n dimethylnitrosamine/sladkorna bolezen

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Pharmacokinetic changes of drugs in a rat model of liver cirrhosis induced by dimethylnitrosamine, alone and in combination with diabetes mellitus induced by streptozotocin.

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Prijava / prijava

Rats with liver cirrhosis induced by N-dimethylnitrosamine (LC) and rats with LC with diabetes mellitus induced by streptozotocin (LCD) have been developed as animal models for human liver cirrhosis and liver cirrhosis with diabetes mellitus, respectively. Changes in the pharmacokinetics of drugs

Pharmacokinetic parameters of chlorzoxazone and its main metabolite, 6-hydroxychlorzoxazone, after intravenous and oral administration of chlorzoxazone to liver cirrhotic rats with diabetes mellitus.

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Prijava / prijava

Protein expression of the hepatic CYP2E1 has been reported to be increased in diabetic rats. This enzyme is the primary metabolizer of chlorzoxazone (CZX) to 6-hydroxychlorzoxazone (OH-CZX). Although patients with liver cirrhosis have a higher prevalence of diabetes mellitus, there have been no

Reactive metabolite formation catalysed by cytochrome P-450j.

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Prijava / prijava

Cytochrome P-450j is induced by ethanol, isoniazid, fasting and in diabetes mellitus; the hepatotoxicity of paracetamol and N,N-dimethylnitrosamine is increased following such induction. We have assessed the potential of liver microsomes isolated from control and isoniazid-treated rats to convert

Pharmacokinetics of oltipraz in diabetic rats with liver cirrhosis.

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OBJECTIVE The incidence of diabetes mellitus is increased in patients with liver cirrhosis. Oltipraz is currently in trials to treat patients with liver fibrosis and cirrhosis induced by chronic hepatitis types B and C and is primarily metabolized via hepatic cytochrome P450 isozymes CYP1A1/2,

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