Choo L K, Mitchelson F
Eur J Pharmacol. 1978 Dec 1;52(3-4):313-22. doi: 10.1016/0014-2999(78)90284-4.
The inhibitory effect of troxypyrrolidinium (trox) (10(-6) to 2 x 10(-3) M) on responses to carbachol (CCh) and acetylcholine (ACh) was investigated in the electrically stimulated left atrium and longitudinal ileal muscle of the guinea pig. In both tissues, trox exhibited antimuscarinic activity causing parallel shifts of the concentration--response curves to both agonists with no depression of maximum responses. Responses to CCh were inhibited by trox (5 x 10(-4) M) to a greater extent than responses to ACh and this difference was maintained following inhibition of cholinesterases with dyflos. In the guinea-pig atrium using CCh as agonist dose ratios produced by the higher concentrations of trox (greater than 5 x 10(-5) M) were less than expected resulting in a non-linear Arunlakshana--Schild (A-S) plot and this effect of trox was maintained in the presence of mecamylamine (2 x 10(-5) M). In longitudinal ileal muscle flattening of the A-S plot with high concentrations of trox did not occur. Although hemicholinium-3 (HC-3) produces a non-linear A-S plot for antimuscarinic activity in atria the A-S plot obtained with the longitudinal ileal strip using HC-3 (2 x 10(-5) to 2 x 10(-3) M) did not exhibit flattening at high concentrations. The dose ratios obtained with HC-3 (5 x 10(-4) M) using CCh as agonist were significantly greater than those obtained with ACh. It is suggested that trox, like HC-3, acts as a metaffinoid antagonist at the muscarinic receptor.
在豚鼠的电刺激左心房和回肠纵行肌中,研究了曲昔匹铵(trox)(10⁻⁶至2×10⁻³M)对卡巴胆碱(CCh)和乙酰胆碱(ACh)反应的抑制作用。在这两种组织中,曲昔匹铵均表现出抗毒蕈碱活性,使两种激动剂的浓度-反应曲线平行右移,而最大反应无降低。曲昔匹铵(5×10⁻⁴M)对CCh反应的抑制程度大于对ACh反应的抑制程度,在用双氟磷抑制胆碱酯酶后,这种差异仍然存在。在豚鼠心房中,以CCh作为激动剂,较高浓度的曲昔匹铵(大于5×10⁻⁵M)产生的剂量比低于预期,导致阿伦拉克沙纳-席尔德(A-S)图呈非线性,且在存在美加明(2×10⁻⁵M)的情况下,曲昔匹铵的这种作用仍然存在。在回肠纵行肌中,高浓度曲昔匹铵时A-S图不会变平。虽然半胱氨酸-3(HC-3)在心房中产生抗毒蕈碱活性的非线性A-S图,但用HC-3(2×10⁻⁵至2×10⁻³M)处理回肠纵行肌条得到的A-S图在高浓度时并未变平。以CCh作为激动剂时,HC-3(5×10⁻⁴M)得到的剂量比显著大于以ACh作为激动剂时得到的剂量比。提示曲昔匹铵与HC-3一样,在毒蕈碱受体上作为类变态反应拮抗剂起作用。