16,16-dimethyl-PGE2 protection against alpha-naphthylisothiocyanate-induced experimental cholangitis in the rat.

Abstract

Male rats were treated with subcutaneous vehicle or 16,16-dimethyl-PGE2 (dmPGE2, 100 micrograms per kg), 24, 18 and 0.5 hr prior to and 6, 24 and 30 hr after challenge with oral alpha-naphthylisothiocyanate (ANIT, 30 mg per kg). Forty-eight hours after challenge, rats were sacrificed by decapitation; serum and liver samples were taken for biochemical and histological analysis, respectively. Rats treated with vehicle (2% ethanol in saline) and ANIT exhibited elevations in alkaline phosphatase, SGPT and bilirubin as well as cholangitis and mild parenchymal necrosis. Rats treated with dmPGE2 and ANIT had normal serum biochemical findings, no necrosis and only mild proliferation of bile duct epithelium. Thus, dmPGE2 may be able to protect the rat liver against the deleterious effects of orally administered ANIT.

• Authors: M J Ruwart, B D Rush, N M Friedle, J Stachura, A Tarnawski
• Journal: Hepatology (Baltimore, Md.) (Hepatology) 1984 Jul-Aug Vol. 4 Issue 4 Pg. 658-60 ISSN: 0270-9139 [Print] United States
• PMID: 6745853 (Publication Type: Journal Article)

Chemical References

• Prostaglandins E, Synthetic
• Thiocyanates
• 1-Naphthylisothiocyanate
• Aspartate Aminotransferases
• Alanine Transaminase
• Alkaline Phosphatase
• 16,16-Dimethylprostaglandin E2
• Bilirubin

Topics

• 1-Naphthylisothiocyanate
• 16,16-Dimethylprostaglandin E2 (therapeutic use)
• Alanine Transaminase (blood)
• Alkaline Phosphatase (blood)
• Animals
• Aspartate Aminotransferases (blood)
• Bilirubin (blood)
• Cholangitis (chemically induced, drug therapy, pathology)
• Liver (pathology)
• Male
• Prostaglandins E, Synthetic (therapeutic use)
• Rats
• Rats, Inbred Strains
• Thiocyanates