Brain-wide connections of the parvicellular subdivision of the basolateral and basomedial amygdaloid nuclei in the rats.

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neural Circuits Pub Date : 2025-04-25 eCollection Date: 2025-01-01 DOI:10.3389/fncir.2025.1575232
Ge Zhu, Sheng-Qiang Chen, Run-Zhe Ma, Hui-Ru Cai, Jin-Yuan Zhang, Yi-Min Peng, Dian Lian, Song-Lin Ding
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引用次数: 0

Abstract

As the core area of emotion regulation, the amygdala is involved in and regulates many related behaviors, such as fear, anxiety, depression, as well as reward, learning, and memory. Most previous connectional studies have focused on the anterior and middle parts of the basolateral nucleus (BL) and basomedial nucleus (BM) of the amygdala. Little is known about the brain-wide connections of the posterior part of the BL and BM (termed parvicellular subdivision of the BL and BM, i.e., BLpc and BMpc). In this study, brain-wide afferent and efferent projections of the BLpc and BMpc in the rats are investigated using both retrograde and anterograde tracing methods. Both common and differential connections of the BLpc and BMpc are revealed. Major common inputs of both regions originate from the ventral hippocampal CA1 and prosubiculum, sublenticular extended amygdala, anterior basomedial nucleus, midline thalamic nuclei, endopiriform nucleus, dorsal raphe, piriform cortex and lateral entorhinal cortex. The BLpc receives preferential inputs from agranular insular cortex, amygdalopiriform transition area, periaqueductal gray, parataenial nucleus and anterior cortical nucleus of the amygdala. The BMpc preferentially receives its inputs from the peripeduncular nucleus, paraventricular nucleus of thalamus, ventromedial hypothalamic nucleus (VMH), caudal bed nucleus of stria terminalis (BST), medial amygdaloid nucleus and posterior cortical nucleus of the amygdala. Major differential outputs of the BLpc and BMpc are also obvious. The BLpc projects mainly to nucleus accumbens, rostral BST, lateral central amygdaloid nucleus (Ce), intermediate BL and BM. The BMpc sends its main outputs to VMH, medial Ce, caudal BST, prosubiculum, and perirhinal-ectorhinal cortices. These major findings are further confirmed with anterograde viral tracing in mice. Compared with previous findings in monkeys, our findings in rodents suggest that the BLpc and BMpc have overall similar connectional patterns across species. In addition, some gene markers for BM subdivisions are identified. All these findings would provide an important anatomical basis for the understanding of emotion-related neuronal circuits and diseases and for cross-species comparison of the subcircuits in amygdaloid complex.

大鼠基底外侧和基底内侧杏仁核细胞内亚分裂的全脑连接。
杏仁核是情绪调节的核心区域,参与和调节许多相关行为,如恐惧、焦虑、抑郁,以及奖励、学习、记忆等。以往的连接研究大多集中在杏仁核基底外侧核(BL)的前部和中部以及基底内侧核(BM)。对于脑后段和脑后段的全脑连接知之甚少(称为脑后段和脑后段的细胞细分化,即BLpc和BMpc)。本研究采用逆行示踪和顺行示踪两种方法对大鼠脑内BLpc和BMpc的传入和传出投射进行了研究。揭示了BLpc和BMpc的共连接和差动连接。这两个区域的主要共同输入来自海马腹侧CA1和下丘前区、核泡下延伸杏仁核、基底内侧前核、丘脑中线核、梨状内核、中缝背、梨状皮质和外侧鼻内皮质。BLpc接收的优先输入来自颗粒状岛皮质、杏仁核梨状过渡区、导水管周围灰质、尾轴旁核和杏仁核皮质前部核。BMpc优先接受来自脑梗周围核、丘脑室旁核、下丘脑腹内侧核(VMH)、尾纹尾床核(BST)、杏仁核内侧核和杏仁核后皮质核的输入。BLpc和BMpc的主要输出差异也很明显。BLpc主要投射到伏隔核、喙侧BST、外侧中央杏仁核(Ce)、中间BL和BM。BMpc将其主要输出发送到VMH,内侧Ce,尾侧BST,下丘前和鼻周-鼻外皮层。这些主要发现在小鼠的顺行病毒追踪中得到进一步证实。与之前在猴子身上的发现相比,我们在啮齿动物身上的发现表明,跨物种的BLpc和BMpc总体上具有相似的连接模式。此外,还鉴定了BM细分的一些基因标记。这些发现将为了解情绪相关神经回路和疾病以及跨物种比较杏仁核复合体亚回路提供重要的解剖学基础。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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