Gender Medicine, ISSN 1550-8579, 2005, Volume 2, Issue 3, pp. 137 - 145
Abstract A number of studies have demonstrated a higher prevalence of chronic pain states and greater pain sensitivity among women compared with men. Pain...
nociception | chronic pain | analgesics | pain sensitivity | gender differences | Nociception | Pain sensitivity | Gender differences | Analgesics | Chronic pain | Analgesics - therapeutic use | Receptors, Opioid - genetics | Animals | Pain - drug therapy | Humans | Sex Factors | Rats | Female | Male | Pain Threshold | Treatment Outcome | Mice
nociception | chronic pain | analgesics | pain sensitivity | gender differences | Nociception | Pain sensitivity | Gender differences | Analgesics | Chronic pain | Analgesics - therapeutic use | Receptors, Opioid - genetics | Animals | Pain - drug therapy | Humans | Sex Factors | Rats | Female | Male | Pain Threshold | Treatment Outcome | Mice
Journal Article
1995, Progress in brain research, ISBN 0444817190, Volume 104., xv, 421
Book
Pain, ISSN 0304-3959, 01/2019, Volume 160, Issue 1, pp. 224 - 236
Recent studies have suggested a sexually dimorphic role of spinal glial cells in the maintenance of mechanical hypersensitivity in rodent models of chronic...
Spinal cord | IMMUNOREACTIVITY | PAIN PERCEPTION | TACTILE ALLODYNIA | Arthritis | Sex difference | NEUROSCIENCES | Chronic pain | CLINICAL NEUROLOGY | Microglia | EARLY RHEUMATOID-ARTHRITIS | INHIBITION | RNA-seq | DISEASE | Minocycline | GENE-EXPRESSION | ANESTHESIOLOGY | SEX-DIFFERENCES | HYPERSENSITIVITY | Microglia - metabolism | Microglia - drug effects | Arthritis - pathology | Collagen - immunology | Mice, Inbred C57BL | Antibodies - toxicity | Male | Transcriptome - drug effects | RNA, Messenger - metabolism | Antigens, CD - metabolism | Nerve Tissue Proteins - metabolism | Arthritis - chemically induced | Animals | Time Factors | Spinal Cord - pathology | Hyperalgesia - etiology | Female | Transcriptome - physiology | Disease Models, Animal | Research Paper
Spinal cord | IMMUNOREACTIVITY | PAIN PERCEPTION | TACTILE ALLODYNIA | Arthritis | Sex difference | NEUROSCIENCES | Chronic pain | CLINICAL NEUROLOGY | Microglia | EARLY RHEUMATOID-ARTHRITIS | INHIBITION | RNA-seq | DISEASE | Minocycline | GENE-EXPRESSION | ANESTHESIOLOGY | SEX-DIFFERENCES | HYPERSENSITIVITY | Microglia - metabolism | Microglia - drug effects | Arthritis - pathology | Collagen - immunology | Mice, Inbred C57BL | Antibodies - toxicity | Male | Transcriptome - drug effects | RNA, Messenger - metabolism | Antigens, CD - metabolism | Nerve Tissue Proteins - metabolism | Arthritis - chemically induced | Animals | Time Factors | Spinal Cord - pathology | Hyperalgesia - etiology | Female | Transcriptome - physiology | Disease Models, Animal | Research Paper
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 07/2019, Volume 854, pp. 101 - 108
Management of chronic pain is restricted by the lack of effective tools. This study evaluated the efficacies of sinomenine combined gabapentin or ligustrazine...
Sinomenine | Drug combination | Gabapentin | Ligustrazine hydrochloride | Neuropathic pain | ACTIVATION | RAT | ISCHEMIA | RECEPTOR | COMBINATION | GRADING SYSTEM | INHIBITION | PHARMACOKINETICS | PHARMACOLOGY & PHARMACY | BEHAVIORS | HYPERSENSITIVITY | Medical research | Care and treatment | Pain | Analgesics | Analysis | Medicine, Experimental | Models | Drug therapy, Combination | Chronic pain
Sinomenine | Drug combination | Gabapentin | Ligustrazine hydrochloride | Neuropathic pain | ACTIVATION | RAT | ISCHEMIA | RECEPTOR | COMBINATION | GRADING SYSTEM | INHIBITION | PHARMACOKINETICS | PHARMACOLOGY & PHARMACY | BEHAVIORS | HYPERSENSITIVITY | Medical research | Care and treatment | Pain | Analgesics | Analysis | Medicine, Experimental | Models | Drug therapy, Combination | Chronic pain
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 12/2013, Volume 721, Issue 1-3, pp. 5 - 11
Sinomenine is an alkaloid originally isolated from the root of the plant . It is used in traditional medicine in China to treat rheumatic arthritis. In the...
Herbal medicine | Sinomenine | Analgesia | Morphine | Neuropathic pain | ACTIVATED PROTEIN-KINASE | RATS | RECEPTOR | MODEL | ARTHRITIS | GRADING SYSTEM | INHIBITION | SCIATIC-NERVE | PHOTOCHEMICALLY-INDUCED ISCHEMIA | PHARMACOLOGY & PHARMACY | Inflammation - chemically induced | Analgesics - pharmacology | Analgesics - therapeutic use | Neuralgia - complications | Sciatic Nerve - injuries | Spinal Cord Injuries - drug therapy | Spinal Cord Injuries - complications | Hyperalgesia - complications | Rats | Male | Neuralgia - drug therapy | Animals | Hyperalgesia - drug therapy | Inflammation - drug therapy | Nociception - drug effects | Behavior, Animal - drug effects | Carrageenan - adverse effects | Female | Mice | Sciatic Nerve - drug effects | Spinal Cord Injuries - physiopathology | Morphinans - pharmacology | Morphinans - therapeutic use | Evaluation | Carrageenin | Analgesics | Analysis | Rodents | Arthritis | Inflammation | Neurologi | Farmakologi och toxikologi | Klinisk medicin | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Herbal medicine | Sinomenine | Analgesia | Morphine | Neuropathic pain | ACTIVATED PROTEIN-KINASE | RATS | RECEPTOR | MODEL | ARTHRITIS | GRADING SYSTEM | INHIBITION | SCIATIC-NERVE | PHOTOCHEMICALLY-INDUCED ISCHEMIA | PHARMACOLOGY & PHARMACY | Inflammation - chemically induced | Analgesics - pharmacology | Analgesics - therapeutic use | Neuralgia - complications | Sciatic Nerve - injuries | Spinal Cord Injuries - drug therapy | Spinal Cord Injuries - complications | Hyperalgesia - complications | Rats | Male | Neuralgia - drug therapy | Animals | Hyperalgesia - drug therapy | Inflammation - drug therapy | Nociception - drug effects | Behavior, Animal - drug effects | Carrageenan - adverse effects | Female | Mice | Sciatic Nerve - drug effects | Spinal Cord Injuries - physiopathology | Morphinans - pharmacology | Morphinans - therapeutic use | Evaluation | Carrageenin | Analgesics | Analysis | Rodents | Arthritis | Inflammation | Neurologi | Farmakologi och toxikologi | Klinisk medicin | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Nature Neuroscience, ISSN 1097-6256, 03/2005, Volume 8, Issue 3, pp. 346 - 353
Several studies have reported functional improvement after transplantation of neural stem cells into injured spinal cord. We now provide evidence that grafting...
FUNCTIONAL RECOVERY | NEUROTROPHIC FACTORS | ADULT RATS | PROMOTE RECOVERY | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | CHRONIC CENTRAL PAIN | SCHWANN-CELLS | AXONAL GROWTH | INTRACEREBROVENTRICULAR INFUSION | NEUROSCIENCES | Motor Activity - physiology | Spinal Cord - metabolism | Cell Count | Magnetic Resonance Imaging - methods | Phosphopyruvate Hydratase - metabolism | Green Fluorescent Proteins - genetics | Myelin Sheath - metabolism | Behavior, Animal | Brain - blood supply | Hindlimb - physiopathology | Tubulin - metabolism | Time Factors | Neurons - physiology | Pain - etiology | Recovery of Function - physiology | Female | Functional Laterality - physiology | Bromodeoxyuridine - metabolism | Calcitonin Gene-Related Peptide - metabolism | Spinal Cord Injuries - therapy | Transduction, Genetic - methods | Basic Helix-Loop-Helix Transcription Factors | Disease Models, Animal | Green Fluorescent Proteins - metabolism | Receptors, Atrial Natriuretic Factor - metabolism | Brain - physiopathology | Rats | Hindlimb - innervation | Oligopeptides - metabolism | Nerve Tissue Proteins - genetics | Rats, Sprague-Dawley | Oxygen - blood | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Stem Cell Transplantation - methods | Animals | Analysis of Variance | Pain - physiopathology | Laminin - classification | Neural Pathways - metabolism | Stem Cells - physiology | Spinal Cord - physiopathology | Spinal Cord Injuries - physiopathology | Laminin - metabolism | Neurofilament Proteins - metabolism | Pain Measurement | Stem Cell Transplantation - adverse effects | Complications and side effects | Pain | Stem cells | Physiological aspects | Transplantation | Research | Diagnosis | Cell differentiation | Risk factors | Medical and Health Sciences | Medicin och hälsovetenskap
FUNCTIONAL RECOVERY | NEUROTROPHIC FACTORS | ADULT RATS | PROMOTE RECOVERY | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | CHRONIC CENTRAL PAIN | SCHWANN-CELLS | AXONAL GROWTH | INTRACEREBROVENTRICULAR INFUSION | NEUROSCIENCES | Motor Activity - physiology | Spinal Cord - metabolism | Cell Count | Magnetic Resonance Imaging - methods | Phosphopyruvate Hydratase - metabolism | Green Fluorescent Proteins - genetics | Myelin Sheath - metabolism | Behavior, Animal | Brain - blood supply | Hindlimb - physiopathology | Tubulin - metabolism | Time Factors | Neurons - physiology | Pain - etiology | Recovery of Function - physiology | Female | Functional Laterality - physiology | Bromodeoxyuridine - metabolism | Calcitonin Gene-Related Peptide - metabolism | Spinal Cord Injuries - therapy | Transduction, Genetic - methods | Basic Helix-Loop-Helix Transcription Factors | Disease Models, Animal | Green Fluorescent Proteins - metabolism | Receptors, Atrial Natriuretic Factor - metabolism | Brain - physiopathology | Rats | Hindlimb - innervation | Oligopeptides - metabolism | Nerve Tissue Proteins - genetics | Rats, Sprague-Dawley | Oxygen - blood | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Stem Cell Transplantation - methods | Animals | Analysis of Variance | Pain - physiopathology | Laminin - classification | Neural Pathways - metabolism | Stem Cells - physiology | Spinal Cord - physiopathology | Spinal Cord Injuries - physiopathology | Laminin - metabolism | Neurofilament Proteins - metabolism | Pain Measurement | Stem Cell Transplantation - adverse effects | Complications and side effects | Pain | Stem cells | Physiological aspects | Transplantation | Research | Diagnosis | Cell differentiation | Risk factors | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
NEUROSCIENCE, ISSN 0306-4522, 10/2010, Volume 170, Issue 3, pp. 923 - 928
Here we studied the role of peripheral adenosine A(2A) receptors in mechanical hyperalgesia during inflammation using mice lacking the A(2A) receptors....
SPINAL-CORD | HORN NEURONS | knock-out | KNOCKOUT MICE | ANTINOCICEPTION | NEUROSCIENCES | adenosine | mouse | LACKING | A RECEPTOR | PAIN | carrageenan | RAT DORSAL-ROOT | hyperalgesia | SEX-DIFFERENCES | FORMALIN TEST | sex differences
SPINAL-CORD | HORN NEURONS | knock-out | KNOCKOUT MICE | ANTINOCICEPTION | NEUROSCIENCES | adenosine | mouse | LACKING | A RECEPTOR | PAIN | carrageenan | RAT DORSAL-ROOT | hyperalgesia | SEX-DIFFERENCES | FORMALIN TEST | sex differences
Journal Article
European Journal of Pain, ISSN 1090-3801, 11/2012, Volume 16, Issue 10, pp. 1368 - 1377
Background Chronic pain of neuropathic nature after spinal cord injury (SCI) is common and its underlying mechanisms are poorly understood. Genes, as well as...
QUANTITATIVE TRAIT LOCUS | SENSITIVITY | QTL | RECEPTOR | MAJOR HISTOCOMPATIBILITY COMPLEX | IDENTIFICATION | NEUROSCIENCES | CLINICAL NEUROLOGY | PERIPHERAL-NERVE | ANESTHESIOLOGY | CANDIDATE GENE | EXPRESSION | ANALGESIA | Genetic Predisposition to Disease | Genome-Wide Association Study | Neuralgia - genetics | Spinal Cord Injuries - complications | Rats | Male | Spinal Cord Injuries - genetics | Rats, Inbred Strains | Hyperalgesia - physiopathology | Behavior, Animal | Animals | Hyperalgesia - genetics | Neuralgia - etiology | Sex Factors | Hyperalgesia - etiology | Female | Pain Threshold | Spinal Cord Injuries - physiopathology | Neuralgia - physiopathology | Quantitative Trait Loci | Disease Models, Animal
QUANTITATIVE TRAIT LOCUS | SENSITIVITY | QTL | RECEPTOR | MAJOR HISTOCOMPATIBILITY COMPLEX | IDENTIFICATION | NEUROSCIENCES | CLINICAL NEUROLOGY | PERIPHERAL-NERVE | ANESTHESIOLOGY | CANDIDATE GENE | EXPRESSION | ANALGESIA | Genetic Predisposition to Disease | Genome-Wide Association Study | Neuralgia - genetics | Spinal Cord Injuries - complications | Rats | Male | Spinal Cord Injuries - genetics | Rats, Inbred Strains | Hyperalgesia - physiopathology | Behavior, Animal | Animals | Hyperalgesia - genetics | Neuralgia - etiology | Sex Factors | Hyperalgesia - etiology | Female | Pain Threshold | Spinal Cord Injuries - physiopathology | Neuralgia - physiopathology | Quantitative Trait Loci | Disease Models, Animal
Journal Article
RESTORATIVE NEUROLOGY AND NEUROSCIENCE, ISSN 0922-6028, 2009, Volume 27, Issue 4, pp. 307 - 321
Purpose: Previous reports established that after a contusion injury to the rat spinal cord, locomotor function was enhanced by the transplantation of cells...
FUNCTIONAL RECOVERY | RESPONSES | STEM-CELLS | IN-VITRO | RAT | LOCOMOTOR | CONTUSION MODEL | ALLODYNIA | NEUROSCIENCES | INHIBIT | TRANSPLANTATION | Severity of Illness Index | Spinal Cord Injuries - complications | Ectodysplasins - metabolism | Rats, Inbred Lew | Rats | Glial Fibrillary Acidic Protein - metabolism | Inflammation - etiology | Physical Stimulation - methods | Mesenchymal Stem Cell Transplantation - methods | Exploratory Behavior - physiology | Hindlimb - physiopathology | Animals | Mesenchymal Stromal Cells | Sensory Thresholds - physiology | Time Factors | Female | Multipotent Stem Cells - physiology | Inflammation - surgery | Disease Models, Animal
FUNCTIONAL RECOVERY | RESPONSES | STEM-CELLS | IN-VITRO | RAT | LOCOMOTOR | CONTUSION MODEL | ALLODYNIA | NEUROSCIENCES | INHIBIT | TRANSPLANTATION | Severity of Illness Index | Spinal Cord Injuries - complications | Ectodysplasins - metabolism | Rats, Inbred Lew | Rats | Glial Fibrillary Acidic Protein - metabolism | Inflammation - etiology | Physical Stimulation - methods | Mesenchymal Stem Cell Transplantation - methods | Exploratory Behavior - physiology | Hindlimb - physiopathology | Animals | Mesenchymal Stromal Cells | Sensory Thresholds - physiology | Time Factors | Female | Multipotent Stem Cells - physiology | Inflammation - surgery | Disease Models, Animal
Journal Article
Journal of Comparative Neurology, ISSN 0021-9967, 07/2015, Volume 523, Issue 10, pp. 1505 - 1528
The mechanisms underlying rheumatoid arthritis (RA)‐induced pain are still not fully elucidated, and accumulating data indicate that peripheral inflammation is...
neuropeptides | pain | rheumatoid arthritis | ion channels | nerve injury | dorsal root ganglia | Nerve injury | Neuropeptides | Ion channels | Dorsal root ganglia | Pain | Rheumatoid arthritis | RHEUMATOID-ARTHRITIS | GENE-RELATED PEPTIDE | PRIMARY AFFERENT NEURONS | RECEPTOR-MEDIATED RESPONSES | SODIUM-CHANNELS | NEUROSCIENCES | NEUROPATHIC PAIN | ZOOLOGY | PRIMARY SENSORY NEURONS | GALANIN-LIKE IMMUNOREACTIVITY | SUBSTANCE-P | UP-REGULATION | Arthritis - physiopathology | Spinal Cord - metabolism | Calcium Channels - metabolism | Antibodies - toxicity | Male | Galanin - metabolism | Neuropeptide Y - metabolism | Arthritis - chemically induced | Lectins - metabolism | Time Factors | Spinal Cord - pathology | Arthritis - immunology | Mice, Inbred CBA | Disease Models, Animal | Arthritis - pathology | Collagen - immunology | Activating Transcription Factor 3 - metabolism | Nerve Tissue Proteins - metabolism | Animals | Ganglia, Spinal - pathology | Lipopolysaccharides - pharmacology | Hyperalgesia - etiology | Substance P - metabolism | Mice | Ganglia, Spinal - metabolism | Rheumatoid factor | Arthritis | Collagen | Analysis
neuropeptides | pain | rheumatoid arthritis | ion channels | nerve injury | dorsal root ganglia | Nerve injury | Neuropeptides | Ion channels | Dorsal root ganglia | Pain | Rheumatoid arthritis | RHEUMATOID-ARTHRITIS | GENE-RELATED PEPTIDE | PRIMARY AFFERENT NEURONS | RECEPTOR-MEDIATED RESPONSES | SODIUM-CHANNELS | NEUROSCIENCES | NEUROPATHIC PAIN | ZOOLOGY | PRIMARY SENSORY NEURONS | GALANIN-LIKE IMMUNOREACTIVITY | SUBSTANCE-P | UP-REGULATION | Arthritis - physiopathology | Spinal Cord - metabolism | Calcium Channels - metabolism | Antibodies - toxicity | Male | Galanin - metabolism | Neuropeptide Y - metabolism | Arthritis - chemically induced | Lectins - metabolism | Time Factors | Spinal Cord - pathology | Arthritis - immunology | Mice, Inbred CBA | Disease Models, Animal | Arthritis - pathology | Collagen - immunology | Activating Transcription Factor 3 - metabolism | Nerve Tissue Proteins - metabolism | Animals | Ganglia, Spinal - pathology | Lipopolysaccharides - pharmacology | Hyperalgesia - etiology | Substance P - metabolism | Mice | Ganglia, Spinal - metabolism | Rheumatoid factor | Arthritis | Collagen | Analysis
Journal Article
Drugs, ISSN 0012-6667, 01/1998, Volume 55, Issue 1, pp. 1 - 4
The potential beneficial effect of coadministration of opiates with antagonists of the N-methyl-D-aspartate (NMDA) receptor for glutamate are discussed. There...
Reviews-on-treatment | Opioid-antagonists, therapeutic-use | Analgesics, therapeutic-use | Pain, treatment | NMDA-antagonists, therapeutic-use | Pharmacotherapy | Internal Medicine | Medicine & Public Health | Pharmacology/Toxicology | MK-801 | DEXTROMETHORPHAN | ASPARTATE RECEPTOR ANTAGONISTS | RAT | MORPHINE-TOLERANCE | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | POSTOPERATIVE ANALGESIA | TOXICOLOGY | DORSAL HORN | ANTINOCICEPTION | KETAMINE | Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors | Excitatory Amino Acid Antagonists - therapeutic use | Humans | Drug Tolerance - physiology | Analgesics, Opioid - therapeutic use | Clinical Trials as Topic | Receptors, N-Methyl-D-Aspartate - physiology | Drug Synergism | Pain - drug therapy | Pain - physiopathology | Ketamine - therapeutic use | Drug Therapy, Combination | Morphine - therapeutic use
Reviews-on-treatment | Opioid-antagonists, therapeutic-use | Analgesics, therapeutic-use | Pain, treatment | NMDA-antagonists, therapeutic-use | Pharmacotherapy | Internal Medicine | Medicine & Public Health | Pharmacology/Toxicology | MK-801 | DEXTROMETHORPHAN | ASPARTATE RECEPTOR ANTAGONISTS | RAT | MORPHINE-TOLERANCE | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | POSTOPERATIVE ANALGESIA | TOXICOLOGY | DORSAL HORN | ANTINOCICEPTION | KETAMINE | Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors | Excitatory Amino Acid Antagonists - therapeutic use | Humans | Drug Tolerance - physiology | Analgesics, Opioid - therapeutic use | Clinical Trials as Topic | Receptors, N-Methyl-D-Aspartate - physiology | Drug Synergism | Pain - drug therapy | Pain - physiopathology | Ketamine - therapeutic use | Drug Therapy, Combination | Morphine - therapeutic use
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 06/2008, Volume 65, Issue 12, pp. 1813 - 1819
Since the discovery of galanin in 1983, one of the most frequently mentioned possible physiological functions for this peptide is spinal pain modulation. This...
Nerve injury | Spinal cord | Inflammation | Opioids | Neuropathic pain | FLEXOR REFLEX | BIOCHEMISTRY & MOLECULAR BIOLOGY | DORSAL-ROOT GANGLIA | LEUKEMIA INHIBITORY FACTOR | CELL BIOLOGY | PERIPHERAL-NERVE INJURY | neuropathic pain | SCIATIC-NERVE | inflammation | VASOACTIVE INTESTINAL POLYPEPTIDE | nerve injury | spinal cord | PRIMARY SENSORY NEURONS | C-FIBER STIMULATION | opioids | INTRATHECAL GALANIN | Analgesics - therapeutic use | Sciatic Nerve - injuries | Spinal Cord - drug effects | Galanin - pharmacology | Animals | Galanin - physiology | Pain - drug therapy | Pain - physiopathology | Pain - etiology | Receptors, Galanin - metabolism | Spinal Cord - physiopathology | Neurons, Afferent - metabolism | Spinal Cord - cytology | Peripheral Nerve Injuries
Nerve injury | Spinal cord | Inflammation | Opioids | Neuropathic pain | FLEXOR REFLEX | BIOCHEMISTRY & MOLECULAR BIOLOGY | DORSAL-ROOT GANGLIA | LEUKEMIA INHIBITORY FACTOR | CELL BIOLOGY | PERIPHERAL-NERVE INJURY | neuropathic pain | SCIATIC-NERVE | inflammation | VASOACTIVE INTESTINAL POLYPEPTIDE | nerve injury | spinal cord | PRIMARY SENSORY NEURONS | C-FIBER STIMULATION | opioids | INTRATHECAL GALANIN | Analgesics - therapeutic use | Sciatic Nerve - injuries | Spinal Cord - drug effects | Galanin - pharmacology | Animals | Galanin - physiology | Pain - drug therapy | Pain - physiopathology | Pain - etiology | Receptors, Galanin - metabolism | Spinal Cord - physiopathology | Neurons, Afferent - metabolism | Spinal Cord - cytology | Peripheral Nerve Injuries
Journal Article
NeuroReport, ISSN 0959-4965, 1996, Volume 7, Issue 13, pp. 2092 - 2094
A heptadecapeptide (orphanin FQ or nociceptin) was recently identified as an endogenous ligand for the orphan opioid-like receptor. Here we report that...
Analgesia | Spinal cord | Pain | Rat | Tail flick | Opioids | Antinociception | Flexor reflex | Intrathecal | Orphan receptor | intrathecal | LOCALIZATION | pain | antinociception | rat | analgesia | tail flick | orphan receptor | NEUROSCIENCES | K RU NEUROSCIENCES | MEMBER | PROTEIN-COUPLED RECEPTOR | TISSUE DISTRIBUTION | GENE FAMILY | MOLECULAR-CLONING | spinal cord | flexor reflex | opioids | Injections, Spinal | Receptors, Opioid - agonists | Opioid Peptides - pharmacology | Spinal Cord - drug effects | Adrenergic beta-2 Receptor Antagonists | GABA-A Receptor Antagonists | Rats | Muscle, Skeletal - innervation | Adrenergic alpha-Antagonists - pharmacology | Imidazoles - pharmacology | Opioid Peptides - administration & dosage | Bicuculline - pharmacology | Rats, Sprague-Dawley | Narcotic Antagonists | Animals | Nerve Fibers - physiology | Analysis of Variance | Naloxone - pharmacology | Spinal Cord - physiology | Female | Electromyography | Sural Nerve - physiology | Electroshock
Analgesia | Spinal cord | Pain | Rat | Tail flick | Opioids | Antinociception | Flexor reflex | Intrathecal | Orphan receptor | intrathecal | LOCALIZATION | pain | antinociception | rat | analgesia | tail flick | orphan receptor | NEUROSCIENCES | K RU NEUROSCIENCES | MEMBER | PROTEIN-COUPLED RECEPTOR | TISSUE DISTRIBUTION | GENE FAMILY | MOLECULAR-CLONING | spinal cord | flexor reflex | opioids | Injections, Spinal | Receptors, Opioid - agonists | Opioid Peptides - pharmacology | Spinal Cord - drug effects | Adrenergic beta-2 Receptor Antagonists | GABA-A Receptor Antagonists | Rats | Muscle, Skeletal - innervation | Adrenergic alpha-Antagonists - pharmacology | Imidazoles - pharmacology | Opioid Peptides - administration & dosage | Bicuculline - pharmacology | Rats, Sprague-Dawley | Narcotic Antagonists | Animals | Nerve Fibers - physiology | Analysis of Variance | Naloxone - pharmacology | Spinal Cord - physiology | Female | Electromyography | Sural Nerve - physiology | Electroshock
Journal Article
Journal of Neurotrauma, ISSN 0897-7151, 11/2015, Volume 32, Issue 21, pp. 1645 - 1657
With no currently available drug treatment for spinal cord injury, there is a need for additional therapeutic candidates. We took the approach of repositioning...
Original Articles | cytokines | bladder function | chemokines | locomotor function | glivec | APOPTOSIS | ACTIVATION | NEUROSCIENCES | CLINICAL NEUROLOGY | CHRONIC MYELOID-LEUKEMIA | CONTUSION | KINASE INHIBITOR IMATINIB | CLINICAL-TRIALS | ICCP PANEL | INFLAMMATORY CYTOKINES | RATING-SCALE | SEVERITY | CRITICAL CARE MEDICINE | Spinal Cord Injuries - drug therapy | Recovery of Function - drug effects | Imatinib Mesylate - pharmacology | Rats | Biomarkers - blood | Protein Kinase Inhibitors - adverse effects | Rats, Sprague-Dawley | Protein Kinase Inhibitors - administration & dosage | Animals | Time Factors | Imatinib Mesylate - adverse effects | Imatinib Mesylate - administration & dosage | Recovery of Function - physiology | Female | Protein Kinase Inhibitors - pharmacology | Spinal Cord Injuries - blood | Cytokines - blood | Disease Models, Animal | Spinal cord injuries | Research | Biological markers | Drug therapy | Original
Original Articles | cytokines | bladder function | chemokines | locomotor function | glivec | APOPTOSIS | ACTIVATION | NEUROSCIENCES | CLINICAL NEUROLOGY | CHRONIC MYELOID-LEUKEMIA | CONTUSION | KINASE INHIBITOR IMATINIB | CLINICAL-TRIALS | ICCP PANEL | INFLAMMATORY CYTOKINES | RATING-SCALE | SEVERITY | CRITICAL CARE MEDICINE | Spinal Cord Injuries - drug therapy | Recovery of Function - drug effects | Imatinib Mesylate - pharmacology | Rats | Biomarkers - blood | Protein Kinase Inhibitors - adverse effects | Rats, Sprague-Dawley | Protein Kinase Inhibitors - administration & dosage | Animals | Time Factors | Imatinib Mesylate - adverse effects | Imatinib Mesylate - administration & dosage | Recovery of Function - physiology | Female | Protein Kinase Inhibitors - pharmacology | Spinal Cord Injuries - blood | Cytokines - blood | Disease Models, Animal | Spinal cord injuries | Research | Biological markers | Drug therapy | Original
Journal Article
Scandinavian Journal of Pain, ISSN 1877-8860, 07/2018, Volume 18, Issue 4, p. 687
Background and aims The clinical management of neuropathic pain remains a challenge. We examined the interaction between gabapentin and NMDA receptor...
spinal cord injury | MK-801 | anti-convulsant | dextromethorphan | nerve injury
spinal cord injury | MK-801 | anti-convulsant | dextromethorphan | nerve injury
Journal Article
Journal of Comparative Neurology, ISSN 0021-9967, 06/2015, Volume 523, Issue 10, pp. 1505 - 1528
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 07/2001, Volume 98, Issue 16, pp. 9407 - 9412
Caffeine is believed to act by blocking adenosine A(1) and A(2A) receptors (A(1)R, A(2A)R), indicating that some A receptors are tonically activated. We...
NEONATAL RAT | HIPPOCAMPUS | NERVOUS-SYSTEM | RESPONSES | RESPIRATORY RHYTHM | IN-VITRO | ACTIVATION | MULTIDISCIPLINARY SCIENCES | CAFFEINE | RAT-BRAIN | EXPRESSION | Physiological aspects | Hypoxia | Adenosine | Anxiety | Mice | Caffeine
NEONATAL RAT | HIPPOCAMPUS | NERVOUS-SYSTEM | RESPONSES | RESPIRATORY RHYTHM | IN-VITRO | ACTIVATION | MULTIDISCIPLINARY SCIENCES | CAFFEINE | RAT-BRAIN | EXPRESSION | Physiological aspects | Hypoxia | Adenosine | Anxiety | Mice | Caffeine
Journal Article