Beaston-Wimmer P, Smolen A J
Department of Anatomy, Medical College of Pennsylvania, Philadelphia 19129.
Brain Res Dev Brain Res. 1991 Jan 15;58(1):123-8. doi: 10.1016/0165-3806(91)90244-d.
Sexual dimorphism of neuron number has been observed in several areas in the central and peripheral nervous system. In many of these areas enhanced neuron survival exists in males during the period of naturally occurring cell death. This has been attributed to high levels of circulating testosterone in the perinatal period. The superior cervical ganglion (SCG) of the rat exhibits this sexual dimorphism. The difference in neuron numbers is established by two weeks postnatally and precedes the differences in body weight and sympathetic target mass between the sexes. At this two week time point, fewer SCG neurons in the female rat must supply neurotransmitter to the same mass of sympathetic target as in the male. The present study examined some of the mechanisms used by neurons in the SCGs of male and female rats to compensate in supplying neurotransmitter to their targets. At birth, the SCGs of male and female rats contain equal numbers of neurons. There is also no sex difference at this time in the content of norepinephrine (NE) in these neurons or in the enzyme activity of tyrosine hydroxylase (TH). However, a sex difference does exist in the expression of TH-mRNA, with SCG neurons in female expressing more TH-mRNA than males. At this time, there is no sex difference in either the total body weight of males and females or in the mass of sympathetic target organs. During the first two postnatal weeks, natural neuron death in the SCG results in the loss of significantly more neurons in females than in males. At the end of the period of cell death, neurons in females continue to express more TH-mRNA, and at this time both TH enzyme activity and NE content per neuron are also higher in females. Since the adult sex difference in body weight and sympathetic target mass has not yet been established, the same amount of target mass is innervated by fewer neurons in females. In the adult, the sex difference in SCG neuron number is maintained. However, both overall body weight and sympathetic target mass are significantly greater in males. At this time expression of TH-mRNA is greater in SCG neurons of males, while both TH enzyme activity and NE content per neuron are equal in males and females. One of the challenges presented to the developing nervous system is to match a population of neurons with its targets.(ABSTRACT TRUNCATED AT 400 WORDS)
在中枢神经系统和外周神经系统的多个区域都观察到了神经元数量的性别差异。在这些区域中的许多,在自然发生细胞死亡的时期,雄性存在增强的神经元存活情况。这归因于围产期循环睾酮水平较高。大鼠的颈上神经节(SCG)表现出这种性别差异。神经元数量的差异在出生后两周就已确立,且早于两性之间体重和交感神经靶器官质量的差异。在这个两周的时间点,雌性大鼠中较少的SCG神经元必须向与雄性相同质量的交感神经靶器官提供神经递质。本研究考察了雄性和雌性大鼠SCG中的神经元用于补偿向其靶器官提供神经递质的一些机制。出生时,雄性和雌性大鼠的SCG含有相等数量的神经元。此时,这些神经元中去甲肾上腺素(NE)的含量或酪氨酸羟化酶(TH)的酶活性也没有性别差异。然而,TH - mRNA的表达确实存在性别差异,雌性SCG神经元表达的TH - mRNA比雄性更多。此时,雄性和雌性的总体重或交感神经靶器官的质量均无性别差异。在出生后的前两周,SCG中的自然神经元死亡导致雌性比雄性损失的神经元明显更多。在细胞死亡期结束时,雌性神经元继续表达更多的TH - mRNA,此时雌性每个神经元的TH酶活性和NE含量也更高。由于成年时体重和交感神经靶器官质量的性别差异尚未确立,相同质量的靶器官由雌性中较少的神经元支配。在成年期,SCG神经元数量的性别差异得以维持。然而,雄性的总体重和交感神经靶器官质量都明显更大。此时,雄性SCG神经元中TH - mRNA的表达更高,而雄性和雌性每个神经元的TH酶活性以及NE含量相等。发育中的神经系统面临的挑战之一是使一群神经元与其靶器官相匹配。(摘要截选至400字)