Bovine milk-derived α-lactalbumin inhibits colon inflammation and carcinogenesis in azoxymethane and dextran sodium sulfate-treated mice

Biosci Biotechnol Biochem. 2014;78(4):672-9. doi: 10.1080/09168451.2014.890034. Epub 2014 Apr 16.

Abstract

Cyclooxygenase-2 is expressed early in colon carcinogenesis and plays crucial role in the progress of the disease. Recently, we found that α-lactalbumin had anti-inflammatory activity by inhibiting cyclooxygenase-2. In experiment 1, we investigated the effects of α-lactalbumin on the colon carcinogenesis initiated with azoxymethane (AOM) followed by promotion with dextran sodium sulfate (DSS) in mice. Dietary treatment with α-lactalbumin decreased fecal occult blood score at 3 days after DSS intake. α-Lactalbumin also decreased the colon tumor at week 9. In experiment 2, AOM-treated mice were sacrificed at 7 days after DSS intake. The plasma and colon prostaglandin E2 (PGE2) levels in AOM/DSS-treated mice were higher than those in the DSS-treated mice without initiation by AOM. α-Lactalbumin decreased PGE2 in both plasma and colon. These results suggest that α-lactalbumin effectively inhibited colon carcinogenesis, and the inhibition may be due to the decreased PGE2 by inhibiting cyclooxygenase-2 at cancer promotion stages.

Keywords: colon carcinogenesis; cyclooxygenase; prostaglandin E2; α-lactalbumin.

MeSH terms

  • Adenocarcinoma / chemically induced
  • Adenocarcinoma / pathology
  • Adenocarcinoma / prevention & control
  • Adenoma / chemically induced
  • Adenoma / pathology
  • Adenoma / prevention & control
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Azoxymethane / pharmacology*
  • Carcinogenesis / chemically induced
  • Carcinogenesis / drug effects*
  • Cattle
  • Colon / drug effects*
  • Colon / metabolism
  • Colon / pathology
  • Colonic Neoplasms / chemically induced
  • Colonic Neoplasms / pathology
  • Colonic Neoplasms / prevention & control
  • Dextran Sulfate / pharmacology*
  • Dietary Supplements
  • Dinoprostone / blood
  • Dinoprostone / metabolism
  • Inflammation / blood
  • Inflammation / drug therapy
  • Inflammation / metabolism
  • Inflammation / pathology
  • Interleukin-1beta / metabolism
  • Lactalbumin / pharmacology*
  • Lactalbumin / therapeutic use
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Milk / chemistry*
  • Occult Blood
  • Organ Size / drug effects
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Interleukin-1beta
  • Tumor Necrosis Factor-alpha
  • Lactalbumin
  • Dextran Sulfate
  • Dinoprostone
  • Azoxymethane