Introduction:
Pretreatment with antibiotics is commonly performed prior to surgical implantation of prosthetic materials. We have previously shown that pericardial patches are infiltrated by macrophages and arterial stem cells after implantation into an artery. We hypothesized that antibiotic pretreatment would diminish the number of cells infiltrating into the patch, potentially affecting early neointimal formation.
Methods:
Bovine pericardial patches were pretreated with saline, bacitracin (500 U/ml), or cephalexin (10 mg/ml) for 30 minutes prior to implantation into the Wistar rat infrarenal aorta. Patches were retrieved on day 7 or day 30, and analyzed for histology and cell infiltration; markers of proliferation, apoptosis, vascular cell identity, and M1 and M2 macrophage subtypes were examined using immunofluorescence and immunohistochemistry. Extracted proteins were analyzed by Western blot.
Results:
At day 7, pericardial patches pretreated with either bacitracin or cephalexin showed similar amounts of neointimal thickening (p=0.55) and cellular infiltration (p=0.42) compared to control patches. Patches pretreated with antibiotics showed similar proliferation (p=0.09) and apoptosis (p=0.84) as control patches. The cell composition of the neointima in pretreated patches was similar to control patches, with a thin endothelial layer overlying a thin layer of SMC (p=0.45), and containing similar numbers of CD34-positive (p=0.26) and VEGFR2-positive (p=0.31) cells. Interestingly, within the body of the patch, there were fewer macrophages (p=0.0003) and a trend towards fewer EPC (p=0.051). There were no M1 macrophages in or around any of the patches; M2 macrophages were present around the patches and there was no difference in numbers of M2 macrophages surrounding control patches and patches pretreated with antibiotics (p=0.24). There was no difference in neointimal thickness at day 30 between control patches and patches pretreated with antibiotics (p=0.52).
Conclusions:
Pretreatment of bovine pericardial patches with the antibiotics bacitracin or cephalexin has no detrimental effect on early patch healing, with similar neointimal thickness, cellular infiltration, and numbers of M2 macrophages compared to control patches. These results suggest that the host vessel response to patch angioplasty using pericardial patches is adaptive remodeling, e.g. arterial healing.