Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons

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Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons. / Hansen, H.H.; Schousboe, A.; Hansen, Harald S.; Hansen, S.H.

In: Journal of Neurochemistry, Vol. 75, No. 2, 01.01.2000, p. 861-871.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, HH, Schousboe, A, Hansen, HS & Hansen, SH 2000, 'Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons', Journal of Neurochemistry, vol. 75, no. 2, pp. 861-871. https://doi.org/10.1046/j.1471-4159.2000.0750861.x

APA

Hansen, H. H., Schousboe, A., Hansen, H. S., & Hansen, S. H. (2000). Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons. Journal of Neurochemistry, 75(2), 861-871. https://doi.org/10.1046/j.1471-4159.2000.0750861.x

Vancouver

Hansen HH, Schousboe A, Hansen HS, Hansen SH. Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons. Journal of Neurochemistry. 2000 Jan 1;75(2):861-871. https://doi.org/10.1046/j.1471-4159.2000.0750861.x

Author

Hansen, H.H. ; Schousboe, A. ; Hansen, Harald S. ; Hansen, S.H. / Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons. In: Journal of Neurochemistry. 2000 ; Vol. 75, No. 2. pp. 861-871.

Bibtex

@article{078f6192c7d34d1f8cf0a2c7e7967f92,
title = "Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons",
abstract = "Phospholipase D-mediated hydrolysis of N-acylethanolamine phospholipids (NAPEs) releases anandamide and other N-acylethanolamines, resulting in different actions at cellular targets in the CNS. Recently, we have demonstrated that these N-acyl lipids accumulate in cultured neocortical neurons subjected to sodium azide-induced cell injury. We here extend the information on the NAPE response, reporting on the composition of N-acyl species of NAPE, employing a new methodological approach of HPLC-coupled electrospray ionization mass spectrometry. Exposure to sodium azide (5 mM) increased the total amount of NAPE threefold over control levels; however, no alteration of the relative composition of NAPE species was detected. The anandamide precursor (20:4-NAPE) constituted only 0.1% of all NAPEs detected in the neurons. Total NAPE species in control cells amounted to 956-1,060 pmol/10 cells. Moreover, we detected the presence of an unknown NAPE species with molecular weight identical to 20:4-NAPE. This may suggest the presence of a putative stereoisomer of the anandamide precursor with at least one trans-configured double bond in the N-arachidonoyl moiety. These results show that with the present method, neuronal NAPE species can be identified and quantified with respect to N-acyl composition, including a trans-isomer of the anandamide precursor. The anandamide precursor is up-regulated to the same extent as other NAPEs upon neuronal injury.",
author = "H.H. Hansen and A. Schousboe and Hansen, {Harald S.} and S.H. Hansen",
year = "2000",
month = jan,
day = "1",
doi = "10.1046/j.1471-4159.2000.0750861.x",
language = "English",
volume = "75",
pages = "861--871",
journal = "Journal of Neurochemistry",
issn = "0022-3042",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Determination of the phospholipid precursor of anandamide and other N- acylethanolamine phospholipids before and after sodium azide-induced toxicity in cultured neocortical neurons

AU - Hansen, H.H.

AU - Schousboe, A.

AU - Hansen, Harald S.

AU - Hansen, S.H.

PY - 2000/1/1

Y1 - 2000/1/1

N2 - Phospholipase D-mediated hydrolysis of N-acylethanolamine phospholipids (NAPEs) releases anandamide and other N-acylethanolamines, resulting in different actions at cellular targets in the CNS. Recently, we have demonstrated that these N-acyl lipids accumulate in cultured neocortical neurons subjected to sodium azide-induced cell injury. We here extend the information on the NAPE response, reporting on the composition of N-acyl species of NAPE, employing a new methodological approach of HPLC-coupled electrospray ionization mass spectrometry. Exposure to sodium azide (5 mM) increased the total amount of NAPE threefold over control levels; however, no alteration of the relative composition of NAPE species was detected. The anandamide precursor (20:4-NAPE) constituted only 0.1% of all NAPEs detected in the neurons. Total NAPE species in control cells amounted to 956-1,060 pmol/10 cells. Moreover, we detected the presence of an unknown NAPE species with molecular weight identical to 20:4-NAPE. This may suggest the presence of a putative stereoisomer of the anandamide precursor with at least one trans-configured double bond in the N-arachidonoyl moiety. These results show that with the present method, neuronal NAPE species can be identified and quantified with respect to N-acyl composition, including a trans-isomer of the anandamide precursor. The anandamide precursor is up-regulated to the same extent as other NAPEs upon neuronal injury.

AB - Phospholipase D-mediated hydrolysis of N-acylethanolamine phospholipids (NAPEs) releases anandamide and other N-acylethanolamines, resulting in different actions at cellular targets in the CNS. Recently, we have demonstrated that these N-acyl lipids accumulate in cultured neocortical neurons subjected to sodium azide-induced cell injury. We here extend the information on the NAPE response, reporting on the composition of N-acyl species of NAPE, employing a new methodological approach of HPLC-coupled electrospray ionization mass spectrometry. Exposure to sodium azide (5 mM) increased the total amount of NAPE threefold over control levels; however, no alteration of the relative composition of NAPE species was detected. The anandamide precursor (20:4-NAPE) constituted only 0.1% of all NAPEs detected in the neurons. Total NAPE species in control cells amounted to 956-1,060 pmol/10 cells. Moreover, we detected the presence of an unknown NAPE species with molecular weight identical to 20:4-NAPE. This may suggest the presence of a putative stereoisomer of the anandamide precursor with at least one trans-configured double bond in the N-arachidonoyl moiety. These results show that with the present method, neuronal NAPE species can be identified and quantified with respect to N-acyl composition, including a trans-isomer of the anandamide precursor. The anandamide precursor is up-regulated to the same extent as other NAPEs upon neuronal injury.

UR - http://www.scopus.com/inward/record.url?scp=0033928039&partnerID=8YFLogxK

U2 - 10.1046/j.1471-4159.2000.0750861.x

DO - 10.1046/j.1471-4159.2000.0750861.x

M3 - Journal article

AN - SCOPUS:0033928039

VL - 75

SP - 861

EP - 871

JO - Journal of Neurochemistry

JF - Journal of Neurochemistry

SN - 0022-3042

IS - 2

ER -

ID: 45562245