Figure 4
Figure 4. The influence of PRCP on arterial thrombosis risk. (A) Control C57BL/6 WT and PRCPgt/gt (gt/gt) mice were subjected to the Rose-Bengal and ferric chloride carotid artery thrombosis occlusion models. Data are expressed as the time to complete arterial occlusion. A 1-way analysis of variance was used to determine differences among groups. Data represent the mean ± SEM of 10 WT and 12 PRCPgt/gt mice for the Rose Bengal assay and 4 WT and 5 PRCPgt/gt mice for the ferric chloride assay. (B) The time to carotid artery occlusion on the Rose Bengal assay was determined in C57BL/6 mice that were untreated (WT, open bar graph, n = 13) or treated with the inhibitor to the PRCP, ZPP (n = 4), or plasma kallikrein inhibitors SBTI (n = 4), PFRCK (n = 5), or PKSI 527 (PKSI; n = 6). Data represent the mean ± SEM of 4 to 13 animals in each group. (C) Determination of the IC50 of PFRCK on 2nM plasma kallikrein or factor XIIa. Inhibition studies were performed as indicated in supplemental Methods. Data represent the mean ± SEM of 3 reactions. (D) Determination of the IC50 of SBTI on 5nM plasma kallikrein or factor XIa. Inhibition studies were performed as indicated in supplemental Methods. Data represent the mean ± SEM of 3 reactions. *P < .05.

The influence of PRCP on arterial thrombosis risk. (A) Control C57BL/6 WT and PRCPgt/gt (gt/gt) mice were subjected to the Rose-Bengal and ferric chloride carotid artery thrombosis occlusion models. Data are expressed as the time to complete arterial occlusion. A 1-way analysis of variance was used to determine differences among groups. Data represent the mean ± SEM of 10 WT and 12 PRCPgt/gt mice for the Rose Bengal assay and 4 WT and 5 PRCPgt/gt mice for the ferric chloride assay. (B) The time to carotid artery occlusion on the Rose Bengal assay was determined in C57BL/6 mice that were untreated (WT, open bar graph, n = 13) or treated with the inhibitor to the PRCP, ZPP (n = 4), or plasma kallikrein inhibitors SBTI (n = 4), PFRCK (n = 5), or PKSI 527 (PKSI; n = 6). Data represent the mean ± SEM of 4 to 13 animals in each group. (C) Determination of the IC50 of PFRCK on 2nM plasma kallikrein or factor XIIa. Inhibition studies were performed as indicated in supplemental Methods. Data represent the mean ± SEM of 3 reactions. (D) Determination of the IC50 of SBTI on 5nM plasma kallikrein or factor XIa. Inhibition studies were performed as indicated in supplemental Methods. Data represent the mean ± SEM of 3 reactions. *P < .05.

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