Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo

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Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo. / Kolko, M; Bruhn, T; Christensen, Thomas; Lazdunski, M; Lambeau, G; Bazan, N G; Diemer, Nils Henrik.

In: Neuroscience Letters, Vol. 274, No. 3, 1999, p. 167-170.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kolko, M, Bruhn, T, Christensen, T, Lazdunski, M, Lambeau, G, Bazan, NG & Diemer, NH 1999, 'Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo', Neuroscience Letters, vol. 274, no. 3, pp. 167-170. https://doi.org/10.1016/S0304-3940(99)00709-0

APA

Kolko, M., Bruhn, T., Christensen, T., Lazdunski, M., Lambeau, G., Bazan, N. G., & Diemer, N. H. (1999). Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo. Neuroscience Letters, 274(3), 167-170. https://doi.org/10.1016/S0304-3940(99)00709-0

Vancouver

Kolko M, Bruhn T, Christensen T, Lazdunski M, Lambeau G, Bazan NG et al. Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo. Neuroscience Letters. 1999;274(3):167-170. https://doi.org/10.1016/S0304-3940(99)00709-0

Author

Kolko, M ; Bruhn, T ; Christensen, Thomas ; Lazdunski, M ; Lambeau, G ; Bazan, N G ; Diemer, Nils Henrik. / Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo. In: Neuroscience Letters. 1999 ; Vol. 274, No. 3. pp. 167-170.

Bibtex

@article{4f9bca2074c911dbbee902004c4f4f50,
title = "Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo",
abstract = "The secretory phospholipases A2 (sPLA2) OS2 (10, 20 and 50 pmol) or OS1, (50 pmol) purified from taipan snake Oxyuranus scutellatus scutellatus venom, and the excitatory amino acid glutamate (Glu) (2.5 and 5.0 micromol) were injected into the right striatum of male Wistar rats. Injection of 10 and 20 pmol OS2 caused no neurological abnormalities or tissue damage. OS2 (50 pmol) caused apathy and circling towards the injection side. Histology revealed an infarct at the injection site. Injection of 50 pmol OS1 showed very little or no signs of neurotoxicity. Injection of 2.5 micromol Glu caused no tissue damage or neurological abnormality. After injection of 5.0 micromol Glu, the animals initially circled towards the side of injection, and gradually developed generalized clonic convulsions. These animals showed a well demarcated striatal infarct. When non-toxic concentrations of 20 pmol OS2 and 2.5 micromol Glu were co-injected, a synergistic neurotoxicity was observed. Extensive histological damage occurred in the entire right hemisphere, and in several rats comprising part of the contralateral hemisphere. These animals were apathetic in the immediate hours following injection, with circling towards the side of injection in the following days. Thus, OS2 greatly potentiates glutamate excitoxicity in vivo.",
keywords = "Animals, Behavior, Animal, Cell Death, Cerebral Infarction, Corpus Striatum, Elapid Venoms, Glutamic Acid, Male, Microinjections, Neurons, Neurotoxins, Phospholipases A, Phospholipases A2, Rats, Rats, Wistar, Reptilian Proteins",
author = "M Kolko and T Bruhn and Thomas Christensen and M Lazdunski and G Lambeau and Bazan, {N G} and Diemer, {Nils Henrik}",
year = "1999",
doi = "10.1016/S0304-3940(99)00709-0",
language = "English",
volume = "274",
pages = "167--170",
journal = "Neuroscience letters. Supplement",
issn = "0167-6253",
publisher = "Elsevier Ireland Ltd",
number = "3",

}

RIS

TY - JOUR

T1 - Secretory phospholipase A2 potentiates glutamate-induced rat striatal neuronal cell death in vivo

AU - Kolko, M

AU - Bruhn, T

AU - Christensen, Thomas

AU - Lazdunski, M

AU - Lambeau, G

AU - Bazan, N G

AU - Diemer, Nils Henrik

PY - 1999

Y1 - 1999

N2 - The secretory phospholipases A2 (sPLA2) OS2 (10, 20 and 50 pmol) or OS1, (50 pmol) purified from taipan snake Oxyuranus scutellatus scutellatus venom, and the excitatory amino acid glutamate (Glu) (2.5 and 5.0 micromol) were injected into the right striatum of male Wistar rats. Injection of 10 and 20 pmol OS2 caused no neurological abnormalities or tissue damage. OS2 (50 pmol) caused apathy and circling towards the injection side. Histology revealed an infarct at the injection site. Injection of 50 pmol OS1 showed very little or no signs of neurotoxicity. Injection of 2.5 micromol Glu caused no tissue damage or neurological abnormality. After injection of 5.0 micromol Glu, the animals initially circled towards the side of injection, and gradually developed generalized clonic convulsions. These animals showed a well demarcated striatal infarct. When non-toxic concentrations of 20 pmol OS2 and 2.5 micromol Glu were co-injected, a synergistic neurotoxicity was observed. Extensive histological damage occurred in the entire right hemisphere, and in several rats comprising part of the contralateral hemisphere. These animals were apathetic in the immediate hours following injection, with circling towards the side of injection in the following days. Thus, OS2 greatly potentiates glutamate excitoxicity in vivo.

AB - The secretory phospholipases A2 (sPLA2) OS2 (10, 20 and 50 pmol) or OS1, (50 pmol) purified from taipan snake Oxyuranus scutellatus scutellatus venom, and the excitatory amino acid glutamate (Glu) (2.5 and 5.0 micromol) were injected into the right striatum of male Wistar rats. Injection of 10 and 20 pmol OS2 caused no neurological abnormalities or tissue damage. OS2 (50 pmol) caused apathy and circling towards the injection side. Histology revealed an infarct at the injection site. Injection of 50 pmol OS1 showed very little or no signs of neurotoxicity. Injection of 2.5 micromol Glu caused no tissue damage or neurological abnormality. After injection of 5.0 micromol Glu, the animals initially circled towards the side of injection, and gradually developed generalized clonic convulsions. These animals showed a well demarcated striatal infarct. When non-toxic concentrations of 20 pmol OS2 and 2.5 micromol Glu were co-injected, a synergistic neurotoxicity was observed. Extensive histological damage occurred in the entire right hemisphere, and in several rats comprising part of the contralateral hemisphere. These animals were apathetic in the immediate hours following injection, with circling towards the side of injection in the following days. Thus, OS2 greatly potentiates glutamate excitoxicity in vivo.

KW - Animals

KW - Behavior, Animal

KW - Cell Death

KW - Cerebral Infarction

KW - Corpus Striatum

KW - Elapid Venoms

KW - Glutamic Acid

KW - Male

KW - Microinjections

KW - Neurons

KW - Neurotoxins

KW - Phospholipases A

KW - Phospholipases A2

KW - Rats

KW - Rats, Wistar

KW - Reptilian Proteins

U2 - 10.1016/S0304-3940(99)00709-0

DO - 10.1016/S0304-3940(99)00709-0

M3 - Journal article

C2 - 10548416

VL - 274

SP - 167

EP - 170

JO - Neuroscience letters. Supplement

JF - Neuroscience letters. Supplement

SN - 0167-6253

IS - 3

ER -

ID: 197763