Effect of continuous passive motion initiated after the onset of arthritis on inflammation and secondary hyperalgesia in rats
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu hodnotící studie, časopisecké články
PubMed
26988156
DOI
10.33549/physiolres.933214
PII: 933214
Knihovny.cz E-zdroje
- MeSH
- artritida komplikace MeSH
- bolest etiologie prevence a kontrola MeSH
- fyzické omezení MeSH
- hyperalgezie etiologie prevence a kontrola MeSH
- náhodné rozdělení MeSH
- pasivní pohybová terapie CPM * MeSH
- peptid spojený s genem pro kalcitonin metabolismus MeSH
- potkani Wistar MeSH
- práh bolesti MeSH
- rozsah kloubních pohybů MeSH
- zadní rohy míšní metabolismus MeSH
- zánět etiologie terapie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- Názvy látek
- peptid spojený s genem pro kalcitonin MeSH
This study investigated the effect of continuous passive motion (CPM) initiated after the onset of arthritis in rats. Rats were injected with 3 % kaolin/carrageenan in the knee joint and randomized to the control, immobilization (IM), or CPM group. The knee joints of the IM and CPM groups were immobilized with a cast for 56 days. In the CPM group, CPM exercise was administered for 60 min/day (6 times/week). Joint transverse diameter and pressure pain threshold (PPT) were assessed as indicators of inflammation, and paw withdrawal response (PWR) was assessed as indicator of secondary hyperalgesia. Central sensitization was analyzed by measuring calcitonin gene-related peptide (CGRP) expression levels in the spinal dorsal horn. In the CPM group, the PPT was significantly increased compared with the IM group from 14 to 35 days, and PWR was significantly decreased from 14 to 56 days. Additionally, CGRP expression in the super facial layer (I-II) of the spinal dorsal horn (L4-5) in the CPM group was significantly decreased compared with the IM group. Our study found the CPM initiated after the onset of arthritis promoted the recovery of inflammation and mitigated secondary hyperalgesia.
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