TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466.

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TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 1. Changes of myocyte apoptosis of the heart tissue after trauma. Pentobarbital anesthetized rats were subjected to control or trauma group. Trauma group included five subgroups: posttraumatic 0, 3, 6, 12, and 24 h subgroups. Their hearts were collected at several times, and myocyte apoptosis in the heart tissue was measured by situ DNA TUNEL staining. Representative figures showed myocyte apoptosis in control and traumatized rats. Arrows indicated the positive staining identifying apoptotic nuclei. Magnification (×200). * P<0.05 vs. control. n = 10 rats per group or subgroup. © 2015 S. Karger AG, Basel - CC BY-NC 3.0

TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 2. Changes of isolated myocyte apoptosis after trauma. Pentobarbital anesthetized rats were subjected to control or trauma group. Trauma group included five subgroups: posttraumatic 0, 3, 6, 12, and 24 h subgroups. Their hearts were collected at several times, and isolated myocyte apoptosis was measured by Flow cytometry. * P<0.05 vs. control. n = 10 rats per group or subgroup. © 2015 S. Karger AG, Basel - CC BY-NC 3.0

TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 3. Changes of plasma TNF-α, IL-1β and IFN-γ after trauma. Pentobarbital anesthetized rats were subjected to control or trauma group. Trauma group included five subgroups: posttraumatic 0, 3, 6, 12, and 24 h subgroups. Plasma samples were obtained at the specified time points, and TNF-α (A), IL-1β (B) and IFN-γ (C) levels were measured by ELISA. *P<0.05 vs. control. n = 10 rats per group or subgroup. © 2015 S. Karger AG, Basel - CC BY-NC 3.0

TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 4. Changes of the activities of caspases-3, 8 and 9, and the expression of Bax and Bcl-2 after the incubation of Cytomix, TNF-α, IL-1β and IFN-γ. Cardiomyocytes isolated from traumatized rats (traumatized cardiomyocytes) were incubated with one of the following factors for 12 h: normal plasma; Cytomix (a mixture of 10 ng/mL TNF-α, 1 ng/mL IL-1β, and 1,000 U/mL IFN-γ); 10 ng/mL TNF-α; 1 ng/mL IL-1β; 1,000 U/mL IFN-γ. Caspases-3, 8, and 9 activities, and the expression of Bax and Bcl-2 were assayed by colorimetric assays and western blot, respectively. **P<0.01 vs. NP. n = 3 independent experiments. © 2015 S. Karger AG, Basel - CC BY-NC 3.0

TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 5. Changes of MAPKs activation after the incubation of Cytomix, TNF-α, IL-1β and IFN-γ. Cardiomyocytes isolated from traumatized rats (traumatized cardiomyocytes) were incubated with one of the following factors for 12 h: normal plasma (NP); Cytomix (a mixture of 10 ng/mL TNF-α, 1 ng/mL IL-1β, and 1,000 U/mL IFN-γ); 10 ng/mL TNF-α; 1 ng/mL IL-1β, and 1,000 U/mL IFN-γ. Total- and phos- of p38 and ERK1/2 were measured by western blot. **P < 0.01 vs. NP. n = 3 independent experiments. © 2015 S. Karger AG, Basel - CC BY-NC 3.0

TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 6. Changes of caspases-3, 8, and 9 activities, and p38 activation after the incubation of anti-TNF-α antibody. Cardiomyocytes isolated from traumatized rats (traumatized cardiomyocytes) were incubated with one of the following factors for 12 h: normal plasma (NP); trauma plasma (TP); TP plus 1 μg/mL anti-TNF-α antibody. The activities of caspases-3, 8 and 9, and the expression of total- and phos-p38 were measured by colorimetric assays and western blot, respectively. **P<0.01 vs. NP; <italic>#<italic>P<0.05 vs. TP. n = 3 independent experiments. © 2015 S. Karger AG, Basel - CC BY-NC 3.0

TNF-α- Mediated-p38-Dependent Signaling Pathway Contributes to Myocyte Apoptosis in Rats Subjected to Surgical Trauma Cell Physiol Biochem 2015;35:1454-1466 - DOI:10.1159/000373965 Fig. 7. Changes of caspases-3, 8, and 9 activities, and p38 activation after the incubation of SB203580. Cardiomyocytes isolated from traumatized rats (traumatized cardiomyocytes) were subjected to one of the following treatments for 12 h: normal plasma (NP); trauma plasma (TP); TP plus 10 μM SB203580. The activities of caspases-3, 8 and 9, and the expression of total- and phos-p38 were assayed by colorimetric assays and western blot, respectively. **P<0.01 vs. NP; <italic>#<italic>P<0.05 vs. TP. n = 3 independent experiments. © 2015 S. Karger AG, Basel - CC BY-NC 3.0