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成年雄性大鼠扣带区(腹内侧前额叶皮层和前扣带区,背侧部分)与间脑之间双向连接的拓扑组织。

Topographic organization of bidirectional connections between the cingulate region (infralimbic area and anterior cingulate area, dorsal part) and the interbrain (diencephalon) of the adult male rat.

作者信息

Negishi Kenichiro, Montes Laura P, Navarro Vanessa I, Arzate Lidice Soto, Oliveros Cindy, Khan Arshad M

机构信息

UTEP Systems Neuroscience Laboratory, Department of Biological Sciences, The University of Texas at El Paso, El Paso, Texas, 79968, USA.

Ph.D. Program in Bioscience, Department of Biological Sciences, The University of Texas at El Paso, El Paso, Texas, 79968, USA.

出版信息

bioRxiv. 2024 Oct 1:2024.09.29.615708. doi: 10.1101/2024.09.29.615708.

DOI:10.1101/2024.09.29.615708
PMID:40093037
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11908189/
Abstract

The medial prefrontal cortex [ (Brodmann, 1909) (CNG)] in the rat is a connectionally and functionally diverse structure. It harbors cerebral nuclei that use long-range connections to promote adaptive changes to ongoing behaviors. The CNG is often described across functional and anatomical gradients, a dorsalventral gradient being the most prominent. Topographic organization is a general feature of the nervous system, and it is becoming clear that such spatial arrangements can reflect connectional, functional, and cellular differences. Portions of the CNG are known to form reciprocal connections with cortical areas and thalamus; however, these connectional features have not been described in detail or mapped to standardized rat brain atlases. Here, we used co-injected anterograde ( leucoagglutinin) and retrograde (cholera toxin B subunit) tracers throughout the CNG to identify zones of reciprocal connectivity in the diencephalon [or (Baer, 1837) (IB)]. Tracer distributions were observed using a Nissl-based atlas-mapping approach that facilitates description of topographic organization. This draft report describes CNG connections of the (Rose & Woolsey, 1948) (ILA) and (Krettek & Price, 1977) (ACAd) throughout the IB. We found that corticothalamic connections are predominantly reciprocal, and that ILA and ACAd connections tended to be spatially segregated with minimal overlap. In the (Kuhlenbeck, 1927), we found dense and specific ILA-originating terminals in the following atlas territories: (Swanson, 2004) (LHAd) and (Swanson, 2004) (LHAs) of the (Nissl, 1913), (Wang & Zhang, 1995) (PSTN), (Petrovich et al., 2001) (TUte), and an ill-defined dorsal cap of the (Gudden, 1881) (MM). We discuss these findings in the context of feeding behaviors.

摘要

大鼠的内侧前额叶皮质[(布罗德曼,1909年)(CNG)]是一个在连接和功能上具有多样性的结构。它包含一些脑核,这些脑核利用长距离连接来促进对正在进行的行为的适应性变化。CNG通常根据功能和解剖学梯度来描述,其中背腹梯度最为显著。拓扑组织是神经系统的一个普遍特征,并且越来越清楚的是,这种空间排列可以反映连接、功能和细胞差异。已知CNG的部分区域与皮质区域和丘脑形成相互连接;然而,这些连接特征尚未得到详细描述或映射到标准化的大鼠脑图谱上。在这里,我们在整个CNG中共同注射了顺行(白凝集素)和逆行(霍乱毒素B亚基)示踪剂,以确定间脑[或(贝尔,1837年)(IB)]中的相互连接区域。使用基于尼氏染色的图谱映射方法观察示踪剂分布,该方法有助于描述拓扑组织。本报告草案描述了整个IB中(罗斯和伍尔西,1948年)(ILA)和(克雷泰克和普赖斯,1977年)(ACAd)的CNG连接。我们发现皮质丘脑连接主要是相互的,并且ILA和ACAd连接倾向于在空间上分离,重叠最小。在(库伦贝克,1927年)中,我们在以下图谱区域发现了密集且特定的ILA起源终末:(斯旺森,2004年)(LHAd)和(斯旺森,2004年)(LHA)的(尼氏,1913年)、(王和张,1995年)(PSTN)、(彼得罗维奇等人,2001年)(TUte)以及(古登,1881年)(MM)的一个界限不明确的背帽。我们在进食行为的背景下讨论这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/60b1c72f5e68/nihpp-2024.09.29.615708v1-f0016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/3d736d3ae230/nihpp-2024.09.29.615708v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/da855ffd1ead/nihpp-2024.09.29.615708v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/7e3130d0e067/nihpp-2024.09.29.615708v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/9b89a6a8b991/nihpp-2024.09.29.615708v1-f0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/4b64b38f786b/nihpp-2024.09.29.615708v1-f0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/9586664bf046/nihpp-2024.09.29.615708v1-f0015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/60b1c72f5e68/nihpp-2024.09.29.615708v1-f0016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/3d736d3ae230/nihpp-2024.09.29.615708v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/da855ffd1ead/nihpp-2024.09.29.615708v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/7e3130d0e067/nihpp-2024.09.29.615708v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/9b89a6a8b991/nihpp-2024.09.29.615708v1-f0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/4b64b38f786b/nihpp-2024.09.29.615708v1-f0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/9586664bf046/nihpp-2024.09.29.615708v1-f0015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cebe/11908189/60b1c72f5e68/nihpp-2024.09.29.615708v1-f0016.jpg

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