Bromelain has previously been shown to prevent ischemia-induced necrosis in different
types of tissues. In the present study, we, therefore, evaluated for the first time, the tissue-protective
effects of bromelain in musculocutaneous flaps in mice. Adult C57BL/6N mice were randomly
assigned to a bromelain treatment group and a control group. The animals were treated daily with
intraperitoneal injections of 20 mg/kg bromelain or saline (control), starting 1 h before the flap
elevation throughout a 10-day observation period. The random-pattern musculocutaneous flaps
were raised on the backs of the animals and mounted into a dorsal skinfold chamber. Angiogenesis,
nutritive blood perfusion and flap necrosis were quantitatively analyzed by means of repeated
intravital fluorescence microscopy over 10 days after surgery. After the last microscopy, the flaps
were harvested for additional histological and immunohistochemical analyses. Bromelain reduced
necrosis of the critically perfused flap tissue by ~25%. The bromelain-treated flaps also exhibited
a significantly higher functional microvessel density and an elevated formation of newly devel oped microvessels in the transition zone between the vital and necrotic tissues when compared
to the controls. Immunohistochemical analyses demonstrated a markedly lower invasion of the
myeloperoxidase-positive neutrophilic granulocytes and a significantly reduced number of cleaved
caspase 3-positive apoptotic cells in the transition zone of bromelain-treated musculocutaneous
flaps. These findings indicate that bromelain prevents flap necrosis by maintaining nutritive tissue
perfusion and by suppressing ischemia-induced inflammation and apoptosis. Hence, bromelain may
represent a promising compound to prevent ischemia-induced flap necrosis in clinical practice