Enhanced vasoconstriction to α1-adrenoceptor stimulation during cooling in mouse cutaneous plantar arteries.

Abstract:

:Cutaneous arteries are known to constrict in response to cooling via α2C-adrenoceptors. The involvement of α1-adrenoceptors in the cooling response has also recently been suggested by in vivo studies in mice. The present study was thus aimed to confirm it in the isolated mouse cutaneous plantar artery. Changes in vessel diameter were measured by pressurized arteriography. Myogenic constriction was induced depending on intraluminal pressure, and was nearly abolished by the Ca(2+) channel blocker nifedipine or by lowering bath temperature to 24°C. The α1-adrenoceptor agonist phenylephrine produced two-phase constriction composed of phasic and tonic components, both of which were enhanced by the cooling to 24°C. Nifedipine partly inhibited the phenylephrine constriction at 37°C, and the nifedipine-resistant constriction was further inhibited by the inositol 1,4,5-trisphosphate (IP3) receptor inhibitor xestospongin C. Although the cooling to 24°C still enhanced the phenylephrine constriction in the presence of nifedipine, the enhancement was not observed in the presence of both nifedipine and xestospongin C. In Ca(2+)-free solution, phenylephrine produced two-phase constriction at 37°C, which was abolished by 30-min treatment with thapsigargin, an inhibitor of sarcoplasmic/endoplasmic reticulum Ca(2+)-ATPase (SERCA). In contrast, short-term treatment with thapsigargin for 3min rather enhanced the phenylephrine constriction in Ca(2+)-free solution at 37°C; however, the enhanced constriction by the cooling to 24°C was not further enhanced by the SERCA inhibitor. These results suggest that cooling inhibits Ca(2+) re-uptake by SERCA, thereby enhancing constriction induced by Ca(2+) released via IP3 receptors in the mouse plantar artery.

journal_name

Eur J Pharmacol

authors

Goto K,Saito SY,Ishikawa T

doi

10.1016/j.ejphar.2014.08.014

subject

Has Abstract

pub_date

2014-11-05 00:00:00

pages

1-7

eissn

0014-2999

issn

1879-0712

pii

S0014-2999(14)00619-0

journal_volume

742

pub_type

杂志文章
  • Reduction of vagal pressor reflexes by neurohypophyseal peptides and related compounds.

    abstract::The effects of intracisternal injections of [Lys8]vasopressin and [Arg8]vasopressin (25, 50, 100, 200 mU/kg) and related compounds oxytocin (25, 50, 100, 200 mU/kg), felypressin (25, 50, 100, 200 mU/kg) and vasotocin (100, 200, 400, 800 ng/kg) on the acute neurogenic pressor responses to afferent vagal stimulation (5,...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(85)90009-3

    authors: Montastruc P,Dang Tran L,Montastruc JL

    更新日期:1985-11-19 00:00:00

  • Further evaluation of the selectivity of a novel antihypertensive agent, SGB-1534, for peripheral alpha 1-adrenoceptors in the spinally anesthetized dog.

    abstract::Experiments were designed to examine some characteristics of an orally active antihypertensive agent, SGB-1534 on alpha-adrenoceptors in spinally anesthetized dogs. In the saphenous arterial bed perfused by a constant pump volume, saphenous nerve stimulation and bolus applications of norepinephrine and phenylephrine i...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90579-0

    authors: Imagawa J,Sakai K

    更新日期:1986-11-19 00:00:00

  • Pharmacological modulation of bradykinin-, acetylcholine- and calcium ionophore A23187-induced relaxation of rabbit pulmonary arterial segments.

    abstract::Bradykinin (BK; 10(-10)-10(-7) M) relaxes phenylephrine-contracted rabbit isolated pulmonary arterial rings. The mechanical destruction of the endothelial layer obliterates acetylcholine (ACh) and A23187-induced relaxation without influencing BK-, isoproterenol-, sodium nitroprusside- and papaverine-induced relaxation...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(87)90219-6

    authors: Chand N,Mahoney TP Jr,Diamantis W,Sofia RD

    更新日期:1987-06-04 00:00:00

  • Modification of behavioral response to intra-hippocampal injections of noradrenaline and adrenoceptor agonists by chronic treatment with desipramine and citalopram: functional aspects of adaptive receptor changes.

    abstract::The present study investigated the effects of acute and of chronic treatment with desipramine (DI) and citalopram (CT) on the alterations in rat behavior in the open field and in the forced swim tests produced by intra-hippocampal microinjections of noradrenaline (NA) and adrenoceptor agonists. Chronic but not acute t...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(85)90609-0

    authors: Płaźnik A,Kostowski W

    更新日期:1985-11-05 00:00:00

  • A single dose of benzodiazepine hypnotics alters the sleep EEG in the subsequent drug-free night.

    abstract::All-night spectral analysis of the sleep EEG was used to study the effect and after-effect of a single bedtime dose of flunitrazepam (2 mg), flurazepam (30 mg) or triazolam (0.5 mg) in healthy young males. In the night of drug treatment all 3 hypnotics reduced the EEG slow waves and enhanced the activity in the freque...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(83)90622-2

    authors: Borbély AA,Mattmann P,Loepfe M,Fellmann I,Gerne M,Strauch I,Lehmann D

    更新日期:1983-04-22 00:00:00

  • Studies on beta-adrenoceptors mediating changes in mechanical events and adenosine 3',5'-monophosphate levels. Rat atria.

    abstract::Increasing concentrations of the functional antagonist carbachol resulted in a shift to the right of the dose-response curves for (--)-isoproterenol-induced positive chronotropic and inotropic responses and a reduction of the maximum degree of response that could be produced relative to that produced by theophylline. ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(78)90233-9

    authors: Buckner CK,Torphy T,Costa DJ

    更新日期:1978-02-01 00:00:00

  • A role for M(2) and M(3) muscarinic receptors in the contraction of rat and human small airways.

    abstract::Large airway bronchoconstriction acts mainly through cholinergic pathways via muscarinic M3 receptors with some contribution from M2 receptors. By contrast, the mechanisms of small airway contraction are largely unknown. This study used precision cut lung slices to examine the role of muscarinic M2 and M3 receptors in...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2013.01.054

    authors: Brown SM,Koarai A,Sturton RG,Nicholson AG,Barnes PJ,Donnelly LE

    更新日期:2013-02-28 00:00:00

  • Sodium salicylate acts through direct inhibition of phosphoinositide 3-kinase-like kinases to modulate topoisomerase-mediated DNA damage responses.

    abstract::Chemopreventive non-steroidal anti-inflammatory drugs (NSAIDs) exhibit diverse pharmacological and biological activities mainly through their inhibitory effect on cyclooxygenase (COX). However, COX-independent mechanisms involving kinase inhibition have been proposed to explain certain therapeutic effects of NSAIDs. H...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2010.04.012

    authors: Fan JR,Huang TH,Wen CY,Shen TL,Li TK

    更新日期:2010-07-25 00:00:00

  • Contribution of receptor for advanced glycation end products to vasculature-protecting effects of exercise training in aged rats.

    abstract::The aim of present work was to investigate the underlying mechanism of vasculature-protecting effects of exercise training in aged rats. Experiment 1: aged rats were given moderate-intensity exercise for 12 weeks. Exercise training suppressed advanced glycation evidenced by reduced activity of aldose reductase, increa...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2014.08.017

    authors: Gu Q,Wang B,Zhang XF,Ma YP,Liu JD,Wang XZ

    更新日期:2014-10-15 00:00:00

  • Evidence for a role of human organic anion transporters in the muscular side effects of HMG-CoA reductase inhibitors.

    abstract::The purpose of this study was to elucidate the role of human organic anion transporters (human OATs) in the induction of drug-induced skeletal muscle abnormalities. 3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors have been clinically used for lowering plasma cholesterol levels, and are known to in...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2003.10.017

    authors: Takeda M,Noshiro R,Onozato ML,Tojo A,Hasannejad H,Huang XL,Narikawa S,Endou H

    更新日期:2004-01-12 00:00:00

  • Oxyntomodulin and its (19-37) and (30-37) fragments inhibit histamine-stimulated gastric acid secretion in the conscious rat.

    abstract::Oxyntomodulin, a hormone released from jejuno-ileum and composed of the glucagon sequence extended by a C-terminal octapeptide displays original tissue specificity for the gastric mucosa. The aim of this study was to compare the effect of oxyntomodulin on histamine (0.4 mg/kg per h)-stimulated gastric acid secretion i...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(91)90720-b

    authors: Carles-Bonnet C,Jarrousse C,Niel H,Martinez J,Bataille D

    更新日期:1991-10-15 00:00:00

  • Dopamine receptor plasticity following MPTP-induced nigrostriatal lesions in the mouse.

    abstract::MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) destroys dopamine-containing nigrostriatal neurons and increases the apparent Bmax of both D1 and D2 binding sites in the striatum. However, the changes of Bmax occur at different intervals after the lesion. Up-regulation of D2 sites becomes evident about 3 weeks aft...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(90)90324-y

    authors: Weihmuller FB,Bruno JP,Neff NH,Hadjiconstantinou M

    更新日期:1990-05-16 00:00:00

  • Long lasting effects of prenatal exposure to deltamethrin on cerebral and hepatic cytochrome P450s and behavioral activity in rat offspring.

    abstract::Prenatal exposure to different doses (0.25, or 0.5 or 1.0 mg/kg corresponding to 1/320 th or 1/160 th or 1/80 th of LD50) of deltamethrin to the pregnant Wistar rats from gestation day 5 to 21 were found to produce a dose dependent increase in the activity of cytochrome P450 (CYP) dependent 7-ethoxyresorufin-O-deethyl...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2006.06.042

    authors: Johri A,Yadav S,Singh RL,Dhawan A,Ali M,Parmar D

    更新日期:2006-08-21 00:00:00

  • Pharmacological profile of YM358, a novel nonpeptide angiotensin AT1 receptor antagonist.

    abstract::The pharmacological profile of YM358, 2,7-diethyl-5-[[2'-(1 H-tetrazol-5-yl)biphenyl-4-yl]methyl]-5H-pyrazolo[1,5-b][1,2,4]tri azole potassium salt monohydrate, a novel non-peptide angiotensin AT1 receptor antagonist, was studied in vitro and in vivo. YM358 competed with [125I][Sar1, Ile8]angiotensin II for angiotensi...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(97)01189-8

    authors: Shibasaki M,Fujimori A,Takanashi M,Kusayama T,Tokioka T,Satoh Y,Okazaki T,Uchida W,Inagaki O,Yanagisawa I

    更新日期:1997-09-24 00:00:00

  • Activation of the retrohippocampal region in the rat causes dopamine release in the nucleus accumbens: disruption by fornix section.

    abstract::There is a well-described projection from the retrohippocampus (subiculum and entorhinal cortex) to the nucleus accumbens that is involved in the control of psychomotor behaviour, and is implicated in the aetiology of schizophrenia. Cortical abnormalities are widely reported in the brains of schizophrenic patients, bu...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(00)00741-x

    authors: Mitchell SN,Yee BK,Feldon J,Gray JA,Rawlins JN

    更新日期:2000-10-27 00:00:00

  • Neurobiology of the metabolic syndrome: an allostatic perspective.

    abstract::The metabolic syndrome is a cluster of more or less related metabolic and cardiovascular derangements including visceral obesity, insulin resistance, blood and tissue dislipidemia, high blood pressure and it is often associated with neuroendocrine and immunological dysregulations. The aetiology of this syndrome is cli...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章,评审

    doi:10.1016/j.ejphar.2007.11.079

    authors: van Dijk G,Buwalda B

    更新日期:2008-05-06 00:00:00

  • 2-Aminoethylmethyl-sulfone (AEMS): a potent stimulator of ATP-dependent calcium uptake.

    abstract::Retinal ATP-dependent calcium ion uptake is stimulated by a number of agents, but none are previously reported to be as potent as taurine. We have evaluated the effects of 2-aminoethylmethyl-sulfone (AEMS), thiomorpholine-1,1-dioxide (TMS), and N-methyl-thiomorpholine-1,1-dioxide (M-TMS) on calcium ion uptake. AEMS is...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(86)90648-5

    authors: Liebowitz SM,Lombardini JB,Allen CI

    更新日期:1986-01-14 00:00:00

  • Exploration of Emodin to treat alpha-naphthylisothiocyanate-induced cholestatic hepatitis via anti-inflammatory pathway.

    abstract::Emodin, 1,3,8-trihydroxy-6-methyl-anthraquinone, is an anthraquinone derivative from the roots of Rheum officinale Baill that has been used to treat many diseases in digestive system for thousands of years. This study is to disclose the mechanism of Emodin to treat cholestatic hepatitis via anti-inflammatory pathway. ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2008.06.044

    authors: Ding Y,Zhao L,Mei H,Zhang SL,Huang ZH,Duan YY,Ye P

    更新日期:2008-08-20 00:00:00

  • Confirming whether novel rhein derivative 4a induces paraptosis-like cell death by endoplasmic reticulum stress in ovarian cancer cells.

    abstract::Ovarian cancer is the leading cause of death among gynecologic cancer patients. Although platinum-based chemotherapy as a frontline treatment for ovarian cancer has been widely used in clinical settings, its clinical efficacy is not satisfactory due to the resistance of ovarian cancer cells to apoptosis. Therefore, it...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2020.173526

    authors: Pang HF,Li XX,Zhao YH,Kang JK,Li JY,Tian W,Wang CM,Hou HX,Li DR

    更新日期:2020-11-05 00:00:00

  • 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

  • Endomorphins 1 and 2 induce amnesia via selective modulation of dopamine receptors in mice.

    abstract::The involvement of dopamine receptors in the amnesic effects of the endogenous micro-opioid receptor agonists endomorphins 1 and 2 was investigated by observing step-down type passive avoidance learning in mice. Although the dopamine D1 receptor agonist R(+)-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol hydroc...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(02)01760-0

    authors: Ukai M,Lin HP

    更新日期:2002-06-20 00:00:00

  • Conditioned taste aversion: modulation by 5-HT receptor activity and corticosterone.

    abstract::Two experiments were designed to elucidate the involvement of the hypothalamic-pituitary-adrenal axis and the 5-hydroxytryptamine (5-HT) system in the acquisition of lithium chloride-conditioned taste aversion. In Experiment 1, rats were administered either vehicle or 50 mg/kg nefazodone daily for 4 weeks. Rats were t...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/s0014-2999(03)01790-4

    authors: Gorzalka B,Hanson L,Harrington J,Killam S,Campbell-Meiklejohn D

    更新日期:2003-06-20 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

  • Heterologous desensitization and reduced G protein ADP-ribosylation following exposure to alpha 2-adrenoceptor and muscarinic receptor agonists.

    abstract::We investigated the acute and chronic effects of alpha 2-adrenoceptor and muscarinic receptor agonists on dihydropyridine-sensitive voltage-dependent Ca2+ channels in spinal cord-dorsal root ganglion cocultures. Clonidine and oxotremorine inhibited the voltage-dependent Ca2+ influx (42 +/- 2% and 35 +/- 6% with 100 mi...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0922-4106(93)90060-m

    authors: Nah SY,Attali B,Vogel Z

    更新日期:1993-01-04 00:00:00

  • Potentiation of MK-801-induced breathing impairment by 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline.

    abstract::The purpose of our study was to examine whether a significant interaction occurs between NMDA and non-NMDA receptor antagonists on respiratory function. For this purpose chloralose-anesthetized cats were used and respiratory minute volume (VE), tidal volume (Vt) respiratory rate (f), inspiratory and expiratory duratio...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(94)90569-x

    authors: McManigle JE,Taveira DaSilva AM,Dretchen KL,Gillis RA

    更新日期:1994-01-24 00:00:00

  • The effect of sub-anesthetic and anesthetic ketamine on water maze memory acquisition, consolidation and retrieval.

    abstract::Ketamine, a non-selective inhibitor of NMDA (N-methyl-D-aspartate) channels is used in anesthetic or sub-anesthetic doses to induce analgesia, amnesia, to suppress fear, anxiety and depression. Although the ketamine's effect on memory acquisition is known, its effects on other aspects of memory are controversial. Morr...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2011.12.021

    authors: Moosavi M,Yadollahi Khales G,Rastegar K,Zarifkar A

    更新日期:2012-02-29 00:00:00

  • Inhibitory and stimulatory actions of danazol in rat ovarian and uterine tissues.

    abstract::We examined whether danazol has a direct action on ovarian steroid secretion and/or uterine prostaglandin (PG) F2 alpha catabolic activity in immature rats in which the first ovulation was induced and in adult ovariectomized rats. The preovulatory surge of estradiol and progesterone was markedly suppressed together wi...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/0014-2999(92)90264-5

    authors: Kogo H,Takasaki K,Yatabe Y,Nishikawa M,Takeo S,Tamura K

    更新日期:1992-01-28 00:00:00

  • Rapid human melanoma cell death induced by sanguinarine through oxidative stress.

    abstract::Sanguinarine is a natural isoquinoline alkaloid derived from the root of Sanguinaria canadensis and from other poppy fumaria species, and is known to have a broad spectrum of pharmacological properties. Here we have found that sanguinarine, at low micromolar concentrations, showed a remarkably rapid killing activity a...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2013.02.035

    authors: Burgeiro A,Bento AC,Gajate C,Oliveira PJ,Mollinedo F

    更新日期:2013-04-05 00:00:00

  • Anti-leukemic effects of histone deacetylase (HDAC) inhibition in acute lymphoblastic leukemia (ALL) cells: Shedding light on mitigating effects of NF-κB and autophagy on panobinostat cytotoxicity.

    abstract::Identification of the roles of epigenetic alterations in cancers has suggested that different molecules involved in this process are potentially therapeutic targets. Given the role of histone deacetylases (HDACs) enzymes in leukemogenesis, we designed a study to investigate the anti-leukemic property of panobinostat, ...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2020.173050

    authors: Mehrpouri M,Safaroghli-Azar A,Pourbagheri-Sigaroodi A,Momeny M,Bashash D

    更新日期:2020-05-15 00:00:00

  • In vivo efficiency of the collagen coated nanofibrous scaffold and their effect on growth factors and pro-inflammatory cytokines in wound healing.

    abstract::Exploring the importance of nanofibrous scaffold with traditionally important medicine as a wound dressing material prevents infection and aids in faster healing of wounds. In the present study, the Collagen (COL) from the marine fish skin was extracted and employed for coating the Poly(3-hydroxybutyric acid) (P)-Gela...

    journal_title:European journal of pharmacology

    pub_type: 杂志文章

    doi:10.1016/j.ejphar.2017.08.003

    authors: Ramanathan G,Muthukumar T,Tirichurapalli Sivagnanam U

    更新日期:2017-11-05 00:00:00