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1.
Brain Res ; 1648(Pt A): 11-18, 2016 10 01.
Article in English | MEDLINE | ID: mdl-27378583

ABSTRACT

The systemic administration of opioids can be used for their strong analgesic effect. However, extensive activation of opioid receptors (ORs) beyond the targeted tissue can cause dysphoria, pruritus, and constipation. Therefore, selective activation of peripheral ORs present in the afferent fibers of the targeted tissue can be considered a superior strategy in opioid analgesia to avoid potential adverse effects. The purpose of this study was to clarify the role of peripheral kappa opioid receptors (kORs) in arthritic pain for the possible use of peripheral ORs as a target in anti-nociceptive therapy. We administered U50488 or nor-BNI/DIPPA, a selective agonist or antagonist of kOR, respectively into arthritic rat knee joints induced using 1% carrageenan. After the injection of U50488 or U50488 with nor-BNI or DIPPA into the inflamed knee joint, we evaluated nociceptive behavior as indicated by reduced weight-bearing on the ipsilateral limbs of the rat and recorded the activity of mechanosensitive afferents (MSA). In the inflamed knee joint, the intra-articular application of 1µM, 10nM, or 0.1nM U50488 resulted in a significant reduction in nociceptive behavior. In addition, 1µM and 10nM U50488 decreased MSA activity. However, in a non-inflamed knee joint, 1µM U50488 had no effect on MSA activity. Additionally, intra-articular pretreatment with 20µM nor-BNI or 10µM DIPPA significantly blocked the inhibitory effects of 1µM U50488 on nociceptive behavior and MSA activity in the inflamed knee joint. These results implicate that peripheral kORs can contribute to anti-nociceptive processing in an inflamed knee joint.


Subject(s)
Knee Joint/metabolism , Receptors, Opioid, kappa/metabolism , 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer/metabolism , 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer/therapeutic use , Analgesics, Opioid/pharmacology , Animals , Inflammation , Knee Joint/physiopathology , Male , Nociception/drug effects , Nociceptors/drug effects , Pain , Rats , Rats, Sprague-Dawley , Receptors, Opioid , Receptors, Opioid, kappa/drug effects , Receptors, Opioid, kappa/physiology
2.
Clin Orthop Surg ; 2(4): 256-9, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21119944

ABSTRACT

Necrotizing fasciitis (NF) is a deep infection of the subcutaneous tissue that progressively destroys fascia and fat; it is associated with systemic toxicity, a fulminant course, and high mortality. NF most frequently develops from trauma that compromises skin integrity, and is more common in patients with predisposing medical conditions such as diabetes mellitus, atherosclerosis, alcoholism, renal disease, liver disease, immunosuppression, malignancy, or corticosteroid use. Most often, NF is caused by polymicrobial pathogens including aerobic and anaerobic bacteria. NF caused by Staphylococcus aureus as a single pathogen, however, is rare. Here we report a case of NF that developed in a healthy woman after an isolated shoulder sprain that occurred without breaking a skin barrier, and was caused by Staphylococcus aureus as a single pathogen.


Subject(s)
Arm , Fasciitis, Necrotizing/etiology , Shoulder Injuries , Sprains and Strains/complications , Staphylococcal Infections/etiology , Coagulase/metabolism , Fasciitis, Necrotizing/microbiology , Fasciitis, Necrotizing/pathology , Fasciitis, Necrotizing/surgery , Female , Humans , Middle Aged , Staphylococcal Infections/microbiology , Staphylococcus aureus/enzymology , Staphylococcus aureus/isolation & purification
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