Figure 5
Figure 5. Amidolytic activity associated with carotid arteries. The left (injured) and right (uninjured) carotid arteries were harvested 30 minutes after injury, opened longitudinally, rinsed, and incubated with the chromogenic substrate tosyl-Gly-Pro-Arg-p-nitroanilide. The rate of substrate hydrolysis was determined by the change in absorbance at 405 nm. Changes in A405 were linear over the time course of the experiment. Phe-Pro-Arg-chloromethylketone (PPACK, 10 nM) or recombinant hirudin (10 units/mL) was added along with the substrate as indicated. Mean values are indicated. Error bars equal 1 SD.

Amidolytic activity associated with carotid arteries. The left (injured) and right (uninjured) carotid arteries were harvested 30 minutes after injury, opened longitudinally, rinsed, and incubated with the chromogenic substrate tosyl-Gly-Pro-Arg-p-nitroanilide. The rate of substrate hydrolysis was determined by the change in absorbance at 405 nm. Changes in A405 were linear over the time course of the experiment. Phe-Pro-Arg-chloromethylketone (PPACK, 10 nM) or recombinant hirudin (10 units/mL) was added along with the substrate as indicated. Mean values are indicated. Error bars equal 1 SD.

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