Nicotine potentiates the nitrergic relaxation responses of rabbit corpus cavernosum tissue via nicotinic acetylcholine receptors.

Abstract:

:The presence of neuronal nicotinic acetylcholine receptors in rabbit corpus cavernosum tissue and possible mechanisms underlying the potentiation of electrical field stimulation induced relaxation by nicotine were analyzed. In corpus cavernosum tissue strips nicotine (3 x 10(-5) M) and acetylcholine (10(-3) M) produced potentiation on electrical field stimulation (amplitude 50 V; frequency 4 Hz; width 0.8 ms) induced relaxation responses. This nicotine-induced potentiation was not altered by atropine (10(-6) M), guanethidine (5 x 10(-6) M) and indomethacin (10(-5) M), but abolished by hexamethonium chloride (10(-5) M) and L-nitro arginine methyl ester (10(-5) M). Nicotine did not cause any alteration on a single dose of carbachol (3 x 10(-5) M) and sodium nitroprusside (10(-5) M) induced relaxation responses. The results suggest that, nicotine-induced potentiation is NO and nicotinic acetylcholine receptor dependent but independent from prostaglandin synthesis, activation of muscarinic receptors and does not require intact adrenergic neurons. Nicotine did not affect smooth muscle and endothelium directly. In conclusion, in this study we showed for the first time that, nicotine acts on the nicotinic acetylcholine receptors located on the nitrergic nerves, thereby evoking the release of NO from these nerve terminals inducing relaxation response in rabbit corpus cavernosum tissue.

journal_name

Eur J Pharmacol

authors

Bozkurt NB,Vural IM,Sarioglu Y,Pekiner C

doi

10.1016/j.ejphar.2006.11.053

subject

Has Abstract

pub_date

2007-03-08 00:00:00

pages

172-8

issue

1-3

eissn

0014-2999

issn

1879-0712

pii

S0014-2999(06)01313-6

journal_volume

558

pub_type

杂志文章
  • Membrane activity of class III antiarrhythmic compounds; a comparison between ibutilide, d-sotalol, E-4031, sematilide and dofetilide.

    abstract::This study compares the membrane activity of ibutilide, d-sotalol, sematilide, E-4031 and dofetilide on single ventricular cells under identical experimental conditions. We found that ibutilide and dofetilide produced a 'bell-shaped' concentration-dependent effect on action potential duration. Ionic current measuremen...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(93)90704-l

    authors: Lee KS,Tsai TD,Lee EW

    更新日期:1993-03-30 00:00:00

  • Depression of automaticity of the rabbit SA node by bepridil and nifedipine.

    abstract::The effects of bepridil and nifedipine, newly developed Ca2+ antagonists, were studied on the spontaneous action potentials of the true pacemaker cell preparations (0.5 X 0.5 mm) obtained from the rabbit sino-atrial (SA) node. At the lower concentrations, bepridil (10(-6) M) and nifedipine (10(-8) M) decreased the spo...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(84)90245-0

    authors: Goto J,Sperelakis N

    更新日期:1984-03-23 00:00:00

  • Inhibition of hERG K+ currents by antimalarial drugs in stably transfected HEK293 cells.

    abstract::Several antimalarial drugs are known to produce a QT interval prolongation via a blockade of the rapidly activating delayed rectifier K+ current (IKr), encoded by the human-ether-a-go-go-related gene (hERG). We investigated the influence of lumefantrine and its major metabolite desbutyl-lumefantrine, as well as halofa...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2003.11.003

    authors: Traebert M,Dumotier B,Meister L,Hoffmann P,Dominguez-Estevez M,Suter W

    更新日期:2004-01-19 00:00:00

  • Withaferin A inhibits iNOS expression and nitric oxide production by Akt inactivation and down-regulating LPS-induced activity of NF-kappaB in RAW 264.7 cells.

    abstract::Induction of inducible nitric oxide synthase (iNOS) expression and nitric oxide (NO) production is thought to have beneficial immunomodulatory effects in acute and chronic inflammatory disorders. In Raw 264.7 cells stimulated with lipopolysaccharide (LPS) to mimic inflammation, withaferin A inhibited LPS-induced expre...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2008.09.017

    authors: Oh JH,Lee TJ,Park JW,Kwon TK

    更新日期:2008-12-03 00:00:00

  • The actions of cimetidine hydrochloride and mepyramine maleate in rat adjuvant arthritis.

    abstract::Adjuvant arthritis in rats was induced by a single subcutaneous injection of Freund adjuvant into a hind paw. The injected paws' mean volume increased continuously by 80 +/- 26% after 6 h (acute local response). The injected paw displayed a biphasic response peaking at day 1-2 decreasing to day 5, then increased to da...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(82)90234-5

    authors: Al-Haboubi HA,Zeitlin IJ

    更新日期:1982-02-26 00:00:00

  • Regional distribution of myocardial beta-adrenoceptors in the cat.

    abstract::The purpose of this study was to delineate the distribution of beta-adrenoceptor density in the cat heart, with an emphasis on areas within the left ventricle. beta-Adrenoceptor densities, determined for hearts obtained from five cats, were not significantly different in the left and rights atria, i.e. 47.6 +/- 7.2 an...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90189-5

    authors: Lathers CM,Levin RM,Spivey WH

    更新日期:1986-10-14 00:00:00

  • The actions of receptor-selective substance P analogs on myenteric neurons: an electrophysiological investigation.

    abstract::Intracellular recordings were made from myenteric neurons of the guinea-pig duodenum and the responses to local ejection of several substance P (SP) analogs were examined. It was found that senktide (succinyl-[Asp6,Me-Phe8]SP-(6-11)), a selective analog for the NK-3 (SP-N) receptor, was particularly effective in depol...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(88)90612-7

    authors: Hanani M,Chorev M,Gilon C,Selinger Z

    更新日期:1988-08-24 00:00:00

  • Allosteric modulation of nicotinic acetylcholine receptors as a treatment strategy for Alzheimer's disease.

    abstract::The basic symptoms of Alzheimer's dementia, i.e., a loss in cognitive function, are due to impaired nicotinic cholinergic neurotransmission. To compensate for this impairment by drug treatment, blockers of the acetylcholine-degrading enzyme acetylcholinesterase are applied, even though this approach obviously is prone...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00093-5

    authors: Maelicke A,Albuquerque EX

    更新日期:2000-03-30 00:00:00

  • Block of rat brain recombinant SK channels by tricyclic antidepressants and related compounds.

    abstract::SK channels are small conductance, Ca(2+)-activated K(+) channels that underlie neuronal slow afterhyperpolarization and mediate spike frequency adaptation. Using the patch clamp technique, we tested the effects of eight clinically relevant psychoactive compounds structurally related to the tricyclic antidepressants, ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00401-5

    authors: Dreixler JC,Bian J,Cao Y,Roberts MT,Roizen JD,Houamed KM

    更新日期:2000-07-28 00:00:00

  • Estrogen alone or combined with medroxyprogesterone but not raloxifene reduce myocardial infarct size.

    abstract::We investigated whether estrogen protects the ischemic myocardium in oophorectomized female rabbits fed with a cholesterol-enriched diet, whether the addition of a progestin compound attenuates the beneficial effect of estrogen and whether raloxifene also limits myocardial necrosis. We treated 32 female oophorectomize...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(03)01627-3

    authors: Sbarouni E,Iliodromitis EK,Bofilis E,Kyriakides ZS,Kremastinos DT

    更新日期:2003-04-25 00:00:00

  • Pharmacological regulation of descending cortical control of the nociceptive processing.

    abstract::Clinical and experimental data indicate that the cerebral cortex plays an important role in pain perception and endogenous antinociceptive system function. Moreover, the enhancement of descending inhibitory cortical control may be involved in the mechanisms of analgetic effect of some agents. The present study was des...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(99)00264-2

    authors: Kharkevich DA,Churukanov VV

    更新日期:1999-06-30 00:00:00

  • Evidence that the NH2-terminus of substance P modulates N-methyl-D-aspartate-induced activity by an action involving sigma receptors.

    abstract::Behaviors induced in mice by intrathecal injections of either N-methyl-D-aspartate (NMDA) or kainic acid are modulated by NH2-terminal fragments of substance P, such as substance P-(1-7). The action of substance P-(1-7) on kainic acid depends on sigma receptor activity. The present study was designed to test the hypot...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(96)00199-9

    authors: Hornfeldt CS,Kitto KF,Larson AA

    更新日期:1996-06-13 00:00:00

  • Serotonin-like actions of quipazine and CPP on spinal motoneurones.

    abstract::The actions of iontophoretically applied quipazine (QPZ) and 6-chloro-2-[1-piperazinyl]-pyrazine (CPP) were compared with those of serotonin (5-HT) on rat spinal motoneurones. QPZ and CPP qualitatively resembled 5-HT in that both facilitated single unit activity evoked by glutamate. Like 5-HT, the facilitation they pr...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(82)90600-8

    authors: Neuman RS,White SR

    更新日期:1982-06-16 00:00:00

  • Dopamine antagonists induce gastric lesions in rats.

    abstract::Gastric lesions were provoked in all rats that had received intraperitoneally a single dose of the dopamine antagonists haloperidol, metoclopramide or domperidone 24 h before. Dose-dependence was demonstrated for haloperidol. This drug induced gastric lesions as early as 90 min after its application. The ulcerogenic e...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90522-4

    authors: Sikirić P,Geber J,Ivanović D,Suchanek E,Gjuris V,Tućan-Foretić M,Mise S,Cvitanović B,Rotkvić I

    更新日期:1986-11-12 00:00:00

  • Effects of central administration of tachykinin receptor agonists and antagonists on plus-maze behavior in mice.

    abstract::This study assessed the effects of intracerebroventricular administration of selective agonists and antagonists for tachykinin NK1 and NK2 receptors on performance of mice in the elevated plus-maze, an ethological model of anxiety. Mice were treated with either vehicle (5 microliters) or 1, 10, 100 or 500 pmol of subs...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(96)00390-1

    authors: Teixeira RM,Santos AR,Ribeiro SJ,Calixto JB,Rae GA,De Lima TC

    更新日期:1996-09-05 00:00:00

  • Studies on the role of 5-HT2C and 5-HT2B receptors in regulating generalised seizure threshold in rodents.

    abstract::The present studies were conducted to investigate the role of 5-HT2C and 5-HT2B receptors in the generation of pentylenetetrazol and electroshock-evoked seizures. The 5-HT2C/2B receptor-preferring agonist 1-(m-chlorophenyl)-piperazine (mCPP; 2.5-7 mg/kg i.p.) weakly elevated seizure threshold in the mouse (but not the...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(98)00621-9

    authors: Upton N,Stean T,Middlemiss D,Blackburn T,Kennett G

    更新日期:1998-10-16 00:00:00

  • Cytotrienin A, a translation inhibitor that induces ectodomain shedding of TNF receptor 1 via activation of ERK and p38 MAP kinase.

    abstract::Cytotrienin A, a member of the triene-ansamycin family, was initially identified to be an inducer of apoptosis and recently shown to be an inhibitor of translation that interferes with eukaryotic elongation factor 1A function. In human lung carcinoma A549 cells, cytotrienin A was found to inhibit more strongly the cel...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2011.05.072

    authors: Yamada Y,Taketani S,Osada H,Kataoka T

    更新日期:2011-09-30 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

  • Diazepam induces tolerance in the isolated skin of Pleurodema thaul.

    abstract::The effects of the long-term administration of diazepam on the potential difference and short-circuit current of the isolated skin of the toad Pleurodema thaul (P. thaul) were investigated. Diazepam applied in a concentration range of 4.6 x 10(-6) to 5.2 x 10(-5) M decreased both electrical parameters. This response w...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00252-g

    authors: Norris B,Contreras E,Nunez G,Contreras G

    更新日期:1995-07-04 00:00:00

  • A novel carbazole derivative, MHY407, sensitizes cancer cells to doxorubicin-, etoposide-, and radiation treatment via DNA damage.

    abstract::In this study, we synthesized a novel carbazole derivative, MHY407, as a sensitizer of cancer cells to increase DNA damage. We then evaluated the anticancer effects of MHY407 and identified the molecular mechanism for the sensitization of breast cancer cell lines. MHY407 significantly increased DNA damage as determine...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2012.10.001

    authors: Yoon S,Kim JH,Lee YJ,Ahn MY,Choi G,Kim WK,Yang Z,Lee HJ,Moon HR,Kim HS

    更新日期:2012-12-15 00:00:00

  • Caprolactam-barbiturate interaction at the GABAA receptor complex in the guinea-pig intestine.

    abstract::4,6,6-Trimethylcaprolactam antagonised GABAA receptor-mediated contractile responses in guinea-pig isolated ileum, displacing the GABA dose-response curve to the right in a non-parallel manner, and causing a depression of the maximum response. Pentobarbitone not only potentiated the GABAA receptor-mediated contraction...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90146-9

    authors: Kerr DI,Ong J,Prager RH,Ward DA

    更新日期:1986-05-13 00:00:00

  • The cardiovascular protective role of docosahexaenoic acid.

    abstract::Dietary fish oils rich in n-3 polyunsaturated fatty acids can modulate a diverse range of factors contributing to cardiovascular disease. This study examined the relative roles of eicosapentaenoic acid (20:5 n-3; EPA) and docosahexaenoic acid (22:6 n-3; DHA) which are the principal n-3 polyunsaturated fatty acids rega...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00861-6

    authors: McLennan P,Howe P,Abeywardena M,Muggli R,Raederstorff D,Mano M,Rayner T,Head R

    更新日期:1996-04-04 00:00:00

  • Mechanism of inhibition of platelet aggregation by rutaecarpine, an alkaloid isolated from Evodia rutaecarpa.

    abstract::In this study, rutaecarpine was tested for its antiplatelet activities in human platelet-rich plasma. In human platelet-rich plasma, rutaecarpine (40-200 microM) inhibited aggregation stimulated by a variety of agonists (i.e., collagen, ADP, adrenaline and arachidonic acid). The antiplatelet activity of rutaecarpine (...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(96)00789-3

    authors: Sheu JR,Hung WC,Lee YM,Yen MH

    更新日期:1996-12-30 00:00:00

  • Intradermal application of nociceptin increases vascular permeability in rats: the possible involvement of histamine release from mast cells.

    abstract::Intradermal application of nociceptin was used to investigate its in vivo effect on the inflammatory response in rats. Intradermal nociceptin (5 pmol/site-5 nmol/site) increased vascular permeability in a dose-dependent manner. The increased vascular permeability by nociceptin (5 nmol/site) was dose-dependently inhibi...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00746-9

    authors: Kimura T,Kitaichi K,Hiramatsu K,Yoshida M,Ito Y,Kume H,Yamaki K,Suzuki R,Takagi K

    更新日期:2000-11-03 00:00:00

  • 2-[125I]iodo-5-methoxycarbonylamino-N-acetyltryptamine: a selective radioligand for the characterization of melatonin ML2 binding sites.

    abstract::We now describe the preparation and characterization of a novel radioligand, 2-[125I]iodo-5-methoxy-carbonylamino-N-acetyltryptamine (2-[125I]MCA-NAT), with high affinity and pharmacological selectivity for melatonin ML2 receptor sites. 2-[125I]MCA-NAT was prepared by introducing an [125I]iodine molecule on carbon 2 o...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00870-5

    authors: Molinari EJ,North PC,Dubocovich ML

    更新日期:1996-04-22 00:00:00

  • Unchanged cardiac angiotensin II levels accompany losartan-sensitive cardiac injury due to nitric oxide synthase inhibition.

    abstract::Chronic nitric oxide synthase (NOS) inhibition results in hypertension and myocardial injury. In a rapid and severe model of chronic NOS inhibition, we determined the role of angiotensin II in these effects by using angiotensin II receptor blockade and by measuring cardiac angiotensin II concentrations before and duri...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00384-8

    authors: Verhagen AM,Hohbach J,Joles JA,Braam B,Boer P,Koomans HA,Gröne H

    更新日期:2000-07-21 00:00:00

  • Effect of 4-(4-bromophenyl)-5-(3-chlorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione on the anticonvulsant action of different classical antiepileptic drugs in the mouse maximal electroshock-induced seizure model.

    abstract::The aim of this study was to determine the effects of 4-(4-bromophenyl)-5-(3-chlorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (TP4-a new S-triazole derivative possessing anticonvulsant properties in preclinical studies) on the protective action of four different classical antiepileptic drugs (carbamazepine, phenob...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2012.06.023

    authors: Luszczki JJ,Plech T,Wujec M

    更新日期:2012-09-05 00:00:00

  • Pharmacology of an original and selective nonpeptide antagonist ligand for the human tachykinin NK2 receptor.

    abstract::The pharmacological outline of a novel and original antagonist at the human tachykinin NK2 receptor is presented, namely MEN13510 (N-N'-bis-[2-(1H-indol-3-yl)-ethyl]-N,N'-bis-(3-thiomorpholin-4-yl-propyl)-phthalamide). MEN13510 retained nanomolar affinity for the human tachykinin NK2 receptor (Ki 6.4 nM), and micromol...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2005.04.033

    authors: Meini S,Catalani C,Bellucci F,Cucchi P,Giuliani S,Zappitelli S,Rotondaro L,Pasqui F,Guidi A,Altamura M,Giolitti A,Maggi CA

    更新日期:2005-06-01 00:00:00

  • Stimulation of kappa-opioid receptor reduces isoprenaline-induced cardiac hypertrophy and fibrosis.

    abstract::The aim of the present study was to determine whether U50,488H (a selective kappa-opioid receptor agonist) inhibits cardiac hypertrophy and fibrosis induced by beta-adrenoceptor stimulation in a rat model. Cardiac hypertrophy and fibrosis were developed by intraperitoneal administration of isoprenaline (ip. 3.0 mg/kg/...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2009.01.050

    authors: Yin W,Zhang P,Huang JH,Zhang QY,Fan R,Li J,Zhou JJ,Hu YZ,Guo HT,Zhang SM,Wang YM,Kaye AD,Gu CH,Liu JC,Cheng L,Cui Q,Yi DH,Pei JM

    更新日期:2009-04-01 00:00:00

  • Neuromodulatory effects of the dorsal hippocampal endocannabinoid system in dextromethorphan/morphine-induced amnesia.

    abstract::Dextromethorphan which is an active ingredient in many cough medicines has been previously shown to potentiate amnesic effect of morphine in rats. However, the effect of dextromethorphan, that is also a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist, in combination with morphine on hippocampus-based lo...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2016.11.025

    authors: Ghasemzadeh Z,Rezayof A

    更新日期:2017-01-05 00:00:00