Search Results - "Entrena, J M"
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Pharmacology and therapeutic potential of sigma(1) receptor ligands
Published in Current neuropharmacology (01-12-2008)“…Sigma (sigma) receptors, initially described as a subtype of opioid receptors, are now considered unique receptors. Pharmacological studies have distinguished…”
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Sigma-1 receptor inhibition reverses acute inflammatory hyperalgesia in mice: role of peripheral sigma-1 receptors
Published in Psychopharmacology (01-10-2014)“…Rationale Sigma-1 (σ 1 ) receptor inhibition ameliorates neuropathic pain by inhibiting central sensitization. However, it is unknown whether σ 1 receptor…”
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3
Sigma-1 Receptor Agonism Promotes Mechanical Allodynia After Priming the Nociceptive System with Capsaicin
Published in Scientific reports (25-11-2016)“…Sigma-1 receptor antagonists promote antinociception in several models of pain, but the effects of sigma-1 agonists on nociception (particularly when the…”
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4
Pharmacology and Therapeutic Potential of Sigma1 Receptor Ligands
Published in Current neuropharmacology (01-12-2008)“…Sigma () receptors, initially described as a subtype of opioid receptors, are now considered unique receptors. Pharmacological studies have distinguished two…”
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5
Push and pull reasons underpinning vulnerable young people’s decisions regarding re-engagement with education and training
Published in Children and youth services review (01-12-2022)“…Leaving school early is an issue of global concern and various measures have been taken to help early school leavers return to and re-engage with education and…”
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Potassium channels and pain: present realities and future opportunities
Published in European journal of pharmacology (01-10-2004)“…Four families of potassium channels with different structures, functional characteristics and pharmacological sensitivity, are distinguished in neurons:…”
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Grip strength in mice with joint inflammation: A rheumatology function test sensitive to pain and analgesia
Published in Neuropharmacology (01-10-2017)“…Grip strength deficit is a measure of pain-induced functional disability in rheumatic disease. We tested whether this parameter and tactile allodynia, the…”
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8
Sigma-1 Receptor Antagonists: A New Class of Neuromodulatory Analgesics
Published in Advances in experimental medicine and biology (01-01-2017)“…The sigma-1 receptor is a unique ligand-operated chaperone present in key areas for pain control, in both the peripheral and central nervous system. Sigma-1…”
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Contilisant, a Tetratarget Small Molecule for Alzheimer’s Disease Therapy Combining Cholinesterase, Monoamine Oxidase Inhibition, and H3R Antagonism with S1R Agonism Profile
Published in Journal of medicinal chemistry (09-08-2018)“…Contilisant, a permeable, antioxidant, and neuroprotectant agent, showing high nM affinity at H3R and excellent inhibition of the monoamine oxidases and…”
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Sigma-1 receptors are essential for capsaicin-induced mechanical hypersensitivity: Studies with selective sigma-1 ligands and sigma-1 knockout mice
Published in Pain (Amsterdam) (01-06-2009)“…We evaluated the role of σ1 receptors on capsaicin-induced mechanical hypersensitivity and on nociceptive pain induced by punctate mechanical stimuli, using…”
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Role of sigma-1 receptors in paclitaxel-induced neuropathic pain in mice
Published in The journal of pain (01-11-2012)“…Sigma-1 (σ(1)) receptors play a role in different types of pain and in central sensitization mechanisms; however, it is unknown whether they are involved in…”
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Enhanced antitumor activity of doxorubicin in breast cancer through the use of poly(butylcyanoacrylate) nanoparticles
Published in International journal of nanomedicine (01-01-2015)“…The use of doxorubicin (DOX), one of the most effective antitumor molecules in the treatment of metastatic breast cancer, is limited by its low tumor…”
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Tetrodotoxin inhibits the development and expression of neuropathic pain induced by paclitaxel in mice
Published in Pain (Amsterdam) (31-07-2008)“…We evaluated the effect of low doses of systemically administered tetrodotoxin (TTX) on the development and expression of neuropathic pain induced by…”
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The antinociceptive effect of morphine is reversed by okadaic acid in morphine-naive but not in morphine-tolerant mice
Published in Pharmacology, biochemistry and behavior (2007)“…The activation of specific subtypes of serine/threonine protein phosphatases (PPs) plays a role in the antinociceptive effect of acute morphine, but it is not…”
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