thiobenzamide and Body-Weight

thiobenzamide has been researched along with Body-Weight* in 2 studies

Other Studies

2 other study(ies) available for thiobenzamide and Body-Weight

ArticleYear
Changes in the rat liver drug metabolizing system during a short thiobenzamide feeding cycle.
    Archives of toxicology, 1987, Volume: 61, Issue:2

    The changes in the hepatic drug metabolizing enzymes induced by the liver tumor promoter thiobenzamide (TB) were investigated. Feeding of TB to rats at a promoting regimen (1 g/kg of diet for 2 weeks) resulted in a significant decrease in the amount of liver microsomal cytochrome P-450 and of total heme. Also, the activity of cytochrome P-450 dependent monooxygenases (aminopyrine demethylase, arylhydrocarbonmonooxygenase and ethoxycoumarindeethylase) and FAD-containing monoxygenase (N,N-dimethylaniline N-oxidase and TB S-oxidase) were depressed. By contrast, phase II enzymes such as epoxide hydrase, UDP-glucuronyl transferase and GSH-transferase were significantly induced. This overall change in the drug metabolizing system was associated with tolerance of the liver towards a high necrogenic dose of TB itself as well as with an increase of mitoses and apoptosis of the hepatocytes. The findings suggest a possible relationship between this TB-induced adaptive response and the promoting activity of the compound on liver carcinogenesis.

    Topics: Adaptation, Biological; Amides; Animals; Body Weight; Cytochrome P-450 Enzyme System; DNA; Liver; Male; Mitosis; Mixed Function Oxygenases; NADH Dehydrogenase; Organ Size; Rats; Rats, Inbred Strains; Thioamides

1987
Biliary cirrhosis and tumors induced by chronic administration of thiobenzamide to rats.
    Archives of toxicology, 1984, Volume: 55, Issue:1

    Thiobenzamide (TB), a thiono-containing compound, was administered for 38 weeks to female Sprague-Dawley rats at a dose of 1 g/kg standard diet; the resulting liver pathology was followed up to 8 months after withdrawal of the compound from the diet. TB administration induced the appearance of biliary cirrhosis. In the first weeks of intoxication the progressive distortion of the liver architecture was mainly due to significant proliferation of the bile ductules. Later, the liver assumed a macronodular appearance. In addition to regenerative and degenerative changes of the hepatocytes, preneoplastic lesions were also detected, and some enzymic markers of the mixed-function monooxygenase system were decreased. Cholangiofibrotic areas were evident, and many biliary tubules within them showed mucous metaplasia. At the end of the intoxication period, as well as 4 months after drug suspension, large portions of the liver or entire lobes were substituted by connective tissue surrounding nests of bile ductules and atrophied hepatocellular nodules. Four months later, in the virtual absence of cirrhotic changes, each animal harboured one or more tumors (mainly cholangiomas).

    Topics: Adenoma, Bile Duct; Amides; Animals; Body Weight; Carcinoma, Hepatocellular; Diet; Female; Liver; Liver Cirrhosis, Biliary; Liver Neoplasms; Organ Size; Rats; Rats, Inbred Strains; Thioamides

1984