Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0184567 (acute pain)
 3,962 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The experience of acute pain serves a crucial biological purpose: it alerts a living organism to environmental dangers, inducing behavioural responses which protect the organism from further damage. In contrast, chronic pain arising from disease states and/or pathological functioning of the nervous system offers no advantage and may be debilitating to those afflicted. Despite recent advances in our understanding of pain mechanisms, the satisfactory management of pathological pain eludes current treatment strategies. We have demonstrated in a previous study on dream deficient mice the pivotal role of downstream regulatory element antagonistic modulator (DREAM) in modulating pain sensitivity in a number of behavioural models, including acute and chronic neuropathic pain. DREAM is a novel calcium binding transcriptional repressor for the prodynorphin gene in spinal cord neurones. The marked attenuation in pain behaviour exhibited by dream-/- mice was shown, by pharmacological and biochemical analyses, to be due to increased activation of the endogenous kappa-opioid system. Importantly, loss of DREAM also attenuated inflammatory pain. Thus, DREAM and the DREAM pathway constitute a novel therapeutic paradigm for the treatment of chronic pain in arthritis.
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PMID:DREAMing about arthritic pain. 1547 77

Research of analgesic action of electromagnetic waves (EMWs) of red (1 = 640 +/- 30 nm) and infra-red (1 = 880 +/- 30 nm) light-emitting diodes of device "MEDOLIGHT" on a tonic and acute pain of white outbreed male mice is carried out. The tonic pain was caused by hypodermic injection of 20 ml of 5% formalin solution in a back surface pad of a hinder leg. Acupuncture point (AP) E-36 or the center of pain were exposed to the action of red or infrared light-emitting diodes in cumulative density of steam radiation capacity during 10 min by 26 mWt/ cm2 in continuous or pulse regimen for frequencies 10, 600, 8000 Hz. Quantitative intensity of a painful syndrome was estimated by average group duration or quantity of painful (licking of the center of a pain, twitching of a hinder leg) and non-painful (dream, grooming, eating) behaviour manifistation of animals for the certain intervals of observation. Sensitivity of animals to acute pain--"a painful threshold"--was deter- mined in experiences with "an electric floor" on size of the electric voltage caused vocalization. The analgesic action both continuous, and pulse light-emitting diode EMWs, features of their action in relation to the place of the application and modes of influence were shown. Thus, the continuous stimulation of AP E-36 only by red EMW decreased the duration of pain paw licking on 33% and quantities of twitching of animals paw on 37% while the duration of grooming, dream, and consumption of feed raised. Such changes of painful and nonpainful behaviour unequivocally specify reduction of a tonic pain. Combined action of red and infrared EMWs caused diverse changes of painful reactions of animals and increase of extremity hyperemia. Thus at summary action of EMWs on AP E-36 of mice the long increase of painful sensitivity was observed. Exposure of EMWs to the center of a pain reduced the intensity of painful reactions of mice on 30% in average, time of their movings in a cage increased twice and duration of dream increased by 39%. Thus, summary action of red and infrared EMWs on AP E-36 promoted only to improvement of a blood circulation and increase painful sensitivity. In experiments with a tonic pain the summary pulse action on AP E-36 of the red and infrared EMWs with frequencies 10, 600, 8000 Hz reduced twice quantity of paw twitchings of animals with pain. The greatest efficiency in suppression of tonic pain syndrome observed for frequencies of 10 and 8000 Hz. The data received testify that the hypoanalgesic effect of light-emitting diode EMWs depends on area of influence, lengths of wave and the modes of an irradiation chosen in view of intensity and duration of stimulation.
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PMID:[Action of the red and infrared electromagnetic waves of light-emitting diodes on the behavioral manifestation of somatic pain]. 1772 44

Downstream Regulatory Element Antagonist Modulator (DREAM) protein modulates pain by regulating prodynorphin gene transcription. Therefore, we investigate the changes of mRNA and DREAM protein in relation to the mRNA and prodynorphin protein expression on the ipsilateral side of the rat spinal cord after formalin injection (acute pain model). DREAM like immunoreactivity (DLI) was not significantly different between C and F groups. However, we detected the upregulation of mean relative DREAM protein level in the nuclear but not in the cytoplasmic extract in the F group. These effects were consistent with the upregulation of the relative DREAM mRNA level. Prodynorphin like immunoreactivity (PLI) expression increased but the relative prodynorphin mRNA level remained unchanged. In conclusion, we suggest that upregulation of DREAM mRNA and protein expression in the nuclear compartment probably has functional consequences other than just the repression of prodynorphin gene. It is likely that these mechanisms are important in the modulation of pain.
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PMID:Increases in mRNA and DREAM protein expression in the rat spinal cord after formalin induced pain. 2118 15