选择最佳大鼠种群作为雄性性功能障碍药物矫正研究的模型

Z. Zhuravleva, N. A. Titova, I. Mukhina, M. Druzin
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摘要

本研究旨在探讨Sprague Dawley大鼠和Wistar大鼠性行为差异的机制,为雄性性功能障碍的药物矫正研究选择最佳的研究对象。材料与方法选用3 ~ 6月龄、体重350 ~ 450 g的Sprague Dawley和Wistar两组性成熟雄性大鼠。动物行为的比较研究采用社会互动、运动活动、焦虑水平以及雄性交配行为模式的标准测试进行。为了确定下丘脑甘氨酸受体在雄性性行为中的作用,通过在雄性大鼠前下丘脑内侧视前区(mPOA)植入双侧脑内微管,对雄性大鼠与雌性交配时甘氨酸受体的活性进行药理学操纵。结果实验结果显示,未受影响的大鼠和经药理激活后的大鼠在性行为上的差异有统计学意义。在开放场地测试中,与焦虑相关的梳理模式的数量在未受药物激活的动物和经甘氨酸受体激活的动物之间存在显著差异;阻断mPOA甘氨酸受体后,观察到的差异消失。在Crowley社会互动测验中,两组间无显著差异。因此,Sprague Dawley和Wistar雄性大鼠在性行为上的差异可能是由于焦虑水平的差异,而焦虑水平的差异又可能与这些大鼠下丘脑mpoa中甘氨酸能神经传递机制的差异有关。结论在研究焦虑水平与性行为的关系时,选择Wistar大鼠为最佳选择,因为该大鼠的雄性性行为对应激的敏感性高于Sprague Dawley大鼠。然而,为了模拟与焦虑无关的雄性性功能障碍,应该优先使用Sprague Dawley雄性大鼠,因为这些动物表现出更稳定的性行为,这对焦虑水平的依赖性较小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Choosing the Optimal Rat Stock as a Model for Research into Pharmacological Correction of Male Sexual Dysfunction
The aim of the study is to identify the mechanisms mediating differences in sexual behavior between Sprague Dawley and Wistar rats, in order to choose the optimal stock for research into pharmacological correction of male sexual dysfunction. Materials and Methods The experiments were carried out on sexually mature male rats of two stocks (Sprague Dawley and Wistar) weighing 350–450 g and aged 3 to 6 months. The comparative study of animal behavior was performed using standard tests for social interaction, locomotor activity, and anxiety level, as well as male mating behavior patterns. In order to determine the role of hypothalamic glycine receptors in the male sexual behavior, pharmacological manipulations of glycine receptor activity during mating with receptive females were conducted via bilateral intracerebral microcannulas implanted in the medial preoptic area (mPOA) of the male rat anterior hypothalamus. Results The obtained results revealed statistically significant inter-stock differences in sexual behavior at the final consummatory stage of both intact animals and those after pharmacological activation of glycine receptors in the mPOA. The number of anxiety-related grooming patterns in the Open Field test significantly differed between the stocks for both intact animals and those after pharmacological activation of glycine receptors; the observed differences disappeared after the mPOA glycine receptors were blocked. In the Crowley test of social interaction, no significant difference was found between the stocks. Thus, the revealed difference in sexual behavior between Sprague Dawley and Wistar male rats is likely due to the difference in the level of anxiety, which, in turn, may be associated with difference in the mechanisms of glycinergic neurotransmission in the hypothalamic mPOAs of these rats. Conclusion To study the relationship between the level of anxiety and sexual behavior, the choice of the Wistar rat stock is optimal since the male sexual behavior in this stock is more sensitive to stress than that in Sprague Dawley rats. However, to model male sexual dysfunction not associated with anxiety, the use of Sprague Dawley male rats should be preferred as these animals show more stable sexual behavior, which is less dependent on the level of anxiety.
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