Rivest R W
University of Geneva, Department of Medicine, Switzerland.
Experientia. 1991 Oct 15;47(10):1027-38. doi: 10.1007/BF01923338.
Two physiological components of sexual maturation, vaginal opening and first estrus, apparently evolve similarly in Wistar and Sprague-Dawley rats. However, a bimodal distribution in the frequency of the days of vaginal opening is observed within a given strain, which is less related to heredity than to the timing and type of experiment. In addition, when the modulators of sexual maturation are reviewed, it can be observed that sensitivity to external stimuli can vary even within a strain. For a defined set of breeding conditions, one group of rats can be more susceptible to changes in the lighting regimen and not be affected by controlled stressors, while another group responds more to stress and less to light. The reason for susceptibility to one rather than another environmental factor under similar breeding conditions is not understood. In that context, it is difficult to evaluate the role of heredity when we cannot understand the full impact of the environment, not to mention maternal influence in fetal and early life. Using two lines of psychogenetically selected rats, it was possible to show that they had differences in sexual maturation, which strongly suggested a genetic predisposition. Nevertheless, the question arises as to whether the genetic locus directly affects organs implicated in sexual maturation or whether it acts on some unknown factor which only secondarily modifies sexual maturation. In summary, there is more need to understand the role of the environment, including that of the mother early in fetal and neonatal life. It is suggested that the mechanisms underlying organ growth are set for a given species, while developmental and environmental factors fix the timing of vaginal opening and first ovulation. In the rat, there appear to be two times which are preferred for vaginal opening, given the laboratory conditions that have been used in the last 20 or so years: an early period, at 31-35 days, and a late period, at 36-40 days. An explanation for this dichotomy would be that a combination of parameters (not necessarily always the same) is needed for vaginal opening. These parameters oscillate during sexual maturation with different frequencies, which can achieve resonance to lead to vaginal opening and ovulation only during given periods.
性成熟的两个生理指标,即阴道开口和首次发情,在Wistar大鼠和Sprague-Dawley大鼠中显然以相似的方式演变。然而,在给定品系中观察到阴道开口天数的频率呈双峰分布,这与遗传的关系较小,而与实验的时间和类型有关。此外,当回顾性成熟的调节因素时,可以观察到即使在同一品系内,对外部刺激的敏感性也可能有所不同。对于一组确定的繁殖条件,一组大鼠可能对光照方案的变化更敏感,而不受可控应激源的影响,而另一组对压力的反应更大,对光照的反应更小。在相似的繁殖条件下,对一种而非另一种环境因素敏感的原因尚不清楚。在这种情况下,当我们无法理解环境的全部影响时,就很难评估遗传的作用,更不用说母体在胎儿期和生命早期的影响了。使用两系心理遗传学选择的大鼠,可以证明它们在性成熟方面存在差异,这强烈表明存在遗传易感性。然而,问题在于基因位点是直接影响与性成熟相关的器官,还是作用于一些未知因素,而这些因素只是间接影响性成熟。总之,更需要了解环境的作用,包括母亲在胎儿期和新生儿期早期的作用。有人认为,给定物种的器官生长潜在机制是固定的,而发育和环境因素决定了阴道开口和首次排卵的时间。在大鼠中,考虑到过去20年左右使用的实验室条件,似乎有两个时间段是阴道开口的首选时间:一个早期,在31-35天,一个晚期,在36-40天。这种二分法的解释可能是阴道开口需要一组参数(不一定总是相同)的组合。这些参数在性成熟过程中以不同频率振荡,只有在特定时期才能达到共振,从而导致阴道开口和排卵。