Inhibition of platelet aggregation in whole blood after exposure of rats to alcohol by inhalation

• Published in: Alcohol (Fayetteville, N.Y.) Vol. 14; no. 1; pp. 49 - 54
• Main Authors: Dong, Quan Sheng, Karanian, John W., Wesely, Lori, Myers, Adam K.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.01.1997; Elsevier Science
• Subjects: Administration, Inhalation; Alcoholic Intoxication - blood; Alcoholism and acute alcohol poisoning; Animals; Biological and medical sciences; Blood alcohol concentration; Dose-Response Relationship, Drug; Ethanol - administration & dosage; Ethanol - blood; Ethanol - pharmacology; Inhalation; Male; Medical sciences; Platelet aggregation; Platelet Aggregation - drug effects; Platelet Aggregation Inhibitors - administration & dosage; Platelet Aggregation Inhibitors - pharmacology; Rats; Rats, Wistar; Toxicology; Platelet aggregation; Blood alcohol concentration; Inhalation; Blood coagulation; Ethanol; Rat; Toxicity; Rodentia; In vitro; Dose activity relation; Aggregation; Vertebrata; Platelet; Mammalia; Animal; Alcoholemia; Platelet function
• ISSN: 0741-8329; 1873-6823
• DOI: 10.1016/S0741-8329(96)00105-X

The dose-effect relationship between blood alcohol concentration (BAC) and altered platelet function was examined in whole blood in a rat model of alcohol exposure by inhalation, using the impedance method of ex vivo whole blood platelet aggregation. With rates of alcohol addition to the chamber air inflow from 29 to 56 mg ethanol/l air/min, BAC was dependent on duration of exposure and concentration of alcohol in the air. Next, 3, 6, and 9 h exposures to the highest delivery rate were used, and platelet aggregability was tested. After 9h, BAC reached 453 ± 16 mg% and aggregation responses to three doses of collagen were significantly lower than in control blood ( p < 0.01). Less consistent inhibition was observed with arachidonic acid and ADP, and also when exposure duration was reduced. However, some significant inhibition of collagen-induced aggregation ( p < 0.05) was observed with BAC as low as 127 ± 15 mg%. These experiments demonstrate that in vivo alcohol exposure inhibits, in a concentration-dependent manner, ex vivo rat whole blood platelet aggregation, at BACs readily attained in humans by ingestion.