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Qualitative and quantitative analysis of glycine- and GABA-immunoreactive nerve terminals on motoneuron cell bodies in the cat spinal cord : A postembedding electron microscopic study. / Örnung, Göran; Shupliakov, Oleg; Lindå, Hans; Ottersen, Ole Petter; Storm-Mathisen, Jon; Ulfhake, Brun; Cullheim, Staffan.

в: Journal of Comparative Neurology, Том 365, № 3, 12.02.1996, стр. 413-426.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Örnung, Göran ; Shupliakov, Oleg ; Lindå, Hans ; Ottersen, Ole Petter ; Storm-Mathisen, Jon ; Ulfhake, Brun ; Cullheim, Staffan. / Qualitative and quantitative analysis of glycine- and GABA-immunoreactive nerve terminals on motoneuron cell bodies in the cat spinal cord : A postembedding electron microscopic study. в: Journal of Comparative Neurology. 1996 ; Том 365, № 3. стр. 413-426.

BibTeX

@article{3bdccfc3ed8d4b43b47b7cefe280129f,
title = "Qualitative and quantitative analysis of glycine- and GABA-immunoreactive nerve terminals on motoneuron cell bodies in the cat spinal cord: A postembedding electron microscopic study",
abstract = "The distribution of glycine- and gamma-aminobutyric acid (GABA)-like immunoreactivity (LI) in nerve terminals on the call soma of motoneurons in the aldehyde-fixed cat L7 spinal cord was examined using postembedding immunogold histochemistry in serial ultrathin sections. Quantitative examination of 405 terminals on eight neurons of α-motoneuron size in the L7 motor nuclei from one animal was performed. A majority of the terminals (69%) were immunoreactive to glycine and/or GABA. These terminals contained flat or oval synaptic vesicles, thus classifying them as F type or as C type in one case. In no case was a type-F terminal unlabeled for both glycine and GABA. Most of the immunolabeled terminals were immunoreactive to glycine only (62.5%), whereas 35.4% contained both glycine- and GABA-LI. A very small number of immunolabeled terminals (2%) were immunoreactive to GABA only. In those terminals, where glycine- and GABA-LI coexisted, the gold particle density for each amino acid was only half of that seen in boutons containing only one of the two amino acids. The involvement of glycine and GABA in postsynaptic inhibition of spinal α-motoneurons is discussed, with particular reference to the possibility that these two inhibitory amino acids may be coreleased from a significant proportion of the nerve terminals impinging on the cell bodies.",
keywords = "bouton, immunohistochemistry, synaptic input, ultrastructure",
author = "G{\"o}ran {\"O}rnung and Oleg Shupliakov and Hans Lind{\aa} and Ottersen, {Ole Petter} and Jon Storm-Mathisen and Brun Ulfhake and Staffan Cullheim",
year = "1996",
month = feb,
day = "12",
doi = "10.1002/(SICI)1096-9861(19960212)365:3<413::AID-CNE6>3.3.CO;2-N",
language = "English",
volume = "365",
pages = "413--426",
journal = "Journal of Comparative Neurology",
issn = "0021-9967",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Qualitative and quantitative analysis of glycine- and GABA-immunoreactive nerve terminals on motoneuron cell bodies in the cat spinal cord

T2 - A postembedding electron microscopic study

AU - Örnung, Göran

AU - Shupliakov, Oleg

AU - Lindå, Hans

AU - Ottersen, Ole Petter

AU - Storm-Mathisen, Jon

AU - Ulfhake, Brun

AU - Cullheim, Staffan

PY - 1996/2/12

Y1 - 1996/2/12

N2 - The distribution of glycine- and gamma-aminobutyric acid (GABA)-like immunoreactivity (LI) in nerve terminals on the call soma of motoneurons in the aldehyde-fixed cat L7 spinal cord was examined using postembedding immunogold histochemistry in serial ultrathin sections. Quantitative examination of 405 terminals on eight neurons of α-motoneuron size in the L7 motor nuclei from one animal was performed. A majority of the terminals (69%) were immunoreactive to glycine and/or GABA. These terminals contained flat or oval synaptic vesicles, thus classifying them as F type or as C type in one case. In no case was a type-F terminal unlabeled for both glycine and GABA. Most of the immunolabeled terminals were immunoreactive to glycine only (62.5%), whereas 35.4% contained both glycine- and GABA-LI. A very small number of immunolabeled terminals (2%) were immunoreactive to GABA only. In those terminals, where glycine- and GABA-LI coexisted, the gold particle density for each amino acid was only half of that seen in boutons containing only one of the two amino acids. The involvement of glycine and GABA in postsynaptic inhibition of spinal α-motoneurons is discussed, with particular reference to the possibility that these two inhibitory amino acids may be coreleased from a significant proportion of the nerve terminals impinging on the cell bodies.

AB - The distribution of glycine- and gamma-aminobutyric acid (GABA)-like immunoreactivity (LI) in nerve terminals on the call soma of motoneurons in the aldehyde-fixed cat L7 spinal cord was examined using postembedding immunogold histochemistry in serial ultrathin sections. Quantitative examination of 405 terminals on eight neurons of α-motoneuron size in the L7 motor nuclei from one animal was performed. A majority of the terminals (69%) were immunoreactive to glycine and/or GABA. These terminals contained flat or oval synaptic vesicles, thus classifying them as F type or as C type in one case. In no case was a type-F terminal unlabeled for both glycine and GABA. Most of the immunolabeled terminals were immunoreactive to glycine only (62.5%), whereas 35.4% contained both glycine- and GABA-LI. A very small number of immunolabeled terminals (2%) were immunoreactive to GABA only. In those terminals, where glycine- and GABA-LI coexisted, the gold particle density for each amino acid was only half of that seen in boutons containing only one of the two amino acids. The involvement of glycine and GABA in postsynaptic inhibition of spinal α-motoneurons is discussed, with particular reference to the possibility that these two inhibitory amino acids may be coreleased from a significant proportion of the nerve terminals impinging on the cell bodies.

KW - bouton

KW - immunohistochemistry

KW - synaptic input

KW - ultrastructure

UR - http://www.scopus.com/inward/record.url?scp=0030026999&partnerID=8YFLogxK

U2 - 10.1002/(SICI)1096-9861(19960212)365:3<413::AID-CNE6>3.3.CO;2-N

DO - 10.1002/(SICI)1096-9861(19960212)365:3<413::AID-CNE6>3.3.CO;2-N

M3 - Article

C2 - 8822179

AN - SCOPUS:0030026999

VL - 365

SP - 413

EP - 426

JO - Journal of Comparative Neurology

JF - Journal of Comparative Neurology

SN - 0021-9967

IS - 3

ER -

ID: 40836123