1979
DOI: 10.1016/0006-2952(79)90698-1
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Determination of platelet monoamine oxidase activity in human platelet-rich plasma— A new microfluorescent assay utilizing kynuramine as substrate

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Cited by 16 publications
(4 citation statements)
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“…To our knowledge, this is the first study to report Km and Vmax of platelet MAO in PMS. Previously, it has been reported that, using kynuramine, the Km and Vmax of platelet MAO in normal volunteers was 30 \iM and 10.9 nmol 4-hydroxyquinoline/108 platelets/h, respectively [McEntire et al, 1979], This is similar to our findings in control patients, al though the Vmax in our study was lower, which could be ascribed to methodological differences, such as prepara tion of PRP and pH of assay buffer.…”
Section: Discussionsupporting
confidence: 89%
See 1 more Smart Citation
“…To our knowledge, this is the first study to report Km and Vmax of platelet MAO in PMS. Previously, it has been reported that, using kynuramine, the Km and Vmax of platelet MAO in normal volunteers was 30 \iM and 10.9 nmol 4-hydroxyquinoline/108 platelets/h, respectively [McEntire et al, 1979], This is similar to our findings in control patients, al though the Vmax in our study was lower, which could be ascribed to methodological differences, such as prepara tion of PRP and pH of assay buffer.…”
Section: Discussionsupporting
confidence: 89%
“…MAO activity was determined using a previously reported method [McEntire et al, 1979], Briefly. 100 pi of PRP incubated with 10 mA/ potassium phosphate buffer (pH 7.4) and either 7.5.…”
Section: Mao Assaymentioning
confidence: 99%
“…Platelet MAO activity in PRP samples was assayed with kynuramine as a substrate, by a method similar to that described by McEntire et al 39 with modifications as follows: platelet suspension (100 μL of PRP, 20 to 40 × 10 6 platelets) was preincubated (for 5 minutes at 37°C) with buffer (Na‐borate‐HCl, pH 8.3) and was then incubated with a saturating concentration of substrate (32 μM) in a final volume of 2 mL for 60 minutes. The reaction was stopped by adding trichloroacetic acid (1 mL, 30%), the mixture was centrifuged, and the formed 4‐hydroxyquinoline (4‐HQ) was measured fluorimetrically at 310 nm excitation and 362 nm emission.…”
Section: Methodsmentioning
confidence: 99%
“…[17] Platelet MAO activity was calculated in terms of nmol/h/mg protein. The COMT activity in erythrocytes was determined by the fluorimetric method of Axerod and Tomchick.…”
Section: Methodsmentioning
confidence: 99%