نتایج جستجو برای: adrenoceptor agonists

تعداد نتایج: 46019  

Journal: :Journal of applied physiology 1997
Y S Prakash H F van der Heijden M S Kannan G C Sieck

Relaxation of airway smooth muscle (ASM) by beta-adrenoceptor agonists involves reduction of intracellular Ca2+ concentration ([Ca2+]i). In porcine ASM cells, acetylcholine induces [Ca2+]i oscillations that display frequency modulation by agonist concentration and basal [Ca2+]i. We used real-time confocal microscopy to examine the effect of salbutamol (1 nM to 1 microM), a beta 2-adrenoceptor a...

2011
Sinan Gursoy Ercan Ozdemir Ihsan Bagcivan Ahmet Altun Nedim Durmus

BACKGROUND Alpha 2 (α(2))-adrenoceptor agonists may be useful for their potential to increase or prolong opioid analgesia while attenuating the development of opioid tolerance. The purpose of this study was to investigate the effects of dexmedetomidine and guanfacine (α(2)-adrenoceptor agonists) on morphine analgesia and tolerance in rats. METHODS Adult male Wistar albino rats weighing 195-20...

Journal: :The American journal of physiology 1998
Michael P Massett Stephen J Lewis Kevin C Kregel

During hyperthermia, vasoconstrictor tone in the viscera is lost despite high levels of sympathetic neural outflow and plasma catecholamines, suggesting that vascular responsiveness to adrenergic receptor stimulation is reduced. The purpose of this study was to determine whether adrenoceptor-mediated control of vascular resistance is altered at high body core temperatures. The hemodynamic respo...

Journal: :Molecular pharmacology 2014
Jillian G Baker Richard G W Proudman Stephen J Hill

The β1-adrenoceptor exists in two agonist conformations/states: 1) a high-affinity state where responses to catecholamines and other agonists (e.g., cimaterol) are potently inhibited by β1-adrenoceptor antagonists, and 2) a low-affinity secondary conformation where agonist responses, particularly CGP12177 [(-)-4-(3-tert-butylamino-2-hydroxypropoxy)-benzimidazol-2-one] are relatively resistant t...

Journal: :European journal of pharmacology 2002
Lee K Chong Russell Chess-Williams Peter T Peachell

The nonselective beta-adrenoceptor agonist, isoprenaline (pD2; 8.8 +/- 0.2), and selective beta2-adrenoceptor agonists, clenbuterol (9.2 +/- 0.4) and salbutamol (7.1 +/- 0.1), inhibited the immunoglobulin E-mediated release of histamine from human lung mast cells in a concentration-dependent manner. The beta2-adrenoceptor-selective antagonist, ICI118551 (erythro-(+/- )-1-(7-methylindan-4-yloyl)...

Journal: :Hypertension 2005
Leonid Luksha Lucilla Poston Jan-Ake Gustafsson Lusine Aghajanova Karolina Kublickiene

Estrogen receptor-beta knockout mice become hypertensive as they age, and males have a higher blood pressure than females. We hypothesized that the absence of estrogen receptor-beta may contribute to development of cardiovascular dysfunction by modification of adrenergic responsiveness in the peripheral vasculature. Small femoral arteries (internal diameter <200 microm) were isolated from estro...

Journal: :American journal of respiratory cell and molecular biology 2008
Long P Nguyen Ozozoma Omoluabi Sergio Parra Joanna M Frieske Cecilia Clement Zoulikha Ammar-Aouchiche Samuel B Ho Camille Ehre Mehmet Kesimer Brian J Knoll Michael J Tuvim Burton F Dickey Richard A Bond

Single-dose administration of beta-adrenoceptor agonists produces bronchodilation and inhibits airway hyperresponsiveness (AHR), and is the standard treatment for the acute relief of asthma. However, chronic repetitive administration of beta-adrenoceptor agonists may increase AHR, airway inflammation, and risk of death. Based upon the paradigm shift that occurred with the use of beta-blockers i...

2006
Cliff Battram Steven J. Charlton Bernard Cuenoud Mark R. Dowling Robin A. Fairhurst David Farr John R. Fozard Juliet R. Leighton-Davies Christine A. Lewis Lorraine McEvoy Robert J. Turner Alexandre Trifilieff

Here, we describe the preclinical pharmacological profile of 5-[(R)-2-(5,6-diethyl-indan-2-ylamino)-1-hydroxy-ethyl]-8hydroxy-1H-quinolin-2-one (indacaterol), a novel, chirally pure inhaled 2 adrenoceptor agonist, in comparison with marketed drugs. Indacaterol is close to a full agonist at the human 2 adrenoceptor (Emax 73 1% of the maximal effect of isoprenaline; pEC50 8.06 0.02), whereas salm...

Journal: :The Journal of experimental biology 2006
Stéphanie Fournier Richard Kinkead

Noradrenaline (NA) is an important modulator of respiratory activity. Results from in vitro studies using immature rodents suggest that the effects exerted by NA change during development, but these investigations have been limited to neonatal stages. To address this issue, we used in vitro brainstem preparations of an ectotherm, Rana catesbeiana, at three developmental stages: pre-metamorphic ...

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