Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Bror Jonzon"'
Publikováno v:
European Journal of Pain. 23:1767-1779
Background Three TRPV1 (Transient Receptor Potential Vanilloid Receptor 1) antagonists were developed for testing in situ in human skin (Sjogren et al., 2016; Sjogren et al., 2018; Sjogren et al., 2018). The first human study using these compounds an
Autor:
Bror Jonzon, Christina Branting-Ekenback, Stephen H. Butler, Bahman Farahmand, Cecilia Wadell
Publikováno v:
Pain. 154:141-146
The influence of pain descriptors and mechanical hypersensitivity on pain severity in neuropathic pain has not been well researched and is poorly understood. The aim of this study was to determine the relationship between pain severity and other fact
Autor:
Per Agvald, Bror Jonzon, Janet Hoogstraate, L. Christofer Adding, Lars I. Andersson, Lars E. Gustafsson
Publikováno v:
British Journal of Pharmacology. 145:679-687
1 AZD3582 [4-(nitrooxy)butyl-(2S)-2-(6-methoxy-2-naphthyl)propanoate] is a COX-inhibiting nitric oxide donor that inhibits COX-1 and COX-2. It is as effective as naproxen in models of pain and inflammation, but causes less gastroduodenal damage. Nitr
Autor:
D. Craig Brater, Maria Malmenäs, Ann Hedman, Bo Odlind, Lars I. Andersson, Gunilla Huledal, Bror Jonzon
Publikováno v:
Clinical Pharmacology & Therapeutics. 77:437-450
Background Nonsteroidal anti-inflammatory drugs (NSAIDs) inhibit cyclooxygenase (COX) and can thereby reduce renal function, especially with respect to solute excretion and renal perfusion. AZD3582 [4-(nitrooxy)butyl-(2S)-2-(6-methoxy-2-naphthyl)prop
Publikováno v:
Cell Biochemistry and Function. 15:153-162
We have previously described the mitogenic and wound-healing properties of keratinocyte-conditioned medium (KCM). In this study we investigated the effect of KCM on the activation of second messenger systems and the expression of proto-oncogene in cu
Autor:
Britta Eriksson, Bror Jonzon, Marcin Janecki, Jarkko Kalliomäki, Stuart Ratcliffe, Didier Bouhassira, Karin Huizar, Danilov Ab, Flemming W. Bach, Nadine Attal
Publikováno v:
Kalliomäki, J, Attal, N, Jonzon, B, Bach, F W, Huizar, K, Ratcliffe, S, Eriksson, B, Janecki, M, Danilov, A, Bouhassira, D & AZD2423 PTN Study Group 2013, ' A randomized, double-blind, placebo-controlled trial of a chemokine receptor 2 (CCR2) antagonist in posttraumatic neuralgia ', Pain, vol. 154, no. 5, pp. 761-7 . https://doi.org/10.1016/j.pain.2013.02.003
We evaluated the analgesic efficacy, safety and tolerability of a novel chemokine receptor 2 (CCR2) antagonist, AZD2423, in posttraumatic neuralgia. This was a double-blind, randomized, parallel-group, multicentre study. One hundred thirty-three pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e828b5b1c937f3a5b188b592fa9946c
https://vbn.aau.dk/da/publications/725566ef-817e-4c73-a872-1ffab846fb18
https://vbn.aau.dk/da/publications/725566ef-817e-4c73-a872-1ffab846fb18
Autor:
Hanna Svensson, Bror Jonzon, Hans Quiding, Christian Åkermark, Märta Segerdahl, Ingalill Reinholdsson
Publikováno v:
PainReferences. 154(11)
A randomized, double-blind, three-period cross-over study was performed to characterize the sensory phenotype and pain demographics in patients with Morton neuroma ( n = 27) and to explore the effects of local administration (2 mL) of placebo and lid
Autor:
Jarkko Kalliomäki, Bror Jonzon, Anita Andersson, Michael O’Malley, Karin Huizar, David M. Simpson
Publikováno v:
Scandinavian journal of pain. 4(2)
Background and aims Preclinical data suggest that the chemokine receptor 2 (CCR2) is involved in the pathophysiology of neuropathic pain through modulation of neuronal excitability, synaptic transmission and activation of spinal cord microglia. CCR2-
Publikováno v:
European Journal of Oral Sciences. 100:366-370
The cyclosporin-A (CsA) level in human unstimulated whole saliva was studied in 5 children, aged 9-16 yr, receiving the immunosuppressive drug CsA following renal allograft transplantation. The time-concentration relationship of CsA in saliva was det
Publikováno v:
Journal of Cellular Physiology. 151:555-560
The effects of two adenosine analogs on cyclic AMP (cAMP) accumulation and DNA synthesis were studied in cultured smooth muscle cells (SMCs) isolated from adult and neonatal rat arteries. N-ethylcarboxamido adenosine (NECA) dose-dependently increased