K

    更新日期:2016-12-15 00:00:00

  • Muscarinic receptors modulate the afterhyperpolarizing potential in neostriatal neurons.

    abstract::The actions of carbachol were studied on the firing response of neostriatal neurons recorded intracellularly from in vitro slice preparations of the rat brain. Carbachol (1-10 microM) reversibly reduced the afterhyperpolarization in neostriatal neurons. This effect was accompanied by an increase in both firing frequen...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00263-k

    authors: Pineda JC,Bargas J,Flores-Hernández J,Galarraga E

    更新日期:1995-08-15 00:00:00

  • An orally active reversible inhibitor of cathepsin S inhibits human trans vivo delayed-type hypersensitivity.

    abstract::Cathepsin S is a major histocompatibility complex (MHC) class II associated invariant chain (Ii) degrading enzyme expressed in antigen presenting cells such as B cells and dendritic cells. This enzyme is essential for MHC class II associated antigen processing and presentation to CD4(+) T cells. Compound I, a selectiv...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2006.03.051

    authors: Desai SN,White DM,O'shea KM,Brown ML,Cywin CL,Spero DM,Panzenbeck MJ

    更新日期:2006-05-24 00:00:00

  • NG-nitro-L-arginine methyl ester protects against lipid peroxidation in the gerbil following cerebral ischaemia.

    abstract::The aim of this study was to assess the role of nitric oxide (NO) in lipid peroxidation following 5 min of bilateral carotid occlusion in the Mongolian gerbil. The study consisted of 4 experimental groups (n = 10). Animals were either sham operated, subjected to bilateral carotid occlusion or administered the NO synth...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00502-c

    authors: Caldwell M,O'Neill M,Earley B,Kelly JP,Leonard BE

    更新日期:1995-10-16 00:00:00

  • Inhibition of nitric oxide synthase delays healing of chronic gastric ulcers.

    abstract::We investigated the influence of inhibition of nitric oxide (NO) synthase, using NG-nitro-L-arginine (L-NNA) or NG-mono-methyl-L-arginine (L-NMMA), and the effects of exogenous donor of NO, such as glyceryl trinitrate (GTN), on the healing of chronic gastric ulcers induced by acetic acid, on gastric blood flow around ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(93)90997-v

    authors: Konturek SJ,Brzozowski T,Majka J,Pytko-Polonczyk J,Stachura J

    更新日期:1993-08-03 00:00:00

  • Cholecystokinin facilitates ejaculation in male rats: blockade with proglumide and apomorphine.

    abstract::Systemic administration of the active, sulfated form of cholecystokinin-octapeptide (CCK-8S), at a dose known to inhibit dopamine (DA) release, significantly reduced the latency to ejaculate and number of intromissions preceding ejaculation in sexually active male rats. This effect was identical to that reported for l...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(87)90549-8

    authors: Pfaus JG,Phillips AG

    更新日期:1987-09-23 00:00:00

  • Pharmacological properties of TD-6301, a novel bladder selective muscarinic receptor antagonist.

    abstract::Existing antimuscarinic drugs for overactive bladder have high affinity for M(3)/M(1) muscarinic receptors and consequently produce M(3)/M(1)-mediated adverse effects including dry mouth, constipation, mydriasis and somnolence. TD-6301 is a M(2/4) muscarinic receptor-selective antagonist developed for the treatment of...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2008.12.043

    authors: McNamara A,Pulido-Rios MT,Sweazey S,Obedencio GP,Thibodeaux H,Renner T,Armstrong SR,Steinfeld T,Hughes AD,Wilson RD,Jasper JR,Mammen M,Hegde SS

    更新日期:2009-03-01 00:00:00

  • Selective glucocorticoid receptor (type II) antagonists prevent weight gain caused by olanzapine in rats.

    abstract::The use of antipsychotic medication has consistently been associated with serious side effects including weight gain and metabolic abnormalities. Strategies for mitigating these side effects have been tested, yet effective interventions have not been identified. The current study tested whether two recently identified...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2011.01.019

    authors: Belanoff JK,Blasey CM,Clark RD,Roe RL

    更新日期:2011-03-25 00:00:00

  • 7-Nitroindazole reduces nitric oxide concentration in rat hippocampus after transient forebrain ischemia.

    abstract::We investigated the effects of 7-nitroindazole, a specific inhibitor of neuronal nitric oxide (NO) synthase, on NO concentration and on blood flow in rat hippocampus after transient forebrain ischemia which was induced by 4-vessel occlusion for 10 min. NO concentration was measured directly by an NO-selective electrod...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(99)00555-5

    authors: Jiang MH,Kaku T,Hada J,Hayashi Y

    更新日期:1999-09-10 00:00:00

  • Influence of acute treatment with sibutramine on the sympathetic neurotransmission of the young rat vas deferens.

    abstract::The effects of acute treatment with sibutramine on the peripheral sympathetic neurotransmission in vas deferens of young rats were still not evaluated. Therefore, we carried out this study in order to verify the effects of acute sibutramine treatment on the neuronal- and exogenous agonist-induced contractions of the y...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.05.035

    authors: de Souza BP,da Silva ED Jr,Jurkiewicz A,Jurkiewicz NH

    更新日期:2014-09-05 00:00:00

  • Effect of isoproterenol on the isolated pregnant rat myometrium.

    abstract::In pregnant rat myometrium, isoproterenol (10(-8) M) inhibited spontaneous contractions without causing hyperpolarization. Isoproterenol (10(-6) M) relaxed the depolarized muscle without affecting the membrane potential. The presence of 80 mM Na+ did not affect the degree of high-K+ depolarization. It was also without...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(79)90045-1

    authors: Meisheri KD,McNeill JH,Marshall JM

    更新日期:1979-11-23 00:00:00

  • Submaxillary secretion in rats treated with guanethidine.

    abstract::The composition of final submaxillary saliva and of whole gland homogenates were compared in rats treated with 14 daily doses of guanethidine (20 mg/kg body weight) and in untreated controls after stimulation with pilocarpine (10 mg/kg) or carbamylcholine (50-100 mg/kg). A 44% reduction in the volume of saliva and ele...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(77)90200-x

    authors: Eccher S,Dodson C,Quissell DO,Martinez JR

    更新日期:1977-01-21 00:00:00

  • Autoradiographic analysis of muscarinic receptors in rat nasal glands.

    abstract::An in vitro method was developed for the biochemical and autoradiographic demonstration of low muscarinic receptor densities in peripheral tissue. Histological criteria point clearly to the necessity for fixation to preserve tissue quality. [3H]l-Quinuclidinylbenzilate bound specifically to a homogeneous class of bind...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(88)90342-1

    authors: Van Megen YJ,Teunissen MJ,Klaassen AB,Rodrigues de Miranda JF

    更新日期:1988-01-05 00:00:00

  • MPP+ inhibits mGluR1/5-mediated long-term depression in mouse hippocampus by calpain activation.

    abstract::Neurotoxins are harmful to nervous system and cause either neuronal cell death or impairment of synaptic activity, which contributes to Parkinson's disease or other neuronal disorders. Hippocampal synaptic plasticity was proposed as a cellular model for memory processing. In this study, we reported a novel effect of n...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2016.11.048

    authors: Li J,Chen H,Wu S,Cheng Y,Li Q,Wang J,Zhu G

    更新日期:2017-01-15 00:00:00

  • Peripheral kappa 1-opioid receptor-mediated analgesia in mice.

    abstract::When injected directly into the tail, U50,488H is a potent analgesic in the tailflick assay (ED50 3.1 micrograms). The analgesic activity is lost if the radiant heat is focused 1 cm away from the site of injection. The kappa 1-opioid receptor antagonist nor-binaltorphimine given systemically reverses the local analges...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(96)00520-1

    authors: Kolesnikov Y,Jain S,Wilson R,Pasternak GW

    更新日期:1996-08-29 00:00:00

  • The hypotensive agent dodoneine inhibits L-type Ca2+ current with negative inotropic effect on rat heart.

    abstract::Agelanthus dodoneifolius is one of the medicinal plants used in African pharmacopeia and traditional medicine for the treatment of cardiovascular diseases. A chemical analysis has identified one of the active principles: Dodoneine (Ddn). It is a new dihydropyranone which exerts hypotensive and vasorelaxant effects on ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.01.059

    authors: Carré G,Carreyre H,Ouedraogo M,Becq F,Bois P,Thibaudeau S,Vandebrouck C,Bescond J

    更新日期:2014-04-05 00:00:00

  • Excitatory amino acid receptor antagonist kynurenic acid attenuates rewarding potential of morphine.

    abstract::The effect of the non-selective antagonist of excitatory amino acid receptors kynurenic acid (50, 100 and 150 mg/kg, i.p.) on morphine-derived reward was studied in rats. Kynurenic acid dose dependently blocked the acquisition of morphine conditioned place preference when injected before conditioning. The expression o...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(94)00462-5

    authors: Bespalov A,Dumpis M,Piotrovsky L,Zvartau E

    更新日期:1994-11-03 00:00:00

  • Characterization of endothelium-dependent relaxation and modulation by treatment with pioglitazone in the hypercholesterolemic rabbit renal artery.

    abstract::The present study was undertaken to investigate vascular function in hypercholesterolemic rabbits and also to characterize the effects of pioglitazone on it. Rabbits were fed normal, 0.5% cholesterol chow, or 0.5% cholesterol chow plus 300 ppm pioglitazone for 5 or 10 weeks. The tension of isolated renal artery rings ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2004.06.062

    authors: Moroe H,Fujii H,Honda H,Arai K,Kanazawa M,Notoya Y,Kogo H

    更新日期:2004-08-30 00:00:00

  • Dinitrosyl iron complexes with glutathione suppress experimental endometriosis in rats.

    abstract::Dinitrosyl iron complexes (DNIC) with glutathione exert a cytotoxic effect on endometrioid tumours in rats with surgically induced experimental endometriosis. Intraperitoneal treatment of rats (Group 1) with DNIC (12.5μmoles/kg, daily, for 12 days), beginning with day 4 after the surgical operation (implantation of tw...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.01.002

    authors: Burgova EN,Tkachev NА,Adamyan LV,Mikoyan VD,Paklina OV,Stepanyan AA,Vanin AF

    更新日期:2014-03-15 00:00:00

  • Effect of propionyl-L-carnitine on oscillatory potentials in electroretinogram in streptozotocin-diabetic rats.

    abstract::The effect of propionyl-L-carnitine, an analogue of L-carnitine, and insulin on the oscillatory potentials of the electroretinogram was determined in rats with streptozotocin-induced diabetes. Propionyl-L-carnitine was administered at a daily dose of 0.5 g/kg by gavage for 4 weeks, while other rats were treated with s...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(96)00420-7

    authors: Hotta N,Koh N,Sakakibara F,Nakamura J,Hamada Y,Hara T,Fukasawa H,Kakuta H,Sakamoto N

    更新日期:1996-09-12 00:00:00

  • 4-Phenylbutyric acid regulates CCl4-induced acute hepatic dyslipidemia in a mouse model: A mechanism-based PK/PD study.

    abstract::Endoplasmic reticulum (ER) stress and associated protein aggregation are closely associated with human diseases, including alterations in hepatic lipid metabolism. Inhibition of ER stress can have a significant effect on the prevention of hepatic dyslipidemia. Here, we studied the role of 4-phenylbutyric acid (4-PBA),...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2016.02.068

    authors: Lee HY,Marahatta A,Bhandary B,Kim HR,Chae HJ

    更新日期:2016-04-15 00:00:00

  • Effect of a decrease in pH on responses mediated by P2 receptors in the rat mesenteric arterial bed.

    abstract::The present study investigated the effect of acidosis (reduction in pH of the Krebs' solution from 7.4 to 6.9) on responses to vasoconstrictors and vasodilators, with a focus on purines, in the rat isolated perfused mesenteric arterial bed. alpha,beta-Methylene ATP (alpha,beta-meATP) (10 microM), a selective P2X recep...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00631-2

    authors: Ralevic V

    更新日期:2000-10-06 00:00:00

  • The effect of cismethrin on the rat dorsal root potentials.

    abstract::Dorsal root potentials were recorded from urethane-anaesthetised rats. Bicuculline, a recognised GABA antagonist, reduced the amplitude of the potential to 67% of control. Cismethrin, a synthetic pyrethroid insecticide, enhanced the potential to 142% of control values. The convulsions associated with cismethrin poison...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(80)90304-0

    authors: Smith PR

    更新日期:1980-08-22 00:00:00

  • Ex vivo studies after oral treatment of the beagle with dihydroergotamine.

    abstract::Plasma concentrations of unchanged dihydroergotamine (DHE) were measured in beagle dogs on days 1 and 7 of a 1 week treatment with daily oral doses of DHE. Responses to both 5-HT and noradrenaline were monitored isometrically on spiral strips from saphenous arteries and femoral veins removed 24 and 72 h after the last...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(83)90601-5

    authors: Müller-Schweinitzer E,Rosenthaler J

    更新日期:1983-04-22 00:00:00

  • Enhanced endothelial nitric oxide activity contributes to the reduced responsiveness of vascular alpha1-adrenoceptors following aortic barodenervation.

    abstract::We have recently shown that short-term aortic barodenervation diminishes constrictor responses to activation of alpha1-adrenoceptors in rat aortic smooth muscle. This study investigated the potential role of vascular endothelium and its derived vasoactive substances, nitric oxide and prostaglandins, in the reduced alp...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(97)01283-1

    authors: El-Mas MM,Daabees TT,El-Gowelli HM,Abdel-Galil AG

    更新日期:1997-10-22 00:00:00

  • Discriminative stimulus effects of BAY 38-7271, a novel cannabinoid receptor agonist.

    abstract::BAY 38-7271 [(-)-(R)-3-(2-hydroxymethylindanyl-4-oxy)phenyl-4,4,4-trifluoro-1-sulfonate] is a novel, highly potent and selective cannabinoid CB(1)/CB(2) receptor agonist with neuroprotective properties. It was the aim of the present study to further confirm its cannabinoid CB(1) receptor agonist properties in a highly...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(02)02697-3

    authors: De Vry J,Rüdiger Jentzsch K

    更新日期:2002-12-20 00:00:00