PhTx4, a new class of toxins from Phoneutria nigriventer spider venom, inhibits the glutamate uptake in rat brain synaptosomes-Reference-Cited by-同舟云学术

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PhTx4, a new class of toxins from Phoneutria nigriventer spider venom, inhibits the glutamate uptake in rat brain synaptosomes

Published:1999-06 Issue:1-2 Volume:831 Page:297-300
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Mafra Roberta Amaral,Figueiredo Suely Gomes,Diniz Carlos Ribeiro,Cordeiro Marta Nascimento,Dos Santos Cruz Jáder,De Lima Maria Elena

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference34 articles.

1. Prolonged presence of glutamate during excitatory synaptic transmission to cerebellar Purkinje cells;Barbour;Neuron,1994

2. Postsynaptic block of glutamatergic synapse by low molecular weight fractions of spider venom;Bateman;Brain Res.,1985

3. Synaptic activation of glutamate transporters in hippocampal astrocytes;Bergles;Neuron,1997

4. Currents evoked in Bergmann glial cells by parallel fiber stimulation in rat cerebellar slices;Clark;J. Physiol. (Lond.),1997

5. Properties of the venom from the south American `Armed' spider Phoneutria nigriventer;Cordeiro;J. Toxicol.-Toxicon Reviews,1995

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1. Intravitreal injection of peptides PnPa11 and PnPa13, derivatives of Phoneutria nigriventer spider venom, prevents retinal damage;Journal of Venomous Animals and Toxins including Tropical Diseases;2020

2. Spider toxins targeting ligand-gated ion channels;Toxin Reviews;2019-03-07

3. Antinociceptive effect of PnTx4(5-5), a peptide from Phoneutria nigriventer spider venom, in rat models and the involvement of glutamatergic system;Journal of Venomous Animals and Toxins including Tropical Diseases;2019

4. Phoneutria nigriventer venom: A pharmacological treasure;Toxicon;2018-09

5. PnPP-19, a spider toxin peptide, induces peripheral antinociception through opioid and cannabinoid receptors and inhibition of neutral endopeptidase;British Journal of Pharmacology;2016-03-10

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