Pertussis toxin differentially reduces the efficacy of opioids to produce supraspinal analgesia in the mouse.

Abstract:

:The i.c.v. administration of 0.5 microgram pertussis toxin to mice led to a non-competitive reduction (approximately 60 to 70%) of the supraspinal analgesia evoked by i.c.v. injection of ED90 doses of [D-Ala2,N-MePhe4,Gly-ol5]enkephalin, [D-Ala2,N-MePhe4,Met-(O)5-ol]enkephalin, [D-Ala2,Met5]enkephalinamide, [D-Ala2,D-Leu5]enkephalin or [D-Pen2,D-Pen5]enkephalin, whereas the analgesic effect of ED90 doses of morphine, etorphine, beta-casomorphin-(1-4) amide or human beta-endorphin was reduced to a lesser extent (about 20 to 30%). The co-administration of any of the opioids from the first group together with morphine resulted in antagonism of the effect elicited by the alkaloid. It is suggested that pertussis toxin treatment reduces differentially the efficacy displayed by various opioids when acting via mu receptors to produce supraspinal analgesia.

journal_name

Eur J Pharmacol

authors

Sánchez-Blázquez P,Garzón J

doi

10.1016/0014-2999(88)90732-7

subject

Has Abstract

pub_date

1988-08-02 00:00:00

pages

357-61

issue

3

eissn

0014-2999

issn

1879-0712

pii

0014-2999(88)90732-7

journal_volume

152

pub_type

杂志文章
  • Diallyl disulfide ameliorates gentamicin-induced oxidative stress and nephropathy in rats.

    abstract::Experimental evidences suggest a role of reactive oxygen species in gentamicin-induced nephropathy in rats. Therefore, we investigated if diallyl disulfide, a garlic-derived compound with antioxidant properties, has a renoprotective effect in this experimental model. Four groups of rats were studied: (1) control, (2) ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(03)01948-4

    authors: Pedraza-Chaverrí J,González-Orozco AE,Maldonado PD,Barrera D,Medina-Campos ON,Hernández-Pando R

    更新日期:2003-07-18 00:00:00

  • Increase in renal phorbol ester receptors in rats with cyclosporine A-induced nephrotoxicity.

    abstract::Treatment of rats with cyclosporine A (50 mg/kg i.p.) for 4 days resulted in the impairment of renal function. Renal membrane and soluble phorbol ester receptor densities were significantly higher in cyclosporine A-treated rats compared to vehicle-treated rats. These data suggest that increased phorbol ester receptor ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(91)90396-8

    authors: Nambi P,Pullen M,Wu HL,Brooks DP

    更新日期:1991-03-19 00:00:00

  • New opioid receptor antagonist: Naltrexone-14-O-sulfate synthesis and pharmacology.

    abstract::Opioid antagonists, naloxone and naltrexone have long been used in clinical practice and research. In addition to their low selectivity, they easily pass through the blood-brain barrier. Quaternization of the amine group in these molecules, (e.g. methylnaltrexone) results in negligible CNS penetration. In addition, zw...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2017.05.024

    authors: Zádor F,Király K,Váradi A,Balogh M,Fehér Á,Kocsis D,Erdei AI,Lackó E,Zádori ZS,Hosztafi S,Noszál B,Riba P,Benyhe S,Fürst S,Al-Khrasani M

    更新日期:2017-08-15 00:00:00

  • AG490, a Jak2 inhibitor, suppressed the progression of murine ovarian cancer.

    abstract::Ovarian cancer is the major cause of cancer death among female genital malignancies, and requires developing novel therapeutic measures. Immune escape and acquisition of tolerance by tumor cells are essential for cancer growth and progression. An immunoregulatory enzyme indoleamine 2,3-dioxygenase (IDO) overexpression...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2015.09.039

    authors: Kobayashi A,Tanizaki Y,Kimura A,Ishida Y,Nosaka M,Toujima S,Kuninaka Y,Minami S,Ino K,Kondo T

    更新日期:2015-11-05 00:00:00

  • The specific effect of Mn2+ on the tonic components of receptor-mediated contractions in isolated vas deferens of the guinea pig.

    abstract::Intracellular accumulation of Mn2+ augmented the contractions induced by norepinephrine and acetylcholine in the guinea pig isolated vas deferens. Contractions repeatedly induced by norepinephrine, acetylcholine, or a high concentration of K+ decreased depending on the incubation time in Ca(2+)-free medium. The rate o...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00664-8

    authors: Tsunobuchi-Ushijima H,Gomi Y

    更新日期:1996-01-11 00:00:00

  • Histamine H3 receptor-mediated inhibition of sympathetically evoked mydriasis in rats.

    abstract::This study was designed to determine if the histamine H3 receptor agonist R-alpha-methylhistamine would play a role in modulation of sympathetically evoked mydriasis in anesthetized rats, and if so, to ascertain the specific receptor subtype(s) involved. Reproducible frequency-response curves of pupillary dilation wer...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(01)00977-3

    authors: Yu Y,Kawarai M,Koss MC

    更新日期:2001-05-04 00:00:00

  • Antidepressant-like activity of corticotropin-releasing factor type-1 receptor antagonists in mice.

    abstract::The development of selective corticotropin-releasing factor type-1 (CRF1) receptor antagonists represents a potential novel treatment for depression. These studies evaluated CRF1 receptor antagonists for antidepressant-like activity in mice. Subchronic dosing of both R 121919 (3-[6-(dimethylamino)-4-methyl-pyrid-3-yl]...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2004.07.091

    authors: Nielsen DM,Carey GJ,Gold LH

    更新日期:2004-09-19 00:00:00

  • The influence of delta9-tetrahydrocannabinol on pilocarpine-induced parotid secretions of the rat.

    abstract::The effects of delta9-THC and its ethanol vehicle on pilocarpine-induced parotid gland secretions were investigated in rats. Single doses of delta9-THC (1, 2.5, 5 and 10 mg/kg) or 95% ethanol were administered i.v. prior to pilocarpine stimulation of saliva. Total flow, alpha-amylase and cation content of the induced ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(76)90071-6

    authors: Nagle B,Tomassone BM,Digregorio J,Piraino A

    更新日期:1976-12-01 00:00:00

  • Effects of encainide on myocardial contractility of cat papillary muscle.

    abstract::The action of a new effective antiarrhythmic agent, encainide, was studied with respect to the mechanical performance of isolated cat papillary muscle. Encainide (0.1-10 micrograms/ml) did not alter the performance of cardiac muscle during either the contraction or relaxation phase. By contrast, lidocaine (1-5 microgr...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(81)90511-2

    authors: Brutsaert DL

    更新日期:1981-12-03 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

  • Linoleic and dihomo-gamma-linolenic acids modulate granuloma growth and granuloma macrophage eicosanoid release.

    abstract::We have already demonstrated that arachidonic acid (AA) inhibits carrageenin-induced granuloma growth in vivo and that this effect is related to an increase in prostaglandin E2 formation. As prostaglandin E1 has been shown to be more effective in inhibiting granuloma growth than prostaglandin E2 we investigated the ef...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90234-7

    authors: Elliott GR,Adolfs MJ,Van Batenburg M,Bonta IL

    更新日期:1986-05-27 00:00:00

  • Mangiferin alleviates lipopolysaccharide and D-galactosamine-induced acute liver injury by activating the Nrf2 pathway and inhibiting NLRP3 inflammasome activation.

    abstract::Mangiferin, a glucosylxanthone from Mangifera indica, has been reported to have anti-inflammatory effects. However, the protective effects and mechanisms of mangiferin on liver injury remain unclear. This study aimed to determine the protective effects and mechanisms of mangiferin on lipopolysaccharide (LPS) and D-gal...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2015.12.006

    authors: Pan CW,Pan ZZ,Hu JJ,Chen WL,Zhou GY,Lin W,Jin LX,Xu CL

    更新日期:2016-01-05 00:00:00

  • Role of ERK1/2 signaling pathways in 4-aminopyridine-induced rat pulmonary vasoconstriction.

    abstract::The aim of the present study was to investigate the contribution of extracellular signal regulated kinase-1/2 (ERK1/2) to pulmonary artery contraction in response to 4-aminopyridione (4-AP), an inhibitor of a voltage-gated K(+) channels that regulate pulmonary vascular tone. Pulmonary artery rings 1-1.5 mm in diameter...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2007.04.042

    authors: Han W,Tang X,Wu H,Liu Y,Zhu D

    更新日期:2007-08-13 00:00:00

  • Effects of amiloride on the neurally mediated contraction of rat mesenteric artery.

    abstract::The effects of amiloride on contraction evoked by perivascular nerve stimulation were studied in a ring preparation of rat mesenteric artery. The contraction evoked by nerve stimulation was abolished by tetrodotoxin or prazosin. Amiloride depressed the nerve-induced contraction concentration dependently. Noradrenaline...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(96)00879-5

    authors: Shimamura K,Zou LB,Moriyama K,Yamamoto K,Sekiguchi F,Sunano S

    更新日期:1997-02-05 00:00:00

  • Enrichment and characterization of specific [3H]PGE2 binding sites in the porcine gastric mucosa.

    abstract::[3H]Prostaglandin E2 (PGE2) binding sites were 10-fold enriched from a porcine fundic mucosal homogenate by differential centrifugation and subsequent discontinuous sucrose gradient separation. PGE2 bound with an activation energy of 66 kJ/mol to a single class of sites with an affinity of 1.5 +/- 0.4 nM and a capacit...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(88)90780-7

    authors: Beinborn M,Netz S,Staar U,Sewing KF

    更新日期:1988-03-01 00:00:00

  • Hydralazine-induced vasodilation involves opening of high conductance Ca2+-activated K+ channels.

    abstract::The purpose of this study was to investigate whether high conductance Ca2+-activated K+ channels (BK(Ca)) are mediating the vasodilator action of hydralazine. In isolated porcine coronary arteries, hydralazine (1-300 microM), like the K+ channel opener levcromakalim, preferentially relaxed contractions induced by K+ (...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(98)00701-8

    authors: Bang L,Nielsen-Kudsk JE,Gruhn N,Trautner S,Theilgaard SA,Olesen SP,Boesgaard S,Aldershvile J

    更新日期:1998-11-13 00:00:00

  • Anti-cancer activity of two novel heterocyclic compounds through modulation of VEGFR and miR-122 in mice bearing Ehrlich ascites carcinoma.

    abstract::Metastasis in breast cancer is a leading cause of mortality among women in many countries. This study investigated the anti-cancer role of benzoimidazoquinazoline and benzimidazotriazin; two novel compounds that were designed, synthesized, structurally elucidated, and biologically evaluated as potent anti-angiogenic a...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2020.173747

    authors: Hazem RM,Mohamed AA,Ghareb N,Mehanna ET,Mesbah NM,Abo-Elmatty DM,Elgawish MS

    更新日期:2021-02-05 00:00:00

  • A role for protein kinase C in the attenuated response to 5-hydroxytryptamine in aortas from streptozotocin-diabetic rats.

    abstract::We investigated protein kinase C participation in the contractile response to 5-hydroxytryptamine (5-HT), and in the interaction between 5-HT and endothelin-1, in aortas from control and diabetic rats. Diabetic rats display attenuated reactivity to 5-HT (i.e., approximately 47% of control maximum). The protein kinase ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(96)00986-7

    authors: James GM,Hodgson WC

    更新日期:1997-03-12 00:00:00

  • B-973, a novel piperazine positive allosteric modulator of the α7 nicotinic acetylcholine receptor.

    abstract::The alpha7 (α7) nicotinic acetylcholine receptor is a therapeutic target for cognitive disorders. Here we describe 3-(3,4-difluorophenyl)-N-(1-(6-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)ethyl)propanamide (B-973), a novel piperazine-containing molecule that acts as a positive allosteric modulator of the α7 recepto...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2017.01.037

    authors: Post-Munson DJ,Pieschl RL,Molski TF,Graef JD,Hendricson AW,Knox RJ,McDonald IM,Olson RE,Macor JE,Weed MR,Bristow LJ,Kiss L,Ahlijanian MK,Herrington J

    更新日期:2017-03-15 00:00:00

  • Effects on feline pial arterioles in situ of bosentan, a non-peptide endothelin receptor antagonist.

    abstract::The cerebrovascular actions of bosentan, a novel endothelin antagonist with effects at endothelin ETA and ETB receptors, have been examined in individual pial arterioles on the cortical surface of chloralose-anaesthetised cats. Subarachnoid perivascular microapplication of bosentan (0.3-300 microM) had minimal effect ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(94)90010-8

    authors: Patel TR,McAuley MA,McCulloch J

    更新日期:1994-07-21 00:00:00

  • (S)YS-51, a novel isoquinoline alkaloid, attenuates obesity-associated non-alcoholic fatty liver disease in mice by suppressing lipogenesis, inflammation and coagulation.

    abstract::Obesity-associated non-alcoholic fatty liver disease (NAFLD) increases coagulation and inflammation. We hypothesized that (S)YS-51, an agent found to be beneficial in animal models of sepsis, may reduce NAFLD in high-fat diet (HFD) mice by reducing coagulation and inflammation. C57BL/6 mice were fed either a chow diet...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2016.06.040

    authors: Park EJ,Kim YM,Kim HJ,Jang SY,Oh MH,Lee DH,Chang KC

    更新日期:2016-10-05 00:00:00

  • Anti-tumor necrosis factor agent PEG-sTNFRI improves the growth hormone/insulin-like growth factor-I system in adjuvant-induced arthritic rats.

    abstract::Adjuvant-induced arthritis is associated with body weight loss and decreased pituitary growth hormone (GH) and hepatic insulin-like growth factor-I (IGF-I) synthesis. Cytokines as tumor necrosis factor (TNF) mediate wasting associated with chronic inflammation. The aim of this study was to analyse whether the inhibiti...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2006.02.035

    authors: Granado M,Priego T,Martín AI,Vara E,López-Calderón A,Angeles Villanúa M

    更新日期:2006-04-24 00:00:00

  • Evidence that the purported dopaminergic agonist (3,4-dihydroxyphenylimino)-2-imidazolidine (DPI) may reduce rat striatal dopamine turnover by an alpha 2-adrenergic mechanism.

    abstract::The potent alpha-adrenergic agonist DPI, which has also been claimed to be a selective dopaminergic agonist, was shown to reduce rat striatal dopamine (DA) synthesis, DA utilization and DA metabolism following intraperitoneal administration (25 mumol/kg). An analytical procedure for the determination of DPI was develo...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(82)90603-3

    authors: van Oene JC,Houwing HA,Horn AS

    更新日期:1982-06-16 00:00:00

  • Activation of KATP channels increases anticancer drug delivery to brain tumors and survival.

    abstract::Several anticancer drugs are ineffective against brain tumor and do not impact patient survival because they fail to cross the blood-brain tumor barrier (BTB) effective levels. One such agent temozolomide is commonly used in brain tumor patients, which works better when combined with radiation or other anticancer agen...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2008.10.056

    authors: Ningaraj NS,Sankpal UT,Khaitan D,Meister EA,Vats T

    更新日期:2009-01-14 00:00:00

  • Brivaracetam and seletracetam, two new SV2A ligands, improve paroxysmal dystonia in the dt sz mutant hamster.

    abstract::Previous examinations demonstrated antidystonic effects of the synaptic vesicle protein 2A (SV2A) ligand levetiracetam in the dt(sz) mutant hamster, an animal model of paroxysmal non-kinesiogenic dyskinesia in which dystonic episodes can be induced by stress. In the present study, we examined the effects of the two ne...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2008.10.048

    authors: Hamann M,Sander SE,Richter A

    更新日期:2008-12-28 00:00:00

  • Cardioprotection of salidroside from ischemia/reperfusion injury by increasing N-acetylglucosamine linkage to cellular proteins.

    abstract::The modification of proteins with O-linked N-acetylglucosamine (O-GlcNAc) is increasingly recognized as an important posttranslational modification that modulates cellular function. Recent studies suggested that augmentation of O-GlcNAc levels increase cell survival following stress. Salidroside, one of the active com...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2009.04.012

    authors: Wu T,Zhou H,Jin Z,Bi S,Yang X,Yi D,Liu W

    更新日期:2009-06-24 00:00:00

  • Effects of intrathecally administered THIP, baclofen and muscimol on nociceptive threshold.

    abstract::This study examined whether the antinociceptive activity of THIP (4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol), a GABA agonist, is mediated through an action exerted at the level of the spinal cord. Intrathecal injection of doses of THIP devoid of motor effects (1-2 micrograms) did not increase tail flick or hot pl...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(84)90197-3

    authors: Hammond DL,Drower EJ

    更新日期:1984-08-03 00:00:00

  • Sex differences in the motor inhibitory and stimulatory role of dopamine D1 receptors in rats.

    abstract::We investigated sex differences in the motor responses to the full and selective dopamine D1-like receptor agonist, (+/-)-6-chloro-7,8-dihydroxyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide (SKF-81297; 0.3, 3, and 10 mg/kg, s.c.), in non-habituated adult rats. In general, SKF-81297 produced a biphasic ef...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(02)01716-8

    authors: Heijtz RD,Beraki S,Scott L,Aperia A,Forssberg H

    更新日期:2002-06-07 00:00:00

  • In vitro binding of the very potent and selective D-2 dopamine agonist, [3H]N-0437 to calf caudate membranes.

    abstract::N-0437, a non-catecholic aminotetralin has recently been described as a very potent and selective dopamine D-2 agonist. In this study the in vitro binding of [3H]N-0437 (specific activity 80.6 Ci/mmol) to calf caudate membranes is described. It was found that [3H]N-0437 binds with a high affinity (KD = 0.17 nM) and a ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(87)90167-1

    authors: Van der Weide J,De Vries JB,Tepper PG,Horn AS

    更新日期:1987-02-10 00:00:00

  • Crocetin, a carotenoid derivative, inhibits retinal ischemic damage in mice.

    abstract::Crocetin, an aglycone of crocin, is found both in the saffron crocus (Crocus starus L.) and in gardenia fruit (Gardenia jasminoides Ellis). We evaluated the protective effects of crocetin against the retinal ischemia induced by 5h unilateral ligation of both the pterygopalatine artery (PPA) and the external carotid ar...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2013.02.007

    authors: Ishizuka F,Shimazawa M,Umigai N,Ogishima H,Nakamura S,Tsuruma K,Hara H

    更新日期:2013-03-05 00:00:00