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. 2017 Nov 30;5(23):e13529. doi: 10.14814/phy2.13529

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© 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Cyclic AMP and TUDC inhibit TLC‐induced phosphorylation of myristoylated alanine‐rich C kinase substrate (MARCKS) in rat hepatocytes. Hepatocytes were treated with 10 μmol/L TLC, 100 μmol/L CPT‐cAMP, 10 μmol/L TLC + 100 μmol/L CPT‐cAMP, 25 μmol/L TUDC, or 10 μmol/L TLC + 25 μmol/L TUDC for different time periods. Untreated cell incubated for 25 min served as controls (Con) in each case. Actin was used as the loading control for phospho MARCKS. The relative values of phospho MARCKS (pMARCKS/actin) are expressed as mean ± SE (n = 4–6). Top: Typical immunoblots. Bottom: Bar graph with results of densitometric analysis. *Significantly different (P < 0.05) from control values.