AI Article Synopsis

  • - Cellulite is a common condition mainly affecting women, and CCH-aaes injections help improve its appearance by disrupting collagen structures, although bruising at the injection site is a common side effect.
  • - An animal study was conducted on female Yorkshire pigs to investigate the tissue changes after CCH-aaes injections, with pigs receiving either the treatment or a placebo at various time points.
  • - Results showed that CCH-aaes led to the breakdown of collagen in the subcutaneous layer soon after injection, with signs of inflammation early on, followed by new collagen formation and tissue remodeling observed by Day 21.

Article Abstract

Background: Cellulite is a common aesthetic condition that affects predominantly females. Collagenase clostridium histolyticum-aaes (CCH-aaes) injections disrupt native collagen structures, resulting in an improvement in cellulite appearance. However, injection-site bruising is a frequently occurring adverse event with CCH-aaes treatment.

Objectives: To characterize tissue histology following CCH-aaes injection in Yorkshire pigs.

Methods: In an animal study, female swine with 10 defined dosing sites on the ventral-lateral aspect received 1 or 2 CCH-aaes (0.07 mg/0.3 mL) or placebo subcutaneous injections at a single site at designated time points before tissue sampling.

Results: Injection with CCH-aaes was associated with lysis of mature, collagen-rich septa in the subcutaneous layer at and adjacent to the injection site as early as Day 1. On Day 4, an increase in inflammatory cells and a decrease in hemorrhage (vs Day 2) were observed, with inflammation and hemorrhage decreased by Day 8. By Day 21, deposition of new collagen and reorganization of fat lobules were observed. Observations with repeat CCH-aaes treatment were comparable with 1 course of CCH-aaes treatment.

Conclusions: In this animal study, targeted enzymatic subcision of collagenous bands and remodeling of subcutaneous tissue were observed following CCH-aaes injection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270649PMC
http://dx.doi.org/10.1093/asjof/ojad034DOI Listing

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