The influence of gastric pentadecapeptide BPC 157 on acute and chronic ethanol administration in mice

Eur J Pharmacol. 2004 Sep 24;499(3):285-90. doi: 10.1016/j.ejphar.2004.07.112.

Abstract

The stable gastric pentadecapeptide BPC 157 (GEPPPGKPADDAGLV, M.W.1419), which was promising in inflammatory bowel disease (PL-10, PLD-116, PL-14736, Pliva) trials, protects against both acute and chronic alcohol-induced lesions in stomach and liver, but also, given peripherally, affects various centrally mediated disturbances. Now, in male NMRI mice BPC 157 (10 pg intraperitoneally, 10 ng and 10 microg, intraperitoneally or intragastrically) (i) strongly opposed acute alcohol (4 g/kg intraperitoneally) intoxication (i.e., quickly produced and sustained anesthesia, hypothermia, increased ethanol blood values, 25% fatality, 90-min assessment period) given before or after ethanol, and (ii) when given after abrupt cessation of ethanol (at 0 or 3 or 7 h withdrawal time), attenuated withdrawal (assessed through 24 hours) after 20%-alcohol drinking (7.6 g/kg) through 13 days, with provocation on the 14th day.

Publication types

  • Comparative Study

MeSH terms

  • Alcohol Withdrawal Seizures / chemically induced
  • Alcohol Withdrawal Seizures / prevention & control
  • Alcoholism / etiology
  • Alcoholism / prevention & control
  • Animals
  • Anti-Ulcer Agents / administration & dosage
  • Anti-Ulcer Agents / pharmacology*
  • Dose-Response Relationship, Drug
  • Ethanol / administration & dosage*
  • Ethanol / blood
  • Ethanol / toxicity
  • Injections, Intraperitoneal
  • Male
  • Mice
  • Mice, Inbred Strains
  • Peptide Fragments / administration & dosage
  • Peptide Fragments / pharmacology*
  • Proteins / administration & dosage
  • Proteins / pharmacology*
  • Stomach / drug effects
  • Substance Withdrawal Syndrome / etiology
  • Substance Withdrawal Syndrome / prevention & control
  • Time Factors

Substances

  • Anti-Ulcer Agents
  • Peptide Fragments
  • Proteins
  • Ethanol
  • BPC 157