Orts A, Martí J L, Marco J, Baltar I, Castejón J
Rev Esp Fisiol. 1979 Sep;35(3):269-72.
The action of orciprenaline, tolazoline, propanolol and inpea on platelet aggregation induced by ADP epinephrine and norepinephrine was studied in vitro in human platelet-rich plasma. Orciprenaline did not significantly affect aggregation induced by ADP. Tolazoline inhibits the aggregation induced by epinephrine and norepinephrine more intensely than the beta-blockers. Inpea blocks the platelet aggregation induced by epinephrine and norepinephrine to a greater extent than propanolol at similar concentrations. The beta-blockers inhibit platelet aggregation non-specifically.
在体外人富含血小板血浆中研究了间羟异丙肾上腺素、妥拉唑啉、普萘洛尔和吲哌胺对由二磷酸腺苷(ADP)、肾上腺素和去甲肾上腺素诱导的血小板聚集的作用。间羟异丙肾上腺素对ADP诱导的聚集无明显影响。妥拉唑啉比β受体阻滞剂更强烈地抑制肾上腺素和去甲肾上腺素诱导的聚集。在相似浓度下,吲哌胺比普萘洛尔更大程度地阻断肾上腺素和去甲肾上腺素诱导的血小板聚集。β受体阻滞剂非特异性地抑制血小板聚集。