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Fig. 1 | BMC Nephrology

Fig. 1

From: Molecular mechanisms of hydrogen sulfide against uremic accelerated atherosclerosis through cPKCβII/Akt signal pathway

Fig. 1

Effects of CSE/H2S system on the membrane translocation of cPKCβII in mouse aorta. The membrane translocation of cPKCβII in control, sham, UAAS, UAAS+L-cys, UAAS+NaHS and UAAS+PPG group. (a) The protein contents in cytosolic and particulate fraction of mouse aorta were tested by Western blot; (b) Quantitative analysis showed that cPKCβII membrane translocation in UAAS group increased significantly compared with sham group (*P < 0.05 vs. sham group, n = 6 per group). L-cys or NaHS injection could suppress the membrane translocation, but PPG treatment resulted in more membrane translocation of cPKCβII (#P < 0.05 vs. UAAS group, n = 6 per group)

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