Klotho Improves Cardiac Function by Suppressing Reactive Oxygen Species (ROS) Mediated Apoptosis by Modulating Mapks/Nrf2 Signaling in Doxorubicin-Induced Cardiotoxicity

Figure 1. Klotho reduced DOX-induced ROS in myocardium and myocytes which was reversed by MAPKs inhibitors or siRNAs. (A) Left panel demonstrates the captured fluorescent images of DHE stained myocardium. Intracellular ROS is tagged red. Columns on the right side indicate the mean fluorescence intensities of ROS in myocardium harvested from control, DOX, DOX+KL, DOX+KL+JNKi, DOX+KL+ERKi and DOX+KL+p38i respectively. (B) Images on the left side are DHE staining of cultured myocytes. Columns on the right side indicate the mean fluorescence intensities of ROS in myocardium harvested from control, DOX, DOX+KL, DOX+KL+JNKi, DOX+KL+ERKi, DOX+KL+p38i, DOX+KL+JNK-siRNA, DOX+KL+ERK-siRNA, and DOX+KL+p38-siRNA respectively. a Differences were significant when compared with control (p<0.05); b differences were significant when compared with DOX (p<0.05); c differences were significant when compared with DOX+KL (p<0.05).

Figure 2. Klotho activated MAPKs in DOX-treated myocardium and myocytes which was reversed by MAPKs inhibitors or siRNAs. (A, B) The left panels show the immunoblots of p-p38 MAPK, p38 MAPK, p-ERK1/2, ERK1/2, p-JNK, JNK, and GAPDH in cytoplasmic protein samples extracted from myocardium and myocytes. Columns on the right panels indicate the ratio of p-p38MAPK/p38MAPK (light blue), p-ERK2/1/ERK1/2 (blue), and p-JNK/JNK (dark blue) in myocardium and cultured myocytes respectively. a Differences were significant when compared with control (p<0.05); b differences were significant when compared with DOX (p<0.05); c differences were significant when compared with DOX+KL (p<0.05).

Figure 3. Klotho improved nuclear translocation of Nrf2 in DOX-exposed myocardium and myocytes which was reversed by MAPKs inhibitors or siRNAs. (A, B) The left panels show the immunoblots of Nrf2 and Histone H3 in nuclear protein samples extracted from myocardium and myocytes. Columns on the right panels indicate the ratio of Nrf2/histone H3 in myocardium and cultured myocytes respectively. (C) The left panel demonstrates the captured fluorescent images of Nrf2, DAPI, and their merged images in cultured myocytes. Columns on the right part indicate the Nrf2 nuclear translocation rate in different groups. a Differences were significant when compared with control (p<0.05); b differences were significant when compared with DOX (p<0.05); c differences were significant when compared with DOX+KL (p<0.05).

Figure 4. Klotho increased expression levels of anti-oxidant enzymes in DOX-treated myocardium and myocytes which was reversed by MAPKs inhibitors or siRNAs. (A, B) The immunoblots of HO1, Prx1, and GAPDH in myocardium and cultured myocytes in different groups are shown on the left panels. Columns on the right part indicate the ratio of HO/GAPDH and Prx1/GAPDH in myocardium and cultured myocytes respectively. a Differences were significant when compared with control (p<0.05); b differences were significant when compared with DOX (p<0.05); c differences were significant when compared with DOX+KL (p<0.05).

Figure 5. Klotho attenuated DOX-induced apoptosis and cardiac dysfunction which were reversed by treatment of MAPKs and siRNAs. (A) Left panel demonstrates the captured images of TUNEL assay in myocardium. Apoptotic cells are stained brown. Columns on the right part indicate the cell apoptotic rate in different groups. (B) Charts of flow cytometry of apoptosis in cultured myocytes in different groups are shown on the left side. Columns on the right part indicate the cell apoptotic rate in different groups. (C) Columns in this panel indicate the detected LVSP (left side) and LVDP (right side) by hemodynamic method in rats from different groups. a Differences were significant when compared with control (p<0.05); b differences were significant when compared with DOX (p<0.05); c differences were significant when compared with DOX+KL (p<0.05).