Inhibitory actions of ropivacaine on tumor necrosis factor-alpha-induced leukocyte adhesion and tissue accumulation in vivo.

Abstract:

:We have examined the effect of ropivacaine, a local anesthetic, on leukocyte-endothelium interactions induced by tumor necrosis factor-alpha (TNF-alpha) in vivo by the use of intravital microscopy in the mouse cremaster microcirculation. It was found that ropivacaine markedly reduced venular leukocyte adhesion and tissue recruitment in response to TNF-alpha challenge, whereas leukocyte rolling was unchanged. Thus, treatment with ropivacaine may be a useful pharmacological tool to control acute inflammation.

journal_name

Eur J Pharmacol

authors

Zhang XW,Thorlacius H

doi

10.1016/s0014-2999(00)00108-4

keywords:

subject

Has Abstract

pub_date

2000-03-24 00:00:00

pages

R1-3

issue

1-2

eissn

0014-2999

issn

1879-0712

pii

S0014-2999(00)00108-4

journal_volume

392

pub_type

杂志文章
  • Mechanisms of phenylalanine-induced pressor effects in conscious rats.

    abstract::Phenylalanine and tyrosine reportedly decrease blood pressure in conscious restrained rats. However, tyrosine has recently been found to increase blood pressure in anesthetized animals, questioning the generality of findings obtained in restrained animals. The present study therefore evaluated the effects of phenylala...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(89)90494-9

    authors: Yourick DL,Tessel RE

    更新日期:1989-01-31 00:00:00

  • Tissue kallikrein (kallidinogenase) protects against retinal ischemic damage in mice.

    abstract::Ocular ischemic syndrome is likely stem from retinal ischemia, and which causes visual disorder. The pathological mechanism of ocular ischemic syndrome is still unknown, therefore the optimal treatment for ocular ischemic syndrome remains to be established. Then, this study aimed to evaluate the effects of tissue-deri...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.05.033

    authors: Masuda T,Shimazawa M,Ishizuka F,Nakamura S,Tsuruma K,Hara H

    更新日期:2014-09-05 00:00:00

  • Glycine regulates the production of pro-inflammatory cytokines in lean and monosodium glutamate-obese mice.

    abstract::Fat tissue plays an important role in the regulation of inflammatory processes. Increased visceral fat has been associated with a higher production of cytokines that triggers a low-grade inflammatory response, which eventually may contribute to the development of insulin resistance. In the present study, we investigat...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2008.09.047

    authors: Alarcon-Aguilar FJ,Almanza-Perez J,Blancas G,Angeles S,Garcia-Macedo R,Roman R,Cruz M

    更新日期:2008-12-03 00:00:00

  • Discrepancies in characterization of sigma sites in the mouse central nervous system.

    abstract::The characteristics of [3H](+)-pentazocine and [3H]1,3-di(2-tolyl) guanidine (DTG) binding to mouse whole brain, cortex, cerebellum and spinal cord membranes were investigated in radioreceptor assays. [3H](+)-Pentazocine bound to a single, high affinity site (Kd = 1.2-1.6 nM) with increasing density along the neuraxis...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00383-v

    authors: Kovács KJ,Larson AA

    更新日期:1995-10-16 00:00:00

  • Mast cells, brain inflammation and autism.

    abstract::Increasing evidence indicates that brain inflammation is involved in the pathogenesis of neuropsychiatric diseases. Mast cells (MCs) are located perivascularly close to neurons and microglia, primarily in the leptomeninges, thalamus, hypothalamus and especially the median eminence. Corticotropin-releasing factor (CRF)...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章,评审

    doi:10.1016/j.ejphar.2015.03.086

    authors: Theoharides TC,Stewart JM,Panagiotidou S,Melamed I

    更新日期:2016-05-05 00:00:00

  • Inhibition of synaptosomal [3H]noradrenaline uptake by beta-adrenoceptor blocking drugs: influence of lipophilicity.

    abstract::Ten beta-adrenoceptor blocking drugs varying in lipophilicity and beta-adrenoceptor blocking potency were examined for inhibitory effects on synaptosomal [3H]noradrenaline uptake. All compounds produced a concentration-dependent inhibition of noradrenaline uptake, but were at least one order of magnitude less potent t...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(84)90263-2

    authors: Street JA,Walsh A

    更新日期:1984-07-13 00:00:00

  • Effects of spinorphin and tynorphin on synaptic transmission in rat hippocampal slices.

    abstract::Spinorphin has been isolated from the bovine spinal cord as an endogenous inhibitor of enkephalin-degrading enzymes (aminopeptidase, dipeptidyl aminopeptidase III, angiotensin-converting enzyme and enkephalinase), and tynorphin has been synthesized as a more potent inhibitor of dipeptidyl aminopeptidase III. In this s...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(01)00742-7

    authors: Yamazaki T,Honda M,Yamamoto Y,Hazato T,Ono H

    更新日期:2001-02-16 00:00:00

  • Regulation of acetylcholine hydrolysis in canine tracheal smooth muscle.

    abstract::The regulation of acetylcholine (ACh) lifetime by acetylcholinesterase (AChE, EC 3.1.1.7) and butyrylcholinesterase (BuChE, EC 3.1.1.8) was evaluated in vitro in canine tracheal smooth muscle preparations. Selective inhibition of AChE by low concentrations of 1,5-bis(N-allyl-N,N-dimethyl-4-ammoniumphenyl)-pentane-3-on...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(91)90772-i

    authors: Adler M,Reutter SA,Moore DH,Filbert MG

    更新日期:1991-11-19 00:00:00

  • Inhibitory effect of sevoflurane on nitric oxide release from cultured endothelial cells.

    abstract::We investigated the effect of sevoflurane (fluoromethyl-2,2,2-trifluoro-1-(trifluoromethyl) ethylether) on intracellular calcium concentration ([Ca2+]i) and nitric oxide (NO) release from cultured porcine aortic endothelial cells using fura-2 fluorometry, and direct (ESR spectrometry with NO-trapping by 2-(4-carboxyph...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0922-4106(95)90165-5

    authors: Az-ma T,Fujii K,Yuge O

    更新日期:1995-03-15 00:00:00

  • Failure to detect 6-hydroxydopamine in rat striatum after the dopamine releasing drugs dexamphetamine, methylamphetamine and MPTP.

    abstract::Large doses of dexamphetamine, methylamphetamine and MPTP failed to induce the formation of 6-hydroxydopamine (6-OHDA) in rat striatum. The potent dopamine (DA) releasing actions of these drugs and of the MPTP metabolite MPP+ were shown by intracerebral dialysis of DA in conscious rats but 6-OHDA was not detectable in...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90011-7

    authors: Rollema H,De Vries JB,Westerink BH,Van Putten FM,Horn AS

    更新日期:1986-12-02 00:00:00

  • Stimulation of peripheral cholinergic nerves by glutamate indicates a new peripheral glutamate receptor.

    abstract::The bronchial smooth muscle of the rat was examined for contractile responses to excitatory amino acids. The nerve-mediated contraction induced by electrical field stimulation was enhanced by exogenous L-glutamate (L-Glu). The apparent affinity (ED50) of L-Glu was 3.5 +/- 0.1 mM. Both tetrodotoxin and hemicholinium-3 ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(89)90235-5

    authors: Aas P,Tansø R,Fonnum F

    更新日期:1989-05-02 00:00:00

  • Increase of myocardial pH by 1- and d-propranolol during ischemia of the heart in dogs.

    abstract::Myocardial pH was measured continuously with a micro pH electrode inserted into the left ventricular wall in dogs. Anterior descending coronary flow was reduced to about 1/3 of the original flow by partial occlusion of the coronary artery. Myocardial pH decreased from 7.50--7.60 to 7.06--7.24 after partial occlusion. ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(80)90231-9

    authors: Abiko Y,Sakai K

    更新日期:1980-06-27 00:00:00

  • Influence of pH changes on the actions of verapamil on cardiac excitation-contraction coupling.

    abstract::Langendorff preparations of Sprague-Dawley rat hearts were perfused with calcium-free Krebs solution of pH 7.48 (control), 7.26 (acidosis) or 7.69 (alkalosis) containing either adrenaline or potassium. The responses of the force of contraction, coronary perfusion pressure and heart rate to graded doses of calcium prec...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(91)90411-i

    authors: Achike FI,Dai S

    更新日期:1991-04-10 00:00:00

  • A comparative study of electrical field stimulation of the guinea-pig, ferret and marmoset urinary bladder.

    abstract::The spontaneous and electrically evoked activity was examined in guinea-pig, ferret and marmoset urinary bladder. Electrical field stimulation of detrusor strips in vitro induced a rapid, frequency-dependent contraction with a maximum response at 40 Hz. This contraction was partly decreased by either atropine (0.29 mi...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(85)90375-9

    authors: Moss HE,Burnstock G

    更新日期:1985-08-27 00:00:00

  • Novel persistent activation of muscarinic M1 receptors by xanomeline.

    abstract::The muscarinic agonists, xanomeline and carbachol, displayed similar intrinsic activities in stimulating neuronal nitric oxide synthase at muscarinic M1 receptors in Chinese hamster ovary (CHO) cells, with xanomeline being more potent. Pre-incubation (1 h) with 1 microM xanomeline, followed by extensive washing, resul...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(97)01162-x

    authors: Christopoulos A,El-Fakahany EE

    更新日期:1997-09-03 00:00:00

  • Pharmacological evidence for selective inhibition of gastric acid secretion by telenzepine, a new antimuscarinic drug.

    abstract::The new antisecretory drug, telenzepine (4,9-dihydro-3-methyl-4-[(4-methyl-1-piperazinyl)acetyl]-10H-thieno-[3,4 - b][1,5]benzodiazepin-10-one), was investigated for its inhibition of functionally intact muscarinic receptors involved in gastric acid secretion in rabbit fundic glands, perfused mouse stomach in vitro, p...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(85)90498-4

    authors: Eltze M,Gönne S,Riedel R,Schlotke B,Schudt C,Simon WA

    更新日期:1985-06-07 00:00:00

  • ATP non-competitive IGF-1 receptor kinase inhibitors as lead anti-neoplastic and anti-papilloma agents.

    abstract::The insulin-like growth factor-1 receptor (IGF-1 receptor) is a receptor tyrosine kinase, highly homologous to the insulin receptor. In contrast to the insulin receptor, which is mostly involved in metabolic pathways, the IGF-1 system plays a pivotal role in normal and neoplastic cell growth through anti-apoptotic, pr...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2007.01.052

    authors: Steiner L,Blum G,Friedmann Y,Levitzki A

    更新日期:2007-05-07 00:00:00

  • Cooperation of calcineurin and ERK for UTP-induced IL-6 production in HaCaT keratinocytes.

    abstract::UTP causes IL-6 production in HaCaT keratinocytes, which is partially inhibited by PD98059, a mitogen-activated protein kinase kinase (MEK) inhibitor, suggesting that a pathway other than the extracellular signal-regulated kinase (ERK) pathway is involved in the production. In the present study, we examined the involv...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2007.07.058

    authors: Kobayashi D,Ohkubo S,Nakahata N

    更新日期:2007-11-14 00:00:00

  • Serotonergic effects of dotarizine in coronary artery and in oocytes expressing 5-HT2 receptors.

    abstract::In strips of pig coronary arteries incubated in oxygenated Krebs-bicarbonate solution at 37 degrees C, dotarizine blocked the phasic contractions evoked by 5-HT (0.5 microM) or K+ depolarization (35 mM K+) with an IC50 of 0.22 and 3.7 microM, respectively. Flunarizine inhibited both types of contractions with IC50 val...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(97)01073-x

    authors: Montiel C,Herrero CJ,García-Palomero E,Renart J,García AG,Lomax RB

    更新日期:1997-08-06 00:00:00

  • Characterisation of [3H]gabapentin binding to a novel site in rat brain: homogenate binding studies.

    abstract::The binding characteristics of [3H]gabapentin, the radiolabelled analogue of the novel anticonvulsant gabapentin (1-(aminomethyl)cyclohexaneacetic acid) were studied using purified synaptic plasma membranes prepared from rat cerebral cortex. In 10 mM HEPES buffer [3H]gabapentin bound to a single population of sites wi...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0922-4106(93)90155-3

    authors: Suman-Chauhan N,Webdale L,Hill DR,Woodruff GN

    更新日期:1993-02-15 00:00:00

  • Berberine as a promising anti-diabetic nephropathy drug: An analysis of its effects and mechanisms.

    abstract::Diabetic nephropathy is a progressive kidney disorder and is pathologically characterized by thickened glomerular and tubular basement membranes, accumulation of the extracellular matrix and increased mesangial hypertrophy. Growing evidence has suggested that diabetic nephropathy is induced by multiple factors, such a...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章,评审

    doi:10.1016/j.ejphar.2015.04.017

    authors: Ni WJ,Ding HH,Tang LQ

    更新日期:2015-08-05 00:00:00

  • Chronic mianserin treatment decreases 5-HT2 receptor binding without altering 5-HT2 receptor mRNA levels.

    abstract::Rats were injected with 15 mg/kg (i.p.) mianserin or vehicle (saline) for 4, 10 or 21 days and 5-HT2 receptor binding and mRNA levels measured. Treatment with mianserin induced a substantial decrease in 5-HT2 radioligand binding (44-59% decrease; P less than 0.05 vs. control). No changes in the amount of 5-HT2 or, as ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0922-4106(91)90093-w

    authors: Roth BL,Ciaranello RD

    更新日期:1991-06-19 00:00:00

  • Ramatroban, a TP receptor antagonist, improves vascular responses to acetylcholine in hypercholesterolemic rabbits in vivo.

    abstract::Recent studies show that 8-iso-prostaglandin F(2alpha), a member of F(2)-isoprostane family, acts as a vasoconstrictor via TP receptor activation; and its local release may contribute to an abnormal vasomotor tone associated with hypercholesterolemia. The purpose of this study was to examine whether ramatroban, a TP r...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(03)01626-1

    authors: Ishizuka T,Matsui T,Kurita A

    更新日期:2003-05-02 00:00:00

  • Muscarinic receptor mediated signaling pathways in hepatocytes from CCL4 - induced liver fibrotic rat.

    abstract::The pathological changes of parasympathetic nerves are considered as an independent prognostic factor of the survival rate for patients with chronic liver disease. The non-selective muscarinic acetylcholine receptors (mAchR) agonists and antagonists can affect the proliferation of hepatocytes, but little is known abou...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2017.03.047

    authors: Luo L,Xi C,Xu T,Zhang G,Qun E,Zhang W

    更新日期:2017-07-15 00:00:00

  • Neutrophil infiltration into the ischaemic/reperfused rabbit isolated myocardium: effect of PF-5901 and cycloheximide.

    abstract::The Langendorff-perfused rabbit heart preparation has been used to study the interaction of isolated rabbit neutrophils with regionally ischaemic myocardium. Short durations of regional ischaemia (10-60 min) and subsequent reperfusion (30 min) of the hearts with neutrophils resulted in a significant time-dependent acc...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(92)94835-j

    authors: Lad N,Williams TJ,Booth RF

    更新日期:1992-11-17 00:00:00

  • Involvement of notch signaling pathway in amyloid precursor protein induced glial differentiation.

    abstract::The amyloid precursor protein (APP) has been mainly studied in its role in the production of amyloid β peptides (Aβ), because Aβ deposition is a hallmark of Alzheimer's disease. Although several studies suggest APP has physiological functions, it is still controversial. We previously reported that APP increased glial ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2010.09.015

    authors: Kwak YD,Marutle A,Dantuma E,Merchant S,Bushnev S,Sugaya K

    更新日期:2011-01-10 00:00:00

  • Identification of novel pyrazoloquinazolinecarboxilate analogues to inhibit nerve growth factor in vitro.

    abstract::Nerve growth factor (NGF) is known to regulate the development and survival of select populations of neurons via its binding/activation of the TrkA and p75(NTR) receptors. However, in some physiological circumstances NGF dysregulation can result in debilitating pathologies, including diabetic neuropathies, interstitia...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2013.03.029

    authors: Eibl JK,Strasser BC,Ross GM

    更新日期:2013-05-15 00:00:00

  • The genetic deletion of Mas abolishes salt induced hypertension in mice.

    abstract::The G protein-coupled receptor Mas is a physiological antagonist of the angiotensin II type 1 receptor and is associated with angiotensin-(1-7) signaling. We investigated the effect of Mas-deficiency on blood pressure regulation under physiological conditions and salt load using radiotelemetry. Mas-knockout mice and t...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2012.05.025

    authors: Heringer-Walther S,Gembardt F,Perschel FH,Katz N,Schultheiss HP,Walther T

    更新日期:2012-08-15 00:00:00

  • GABA modulates the release of dopamine and acetylcholine from rat caudate nucleus slices.

    abstract::The effects of GABA on depolarization-induced (26 mM K+) release of radiolabeled dopamine (DA) and acetylcholine (ACh) from slices of rat caudate nucleus were examined with a superfusion method. GABA, in concentrations of 10(-5)--10(-3) M, dose-dependently enhanced the release of DA, either accumulated by high-affinit...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(79)90101-8

    authors: Stoof JC,Den Breejen EJ,Mulder AH

    更新日期:1979-07-15 00:00:00

  • An involvement of alpha-adrenergic stimulation in exercise-induced hypoglycemia.

    abstract::Hypoglycemia developed in fasted rats during forced swimming. This hypoglycemia was mostly abolished by phentolamine, an alpha-adrenolytic agent, or by hexamethonium; was potentiated by propranolol, a beta-adrenolytic agent, of by 5-methoxyindole-2-carboxylic acid, a gluconeogenic inhibitor; and was not affected by an...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(77)90184-4

    authors: Yajima M,Hosokawa T,Ui M

    更新日期:1977-03-07 00:00:00