Peer-reviewed veterinary case report
Platelet-rich plasma protects dog joint cells from lidocaine damage
By Bianchini, Erika et al.·Published in Acta veterinaria Scandinavica·2018·Department of Veterinary Medicine, Italy·View original on PubMed →
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Original publication title: Protective effects of platelet-rich plasma against lidocaine cytotoxicity on canine articular chondrocytes.
- Species:
- dog
Plain-English summary
A study found that lidocaine, a common local anesthetic used in surgeries for dogs, can harm joint cells, specifically chondrocytes, which are important for healthy cartilage. Researchers tested whether platelet-rich plasma (PRP), a treatment derived from the dog's own blood, could protect these cells from damage caused by lidocaine. The results showed that PRP helped restore the health of the chondrocytes and reduced cell death caused by the anesthetic. While more research is needed to confirm these findings in live dogs, PRP shows promise as a protective treatment for dogs receiving lidocaine injections during joint procedures.
People also search for: dog joint surgery lidocaine side effects · platelet-rich plasma for dogs · how to protect dog cartilage during surgery
Abstract
BACKGROUND: Lidocaine (LD) is one of the most commonly used local anesthetics for performing arthroscopic surgery and managing of osteoarthritic pain in both human and veterinary medicine. However, over the last years, several studies have focused on the chondrotoxic effects of LD. In order to ensure that intra-articular lidocaine is safe to use, treatments aimed at mitigating chondrocyte death have recently been investigated. The aim of this study is to evaluate the possible protective effects of platelet-rich plasma (PRP) against LD cytotoxicity on canine articular chondrocytes. RESULTS: Articular canine chondrocytes, were exposed to 1% or 1.8% LD alone or in co-presence with 10% PRP for 30 min. In order to evaluate the effects of PRP pre-treatments, experiments were carried out on cells cultured in serum-free medium-or in medium supplemented with 10% PRP or 10% fetal bovine serum. Cell viability was evaluated by methyl thiazolyl tetrazolium assay and cell apoptosis was analyzed by flow cytometry using annexin V-fluorescein isothiocyanate/propidium iodide. The results showed that LD significantly reduced canine chondrocytes viability, probably due to apoptosis induction. Pre-treatment or the co-presence of PRP in the media restored the number of viable chondrocytes. The PRP also seemed to protect the cells from LD-induced apoptosis. CONCLUSIONS: Pre-treatments and/or the simultaneous administration of PRP reduced LD-induced cytotoxicity in canine chondrocytes. Further in vivo studies are required to determine whether PRP can be used as a save protective treatment for dogs receiving intra-articular LD injections.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/30367652/