Evidence map›Paper›PMID 37187913›Full record

ArticleFrontiers in neural circuits2023

A neural tract tracing study on synaptic connections for cortical glutamatergic terminals and cervical spinal calretinin neurons in rats.

Ziyun Huang, Liping Sun, Xuefeng Zheng, Ye Zhang, Yaxi Zhu, Tao Chen, Zhi Chen, Linju Ja, Lisi OuYang, Yaofeng Zhu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 56% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Ziyun Huang *Department of Anatomy, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Liping Sun *Department of Pathology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xuefeng Zheng *Neuroscience Laboratory for Cognitive and Developmental Disorders, Department of Anatomy, Medical College of Jinan University, Guangzhou, China.
Ye ZhangNeuroscience Laboratory for Cognitive and Developmental Disorders, Department of Anatomy, Medical College of Jinan University, Guangzhou, China.
Yaxi ZhuDepartment of Pathology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Tao ChenDepartment of Anatomy, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Zhi ChenDepartment of Anatomy, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Linju JaDepartment of Anatomy, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Lisi OuYangDepartment of Anatomy, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Yaofeng ZhuCollege of Medicine, Institute of Medical Sciences, Jishou University, Jishou, China.
Si ChenDepartment of Human Anatomy, Histology and Embryology, Zunyi Medical University, Zhuhai, China.
Wanlong LeiDepartment of Anatomy, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CNJishou University · CNJinan University · CNZunyi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cerebral cortex innervates motor neurons in the anterior horn of the spinal cord by regulating of interneurons. At present, nerve tracing, immunohistochemistry, and immunoelectron microscopy are used to explore and confirm the characteristics of synaptic connections between the corticospinal tract (CST) and cervical spinal calretinin (Cr) interneurons. Our morphological results revealed that (1) biotinylated dextran amine labeled (BDA+) fibers from the cerebral cortex primarily presented a contralateral spinal distribution, with a denser distribution in the ventral horn (VH) than in the dorsal horn (DH). An electron microscope (EM) showed that BDA+ terminals formed asymmetric synapses with spinal neurons, and their mean labeling rate was not different between the DH and VH. (2) Cr-immunoreactive (Cr+) neurons were unevenly distributed throughout the spinal gray matter, and were denser and larger in the VH than in the DH. At the single labeling electron microscope (EM) level, the labeling rate of Cr+ dendrites was higher in the VH than in the DH, in which Cr+ dendrites mainly received asymmetric synaptic inputs, and between the VH and DH. (3) Immunofluorescence triple labeling showed obvious apposition points among BDA+ terminals, synaptophysin and Cr+ dendrites, with a higher density in the VH than in the DH. (4) Double labeling in EM, BDA+ terminals and Cr+ dendrites presented the same pattern, BDA+ terminals formed asymmetric synapses either with Cr+ dendrites or Cr negative (Cr-) dendrites, and Cr+ dendrites received either BDA+ terminals or BDA- synaptic inputs. The average percentage of BDA+ terminals targeting Cr+ dendrites was higher in the VH than in the DH, but the percentage of BDA+ terminals targeting Cr- dendrites was prominently higher than that targeting Cr+ dendrites. There was no difference in BDA+ terminal size. The percentage rate for Cr+ dendrites receiving BDA+ terminal inputs was lower than that receiving BDA- terminal inputs, and the BDA+ terminal size was larger than the BDA- terminal size received by Cr+ dendrites. The present morphological results suggested that spinal Cr+ interneurons are involved in the regulatory process of the cortico-spinal pathway.

Indexed as

Motor NeuronsSynapsesAnimalsCalbindin 2Cerebral CortexPresynaptic TerminalsPyramidal TractsRatsCalbindin 2calretinin interneuroncortical glutamatergic terminalscorticospinal tractspinal cordsynaptic connection

Identifiers

PMID37187913
PMCPMC10175624
OpenAlexW4367300180

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.