
FOLLOWUS
1. PUMC Student
2. Institute of Basic Medical Sciences CAMS
3. ,China
纸质出版日期:1990
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[1]李箭,汪钟.EFFECTS OF NIMODIPINE ON PLATELET AGGREGATION AND THE ACTIVITY OF ENZYMES IN ARACHIDONIC ACID METABOLISM[J].Chinese Medical Sciences Journal,1990(01):47-50.
EFFECTS OF NIMODIPINE ON PLATELET AGGREGATION AND THE ACTIVITY OF ENZYMES IN ARACHIDONIC ACID METABOLISM[J]. Chinese medical sciences journal, 1990, (1): 47-50.
[1]李箭,汪钟.EFFECTS OF NIMODIPINE ON PLATELET AGGREGATION AND THE ACTIVITY OF ENZYMES IN ARACHIDONIC ACID METABOLISM[J].Chinese Medical Sciences Journal,1990(01):47-50. DOI:
EFFECTS OF NIMODIPINE ON PLATELET AGGREGATION AND THE ACTIVITY OF ENZYMES IN ARACHIDONIC ACID METABOLISM[J]. Chinese medical sciences journal, 1990, (1): 47-50. DOI:
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The effects of nimodipine on platelet aggregation and arachidonic acid(AA)metabolismwere studied in order to explore its effect on patients with thrombosis or cardiovas-cular disease.The results indicate that nimodipine(50-350μmol/L)significantly inhibitsplatelet aggregation induced by ADP
AA
and ionophore A23187 in a dose dependentmanner.The inhibitory effects induced by ionophore A23187 could be partially antagonizedby calcium(1 mmol/L).When the substrate was AA and the enzyme was supplied bypig lung microsomes
nimodipine(50-400μmol/L)significantly reduced the generation ofTXB
2
and 6-keto-PGF
1a
in parallel.When the substrate was prostaglandin endoperoxide
however
the levels of TXB
2
and 6-keto-PGF
1a
were not significantly altered in the sameconcentration range.The results suggest that nimodipine is a cyclooxygenase inhibitor
andits ability to inhibit platelet aggregation is related to its calcium blocking effect.
The effects of nimodipine on platelet aggregation and arachidonic acid(AA)metabolism were studied in order to explore its effect on patients with thrombosis or cardiovas- cular disease.The results indicate that nimodipine(50-350μmol/L)significantly inhibits platelet aggregation induced by ADP
AA
and ionophore A23187 in a dose dependent manner.The inhibitory effects induced by ionophore A23187 could be partially antagonized by calcium(1 mmol/L).When the substrate was AA and the enzyme was supplied by pig lung microsomes
nimodipine(50-400μmol/L)significantly reduced the generation of TXB
2
and 6-keto-PGF
1a
in parallel.When the substrate was prostaglandin endoperoxide
however
the levels of TXB
2
and 6-keto-PGF
1a
were not significantly altered in the same concentration range.The results suggest that nimodipine is a cyclooxygenase inhibitor
and its ability to inhibit platelet aggregation is related to its calcium blocking effect.
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