Gene expression, localization, and pharmacological characterization of endothelin receptors in diabetic rat bladder dome.

Abstract:

:As there are significant amounts of functional endothelin receptors in the mammalian urinary tract, we examined the effect of experimental diabetes on the expression of endothelin receptors and their mRNAs in the rat bladder dome. The density of endothelin receptors in the rat bladder dome was higher (8 and 16 weeks following the onset of diabetes) than in age-matched controls. Insulin treatment, started 8 weeks after the induction of diabetes, partially reversed the endothelin receptor alterations. The pharmacological profile of the endothelin receptors in the bladder dome was similar in all groups and was consistent with the predominance of the endothelin ET(A) receptor subtype (ET(A):ET(B)=approximately 4:1). Autoradiographic studies demonstrated that the endothelin receptors were located in all tissue components of the bladder, including epithelial and muscular layers. Semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) data indicated that diabetes increased the expression level of gene transcripts for both endothelin receptor subtypes and that insulin treatment reversed the mRNA upregulation.

journal_name

Eur J Pharmacol

authors

Saito M,Wada Y,Ikeda K,Wang Z,Smith SD,Foster HE,Nishi K,Weiss RM,Latifpour J

doi

10.1016/s0014-2999(99)00753-0

keywords:

subject

Has Abstract

pub_date

2000-01-17 00:00:00

pages

253-63

issue

3

eissn

0014-2999

issn

1879-0712

pii

S0014299999007530

journal_volume

387

pub_type

杂志文章
  • Interactions of calmodulin antagonists with calcium antagonists binding sites.

    abstract::Calmodulin antagonists have calcium entry blocking properties. In order to quantitatively investigate the interactions of these drugs with calcium channels, their effect on [3H]nitrendipine and [3H]d-cis-diltiazem binding to rat cerebral cortex membrane preparations was compared to their inhibitory effect on the activ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0922-4106(91)90117-z

    authors: Schaeffer P,Lugnier C,Stoclet JC

    更新日期:1991-04-25 00:00:00

  • Rosuvastatin enhanced functional recovery after sciatic nerve injury in the rat.

    abstract::Posttraumatic nerve recovery remains a challenge in regenerative medicine. As such, there is a need for agents that limit nerve damage and enhance nerve regeneration. Here we investigate rosuvastatin, a 3-hydroxy-3-methylglutaryl coenzyme (HMG-CoA) reductase inhibitor, with anti-inflammatory and antioxidant properties...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2020.173260

    authors: Abdolmaleki A,Zahri S,Bayrami A

    更新日期:2020-09-05 00:00:00

  • Pharmacological properties of ATP-sensitive K+ channels in mammalian skeletal muscle cells.

    abstract::The patch-clamp technique (single-channel recordings) was used to study the effects of glibenclamide and some channel openers on the KATP channel in mouse skeletal muscle. In outside/out membrane patches, glibenclamide reversibly inhibited KATP channel activity in a dose-dependent manner with an apparent Ki of 190 nM....

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(93)90480-6

    authors: Allard B,Lazdunski M

    更新日期:1993-06-04 00:00:00

  • Protective and preventive effects of teprenone on gastric mucosal lesions in rats.

    abstract::We have reported that neutrophil infiltration into gastric mucosa is closely related to gastric mucosal lesion development in rats with water immersion restraint stress. In this study, we examined the effect of teprenone, which is known to prevent gastric mucosal injury through stimulation of gastric mucus synthesis a...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(98)00430-0

    authors: Nishida K,Ohta Y,Ishiguro I

    更新日期:1998-07-31 00:00:00

  • An absence of changes in sigma receptor subtypes in the brains of genetically dystonic (dt) rats.

    abstract::Binding sites for the sigma ligand [3H]di-o-tollylguanidine ([3H]DTG) have been reported to be altered in the brains of genetically dystonic rats. In the present study, selective sigma 1 and sigma 2 assay conditions were utilized in an effort to define which subpopulation of [3H]DTG binding sites is altered in the dys...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(93)90399-3

    authors: Weissman AD,McCann DJ,Lorden JF,Su TP

    更新日期:1993-12-07 00:00:00

  • Pharmacology of muscarinic acetylcholine receptor subtypes (m1-m5): high throughput assays in mammalian cells.

    abstract::Based on the ability of many receptors to amplify NIH 3T3 cells, we developed a high throughput assay of cloned receptor pharmacology. In this assay, receptors are transiently co-expressed with the marker enzyme beta-galactosidase. Receptors that induce cellular proliferation select and amplify the cells that also exp...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00639-7

    authors: Bräuner-Osborne H,Brann MR

    更新日期:1996-01-04 00:00:00

  • The cocaine-like behavioral effects of meperidine are mediated by activity at the dopamine transporter.

    abstract::Meperidine has atypical opioid receptor agonist effects and shares some structural features with the phenyltropane (WIN) analogs of cocaine. In combination with 0.1 mg/kg naltrexone, meperidine produced cocaine-like discriminative stimulus effects in monkeys, whereas morphine was inactive. Both cocaine and meperidine ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(95)00696-6

    authors: Izenwasser S,Newman AH,Cox BM,Katz JL

    更新日期:1996-02-15 00:00:00

  • Thermoregulatory mechanisms and ethanol hypothermia.

    abstract::The mechanisms underlying the hypothermic effect of ethanol have been investigated in rats. At an ambient temperature of 26 degrees C, at which tail skin blood flow will normally be expected to play a role in regulating core temperature, no change in tail cutaneous temperature occurred during the period in which the c...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(81)90193-x

    authors: Lomax P,Bajorek JG,Bajorek TA,Chaffee RR

    更新日期:1981-05-22 00:00:00

  • Validation of a pharmacological model for mitochondrial dysfunction in healthy subjects using simvastatin: A randomized placebo-controlled proof-of-pharmacology study.

    abstract::Proof-of-pharmacology models to study compounds in healthy subjects offer multiple advantages. Simvastatin is known to induce mitochondrial dysfunction at least partly by depletion of co-enzyme Q10. The goal of this study was to evaluate a model of simvastatin-induced mitochondrial dysfunction in healthy subjects and ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章,随机对照试验

    doi:10.1016/j.ejphar.2017.09.031

    authors: van Diemen MPJ,Berends CL,Akram N,Wezel J,Teeuwisse WM,Mik BG,Kan HE,Webb A,Beenakker JWM,Groeneveld GJ

    更新日期:2017-11-15 00:00:00

  • Dopamine agonist-induced hyperglycemia in rats: structure-activity relationships and mechanisms of action.

    abstract::The concentration of blood glucose was measured in rats after administration of a number of drugs characterized as dopamine agonists. Compounds that cause release of dopamine, or agents that block the reuptake of dopamine, did not elevate blood glucose. Some direct dopamine receptor stimulants (lergotrile, bromocripti...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(83)90234-0

    authors: Schmidt MJ,Root MA,Hall JL

    更新日期:1983-06-03 00:00:00

  • In vitro antibacterial and anti-inflammatory effects of honokiol and magnolol against Propionibacterium sp.

    abstract::Honokiol and magnolol, two major phenolic constituents of Magnolia sp., have been known to exhibit antibacterial activities. However, until now, their antibacterial activity against Propionibacterium sp. has not been reported. To this end, the antibacterial activities of honokiol and magnolol were detected using the d...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2004.05.047

    authors: Park J,Lee J,Jung E,Park Y,Kim K,Park B,Jung K,Park E,Kim J,Park D

    更新日期:2004-08-02 00:00:00

  • Long-lasting change in 5-HT2A receptor-mediated behavior in rats after a single footshock.

    abstract::To investigate the long-term functional change in the 5-HT(2A) receptor after acute stress, we examined the effect of single footshock on head shake behavior induced by the 5-HT(2A) receptor agent (+/-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride (DOI) in rats. Head shakes were evoked in a dose-dependent manner by 0...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(02)02302-6

    authors: Izumi T,Suzuki K,Inoue T,Li XB,Maki Y,Muraki I,Kitaichi Y,Hashimoto S,Koyama T

    更新日期:2002-10-04 00:00:00

  • Effects of deficiency of the G protein Gsα on energy and glucose homeostasis.

    abstract::G(s)α is a ubiquitously expressed G protein α-subunit that couples receptors to the generation of intracellular cyclic AMP. The G(s)α gene GNAS is a complex gene that undergoes genomic imprinting, an epigenetic phenomenon that leads to differential expression from the two parental alleles. G(s)α is imprinted in a tiss...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章,评审

    doi:10.1016/j.ejphar.2010.10.105

    authors: Chen M,Nemechek NM,Mema E,Wang J,Weinstein LS

    更新日期:2011-06-11 00:00:00

  • Determination of oxidative stress and effect of erdosteine on rhinitis medicamentosa in a rat model.

    abstract::We aimed to determine the presence of oxidative stress in rhinitis medicamentosa (RM) and to evaluate the effect of erdosteine (ED) on mucosal changes in a rat model. Twenty-four male rats were used in this experimental study. Three groups were created. Group 1 (n=8) was the control group. Two puffs of 0.05% oxymetazo...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.09.009

    authors: Dokuyucu R,Cevik C,Ozler GS,Ozgur T,Arli C,Sefil F,Yonden Z

    更新日期:2014-11-05 00:00:00

  • Role of alpha 1-adrenoceptors and 5-HT2 receptors in serotonin-induced contraction of rat prostate: autoradiographical and functional studies.

    abstract::Urinary obstruction from benign prostatic hyperplasia is a common clinical problem possibly associated with excessive prostatic constriction around the urethra. These studies compared adrenergic and serotonergic functional activity to specific alpha 1 and serotonin (5-hydroxytryptamine; 5-HT) binding sites in the rat ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(94)00613-c

    authors: Killam AL,Watts SW,Cohen ML

    更新日期:1995-01-24 00:00:00

  • The glutathione reductase inhibitor carmustine induces an influx of Ca2+ in PC12 cells.

    abstract::We studied the effects of carmustine (1,3-bis(2-chloroethyl)-1-nitrosourea) on the intracellular Ca(2+) concentration ([Ca(2+)](i)) in PC12 cells using fura-2 fluorescence imaging. Carmustine (100 microM) caused a delayed increase in [Ca(2+)](i) that developed within approximately 3 h. This effect was enhanced in cell...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2004.06.043

    authors: Doroshenko N,Doroshenko P

    更新日期:2004-08-16 00:00:00

  • Methylphenidate modulates the locus ceruleus neuronal activity in freely behaving rat.

    abstract::The electrophysiological properties of the locus coeruleus (LC) neurons in response to acute and chronic administration of methylphenidate (MPD) were investigated. The extracellular LC neuronal activities were recorded from non-anesthetized, freely behaving rats previously implanted bilaterally with permanent semi mic...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2012.08.016

    authors: Tang B,Dafny N

    更新日期:2012-11-15 00:00:00

  • In vivo characterisation of novel efficacious muscarinic receptor agonists.

    abstract::Although a number of muscarinic agonists have been used in clinical trials for Alzheimer's Disease, many of these compounds are low in potency and have only limited intrinsic efficacy. The present study describes four non-quaternary oxadiazole based muscarinic agonists from a quinuclidine and a 1-azanorbornane series....

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(90)90006-r

    authors: Freedman SB,Harley EA,Marwood RS,Patel S

    更新日期:1990-10-09 00:00:00

  • Inhibition of anti-Fas antibody-induced hepatitis by aminoguanidine in mice.

    abstract::Aminoguanidine is an inhibitor of inducible nitric oxide synthase (iNOS) and is of potential clinical usefulness. Treatment of mice with anti-Fas antibodies (150 microg/kg, i.v.) induced elevation of plasma alanine aminotransferase activity at 4 h and this elevation was inhibited by pretreatment of mice with aminoguan...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00479-9

    authors: Okamoto T,Okabe S

    更新日期:2000-09-08 00:00:00

  • Farrerol can attenuate the aortic lesion in spontaneously hypertensive rats via the upregulation of eNOS and reduction of NAD(P)H oxidase activity.

    abstract::Farrerol, a typical natural flavanone, is the major active component of Rhododendron dauricum L. The objective of this study was to evaluate the attenuation effect of farrerol against the aortic lesions in spontaneously hypertensive rats (SHR) for the first time. Twelve-week-old male SHR were orally administered with ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2015.11.020

    authors: Qin X,Hou X,Liang T,Chen L,Lu T,Li Q

    更新日期:2015-12-15 00:00:00

  • Enalapril, a new nonsulfhydryl angiotensin converting enzyme inhibitor, does not potentiate morphine analgesia.

    abstract::Sprague-Dawley rats received oral doses of enalapril maleate (5 mg/kg), a potent, nonsulfhydryl, angiotensin converting enzyme inhibitor, or saline. Sixty min later, morphine sulfate, 5 mg/kg, or saline was injected subcutaneously. Response to a thermal stimulus was monitored before and up to 5 h ter morphine injectio...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(84)90607-1

    authors: Mojaverian P,Swanson BN,Ferguson RK

    更新日期:1984-02-17 00:00:00

  • Role of cyclin-dependent kinase 5 in capsaicin-induced cough.

    abstract::The role of cyclin-dependent kinase 5 (Cdk5) in the capsaicin-induced cough reflex was examined in mice. Pretreatment with inhaled roscovitine, a selective Cdk5 inhibitor, at concentrations of 0.3 to 3 mM inhibited the number of capsaicin-induced coughs in a concentration-dependent manner. Pretreatment with inhaled ro...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2007.03.036

    authors: Kamei J,Hayashi SS,Takahashi Y,Nozaki C

    更新日期:2007-07-02 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

  • Carmoxirole is able to reduce amisulpride-induced hyperprolactinemia without affecting its central effect.

    abstract::Prolactin blood level and apomorphine-induced yawning were studied in rats treated with the substituted benzamide amisulpride in association with bromocriptine or carmoxirole; two dopamine D(2) receptor agonists with high or low propensity to cross the brain-blood barrier, respectively. Administration of amisulpride p...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(02)01896-4

    authors: Marchese G,Ruiu S,Casti P,Bartholini F,Saba P,Gessa GL,Pani L

    更新日期:2002-06-28 00:00:00

  • Effects of tachykinin NK1 or PAF receptor blockade on the lung injury induced by scorpion venom in rats.

    abstract::In cases of severe human scorpion envenoming, lung injury is a common finding and frequently the cause of death. In the rat, two distinct mechanisms account for oedema following the intravenous injection of the venom -- acute left ventricular failure resulting from a massive release of catecholamines and an increase i...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(99)00382-9

    authors: Matos IM,Souza DG,Seabra DG,Freire-Maia L,Teixeira MM

    更新日期:1999-07-09 00:00:00

  • Human platelet 5HT receptors: characterisation and functional association.

    abstract::Normal human blood platelets in plasma were incubated at 2 degrees C with tritiated 5-hydroxytryptamine ([3H]5HT), and the specific receptor binding was displaced by the addition of unlabelled 5HT. The kinetic parameters of this binding were established and a two-site model for the platelet 5HT receptor demonstrated. ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(80)90522-1

    authors: Peters JR,Grahame-Smith DG

    更新日期:1980-12-05 00:00:00

  • Regulation of urokinase plasminogen activator by epigallocatechin-3-gallate in human fibrosarcoma cells.

    abstract::(-)-Epigallocatechin-3-gallate (EGCG), a main flavanol of green tea, potently suppressed the urokinase-type plasminogen activator (uPA) expression in human fibrosarcoma HT 1080 cells. EGCG induced not only the suppression of the uPA promoter activity but also the destabilization of uPA mRNA. EGCG inhibited the phospho...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2003.12.031

    authors: Kim MH,Jung MA,Hwang YS,Jeong M,Kim SM,Ahn SJ,Shin BA,Ahn BW,Jung YD

    更新日期:2004-03-08 00:00:00

  • Neuroprotection afforded by diazepam against oxygen/glucose deprivation-induced injury in rat cortical brain slices.

    abstract::The aim of the present investigation was to assess neuroprotection exerted by diazepam (0.1-25 microM) in rat cortical brain slices subjected to oxygen-glucose deprivation and reoxygenation. Neuronal injury and neuroprotection were assessed by measuring the release of glutamate and lactate dehydrogenase and tissue wat...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2006.12.030

    authors: Ricci L,Valoti M,Sgaragli G,Frosini M

    更新日期:2007-04-30 00:00:00

  • Regulation of NO-dependent acetylcholine relaxation by K+ channels and the Na+-K+ ATPase pump in porcine internal mammary artery.

    abstract::This study was designed to determine whether K+ channels play a role in nitric oxide (NO)-dependent acetylcholine relaxation in porcine internal mammary artery (IMA). IMA segments were isolated and mounted in organ baths to record isometric tension. Acetylcholine-elicited vasodilation was abolished by muscarinic recep...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2010.05.004

    authors: Pagán RM,Prieto D,Hernández M,Correa C,García-Sacristán A,Benedito S,Martínez AC

    更新日期:2010-09-01 00:00:00

  • Interference with visual memory in rats following infusion of the functional NMDA receptor antagonist, HA-966, into temporal regions.

    abstract::Results from lesion studies show that selective damage to the temporal cortex or lateral entorhinal cortex impairs visual memory, whereas damage to the hippocampal region does not affect retention of a visual discrimination task. Major input pathways of the above structures use glutamate as neurotransmitter. The gluta...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(01)01348-6

    authors: Myhrer T,Andersen JM

    更新日期:2001-10-12 00:00:00