Hellegouarch A, Baranès J, Clostre F, Drieu K, Braquet P, DeFeudis F V
Gen Pharmacol. 1985;16(2):129-32. doi: 10.1016/0306-3623(85)90049-7.
Dose-related contractions were elicited in strips of rabbit isolated vena cava by norepinephrine (NE, IC50 approximately equal to 2.3 X 10(-7) M), dopamine (IC50 approximately equal to 6.9 X 10(-6) M), histamine (IC50 approximately equal to 2.1 X 10(-6) M) and extract of Ginkgo biloba (Gb, IC50 approximately equal to 86 micrograms/ml). Serotonin and tyramine elicited very weak contractile effects in this preparation. Phenoxybenzamine (10(-7) M) abolished the contractions elicited by NE, and blocked the effect of Gb by about 50%. Further support is provided for the therapeutic action of Gb in cardiovascular disorders.
去甲肾上腺素(NE,半数抑制浓度[IC50]约等于2.3×10⁻⁷M)、多巴胺(IC50约等于6.9×10⁻⁶M)、组胺(IC50约等于2.1×10⁻⁶M)和银杏提取物(Gb,IC50约等于86微克/毫升)可使兔离体腔静脉条产生剂量相关的收缩。5-羟色胺和酪胺在此制剂中引起非常微弱的收缩作用。酚苄明(10⁻⁷M)可消除NE引起的收缩,并使Gb的作用阻断约50%。这为Gb在心血管疾病中的治疗作用提供了进一步的支持。