Prostaglandin protection of carbon tetrachloride-induced liver cell necrosis in the rat. 1981

J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk

We studied whether 16,16--dimethyl prostaglandin E2 (dmPGE2) may prevent acute liver damage induced by carbon tetrachloride (CCl4) in the rat. One hundred thirty male rats were divided into the following groups: (1) controls, (2) rats given CCl4 6670 mg/kg body wt subcutaneously, (3) rats pretreated with 5 micrograms/kg dmPGE2 given subcutaneously 30 min before, and 8 and 24 h after CCl4 administration, and (4) animals given dmPGE2 only as in group 3. Liver damage was assessed by biochemical studies (SGPT, serum alkaline phosphatase, and bilirubin) and by histology. In rats receiving CCl4 alone, SGPT activities were significantly elevated to 1024 +/- 82 U/L, 1270 +/- 120 U/L, 386 +/- 48 U/L and 208 +/- 20 U/L at 24, 48, 96, and 120 h after CCl4 respectively. In animals pretreated with dmPGE2 before CCl4, SGPT activities were 201 +/- 24 U/L, 55 +/- 4.6 U/L, 28 +/- 4 U/L, and 24 +/- 4 U/L at 24, 48, 96, and 120 h after CCl4, respectively (p less than 0.01, versus animals receiving CCl4 only). Histologically, livers of rats treated with CCl4 alone showed severe centrilobular necrosis at 24 and 48 h. Livers of animals pretreated with dmPGE2 before CCl4 did not show necrosis. It is concluded that dmPGE2 protects the liver against cell necrosis induced by CCl4 in the rat.

UI MeSH Term Description Entries
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008297 Male Males
D009336 Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply.
D011459 Prostaglandins E, Synthetic Analogs or derivatives of prostaglandins E that do not occur naturally in the body. They do not include the product of the chemical synthesis of hormonal PGE. PGE Synthetic,Prostaglandin E Analogs,Prostaglandin E Analogues,Synthetic Prostaglandins E,Analogs, Prostaglandin E,Analogues, Prostaglandin E,Synthetic, PGE
D002251 Carbon Tetrachloride A solvent for oils, fats, lacquers, varnishes, rubber waxes, and resins, and a starting material in the manufacturing of organic compounds. Poisoning by inhalation, ingestion or skin absorption is possible and may be fatal. (Merck Index, 11th ed) Tetrachloromethane,Tetrachloride, Carbon
D000410 Alanine Transaminase An enzyme that catalyzes the conversion of L-alanine and 2-oxoglutarate to pyruvate and L-glutamate. (From Enzyme Nomenclature, 1992) EC 2.6.1.2. Alanine Aminotransferase,Glutamic-Pyruvic Transaminase,SGPT,Alanine-2-Oxoglutarate Aminotransferase,Glutamic-Alanine Transaminase,Alanine 2 Oxoglutarate Aminotransferase,Aminotransferase, Alanine,Aminotransferase, Alanine-2-Oxoglutarate,Glutamic Alanine Transaminase,Glutamic Pyruvic Transaminase,Transaminase, Alanine,Transaminase, Glutamic-Alanine,Transaminase, Glutamic-Pyruvic
D000469 Alkaline Phosphatase An enzyme that catalyzes the conversion of an orthophosphoric monoester and water to an alcohol and orthophosphate. EC 3.1.3.1.
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001663 Bilirubin A bile pigment that is a degradation product of HEME. Bilirubin IX alpha,Bilirubin, (15E)-Isomer,Bilirubin, (4E)-Isomer,Bilirubin, (4E,15E)-Isomer,Bilirubin, Calcium Salt,Bilirubin, Disodium Salt,Bilirubin, Monosodium Salt,Calcium Bilirubinate,Hematoidin,delta-Bilirubin,Bilirubinate, Calcium,Calcium Salt Bilirubin,Disodium Salt Bilirubin,Monosodium Salt Bilirubin,Salt Bilirubin, Calcium,delta Bilirubin
D015064 16,16-Dimethylprostaglandin E2 A synthetic prostaglandin E analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. The protective effect is independent of acid inhibition. It is also a potent inhibitor of pancreatic function and growth of experimental tumors. 16,16-Dimethyl-PGE2,16,16 Dimethyl PGE2,16,16 Dimethylprostaglandin E2,E2, 16,16-Dimethylprostaglandin

Related Publications

J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
August 1973, Laboratory investigation; a journal of technical methods and pathology,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
June 1974, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
February 1968, European journal of pharmacology,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
March 1997, Research communications in molecular pathology and pharmacology,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
January 1982, Gastroenterologia Japonica,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
January 1968, Polskie Archiwum Medycyny Wewnetrznej,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
May 2010, Journal of ethnopharmacology,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
January 1993, Archives of toxicology,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
November 1992, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica,
J Stachura, and A Tarnawski, and K J Ivey, and T Mach, and J Bogdal, and J Szczudrawa, and B klimczyk
November 1976, Gastroenterology,
Copied contents to your clipboard!