Effects of N-methyl- and N-isobutyl-1,2-diphenyl ethanol amines on the spontaneous and evoked contractions in the rat isolated uterus.

K E el Tahir, M A el Nasser, A M Ageel, H A el-Obeid, K A al-Rashood
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引用次数: 2

Abstract

1. The effects of N-methyl- and N-isobutyl-1,2-diphenyl ethanol amine (compounds M & E), respectively and diltiazem (D) were examined on the spontaneous and evoked uterine contractions of pregnant rats in vitro. 2. Addition of compound M (75-300 microM), compound E (15-60 microM) or D (100-400 nM) to the uterine tissues, inhibited the spontaneous contractions in a dose-dependent manner. The potency order was D greater than E greater than M. 3. The inhibitions were reversed by elevating the extracellular Ca2+ concentration by 20 mM. The compounds also antagonised CaCl2-evoked contractions. 4. Treatment of rats with either compound during pregnancy days (1-16) did not affect the implantation process and did not induce any teratogenicity. 5. The uterine inhibitory effects of the compounds may be due to blockade of uterine Ca2+ channels.

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n -甲基和n -异丁基-1,2-二苯基乙醇胺对大鼠离体子宫自发和诱发性收缩的影响。
1. 研究了n -甲基、n -异丁基-1,2-二苯基乙醇胺(化合物M、E)和地尔硫卓(D)对体外妊娠大鼠自发性和诱发性子宫收缩的影响。2. 化合物M (75 ~ 300 μ M)、化合物E (15 ~ 60 μ M)和D (100 ~ 400 μ M)对子宫组织自发收缩的抑制作用呈剂量依赖性。效价顺序为D > E > m。通过将细胞外Ca2+浓度升高20 mM,这种抑制作用被逆转。这些化合物还能拮抗cacl2引起的收缩。4. 在妊娠期(1-16)用这两种化合物处理大鼠不影响着床过程,也不诱导任何致畸性。5. 这些化合物的子宫抑制作用可能是由于阻断子宫Ca2+通道。
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