Nutritional research has shifted recently from alleviating nutrient deficiencies to
chronic disease prevention. We investigated the activity of
indicaxanthin, a bioavailable
phytochemical of the
betalain class from the edible fruit of Opuntia ficus-indica (L. Miller) in a rat model of acute
inflammation. Rat
pleurisy was achieved by injection of 0.2 mL of λ-
carrageenin in the pleural cavity, and rats were killed 4, 24, and 48 h later; exudates were collected to analyze inflammatory parameters, such as
nitric oxide (NO),
prostaglandin E(2) (
PGE(2)), interleukin-1β (IL-1β), and
tumor necrosis factor-α (TNF-α); cells recruited in pleura were analyzed for
cyclooxygenase-2 (COX-2),
inducible nitric oxide synthase (iNOS) expression, and nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) activation.
Indicaxanthin (0.5, 1, or 2 μmol/kg), given orally before
carrageenin, time- and dose-dependently, reduced the exudate volume (up to 70%) and the number of leukocytes recruited in the pleural cavity (up to 95%) at 24 h. Pretreatment with
indicaxanthin at 2 μmol/kg inhibited the
carrageenin-induced release of
PGE(2) (91.4%), NO (67.7%), IL-1β (53.6%), and TNF-α (71.1%), and caused a decrease of IL-1β (34.5%), TNF-α (81.6%), iNOS (75.2%), and COX2 (87.7%)
mRNA, as well as iNOS (71.9%) and COX-2 (65.9%)
protein expression, in the recruited leukocytes.
Indicaxanthin inhibited time- and dose- dependently the activation of NF-κB, a key
transcription factor in the whole inflammatory cascade. A pharmacokinetic study with a single 2 μmol/kg
oral administration showed a maximum 0.22 ± 0.02 μmol/L (n = 15) plasma concentration of
indicaxanthin, with a half-life of 1.15 ± 0.11 h. When considering the high bioavailability of
indicaxanthin in humans, our findings suggest that this dietary pigment has the potential to improve health and prevent
inflammation-based disorders.