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Genomes and Genes | Thomas ChristophSummaryCountry: Germany Publications
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Publications
Synergistic antihypersensitive effects of pregabalin and tapentadol in a rat model of neuropathic painThomas Christoph
Grunenthal GmbH, Global Preclinical Research and Development, Department of Pharmacology, Zieglerstrasse 6, 52078 Aachen, Germany
Eur J Pharmacol 666:72-9. 2011....
Tapentadol, but not morphine, selectively inhibits disease-related thermal hyperalgesia in a mouse model of diabetic neuropathic painThomas Christoph
Global Preclinical Research and Development, Grunenthal GmbH, Aachen, Germany
Neurosci Lett 470:91-4. 2010..It is hypothesized that this superior efficacy profile of tapentadol is due to simultaneous activation of MOR and inhibition of NA reuptake...
Investigation of TRPV1 loss-of-function phenotypes in transgenic shRNA expressing and knockout miceThomas Christoph
Preclinical Research and Development, Department of Pharmacology, Grünenthal, Zieglerstrasse 6, 52078 Aachen, Germany
Mol Cell Neurosci 37:579-89. 2008..The present study provides further evidence for the relevance of TRPV1 in neuropathic pain and characterizes RNA interference as valuable technique for drug target validation in pain research...
(-)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol hydrochloride (tapentadol HCl): a novel mu-opioid receptor agonist/norepinephrine reuptake inhibitor with broad-spectrum analgesic propertiesThomas M Tzschentke
Department of Pharmacology, Grunenthal GmbH, Aachen, Germany
J Pharmacol Exp Ther 323:265-76. 2007..It is suggested that the broad analgesic profile of tapentadol and its relative resistance to tolerance development may be due to a dual mode of action consisting of both MOR activation and NE reuptake inhibition...
Antinociceptive effect of antisense oligonucleotides against the vanilloid receptor VR1/TRPV1Thomas Christoph
Research and Development, Grunenthal GmbH, Zieglerstr 6, 52078 Aachen, Germany
Neurochem Int 50:281-90. 2007....
The antiallodynic effect of NMDA antagonists in neuropathic pain outlasts the duration of the in vivo NMDA antagonismThomas Christoph
Department of Pharmacology, , Zieglerstrasse 6, 52078 Aachen, Germany
Neuropharmacology 51:12-7. 2006..Development of short-acting NMDA antagonists could represent a strategy for improving their tolerability...
Tapentadol hydrochloride: a next-generation, centrally acting analgesic with two mechanisms of action in a single moleculeThomas M Tzschentke
Grunenthal GmbH, Aachen, Germany
Drugs Today (Barc) 45:483-96. 2009....
Differential contribution of opioid and noradrenergic mechanisms of tapentadol in rat models of nociceptive and neuropathic painWolfgang Schroder
Grunenthal GmbH, Global Preclinical Research and Development, Department of Pharmacology, Aachen, Germany
Eur J Pain 14:814-21. 2010....
Tramadol has a better potency ratio relative to morphine in neuropathic than in nociceptive pain modelsThomas Christoph
Biomedical Research, Grunenthal GmbH, Aachen, Germany
Drugs R D 8:51-7. 2007..The effects of tramadol, an atypically acting analgesic with a combined opioid and monoaminergic mechanism of action, and morphine, a prototypical opioid, were tested in rat models of neuropathic and nociceptive pain...
Antiallodynic effects of NMDA glycine(B) antagonists in neuropathic pain: possible peripheral mechanismsThomas Christoph
Department of Pharmacology, , Zieglerstr. 6, 52078 Aachen, Germany
Brain Res 1048:218-27. 2005..Thus, peripheral NMDA receptors may substantially contribute to the efficacy of NMDA antagonists in neuropathic pain...
Silencing of vanilloid receptor TRPV1 by RNAi reduces neuropathic and visceral pain in vivoThomas Christoph
Research and Development, Grunenthal GmbH, Aachen, Germany
Biochem Biophys Res Commun 350:238-43. 2006..Our data demonstrate that TRPV1 antagonists, including TRPV1 siRNAs, have potential in the treatment of both, neuropathic and visceral pain...
The antinociceptive and antihyperalgesic effect of tapentadol is partially retained in OPRM1 (?-opioid receptor) knockout miceBabette Kogel
Grunenthal GmbH, Global Preclinical Research and Development, Department of Pharmacology, Zieglerstrasse 6, 52078 Aachen, Germany
Neurosci Lett 491:104-7. 2011....
Semi-mechanistic pharmacokinetic/pharmacodynamic modelling of the antinociceptive response in the presence of competitive antagonism: the interaction between tramadol and its active metabolite on micro-opioid agonism and monoamine reuptake inhibition, in Horst Beier
Department of Pharmacokinetics, Grunenthal GmbH, 52078, Aachen, Germany
Pharm Res 25:1789-97. 2008....
Broad analgesic profile of buprenorphine in rodent models of acute and chronic painThomas Christoph
Department of Pharmacology, Grünenthal GmbH Research and Development, Zieglerstrasse 6, D 52078 Aachen, Germany
Eur J Pharmacol 507:87-98. 2005..055 and 0.036 mg/kg i.v. and 0.129 and 0.038 mg/kg i.p., respectively). It is concluded that buprenorphine shows a broad analgesic profile and offers the opportunity to treat different pain conditions, including neuropathic pain...
Actions of tramadol on micturition in awake, freely moving ratsRaj Kumar Pandita
Department of Clinical Pharmacology, Lund University Hospital, Lund, , Aachen, Germany
Br J Pharmacol 139:741-8. 2003..7 (+/-)-Tramadol effectively inhibits micturition in conscious rats by stimulating micro -opioid receptors. A synergy between opioid receptor stimulation and monoamine reuptake inhibition may contribute to the micturition effects...
