نتایج جستجو برای: norverapamil

تعداد نتایج: 37  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2005
Ying-Hong Wang David R Jones Stephen D Hall

The genetic basis for polymorphic expression of CYP3A5 has been recently identified, but the significance of CYP3A5 expression is unclear. The purpose of this study is to quantify the capability of verapamil, a mechanism-based inhibitor of CYP3A, and its metabolites to inhibit the activities of CYP3A4 and CYP3A5, and to determine whether CYP3A5 expression in human liver microsomes alters the in...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2011
Nan Hu Shanshan Xie Li Liu Xinting Wang Xian Pan Guanming Chen Lulu Zhang Haiyan Liu Xiang Liu Xiaodong Liu Lin Xie Guangji Wang

The aim of this study was to report the effect of diabetes mellitus on the pharmacokinetics of verapamil in a route-dependent manner. Diabetes in rats was induced by streptozotocin. Plasma concentrations of verapamil and its metabolite, norverapamil, were measured after oral (10 mg/kg) or intravenous (1 mg/kg) administration. The concentrations of verapamil in portal plasma after oral administr...

Journal: :The Journal of infectious diseases 2014
Kristin N Adams John D Szumowski Lalita Ramakrishnan

Drug tolerance likely represents an important barrier to tuberculosis treatment shortening. We previously implicated the Mycobacterium tuberculosis efflux pump Rv1258c as mediating macrophage-induced tolerance to rifampicin and intracellular growth. In this study, we infected the human macrophage-like cell line THP-1 with drug-sensitive and drug-resistant M. tuberculosis strains and found that ...

Journal: :Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics 1996

Journal: :Clinical pharmacology and therapeutics 1982
J G Wagner A P Rocchini J Vasiliades

With data on adults from two previous articles it was found that the average steady-state plasma concentration of verapamil in subjects on long-term oral therapy of 80 mg every 6 hr (Y) correlated strongly with the area under the curve from zero to infinity (AUC0-x/6 (X) where the area refers to that for a single oral dose of 80 mg (Y - 2.41X, n - 15, r - 0.923, P less than 0.001). Steady-state...

Journal: :The Journal of pharmacology and experimental therapeutics 2002
Rajinder K Bhardwaj Hartmut Glaeser Laurent Becquemont Ulrich Klotz Suresh K Gupta Martin F Fromm

Dietary constituents (e.g., in grapefruit juice; NaCl) and phytochemicals (e.g., St. John's wort) are important agents modifying drug metabolism and transport and thereby contribute to interindividual variability in drug disposition. Most of these drug-food interactions are due to induction or inhibition of P-glycoprotein and/or CYP3A4. Preliminary data indicate that piperine, a major component...

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