نتایج جستجو برای: p2x7 receptor antagonists

تعداد نتایج: 615699  

Journal: :Neuropharmacology 2013
Nanette Messemer Christin Kunert Marcus Grohmann Helga Sobottka Karen Nieber Herbert Zimmermann Heike Franke Wolfgang Nörenberg Isabelle Straub Michael Schaefer Thomas Riedel Peter Illes Patrizia Rubini

Neurogenesis requires the balance between the proliferation of newly formed progenitor cells and subsequent death of surplus cells. RT-PCR and immunocytochemistry demonstrated the presence of P2X7 receptor mRNA and immunoreactivity in cultured neural progenitor cells (NPCs) prepared from the adult mouse subventricular zone (SVZ). Whole-cell patch-clamp recordings showed a marked potentiation of...

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 2009
Dayane A Gomes Zhilin Song Wanida Stevens Celia D Sladek

Coexposure of hypothalamo-neurohypophyseal system explants to ATP and phenylephrine [PE; an alpha1-adrenergic receptor (alpha1-AR) agonist] induces an extended elevation in vasopressin and oxytocin (VP/OT) release. New evidence is presented that this extended response is mediated by recruitment of desensitization-resistant ionotropic purinergic receptor subtypes (P2X-Rs): 1) Antagonists of the ...

Journal: :Experimental and Therapeutic Medicine 2023

Release of large amounts adenosine triphosphate (ATP), a gliotransmitter, into the extracellular space by traumatic brain injury (TBI) is considered to activate microglia followed release inflammatory cytokines resulting in excessive response that induces secondary injury. The present study investigated whether antagonists ATP receptors (P2X4 and/or P2X7) on are beneficial for reducing post‑inj...

2012
Susanne Syberg Peter Schwarz Solveig Petersen Thomas H. Steinberg Jens-Erik Beck Jensen Jenni Teilmann Niklas Rye Jørgensen

Macrophages from mouse strains with the naturally occurring mutation P451L in the purinergic receptor P2X7 have impaired responses to agonists (1). Because P2X7 receptors are expressed in bone cells and are implicated in bone physiology, we asked whether strains with the P451L mutation have a different bone phenotype. By sequencing the most common strains of inbred mice, we found that only a fe...

Journal: :The Journal of investigative dermatology 2003
Aina V H Greig Claire Linge Giorgio Terenghi D Angus McGrouther Geoffrey Burnstock

We investigated the expression of P2X5, P2X7, P2Y1 and P2Y2 receptor subtypes in normal human epidermis and in relation to markers of proliferation (PCNA and Ki-67), keratinocyte differentiation (cytokeratin K10 and involucrin) and markers of apoptosis (TUNEL and anticaspase-3). Using immunohistochemistry, we showed that each of the four receptors was expressed in a spatially distinct zone of t...

Journal: :Molecular pharmacology 2006
Susanna Alloisio Rita Aiello Stefano Ferroni Mario Nobile

In the brain, arachidonic acid (AA) plays a critical role in the modulation of a broad spectrum of biological responses, including those underlying neuroinflammation. By using microfluorometry, we investigated the action of extracellular AA in the modulation of the purinoceptor P2X7-mediated elevation of [Ca(2+)](i) in cultured neocortical type-1 astrocytes and P2X7-, P2X2-transfected human emb...

2015
Rômulo José Soares-Bezerra Natiele Carla da Silva Ferreira Anael Viana Pinto Alberto André Gustavo Bonavita Antônio Augusto Fidalgo-Neto Andrea Surrage Calheiros Valber da Silva Frutuoso Luiz Anastacio Alves Jorge Arreola

ATP physiologically activates the P2X7 receptor (P2X7R), a member of the P2X ionotropic receptor family. When activated by high concentrations of ATP (i.e., at inflammation sites), this receptor is capable of forming a pore that allows molecules of up to 900 Da to pass through. This receptor is upregulated in several diseases, particularly leukemia, rheumatoid arthritis and Alzheimer's disease....

Journal: :Neuroscience 2011
K Itoh C-Y Chiang Z Li J-C Lee J O Dostrovsky B J Sessle

Central sensitization is a crucial process underlying the increased neuronal excitability of nociceptive pathways following peripheral tissue injury and inflammation. Our previous findings have suggested that extracellular adenosine 5'-triphosphate (ATP) molecules acting at purinergic receptors located on presynaptic terminals (e.g., P2X2/3, P2X3 subunits) and glial cells are involved in the gl...

2017
Edward Beamer Wolfgang Fischer Tobias Engel

Despite the progress made in the development of new antiepileptic drugs (AEDs), the biggest challenges that epilepsy presents to drug development have remained unchanged for the last 80 years: finding a treatment with potential for modifying disease progression and reducing the percentage of patients resistant to all pharmacological interventions. The mechanism of action of the majority of AEDs...

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