Role of tactile stimulation during the preweaning period on the development of the peripheral sensory sural (SU) nerve in adult artificially reared female rat
Angel I. Melo, Rene Zempoalteca, Gabriela Ramirez-Funez, Arely Anaya-Hernández, Mercedes G. Porras, Elsa L. Aguirre-Benítez, Margarita González del Pliego, Pérez-Torres Armando, Ismael Jiménez-Estrada
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Abstract
Maternal deprivation, as a result of the artificial rearing (AR) paradigm, disturbs electrophysiological and histological characteristics of the peripheral sensory sural (SU) nerve of infant and adult male rats. Such changes are prevented by providing tactile or social stimulation during isolation. AR also affects the female rat's brain and behavior; however, it is unknown whether this early adverse experience also alters their SU nerve development or if tactile stimulation might prevent these possible developmental effects. To assess these possibilities, the electrophysiological and histological characteristics of the SU nerve from adult diestrus AR female rats that: (i) received no tactile stimulation (AR group), (ii) received tactile stimulation in the anogenital and body area (AR-Tactile group), or (iii) were mother reared (MR group) were determined. We found that the amplitude, but not the area, of the evoked compound action potential response in SU nerves of AR rats was lower than those of SU nerves of MR female rats. Tactile stimulation prevented these effects.
Additionally, we found a reduction in the outer diameter and myelin thickness of axons, as well as a large proportion of axons with low myelin thickness in nerves of AR rats compared to the nerves of the MR and AR-Tactile groups of rats; however, tactile stimulation only partially prevented these effects. Our data indicate that maternal deprivation disturbs the development of sensory SU nerves in female rats, whereas tactile stimulation partially prevents the changes generated by AR. Considering that our previous studies have shown more severe effects of AR on male SU nerve development, we suggest that sex-associated factors may be involved in these processes.
人工饲养(AR)模式导致的母体剥夺会干扰幼年和成年雄性大鼠外周感觉神经(SU)的电生理学和组织学特征。在隔离期间,通过提供触觉或社交刺激可以防止这种变化。AR 也会影响雌性大鼠的大脑和行为;然而,这种早期的不良经历是否也会改变其 SU 神经的发育,或者触觉刺激是否可以防止这些可能的发育影响,目前还不得而知。为了评估这些可能性,对以下成年发情 AR 雌鼠的 SU 神经的电生理学和组织学特征进行了研究:(我们测定了(i)未接受触觉刺激(AR 组)、(ii)肛门和身体部位接受触觉刺激(AR-触觉组)或(iii)母鼠饲养(MR 组)的 SU 神经的电生理和组织学特征。我们发现,AR 组雌性大鼠 SU 神经的复合动作电位诱发反应的振幅低于 MR 组雌性大鼠 SU 神经的复合动作电位诱发反应的振幅(而不是面积)。触觉刺激阻止了这些影响。此外,我们还发现,与 MR 组和 AR 触觉组大鼠的神经相比,AR 组大鼠神经中轴突的外径和髓鞘厚度都有所减少,而且髓鞘厚度低的轴突所占比例也很大;不过,触觉刺激只能部分防止这些影响。我们的数据表明,母性剥夺会干扰雌性大鼠感觉 SU 神经的发育,而触觉刺激则能部分防止 AR 所产生的变化。考虑到我们之前的研究显示 AR 对雄性 SU 神经发育的影响更为严重,我们认为性别相关因素可能参与了这些过程。
期刊介绍:
Developmental Psychobiology is a peer-reviewed journal that publishes original research papers from the disciplines of psychology, biology, neuroscience, and medicine that contribute to an understanding of behavior development. Research that focuses on development in the embryo/fetus, neonate, juvenile, or adult animal and multidisciplinary research that relates behavioral development to anatomy, physiology, biochemistry, genetics, or evolution is appropriate. The journal represents a broad phylogenetic perspective on behavior development by publishing studies of invertebrates, fish, birds, humans, and other animals. The journal publishes experimental and descriptive studies whether carried out in the laboratory or field.
The journal also publishes review articles and theoretical papers that make important conceptual contributions. Special dedicated issues of Developmental Psychobiology , consisting of invited papers on a topic of general interest, may be arranged with the Editor-in-Chief.
Developmental Psychobiology also publishes Letters to the Editor, which discuss issues of general interest or material published in the journal. Letters discussing published material may correct errors, provide clarification, or offer a different point of view. Authors should consult the editors on the preparation of these contributions.