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Table 1.

Plasma lipids in the four groups of rats (mean±SD).

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Table 2.

Plasma malondialdehyde (MDA), superoxide dismutase (SOD) and total antioxidant capacity (T-AOC) in the four groups of rats (mean±SD).

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Figure 1.

Pathological changes of ascending aorta of rats from groups M, L, X and C.

(H-E staining, 20x).

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Table 3.

Hemorheological parameters in the four groups of rats (mean±SD).

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Figure 2.

Effect of Xuezhikang on plasma NOx (nitrite and nitrate).

(n = 12/group). *:P<0.05 vs. group C; **:P<0.05 vs. group M; #:P<0.05 vs. group L.

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Figure 3.

Effects of Xuezhikang on cGMP level in aorta wall and erythrocyte cytoplasm.

Hemoglobin in erythrocyte cytoplasm had been removed by ultrafiltration before the assay. *:P<0.05 vs. group C; **:P<0.05 vs. group M.

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Figure 4.

Effect of Xuezhikang on eNOS expression on erythrocyte membrane (n = 6/group).

About a 134 kDa band was identified by anti-eNOS antibody. β-tubulin was used as an internal reference. *:P<0.05 vs. group C; **:P<0.05 vs. group M; #:P<0.05 vs. group L.

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Figure 5.

Effects of Xuezhikang on eNOS expression in aorta.

(A) Protein lysate of aorta wall was used for the detection of eNOS, eNOS p-ser1177 by western blotting (n = 6/group). *:P<0.05 vs. group C; **:P<0.05 vs. group M; #:P<0.05 vs. group L. (B) Immunohistochemistry of aorta wall located eNOS expression in aorta endothelia (brown staining).

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Figure 6.

Effect of Xuezhikang on caveolin-1 expression in aorta wall.

(A) Protein lysate of aorta wall was used for the detection of caveolin-1 (n = 6/group). *:P<0.05 vs. group C; **:P<0.05 vs. group M; #:P<0.05 vs. group L. (B) Immunohistochemistry of aorta wall located caveolin-1 predominantly in aortic endothelia (brown staining).

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Figure 7.

Interaction between eNOS and caveolin-1 in aorta wall.

Protein lysates of aorta wall were incubated with anti-caveolin-1 antibody and protein A resin, and the immuno-precipitated proteins were blotted by anti-eNOS antibody by western blotting. Negative control sample was taken from the mixed supernatant from groups M, L, X and C, and was subjected to immunoprecipitation without the addition of anti-caveolin-1 antibody.

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