Modulation of Calmodulin and Protein Kinase C Activities by Pencillium Mycotoxins
Autor: | I. Pala, Parminder J. S. Vig, Durisala Desaiah, A. Srinivasan |
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Rok vydání: | 1999 |
Předmět: |
chemistry.chemical_classification
animal structures Calmodulin Stimulation 010501 environmental sciences Biology Toxicology 030226 pharmacology & pharmacy 01 natural sciences 03 medical and health sciences Cytosol 0302 clinical medicine Enzyme Mechanism of action Biochemistry chemistry medicine biology.protein Extracellular medicine.symptom Secalonic acid Protein kinase C 0105 earth and related environmental sciences |
Zdroj: | International Journal of Toxicology. 18:91-96 |
ISSN: | 1092-874X 1091-5818 |
DOI: | 10.1080/109158199225657 |
Popis: | Calmodulin (CaM), a calcium-binding protein, is found in high concentrations in mammalian brain where it plays a pivotal role in a large number of cellular functions. Protein kinase C (PKC), a multifunctional cytosolic enzyme, in the presence of both Ca2+ and phospholipids, transduce extracellular signals into intracellu-lar events. Both CaM and PKC are partially involved in maintaining Ca2+ homeostasis in the cell. Any fluctuations in the intracel-lular Ca2+ can modulate cellular functions and may contribute to neuronal dysfunction. Hence, the present investigation was initiated to study the effects of some selected penicillium (naturally occurring tremorgenic) mycotoxins like secalonic acid, citreoviridin, and verruculogen on CaM activity, active conformation of CaM and PKC activity. Stimulation of CaM-deflcient bovine brain 3′-5′ phosphodieste rase (PDE) indicated CaM activity. The modification of CaM active conformation was studied by the binding of fluorescent probe N-phenyl-1-napthylamine (NPN) to CaM. Alterations in the fluorescence of dansyl-CaM was used to study the effect of these compounds on complex formation between CaM and PDE. Rat brain cytosolic PKC was studied using 32P-ATP as a measure of altered protein phosphorylation. The concentrations of mycotoxins used were in the range of 10 to 50 μM. All three mycotoxins inhibited CaM-stimulated PDE activity in a concentration-dependent manner. Citreoviridin and secalonic acid inhibited NPN fluorescence and Ca2+-dependent complex formation of dansyl-CaM and PDE. The IC50 values for NPN fluorescence of citreoviridin and secalonic acid were 13 μM and 19 μM respectively. However, verruculogen showed little effect on NPN fluorescence and the Ca2+-dependent complex formation of dansyl-CaM and PDE. These mycotoxins also inhibited PKC activity in a concentration-dependent manner with IC50 values of 19.8, 25.7, and 38.4 μM for secalonic acid, citreoviridin, and verruculogen, respectively. The results of our study suggest that these mycotoxins at very low concentrations are interacting with CaM and PKC. Such an effect could lead to impairment of neurotransmission and result in neurotoxicity. |
Databáze: | OpenAIRE |
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