The Brain of the African Wild Dog. V. The Somatosensory System and Vestibular Nuclear Complex

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Samson Chengetanai, Adhil Bhagwandin, Mads F. Bertelsen, Therese Hård, Patrick R. Hof, Muhammad A. Spocter, Paul R. Manger
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Abstract

Social behaviors in the African wild dog (Lycaon pictus) commonly involve a range of tactile aspects, including biting, pushing, embracing, mounting, face and muzzle licking, nose–chin and muzzle contact, paw placement, play fighting, and wrestling, supported by the vestibular system. We employed an array of architectural and immunohistochemical stains to provide a qualitative description of the somatosensory and vestibular systems in the brain of one representative African wild dog individual. The appearance of both systems does not appear to differ from that reported in other Carnivora. The six nuclei forming the vestibular system, and their relationship to each other and the incoming vestibular branch of the eighth cranial nerve, appear like those observed in many mammalian species. The location and appearance of the dorsal column nuclei, the trigeminal sensory column, the colliculi, somatosensory nuclei of the dorsal thalamus, and the five somatosensory cortical areas observed in the African wild dog are like those observed in the domestic dog and other Carnivora. This study of the somatosensory and vestibular systems of the African wild dog completes our series of studies describing the major sensory systems in the African wild dog brain. It appears reasonable to conclude that, at the systems level of analysis, no overt specializations of any of the sensory systems are present. Thus, the neural underpinnings of the complex sociality of the African wild dog may be supported by nonsensory neural systems, such as motor, neuromodulatory, limbic, or cognitive systems, or levels of organization like receptor expression patterns or connectivity.

Abstract Image

非洲野狗的大脑。体感觉系统和前庭核复合体
非洲野狗(Lycaon pictus)的社会行为通常涉及一系列触觉方面,包括咬、推、拥抱、攀爬、舔脸和舔口、鼻子-下巴和口部接触、爪子放置、游戏战斗和摔跤,这些都是由前庭系统支持的。我们采用了一系列的建筑和免疫组织化学染色来提供一个具有代表性的非洲野狗个体大脑的体感和前庭系统的定性描述。这两个系统的外观似乎与其他食肉动物的报道没有什么不同。形成前庭系统的六个神经核,以及它们彼此之间的关系,以及第八脑神经前庭神经的传入分支,看起来就像在许多哺乳动物物种中观察到的那样。在非洲野狗身上观察到的背柱核、三叉神经感觉柱、丘丘、丘脑背侧体感觉核和五个体感觉皮质区的位置和外观与在家犬和其他食肉动物身上观察到的相似。这项对非洲野狗体感和前庭系统的研究完成了我们描述非洲野狗大脑主要感觉系统的系列研究。似乎可以合理地得出这样的结论:在系统层面的分析中,没有任何感觉系统存在明显的专门化。因此,非洲野狗复杂社会性的神经基础可能是由非感觉神经系统(如运动、神经调节、边缘或认知系统)或组织水平(如受体表达模式或连通性)支持的。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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