| Literature DB >> 28430368 |
Anna Antolak1, Anna Bodzoń-Kułakowska1, Ewa Cetnarska1, Monika Pietruszka1, Marta Marszałek-Grabska2, Jolanta Kotlińska1, Piotr Suder1.
Abstract
Drug dependence is an escalating problem worldwide and many efforts are being made to understand the molecular basis of addiction. The morphine model is widely used in these investigations. To date, at least 29 studies exploring the influence of morphine on mammals' proteomes have been published. Among various proteins indicated as up- or down-regulated, the expression changes of enzymes engaged in energy metabolism pathways have often been confirmed. To verify whether proteomics-indicated alterations in enzyme levels reflect changes in their activity, four enzymes: PK, MDH, Complex I, and Complex V were investigated in morphine addiction and abstinence models. After analyses of the rat brain mitochondria fraction in the model of morphine dependence, we found that one of the investigated enzymes (pyruvate kinase) showed statistically significant differences observed between morphine, control, and abstinence groups. J. Cell. Biochem. 118: 4323-4330, 2017.Entities:
Keywords: DATABASE; ENZYME ACTIVITY; MORPHINE; PROTEOMICS
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Year: 2017 PMID: 28430368 DOI: 10.1002/jcb.26085
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429