DSP-4 lesioning prevents the enhancement of dopamine and 5-hydroxytryptamine mediated behavioural changes by repeated electroconvulsive shock.

Abstract:

:DSP-4 (N-(2-chloroethyl)-ethyl-2-bromobenzylamine) a novel neurotoxin which destroys central noradrenaline neurones after peripheral injection was administered to rats (50 mg/kg X 2). This procedure did not alter activity responses to quipazine (7.5 mg/kg) or apomorphine (0.2 mg/kg) but prevented their enhancement by repeated electroconvulsive shocks (ECS X 10). This confirms that intact noradrenergic function is required for ECS-induced enhancement of 5-HT and dopamine mediated responses. Furthermore, DSP-4 is shown to provide a simple, effective alternative to centrally injected 6-hydroxydopamine for noradrenergic lesioning.

journal_name

Eur J Pharmacol

authors

Heal DJ,Davies CL,Goodwin GM

doi

10.1016/0014-2999(85)90593-x

subject

Has Abstract

pub_date

1985-09-10 00:00:00

pages

117-21

issue

1

eissn

0014-2999

issn

1879-0712

pii

0014-2999(85)90593-X

journal_volume

115

pub_type

杂志文章
  • Effect of cyclophosphamide on gene expression of cytochromes p450 and beta-actin in the HL-60 cell line.

    abstract::Many studies have demonstrated that cyclophosphamide (CPA) can affect hepatic cytochrome p450 (CYP) isoenzyme activity in animals. We have investigated the effect of CPA on gene expression of various CYP enzymes as well as beta-actin in the human acute promyelocytic leukemia cell line (HL-60S) and its multidrug-resist...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(02)01995-7

    authors: Xie HJ,Lundgren S,Broberg U,Finnström N,Rane A,Hassan M

    更新日期:2002-08-09 00:00:00

  • Characterization of bradykinin B(2) receptor antagonists in human and rat urinary bladder.

    abstract::The effect of three selective bradykinin B(2) receptor antagonists, MEN11270 (H-DArg-Arg-Pro-Hyp-Gly-Thi-c(Dab-DTic-Oic-Arg)c(7gamma-1 0alpha)), Icatibant (H-DArg-Arg-Pro-Hyp-Gly-Thi-Ser-DTic-Oic-Arg-OH), and FR173567 ((E)-3-(6-acetamido-3-pyridyl)-N-[N-[2, 4-dichloro-3-[(2-methyl-8-quinolinyl) oxymethyl] phenyl]-N-me...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(99)00882-1

    authors: Meini S,Patacchini R,Giuliani S,Lazzeri M,Turini D,Maggi CA,Lecci A

    更新日期:2000-01-28 00:00:00

  • Role of tachykinin NK3 receptors in the release and effects of nerve growth factor in human isolated bronchi.

    abstract::The nerve growth factor (NGF) is a neurotrophic factor essential for the development and survival of neurons. It has also been identified as a mediator of inflammation and can cause airway hyperresponsiveness [Frossard et al., Eur. J. Pharmacol. 500, 453 (2004)]. Evidence in rodents suggests a link between tachykinins...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2006.10.068

    authors: Naline E,Höglund CO,Vincent F,Emonds-Alt X,Lagente V,Advenier C,Frossard N

    更新日期:2007-04-10 00:00:00

  • Use of non-peptide tachykinin receptor antagonists to substantiate the involvement of NK1 and NK2 receptors in a spinal nociceptive reflex in the rat.

    abstract::Non-peptide antagonists of the NK1 and NK2 receptors were tested as inhibitors of the reaction time in the rat tail-flick and on the decrease of reaction time induced by the intrathecal injection of the NK1 receptor selective agonist [Sar9,Met(O2)11]SP or of the NK2 selective agonist NKA-(4-10). The decrease in reacti...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(93)90782-d

    authors: Picard P,Boucher S,Regoli D,Gitter BD,Howbert JJ,Couture R

    更新日期:1993-03-02 00:00:00

  • Stereotyped behavior correlates better than ataxia with phencyclidine-receptor interactions.

    abstract::The interaction of phencyclidine, dexoxadrol, their analogs and stereoisomers with phencyclidine receptors was compared to their ability to induce stereotyped behavior and ataxia after i.c.v. administration to rats. The order of potency for binding to phencyclidine receptors revealed that among the stereoisomers of ph...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90386-9

    authors: Contreras PC,Rice KC,Jacobson AE,O'Donohue TL

    更新日期:1986-02-11 00:00:00

  • Efficacy of SR 47436 (BMS-186295), a non-peptide angiotensin AT1 receptor antagonist in hypertensive rat models.

    abstract::The efficacy of SR 47436 (BMS-186295), 2-n-butyl-3-[(2'-(1H-tetrazol-5-yl)- biphenyl-4-yl)methyl]-1,3-diaza-spiro[4,4]non-1-en-4-one, a non-peptide angiotensin AT1 receptor antagonist, was characterized in various conscious hypertensive rat models. In spontaneously hypertensive rats, single intravenous or oral doses o...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(94)00484-6

    authors: Lacour C,Canals F,Galindo G,Cazaubon C,Segondy D,Nisato D

    更新日期:1994-11-03 00:00:00

  • Brain dopamine receptors and sleep in the rat: effects of stimulation and blockade.

    abstract::A high dose of apomorphine, a stimulator of brain dopamine receptors, caused a reduction in total sleep, intermediate sleep and a delayed appearance of paradoxical sleep. With a lower dose, a small and not significant trend toward an increase of paradoxical sleep was observed. Spiroperidol, considered as a specific bl...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(76)90340-x

    authors: Kafi S,Gaillard JM

    更新日期:1976-08-01 00:00:00

  • Cytoskeletal interference - A new mode of action for the anticancer drugs camptothecin and topotecan.

    abstract::The anticancer drugs camptothecin (CPT) and topotecan (TPT) are known DNA topoisomerase I inhibitors which cause DNA damage and lead to cell death. In this study we provide evidence that CPT and TPT also interfere with the elements of cytoskeleton - microtubules and actin filaments which could be partly responsible fo...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2016.07.044

    authors: Wang X,Tanaka M,Krstin S,Peixoto HS,Moura CCM,Wink M

    更新日期:2016-10-15 00:00:00

  • Scutellarin synergistically enhances cisplatin effect against ovarian cancer cells through enhancing the ability of cisplatin binding to DNA.

    abstract::Platinum resistance is a major limitation in the treatment of ovarian cancer. Combination of natural compounds with platinum-based agents is a new strategy for cancer chemotherapy. Recently, we found that scutellarin sensitized the anticancer effect of cisplatin to ovarian cancer cells. How scutellarin interacts with ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2018.11.040

    authors: Xie Z,Guo Z,Lei J,Yu J

    更新日期:2019-02-05 00:00:00

  • Approaches to anorexia in rodents: focus on the anx/anx mouse.

    abstract::Eating disorders constitute major medical health problems in the western world. Even though little is known about the mechanisms behind abnormal eating behavior, it has become clear that the central nervous system (CNS), particularly the hypothalamus, plays a significant role. The anorexic anx/anx mouse is a unique mo...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章,评审

    doi:10.1016/j.ejphar.2003.08.104

    authors: Johansen JE,Fetissov S,Fischer H,Arvidsson S,Hökfelt T,Schalling M

    更新日期:2003-11-07 00:00:00

  • Dantrolene and the neuromuscular junction: evidence for intracellular calcium stores.

    abstract::Dantrolene sodium (DaNa) markedly depressed the frequency of spontaneous miniature potentials at the frog neuromuscular junction. Its action is still observed at low [Ca2+]o and is little affected by temperature; its effect is not readily reversible. Theophylline antagonises the action of DaNa. DaNa prevents the stimu...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(76)90122-9

    authors: Statham HE,Duncan CJ

    更新日期:1976-09-01 00:00:00

  • Effects of KC 2450 on the lower esophageal sphincter in vivo and in vitro.

    abstract::The effect of KC 2450 (racemic 3,5-cis-3-methylamino-2,3,4,5-tetrahydro-1-benzoxepine-5-ol hydrochloride) on lower esophageal sphincter pressure in pentobarbital-anesthetized dogs was determined and compared to the effect of metoclopramide. The ED20 value (i.e. the dose that increased lower esophageal sphincter pressu...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(87)90111-7

    authors: Fowler PJ,Nelson AH,Price WJ,Sarau HM,Grous M,Lombardi DM,Barone FC,Ormsbee HS 3rd

    更新日期:1987-10-13 00:00:00

  • Neurotoxic effect of prenatal exposure to MPTP on the dopaminergic systems of the marmoset brain.

    abstract::MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) was incidentally administered to pregnant marmosets during the whole gestational period, except for the last 15 days before term. The infant monkeys were killed 5 months after birth, and dopamine and its metabolites were measured in the striatum and the nucleus accum...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(92)90873-3

    authors: Pérez-Otaño I,Oset C,Trinidad Herrero M,Luquin MR,Kupsch A,Oertel W,Obeso JA,Del Río J

    更新日期:1992-07-07 00:00:00

  • Hypophysectomy does not prevent development of striatal dopamine receptor supersensitivity induced by repeated neuroleptic treatment.

    abstract::Hruska et al. (1980) reported that hypophysectomy prevented the onset of dopamine receptor supersensitivity. We have repeated this investigation administering haloperidol (0.75 mg/day) or sulpiride (2 X 15 mg/day) or saline for 17 days, followed by a 3 day drug washout period, to sham-operated or hypophysectomised rat...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(81)90006-6

    authors: Jenner P,Rupniak NM,Hall MD,Dyer R,Leigh N,Marsden CD

    更新日期:1981-11-19 00:00:00

  • Novel iboga alkaloid congeners block nicotinic receptors and reduce drug self-administration.

    abstract::18-Methoxycoronaridine, a novel iboga alkaloid congener, reduces drug self-administration in animal models of addiction. Previously, we proposed that these effects are mediated by the ability of 18-methoxycoronaridine to inhibit nicotinic alpha3beta4 acetylcholine receptors. In an attempt to identify more potent 18-me...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2004.03.062

    authors: Pace CJ,Glick SD,Maisonneuve IM,He LW,Jokiel PA,Kuehne ME,Fleck MW

    更新日期:2004-05-25 00:00:00

  • Tolerance to haloperidol-induced increases in dopamine metabolites: fact or artifact?

    abstract::Haloperidol increased 3,4-dihydroxyphenylacetic acid and homovanillic acid concentrations in the striatum, nucleus accumbens and olfactory tubercle of both drug-naive rats and rats pretreated with haloperidol (10 injections). The increases in metabolite concentrations were greater in all brain regions of the naive rat...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(87)90189-0

    authors: Finlay JM,Jakubovic A,Fu DS,Fibiger HC

    更新日期:1987-05-07 00:00:00

  • Kinins are involved in the development of allergic nasal hyperresponsiveness in guinea pigs.

    abstract::We evaluated roles of kinins in allergen-induced nasal blockage and sneezing, and development of nasal hyperresponsiveness to leukotriene D4 in a Japanese cedar pollen-induced allergic rhinitis model of guinea pigs. Sensitised guinea pigs were repeatedly challenged by pollen inhalation once every week. Neither a brady...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(03)02185-x

    authors: Sugahara S,Nabe T,Mizutani N,Takenaka H,Kohno S

    更新日期:2003-08-29 00:00:00

  • Methamphetamine decreases mouse striatal dopamine transporter activity: roles of hyperthermia and dopamine.

    abstract::Multiple methamphetamine administrations rapidly decrease rat striatal dopamine transporter activity. To determine the species specificity of this phenomenon, the present studies examined effects of this stimulant on the dopamine transporter in mice. As in rats, multiple methamphetamine injections rapidly reduced stri...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00871-2

    authors: Sandoval V,Hanson GR,Fleckenstein AE

    更新日期:2000-12-15 00:00:00

  • Pharmacological and pharmacokinetic study of olmesartan medoxomil in animal diabetic retinopathy models.

    abstract::A close relationship between the renin-angiotensin system and the pathophysiology of diabetic retinopathy has been suggested, several angiotensin II type 1 receptor (angiotensin AT1 receptor) antagonists being effective in animal models. Therefore, we examined the efficacy of an angiotensin AT1 receptor antagonist, ol...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2005.02.047

    authors: Nakamura H,Inoue T,Arakawa N,Shimizu Y,Yoshigae Y,Fujimori I,Shimakawa E,Toyoshi T,Yokoyama T

    更新日期:2005-04-11 00:00:00

  • PM101: a cyclodextrin-based intravenous formulation of amiodarone devoid of adverse hemodynamic effects.

    abstract::Intravenous amiodarone (Amiodarone i.v.) is widely used to treat cardiac arrhythmias. The most frequent clinical adverse event associated with Amiodarone i.v. administration is systemic hypotension which has been attributed to the cosolvents used in the formulation, polysorbate 80 and benzyl alcohol. To minimize hypot...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2009.02.009

    authors: Cushing DJ,Kowey PR,Cooper WD,Massey BW,Gralinski MR,Lipicky RJ

    更新日期:2009-04-01 00:00:00

  • Nucleotide receptors on DDT1 MF-2 vas deferens cells.

    abstract::On exposure to triphosphatic nucleotides vas deferens DDT1 MF-2 smooth muscle cells responded with an outward K+ current as measured with the whole-cell patch clamp configuration. The rank order of potency was: ATP greater than UTP greater than TTP greater than CTP = GTP. The responses evoked by these agonists were bl...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(92)90048-9

    authors: Van der Zee L,Nelemans A,Den Hertog A

    更新日期:1992-05-14 00:00:00

  • Cellular electrophysiological effects of changrolin in isolated rat cardiac myocytes.

    abstract::Changrolin (2, 6-bis[pyrrolidin-1-ylmethyl]-4-[quinazolin-4-ylamino] phenol) is an anti-arrhythmic drug derived from β-dichroine, an active component of the Chinese medicinal herb, Dichroa febrifuga Lour. To elucidate the mechanism underlying the anti-arrhythmic effect of changrolin, we used the whole-cell patch-clamp...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2010.08.024

    authors: Chen WH,Yang D,Wang WY,Zhang J,Wang YP

    更新日期:2010-11-25 00:00:00

  • Salvianolic acid B regulates macrophage polarization in ischemic/reperfused hearts by inhibiting mTORC1-induced glycolysis.

    abstract::Macrophages play important roles in the healing and remodeling of cardiac tissues after myocardial ischemia/reperfusion (MI/R) injury. Here we investigated the potential effects of salvianolic acid B (SalB), one of the abundant and bioactive compounds extracted from Chinese herb Salvia Miltiorrhiza (Danshen), on macro...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2020.172916

    authors: Zhao M,Li F,Jian Y,Wang X,Yang H,Wang J,Su J,Lu X,Xi M,Wen A,Li J

    更新日期:2020-03-15 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

  • Characterisation of muscarinic receptor subtypes in avian smooth muscle.

    abstract::The identity of the muscarinic receptor subtype in the chick ileum was investigated in functional and binding studies. Preliminary studies [Choo, L.-K., Mitchelson, F., Napier, P. 1988. J. Auton. Pharmacol. 8, 259-266] suggested apparent avian and mammalian family differences in the muscarinic receptor profile of ilea...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00489-1

    authors: Darroch S,Irving HR,Mitchelson FJ

    更新日期:2000-08-18 00:00:00

  • Genipin attenuates lipopolysaccharide-induced persistent changes of emotional behaviors and neural activation in the hypothalamic paraventricular nucleus and the central amygdala nucleus.

    abstract::Sickness behavior is a series of behavioral and psychological changes that develop in inflammatory disease, including infections and cancers. Administration of the bacterial endotoxin lipopolysaccharide (LPS) induces sickness behavior in rodents. Genipin, an aglycon derived from an iridoid glycoside geniposide extract...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.07.038

    authors: Araki R,Hiraki Y,Yabe T

    更新日期:2014-10-15 00:00:00

  • Affinity cross-linking of bradykinin B2 receptors in guinea pig ileum membranes.

    abstract::Affinity cross-linking of the bradykinin B2 receptor was performed using [125I-Tyr8]bradykinin, disulfosuccinimidyl tartrate as linker and crude membranes from guinea pig ileum smooth muscle immobilized on Whatman GF/B glass fiber filters. After SDS (sodium dodecylsulfate)-polyacrylamide gel electrophoresis under redu...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0922-4106(94)90199-6

    authors: Graness A,Liebmann C

    更新日期:1994-07-15 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

  • The influence of dopamine agonists and antagonists on indomethacin lesions in stomach and small intestine in rats.

    abstract::Dopamine agents (saline in control groups) were coadministered with indomethacin by either single or repeated application. The ulcerogenic effect (erosions and/or ulcers) of repeated given indomethacin on gastric mucosa differed clearly from that on intestinal mucosa. The effect on intestinal mucosa was markedly great...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(88)90253-1

    authors: Sikirić P,Rotkvić I,Mise S,Krizanac S,Gjuris V,Jukić J,Suchanek E,Petek M,Udovicić I,Kalogjera L

    更新日期:1988-12-06 00:00:00

  • Regulatory role of the dopamine and norepinephrine transporters in pentylenetetrazol-kindled mice: association with effect of antidepressants.

    abstract::In clinical practice, patients with epilepsy are frequently associated with psychiatric disorders, including cognitive impairment, depression, and attention deficit hyperactivity disorder. In fact, patients with epilepsy often take centrally acting drugs, such as antidepressants and anxiolytics; however, it remains un...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2011.10.017

    authors: Takechi K,Suemaru K,Kawasaki H,Araki H

    更新日期:2011-12-30 00:00:00