Villar A, Sevilla E, Anselmi E
Arch Int Pharmacodyn Ther. 1985 Oct;277(2):264-71.
We have investigated the effect of three antidepressants and one phenothiazine on the EDTA-treated rat uterus. It was found that these drugs induce a sustained contraction of tissue in a Ca-free medium (called Ca-free contraction) at concentrations between 5 X 10(-5) and 1 X 10(-4) M. These responses allowed the construction of dose-response curves. However, higher concentrations caused a relaxation of strips contracted by lower doses previously applied. Oxytocin 1 X 10(-2) IU/ml accelerates the appearance of this relaxation. The antidepressants and chlorpromazine at high doses inhibit the oxytocin-induced Ca-free contraction. The drugs-induced Ca-free contraction could be repeated in the same preparation with only a slight reduction in magnitude.
我们研究了三种抗抑郁药和一种吩噻嗪对经乙二胺四乙酸(EDTA)处理的大鼠子宫的作用。结果发现,这些药物在浓度为5×10⁻⁵至1×10⁻⁴ M之间时,可在无钙培养基中诱导组织产生持续收缩(称为无钙收缩)。这些反应可用于构建剂量-反应曲线。然而,更高的浓度会导致先前用较低剂量收缩的条带松弛。1×10⁻² IU/ml的催产素会加速这种松弛的出现。高剂量的抗抑郁药和氯丙嗪会抑制催产素诱导的无钙收缩。药物诱导的无钙收缩在同一制剂中可以重复,只是幅度略有降低。