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Region-specific changes in 5-HT1A agonist-induced Extracellular signal-Regulated Kinases 1/2 phosphorylation in rat brain: a quantitative ELISA study

Neuropharmacology, 2009-02, Vol.56 (2), p.350-361

2009

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Effects of the high-efficacy 5-HT1A receptor agonist, F 13640 in the formalin pain model : A c-Fos study

European journal of pharmacology, 2005-05, Vol.514 (2-3), p.121-130

2005

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Involvement of the spinoparabrachial pathway in inflammatory nociceptive processes: A c-Fos protein study in the awake rat

Journal of comparative neurology (1911), 1998-07, Vol.397 (1), p.10-28

1998

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Aspirin and acetaminophen reduced both Fos expression in rat lumbar spinal cord and inflammatory signs produced by carrageenin inflammation

Pain (Amsterdam), 1995-12, Vol.63 (3), p.365-375

1995

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The contribution of NMDA receptor activation to spinal c‐Fos expression in a model of inflammatory pain

British journal of pharmacology, 1995-09, Vol.116 (1), p.1628-1634

1995

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Enhanced effects of co-administered dexamethasone and diclofenac on inflammatory pain processing and associated spinal c-Fos expression in the rat

Pain (Amsterdam), 1996-03, Vol.64 (3), p.559-568

1996

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7-Nitro-indazole, a selective inhibitor of neuronal nitric oxide synthese, reduces formalin evoked c-Fos expression in dorsal horn neurons of the rat spinal cord

Brain research, 1995-10, Vol.697 (1), p.258-261

1995

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When is the maximal effect of pre-administered systemic morphine on carrageenin evoked spinal c-Fos expression in the rat?

Brain research, 1995-12, Vol.705 (1), p.91-96

1995

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Region-specific changes in 5-HT 1A agonist-induced Extracellular signal-Regulated Kinases 1/2 phosphorylation in rat brain: A quantitative ELISA study

Neuropharmacology, 2009, Vol.56 (2), p.350-361

2009

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Antinociceptive effects of RB101, a complete inhibitor of enkephalin-catabolizing enzymes, are enhanced by a cholecystokinin type B receptor antagonist, as revealed by noxiously evoked spinal c-Fos expression in rats

The Journal of pharmacology and experimental therapeutics, 1997-04, Vol.281 (1), p.208

1997

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The contribution of peripheral bradykinin B2 receptors to carrageenan-evoked oedema and spinal c-Fos expression in rats

European journal of pharmacology, 1997-02, Vol.320 (1), p.73-80

1997

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Interactions between NMDA- and prostaglandin receptor-mediated events in a model of inflammatory nociception

European journal of pharmacology, 1996-05, Vol.303 (1), p.91-100

1996

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Effects of nefopam on the spinal nociceptive processes: a c-Fos protein study in the rat

European journal of pharmacology, 2002-04, Vol.441 (1), p.67-74

2002

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The novel analgesic and high-efficacy 5-HT1A receptor agonist, F 13640 induces c-Fos protein expression in spinal cord dorsal horn neurons

Brain research, 2003-06, Vol.974 (1-2), p.212-221

2003

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Effects of the high-efficacy 5-HT sub(1A) receptor agonist, F 13640 in the formalin pain model: A c-Fos study

European journal of pharmacology, 2005-05, Vol.514 (2-3), p.121-130

2005

Volltextzugriff (PDF)

Effects of the high-efficacy 5-HT 1A receptor agonist, F 13640 in the formalin pain model: A c-Fos study

European journal of pharmacology, 2005, Vol.514 (2), p.121-130

2005

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The novel analgesic and high-efficacy 5-HT 1A receptor agonist, F 13640 induces c-Fos protein expression in spinal cord dorsal horn neurons

Brain research, 2003, Vol.974 (1), p.212-221

2003

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Carrageenin-evoked c-Fos expression in rat lumbar spinal cord: the effects of indomethacin

European journal of pharmacology, 1995-01, Vol.272 (2), p.249-259

1995

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Effects of flurbiprofen and its enantiomers on the spinal c-Fos protein expression induced by noxious heat stimuli in the anaesthetized rat

European journal of pharmacology, 2000-10, Vol.406 (1), p.59-67

2000

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RB101(S), a dual inhibitor of enkephalinases does not induce antinociceptive tolerance, or cross-tolerance with morphine: a c-Fos study at the spinal level

European journal of pharmacology, 2002-04, Vol.441 (3), p.141-150

2002

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Urethane anaesthesia could partly mask antinociceptive effects of non-steroidal anti-inflammatory drugs: a spinal c-Fos protein study

Brain research, 2001-02, Vol.891 (1), p.281-284

2001

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Physiological contributions of neurokinin 1 receptor activation, and interactions with NMDA receptors, to inflammatory-evoked spinal c-Fos expression

Journal of neurophysiology, 1996-09, Vol.76 (3), p.1817-1827

1996

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Further evidence for the interaction of μ- and δ-opioid receptors in the antinociceptive effects of the dual inhibitor of enkephalin catabolism, RB101(S): A spinal c-Fos protein study in the rat under carrageenin inflammation

Brain research, 2003-03, Vol.967 (1), p.106-112

2003

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Peripheral and/or central effects of racemic‐, S(+)‐ and R(−)‐flurbiprofen on inflammatory nociceptive processes: a c‐Fos protein study in the rat spinal cord

British journal of pharmacology, 1998-09, Vol.125 (1), p.87-101

1998

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Further evidence for the interaction of μ- and δ-opioid receptors in the antinociceptive effects of the dual inhibitor of enkephalin catabolism, RB101(S)

Brain research, 2003-03, Vol.967 (1-2), p.106-112

2003

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Region-specific changes in 5-HT1A agonist-induced Extracellular signal-Regulated Kinases 1/2 phosphorylation in rat brain: a quantitative ELISA study

Effects of the high-efficacy 5-HT1A receptor agonist, F 13640 in the formalin pain model : A c-Fos study

Involvement of the spinoparabrachial pathway in inflammatory nociceptive processes: A c-Fos protein study in the awake rat

Aspirin and acetaminophen reduced both Fos expression in rat lumbar spinal cord and inflammatory signs produced by carrageenin inflammation

The contribution of NMDA receptor activation to spinal c‐Fos expression in a model of inflammatory pain

Enhanced effects of co-administered dexamethasone and diclofenac on inflammatory pain processing and associated spinal c-Fos expression in the rat

7-Nitro-indazole, a selective inhibitor of neuronal nitric oxide synthese, reduces formalin evoked c-Fos expression in dorsal horn neurons of the rat spinal cord

When is the maximal effect of pre-administered systemic morphine on carrageenin evoked spinal c-Fos expression in the rat?

Region-specific changes in 5-HT 1A agonist-induced Extracellular signal-Regulated Kinases 1/2 phosphorylation in rat brain: A quantitative ELISA study

Antinociceptive effects of RB101, a complete inhibitor of enkephalin-catabolizing enzymes, are enhanced by a cholecystokinin type B receptor antagonist, as revealed by noxiously evoked spinal c-Fos expression in rats

The contribution of peripheral bradykinin B2 receptors to carrageenan-evoked oedema and spinal c-Fos expression in rats

Interactions between NMDA- and prostaglandin receptor-mediated events in a model of inflammatory nociception

Effects of nefopam on the spinal nociceptive processes: a c-Fos protein study in the rat

The novel analgesic and high-efficacy 5-HT1A receptor agonist, F 13640 induces c-Fos protein expression in spinal cord dorsal horn neurons

Effects of the high-efficacy 5-HT sub(1A) receptor agonist, F 13640 in the formalin pain model: A c-Fos study

Effects of the high-efficacy 5-HT 1A receptor agonist, F 13640 in the formalin pain model: A c-Fos study

The novel analgesic and high-efficacy 5-HT 1A receptor agonist, F 13640 induces c-Fos protein expression in spinal cord dorsal horn neurons

Carrageenin-evoked c-Fos expression in rat lumbar spinal cord: the effects of indomethacin

Effects of flurbiprofen and its enantiomers on the spinal c-Fos protein expression induced by noxious heat stimuli in the anaesthetized rat

RB101(S), a dual inhibitor of enkephalinases does not induce antinociceptive tolerance, or cross-tolerance with morphine: a c-Fos study at the spinal level

Urethane anaesthesia could partly mask antinociceptive effects of non-steroidal anti-inflammatory drugs: a spinal c-Fos protein study

Physiological contributions of neurokinin 1 receptor activation, and interactions with NMDA receptors, to inflammatory-evoked spinal c-Fos expression

Further evidence for the interaction of μ- and δ-opioid receptors in the antinociceptive effects of the dual inhibitor of enkephalin catabolism, RB101(S): A spinal c-Fos protein study in the rat under carrageenin inflammation

Peripheral and/or central effects of racemic‐, S(+)‐ and R(−)‐flurbiprofen on inflammatory nociceptive processes: a c‐Fos protein study in the rat spinal cord

Further evidence for the interaction of μ- and δ-opioid receptors in the antinociceptive effects of the dual inhibitor of enkephalin catabolism, RB101(S)

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