TY - JOUR
T1 - Hyaluronic acid as a carrier supports the effects of glucocorticoids and diminishes the cytotoxic effects of local anesthetics in human articular chondrocytes in vitro
AU - Moser, Lukas B.
AU - Bauer, Christoph
AU - Jeyakumar, Vivek
AU - Niculescu‐morzsa, Eugenia Paulina
AU - Nehrer, Stefan
N1 - Funding Information:
Funding: This research was funded by Anika Therapeutics Inc.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/10/25
Y1 - 2021/10/25
N2 - The current study aimed to investigate the cytotoxicity of co‐administrating local anesthetics (LA) with glucocorticoids (GC) and hyaluronic acid (HA) in vitro. Human articular cartilage was obtained from five patients undergoing total knee arthroplasty. Chondrocytes were isolated, expanded, and seeded in 24‐well plates for experimental testing. LA (lidocaine, bupivacaine, ropi-vacaine) were administered separately and co‐administered with the following substances: GC, HA, and GC/HA. Viability was confirmed by microscopic images, flow cytometry, metabolic activity, and live/dead assay. The addition of HA and GC/HA resulted in enhanced attachment and branched appearance of the chondrocytes compared to LA and LA/GC. Metabolic activity was bet-ter in all LA co‐administered with HA and GC/HA than with GC and only LA. Flow cytometry revealed the lowest cell viability in lidocaine and the highest cell viability in ropivacaine. This find-ing was also confirmed by live/dead assay. In conclusion, HA supports the effect of GC and reduces chondrotoxic effects of LA in vitro. Thereby, the co‐administration of HA to LA and GC offers an alternative less chondrotoxic approach for treating patients with symptomatic osteoarthritis of the knee.
AB - The current study aimed to investigate the cytotoxicity of co‐administrating local anesthetics (LA) with glucocorticoids (GC) and hyaluronic acid (HA) in vitro. Human articular cartilage was obtained from five patients undergoing total knee arthroplasty. Chondrocytes were isolated, expanded, and seeded in 24‐well plates for experimental testing. LA (lidocaine, bupivacaine, ropi-vacaine) were administered separately and co‐administered with the following substances: GC, HA, and GC/HA. Viability was confirmed by microscopic images, flow cytometry, metabolic activity, and live/dead assay. The addition of HA and GC/HA resulted in enhanced attachment and branched appearance of the chondrocytes compared to LA and LA/GC. Metabolic activity was bet-ter in all LA co‐administered with HA and GC/HA than with GC and only LA. Flow cytometry revealed the lowest cell viability in lidocaine and the highest cell viability in ropivacaine. This find-ing was also confirmed by live/dead assay. In conclusion, HA supports the effect of GC and reduces chondrotoxic effects of LA in vitro. Thereby, the co‐administration of HA to LA and GC offers an alternative less chondrotoxic approach for treating patients with symptomatic osteoarthritis of the knee.
KW - Anesthetics, Local/adverse effects
KW - Bupivacaine/adverse effects
KW - Cell Survival/drug effects
KW - Cells, Cultured
KW - Chondrocytes/drug effects
KW - Drug Therapy, Combination/methods
KW - Glucocorticoids/pharmacology
KW - Humans
KW - Hyaluronic Acid/pharmacology
KW - Lidocaine/adverse effects
KW - Osteoarthritis/drug therapy
KW - Pain/drug therapy
KW - Ropivacaine/adverse effects
UR - http://www.scopus.com/inward/record.url?scp=85117576868&partnerID=8YFLogxK
U2 - 10.3390/ijms222111503
DO - 10.3390/ijms222111503
M3 - Journal article
C2 - 34768933
AN - SCOPUS:85117576868
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 21
M1 - 11503
ER -