Inhibition of alpha-smooth muscle actin expression in an in vitro wound healing model by certain antibiotics

Objective: This study assesses the effects of antimicrobials on wound heali ng in an in vitro model of chicken flexor tendons in a collagen gel matrix. Two equidistant tendons were bathed in a culture medium for 28 days as fib roblasts (fb) grew from the tendon ends into the collagen gel and migrated toward each other until gap closure. Five groups of 10 paired tendons each included the control and the study groups, which received oxacillin (Ox), c lindamycin (Cl), chloramphenicol (Chl), or tetracycline (Tet) in the cultur e medium to assess their effects on gap closure rate, fl, migration, and my ofibroblast alpha-smooth muscle (alpha-SM) actin expression. Results: Gap closure, by day 27, was 98.5% in the controls compared with 97 %, 92%, 89.5%, 21.75% in the Tet, Cl, Ox, and Chl groups. Chl retarded gap closure (p < 0.05). Fb migration was similar for all groups. In the control and Ox groups, myofibroblast expressed actin at day 5. By day 7, fb cells were clearly visible in the control, Ox, and Cl groups, whereas, only light actin was present in the Chi and Tet groups. Actin band densities fur the Cl, Ox, Tet, and Chl groups were 78.4%, 62.5%, 61.7% and 26.1%, respectivel y, of the control group. Conclusion: These studies suggest that one reason certain antimicrobials im pair wound healing, is due to myofibroblast inhibition of alpha-SM actin.