Marshall K, Senior J
Br J Pharmacol. 1986 Sep;89(1):251-6. doi: 10.1111/j.1476-5381.1986.tb11142.x.
The aims of this study were to elucidate further the role of histamine in the rat uterotrophic response and to investigate the differences between the oestrogen and the anti-oestrogen induced uterine responses. The parameters examined were uterine blood flow (measured by the microsphere technique), uterine wet and dry weights. 17 beta-Oestradiol and the anti-oestrogen, tamoxifen, were used to stimulate the ovariectomised rat uterus and the antihistamines mepyramine (H1) and ranitidine (H2) were employed to modify these responses. The uterine changes evoked by oestradiol proved to be more susceptible to modification by the antihistamines than the tamoxifen-stimulated responses. The results suggest that histamine is involved in the early uterine response to oestradiol but histamine does not appear to play a major role in the uterine response to tamoxifen.
本研究的目的是进一步阐明组胺在大鼠子宫营养反应中的作用,并研究雌激素和抗雌激素诱导的子宫反应之间的差异。所检测的参数包括子宫血流量(通过微球技术测量)、子宫湿重和干重。使用17β-雌二醇和抗雌激素他莫昔芬刺激去卵巢大鼠的子宫,并使用抗组胺药美吡拉敏(H1)和雷尼替丁(H2)来改变这些反应。结果表明,与他莫昔芬刺激的反应相比,雌二醇引起的子宫变化对抗组胺药的改变更敏感。结果提示,组胺参与了子宫对雌二醇的早期反应,但组胺似乎在子宫对他莫昔芬的反应中不起主要作用。