Owman C
Ciba Found Symp. 1981;83:252-79. doi: 10.1002/9780470720653.ch13.
The uterus is supplied with an extensive system of adrenergic nerves. The neurobiological properties of this innervation have been investigated in a series of studies primarily using the guinea-pig as model. The guinea-pig uterus is supplied from three different sources: the paracervical plexus, containing short adrenergic neurons; the inferior mesenteric ganglion; and a cranial source, probably the aorticorenal plexus, via nerves in the uterine suspensory ligaments. The nerve density is higher in the tubal end of the uterine horn and in the cervix than in the main part of the uterine horn. The turnover rate of transmitter is lower in the uterus than in a control organ, such as the heart. Noradrenaline levels in the uterus, but not the heart, are influenced by alterations in the endocrine milieu, e.g. during the oestrous cycle and after treatment with sex steroids. In the uterine tissue surrounding the conceptus during pregnancy, there is an early and drastic decay in various functional parameters related to the adrenergic nerve plexus and primarily reflecting a local, pregnancy-induced axonal degeneration. In the main part of the empty horn, in unilateral pregnancy, there is an extensive decay in various adrenergic functional parameters; these, however, reflect changes in a nerve plexus that has an essentially intact structure. No sign of functional impairment is seen in the adrenergic nerves of the uterine cervix. The increased turnover rate and reduced transmitter content in this region during late pregnancy may reflect increased frequency of firing of the adrenergic nerves. The tubal end of the uterine horn shows no signs of altered sympathetic function. This is the only part of the uterine horn that appears unaffected by pregnancy. The deficient recovery post partum of the changes in the uterine horn that previously contained the fetuses suggests permanent damage to the adrenergic nerve plexus after a pregnancy. The post partum recovery of changes seen in the previously empty horn, however, is more pronounced but still incomplete by comparison with the innervation before pregnancy. Studies on the adult human uterus indicate that similar events to those described for the guinea-pig model occur in human pregnancy.
子宫由广泛的肾上腺素能神经支配系统供应。在一系列主要以豚鼠为模型的研究中,对这种神经支配的神经生物学特性进行了研究。豚鼠子宫的神经来自三个不同的来源:子宫颈旁神经丛,包含短的肾上腺素能神经元;肠系膜下神经节;以及一个颅部来源,可能是主动脉肾神经丛,通过子宫悬韧带中的神经。子宫角的输卵管端和子宫颈的神经密度高于子宫角的主要部分。子宫中递质的周转率低于对照器官,如心脏。子宫中的去甲肾上腺素水平,而非心脏中的,受内分泌环境变化的影响,例如在发情周期和用性类固醇治疗后。在妊娠期间围绕孕体的子宫组织中,与肾上腺素能神经丛相关的各种功能参数会出现早期且剧烈的衰退,主要反映了局部妊娠诱导的轴突退变。在单侧妊娠时,空子宫角的主要部分,各种肾上腺素能功能参数会出现广泛衰退;然而,这些反映的是一个结构基本完整的神经丛的变化。子宫颈的肾上腺素能神经未见到功能受损的迹象。妊娠后期该区域递质周转率增加和递质含量减少可能反映了肾上腺素能神经发放频率的增加。子宫角的输卵管端未显示交感神经功能改变的迹象。这是子宫角中唯一似乎不受妊娠影响的部分。先前容纳胎儿的子宫角变化在产后恢复不足,提示妊娠后肾上腺素能神经丛受到永久性损伤。然而,先前空子宫角中所见变化的产后恢复更为明显,但与妊娠前的神经支配相比仍不完全。对成年人类子宫的研究表明,人类妊娠中发生的事件与豚鼠模型中描述的类似。