## Abstract The regulation of drug metabolic activity of cultured hepatocytes can be applied to the evaluation of pharmacokinetics, analysis of drug delivery and the bioartificial liver system. It is very difficult to maintain the drug metabolic activity mediated by cytochrome Pβ450 (CYP) 3A. Recen
GANGLIOSIDE-MEDIATED METABOLIC SYNCHRONIZATION OF PROTEIN SYNTHESIS ACTIVITY IN CULTURED HEPATOCYTES
β Scribed by Vsevolod Y. Brodsky; Natalia V. Nechaeva; Natalia D. Zvezdina; Tatjana E. Novikova; Inna G. Gvasava; Valentina I. Fateeva; Nina V. Prokazova; Natalia K. Golovanova
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 653 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1065-6995
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β¦ Synopsis
Abstract
An ultradian oscillation of protein synthesis was detected by synchronization of metabolic activity in rat hepatocyte cultures. This oscillation occurs in dense cultures in fresh medium, but not in sparse ones. Metabolic synchronization of sparse cultures, however, was initiated by conditioned medium or addition of 0.3β0.5ΞΌm of a mixture of bovine brain gangliosides to fresh culture medium along with either 0.06β0.2ΞΌm GM1 or 0.1β0.2ΞΌm GDIa. GTIb and GDIb did not produce oscillations, nor did human liver ganglioside GM3. High expression of GM1 ganglioside determinants in hepatocytes maintained in the conditioned medium purified polyclonal antibodies to GM1 was coupled with protein synthetic oscillatory activity, i.e. metabolic synchronization. Incubation of dense cultures with GM1βantibodies for 24h decreased the amplitude of these oscillations. In sparse cultures maintained in fresh medium where protein synthesis showed no oscillatory pattern, GM1 expression was low.
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