Thromb Haemost 1978; 39(01): 135-145
DOI: 10.1055/s-0038-1646663
Original Article
Schattauer GmbH Stuttgart

Contribution of Platelets to the Cardiovascular Effects of ADP in the Rat

Elisabetta Dejana
The Laboratory of Autonomic Nervous System and Laboratory of Cardiovascular Clinical Pharmacology, Istituto di Ricerche Farmacologiche “Mario Negri”, Milan, Italy
,
Maria Grazia Castelli
The Laboratory of Autonomic Nervous System and Laboratory of Cardiovascular Clinical Pharmacology, Istituto di Ricerche Farmacologiche “Mario Negri”, Milan, Italy
,
Giovanni De Gaetano
The Laboratory of Autonomic Nervous System and Laboratory of Cardiovascular Clinical Pharmacology, Istituto di Ricerche Farmacologiche “Mario Negri”, Milan, Italy
,
Aurora Bonaccorsi
The Laboratory of Autonomic Nervous System and Laboratory of Cardiovascular Clinical Pharmacology, Istituto di Ricerche Farmacologiche “Mario Negri”, Milan, Italy
› Author Affiliations
Further Information

Publication History

Received 24 March 1977

Accepted 12 July 1977

Publication Date:
12 July 2018 (online)

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Summary

The contribution of platelets to the cardiovascular effects of ADP was investigated in rats in different experimental conditions. Following rapid i. v. bolus injections of ADP (from 0.001 to 0.03 mg/kg b. w.) only a dose-related fall in blood pressure could be detected. Increasing the dose of ADP (up to 1 mg/kg b. w.), platelet fall and changes in cardiac rhythm (bradycardia, A. V. blocks and ectopic beats) became evident. All these phenomena were rapidly reversed. Inhibition of platelet aggregation by a pyrimido-pyrimidine compound (SH 869) or thrombocytopenia induced by Busulfan or antiplatelet antiserum did not significantly protect the animals from the cardiovascular effects of ADP. The fall in blood pressure, however, was reduced. Adenosine, at equimolar concentrations, caused ECG changes similar to those induced by ADP with no platelet aggregation and a less pronounced blood pressure fall.

These results suggest that most of the cardiovascular modifications induced by rapid injection of ADP are largely independent of platelets. Platelets appeared to play a more important role when ADP was given for a longer period of time. A slow i. v. infusion of ADP (6 mg/kg b. w. for 10 min) was accompanied by platelet fall, cardiovascular collapse and ECG alterations typical of myocardial ischaemia. All these effects persisted throughout the ADP infusion but disappeared soon after its termination. They were almost completely inhibited in rats given SH 869 or made thrombocytopenic.

In conclusion, platelets seem to contribute to the cardiovascular effects of ADP only in certain experimental conditions. In others, the nucleotide’s direct effects seem more important.