Literature DB >> 6784136

Effect of Amrinone, a cardiotonic drug, on hemodynamics and platelet function.

G H Rao, S Einzig, G J Johnson, J G White.   

Abstract

In the present study we have investigated the effect of Amrinone on the hemodynamics, platelet counts, prostacyclin and thromboxane synthesis and platelet function. Results show that infusion of the drug increased the heart rate and lowered left atrial, aortic and pulmonary artery pressures within five minutes after a single bolus injection of 2 mg/kg IV dose. Platelet counts made from the blood obtained from anesthetized dogs after the drug infusion showed severe loss of platelets. However, infusion of a similar dose in awake dogs showed no such detrimental effect on platelets. Examination of formalin fixed blood for aggregates showed no more clumps in the treated samples than in the control. Platelets obtained from canine blood drawn at 30 minutes post infusion of the drug showed no aggregatory response to arachidonate. However, the response of these platelets to ADP was quite normal. Amrinone infusion had no inhibitory effect on the ability of vascular tissue to convert arachidonic acid to prostacyclin. Similarly, no inhibitory action could be observed on platelet cyclo-oxygenase activity at this concentration (2 mg/kg). In vitro studies on human platelets showed significant inhibition of cyclo-oxygenase at high concentrations (0.5 mg/ml). Therefore it is unlikely that the drug caused inhibition of the platelet response to arachidonate by the inhibition of prostaglandin synthesis during infusion, as the dose used was quite low (2 mg/kg) compared to what is required for the inhibition of cyclo-oxygenase.

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Year:  1981        PMID: 6784136     DOI: 10.1016/s0161-4630(81)80009-2

Source DB:  PubMed          Journal:  Prostaglandins Med        ISSN: 0161-4630


  1 in total

1.  The effects of amrinone on platelet count, survival and function in patients with congestive cardiac failure.

Authors:  P T Wilmshurst; S F Al-Hasani; M J Semple; A S Hamblin; P G Kioy; G F Lucas; G F Savidge; M M Webb-Peploe
Journal:  Br J Clin Pharmacol       Date:  1984-03       Impact factor: 4.335

  1 in total

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