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Synergistic induction of metallothionein synthesis by interleukin-6, dexamethasone and zinc in the rat
Affiliation:1. Department of Microbiology and Biotechnology, Bangalore University, Jnana Bharathi, Bengaluru 560 056, Karnataka, India;2. Department of Bioinformatics and Biotechnology, Karnataka State Women''s University, Jnana Shakthi Campus, Vijayapura 586 108, Karnataka, India;3. Department of Biology and Center for Biotechnology and Biomedical Sciences, Norfolk State University, Norfolk, VA, USA;4. Department of Biotechnology, The Oxford College of Science, HSR Layout, Bengaluru 560102, Karnataka, India;1. Department of Life Science, College of Natural Sciences, Hanyang University, Seoul, South Korea;2. Graduate School of Biomedical Science and Engineering, Hanyang University, Seoul, South Korea;3. Department of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon, South Korea;4. College of Medicine, Hanyang University, Seoul 04763, South Korea
Abstract:We investigated the reciprocal effects of interleukin-6 (IL-6), glucocorticoid and zinc (Zn) on metallothionein (MT) synthesis in rats. MT synthesis in the liver, which is a key responsible organ in acute phase responses, was induced by IL-6 or dexamethasone (Dex), and in an additive manner by a combination of IL-6 and Dex 18 h after injection. MT synthesis in the lung and heart was evaluated by immunoassay using a specific antibody to MT-I, because of its low concentration in these tissues. Heart concentrations of MT-I were significantly increased by IL-6, and were further increased by the combination of IL-6 and Dex, although Dex by itself had no effect. This suggests a synergistic effect of IL-6 and Dex on MT-I synthesis in the heart. A similar synergism was observed in the lung. To study the effect of Zn on the induction of MT and acute phase proteins, Zn, IL-6 and Dex were administered in various concentrations. The increase in liver MT induced by the combination of IL-6 and Dex with Zn (130 μg MT/g of liver) was greater than the sum of the increases induced by (IL-6 + Zn) and by (Dex + Zn) (103 μg MT/g), suggesting a synergistic increase. The data indicate that the maximal increase in the induction of MT by a combination of IL-6 and Dex depends on an adequate liver Zn content. Thus, the in vivo synergistic induction of acute phase proteins by IL-6, glucocorticoid and Zn may be required for the maximal and rapid response, not only in liver but also in other tissues including heart and lung. This suggests that the synergistic reaction may be important for an enhancement of the radical scavenging ability of tissues in acute phase responses.
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