Sensitized pain response to bradykinin after sunburn - a human model for ongoing inflammatory pain?

Pain ◽  
2013 ◽  
Vol 154 (6) ◽  
pp. 769-770 ◽  
Author(s):  
Martin Schmelz
Pain ◽  
1998 ◽  
Vol 74 (2) ◽  
pp. 139-151 ◽  
Author(s):  
Juri L Pedersen ◽  
Henrik Kehlet

Author(s):  
Irina P Butkevich ◽  
Viktor A Mikhailenko ◽  
Elena A Vershinina

Abstract: Previously, we have shown that the administration of a selective serotonin reuptake inhibitor fluoxetine or a 5-HT1A receptor agonist buspirone to stressed rats during gestation causes in the offspring alleviation of formalin-induced pain, strengthened by prenatal stress. We have also found that neonatal inflammatory pain strengthens formalin-induced pain in prenatally unstressed rats in later life. In the present study we investigated the effect of neonatal inflammatory pain on the time-course of the biphasic pain response in the formalin test in prenatally stressed adolescent rats of both sexes to evaluate whether neonatal pain affects the antinociceptive properties of these drugs administered to their depressed mothers during gestation. Our findings demonstrate that neonatal pain modulates in prenatally stressed rats the antinociceptive effect of fluoxetine and buspirone depending on the level of organization of pain response in the CNS, the phase of the time-course of the formalin-induced pain, and sex.


1998 ◽  
Vol 89 (1) ◽  
pp. 58-66 ◽  
Author(s):  
Juri L. Pedersen ◽  
Tina S. Galle ◽  
Henrik Kehlet

Unlabelled BACKGROUND. This study examined the analgesic effect of local ketamine infiltration, compared with placebo and systemic ketamine, in a human model of inflammatory pain. Methods Inflammatory pain was induced by a burn (at 47 degrees C for 7 min; wound size, 2.5 x 5 cm) on the calf in 15 volunteers on 3 separate days with 7-day intervals. They received either (1) subcutaneous infiltration with ketamine in the burn area (local treatment) and contralateral placebo injections, or (2) subcutaneous ketamine contralateral to the burn (systemic treatment) and placebo in the burn area, or (3) placebo on both sides. The study was double-blinded and the order of the treatments was randomized. Hyperalgesia to mechanical and heat stimuli was examined by von Frey hairs and contact thermodes (3.75 and 12.5 cm2), and pain was rated using a visual analog scale (0-100). Results The burns produced significant hyperalgesia. Local ketamine infiltration reduced pain during the burn injury compared with systemic treatment and placebo (P < 0.01). Heat pain thresholds were increased by local ketamine treatment compared with placebo immediately after injection (P < 0.03), and so were the mechanical pain thresholds (P = 0.02). Secondary hyperalgesia and suprathreshold pain responses to heat and mechanical stimuli were not significantly affected by local ketamine. No difference between local ketamine and placebo could be detected 1 h and 2 h after the burn. Conclusions Ketamine infiltration had brief local analgesic effects, but several measures of pain and hyperalgesia were unaffected. Therefore, a clinically relevant effect of peripheral ketamine in acute pain seems unlikely.


Life Sciences ◽  
2012 ◽  
Vol 91 (13-14) ◽  
pp. 618-622 ◽  
Author(s):  
Victor K.L. Hung ◽  
Samantha M.Y. Chen ◽  
Lydia W. Tai ◽  
Ann Y.S. Chen ◽  
Sookja K. Chung ◽  
...  

2018 ◽  
Vol 126 (2) ◽  
pp. 661-669 ◽  
Author(s):  
Ya-Chi Lin ◽  
Hung-Tsung Hsiao ◽  
Sheng-Nan Wu ◽  
Yen-Chin Liu

2000 ◽  
Vol 85 (2) ◽  
pp. 228-232 ◽  
Author(s):  
J. Lillesø ◽  
N.A. Hammer ◽  
J.L. Pedersen ◽  
H. Kehlet

Cephalalgia ◽  
2004 ◽  
Vol 24 (6) ◽  
pp. 466-475 ◽  
Author(s):  
H Mørk ◽  
M Ashina ◽  
L Bendtsen ◽  
J Olesen ◽  
R Jensen

A new experimental human model of myofascial pain using intramuscular infusion of a combination of bradykinin, serotonin (5-hydroxytryptamine), histamine, and prostaglandin E2 was applied to patients with episodic tension-type headache (ETTH) in order to examine pain perception. Fifteen patients with ETTH and 15 healthy controls completed the randomized, balanced, double-blinded, placebo-controlled study. Pain intensity, punctate hyperalgesia and allodynia, and pain quality were recorded. The combination induced a moderate and prolonged pain in both patients (median 51 min) ( P = 0.001) and controls (median 22 min) ( P = 0.001). Patients reported more pain than controls both after the combination ( P = 0.045) and after placebo ( P < 0.001). The McGill pain score [PRI(R)] was significantly higher in patients ( P = 0.002) and in controls ( P = 0.001), whereas pain quality and hyperalgesia were similar after the combination compared with placebo in the two groups. Due to side-effects nine subjects did not complete the study. The increased pain response, but similar qualitative pain perception, in ETTH patients may be explained by sensitization of peripheral nociceptors even though central mechanisms may also be involved.


2009 ◽  
Vol 1286 ◽  
pp. 53-59 ◽  
Author(s):  
Irina P. Butkevich ◽  
Victor A. Mikhailenko ◽  
Elena A. Vershinina ◽  
Pavel O. Semionov ◽  
Vladimir A. Otellin ◽  
...  

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