Literature DB >> 19384574

Unconjugated TAT carrier peptide protects against excitotoxicity.

Anne Vaslin1, Coralie Rummel, Peter G H Clarke.   

Abstract

We report in this article for the first time the neuroprotective effects of unconjugated TAT carrier peptide against a mild excitotoxic stimulus both in vitro and in vivo. In view of the widespread use of TAT peptides to deliver neuroprotectants into cells, it is important to know the effects of the carrier itself. Unconjugated TAT carrier protects dissociated cortical neurons against NMDA but not against kainate, suggesting that TAT peptides may interfere with NMDA signaling. Furthermore, a retro-inverso form of the carrier peptide caused a reduction in lesion volume (by about 50%) in a rat neonatal cerebral ischemia model. Thus, even though TAT is designed merely as a carrier, its own pharmacological activity will need to be considered in the analysis of TAT-linked neuroprotectant peptides.

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Year:  2009        PMID: 19384574     DOI: 10.1007/s12640-009-9012-6

Source DB:  PubMed          Journal:  Neurotox Res        ISSN: 1029-8428            Impact factor:   3.911


  12 in total

1.  Excitotoxicity-related endocytosis in cortical neurons.

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3.  Cell-penetrating peptides: a comparative membrane toxicity study.

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4.  In vivo protein transduction: delivery of a biologically active protein into the mouse.

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5.  A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia.

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6.  Specific targeting of pro-death NMDA receptor signals with differing reliance on the NR2B PDZ ligand.

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7.  Identification of a human immunodeficiency virus type 1 Tat epitope that is neuroexcitatory and neurotoxic.

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Journal:  J Virol       Date:  1996-03       Impact factor: 5.103

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9.  Short therapeutic window for MK-801 in transient focal cerebral ischemia in normotensive rats.

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Journal:  Biochim Biophys Acta       Date:  2007-06-14
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  10 in total

1.  Poly-arginine and arginine-rich peptides are neuroprotective in stroke models.

Authors:  Bruno P Meloni; Laura M Brookes; Vince W Clark; Jane L Cross; Adam B Edwards; Ryan S Anderton; Richard M Hopkins; Katrin Hoffmann; Neville W Knuckey
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Review 2.  Peptide Pharmacological Approaches to Treating Traumatic Brain Injury: a Case for Arginine-Rich Peptides.

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3.  Inhibition of N-Methyl-D-aspartate-induced Retinal Neuronal Death by Polyarginine Peptides Is Linked to the Attenuation of Stress-induced Hyperpolarization of the Inner Mitochondrial Membrane Potential.

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4.  Interaction of Arginine-Rich Cell-Penetrating Peptides with an Artificial Neuronal Membrane.

Authors:  Piotr Mucha; Emilia Sikorska; Piotr Rekowski; Jarosław Ruczyński
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5.  The neuroprotective efficacy of cell-penetrating peptides TAT, penetratin, Arg-9, and Pep-1 in glutamic acid, kainic acid, and in vitro ischemia injury models using primary cortical neuronal cultures.

Authors:  Bruno P Meloni; Amanda J Craig; Nadia Milech; Richard M Hopkins; Paul M Watt; Neville W Knuckey
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6.  The R18 Polyarginine Peptide Is More Effective Than the TAT-NR2B9c (NA-1) Peptide When Administered 60 Minutes after Permanent Middle Cerebral Artery Occlusion in the Rat.

Authors:  D Milani; N W Knuckey; R S Anderton; J L Cross; B P Meloni
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7.  The Therapeutic Potential of Naturally Occurring Peptides in Counteracting SH-SY5Y Cells Injury.

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Review 8.  Inhibition of regulated cell death by cell-penetrating peptides.

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Review 9.  Perinatal Hypoxic-Ischemic Encephalopathy and Neuroprotective Peptide Therapies: A Case for Cationic Arginine-Rich Peptides (CARPs).

Authors:  Adam B Edwards; Ryan S Anderton; Neville W Knuckey; Bruno P Meloni
Journal:  Brain Sci       Date:  2018-08-07

10.  Cationic Arginine-Rich Peptides (CARPs): A Novel Class of Neuroprotective Agents With a Multimodal Mechanism of Action.

Authors:  Bruno P Meloni; Frank L Mastaglia; Neville W Knuckey
Journal:  Front Neurol       Date:  2020-02-25       Impact factor: 4.003

  10 in total

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