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Effect of Polyarginine Peptide R18D Following a Traumatic Brain Injury in Sprague-Dawley Rats.
Chiu, Li Shan; Anderton, Ryan S; Clark, Vince W; Cross, Jane L; Knuckey, Neville W; Meloni, Bruno P.
Afiliación
  • Chiu LS; Perron Institute for Neurological and Translational Science, Nedlands, Western Australia, Australia.
  • Anderton RS; Centre for Neuromuscular and Neurological Disorders, The University of Western Australia, Nedlands, Western Australia, Australia.
  • Clark VW; Perron Institute for Neurological and Translational Science, Nedlands, Western Australia, Australia.
  • Cross JL; Centre for Neuromuscular and Neurological Disorders, The University of Western Australia, Nedlands, Western Australia, Australia.
  • Knuckey NW; School of Heath Sciences, The University Notre Dame Australia, Fremantle, Western Australia, Australia.
  • Meloni BP; Institute for Health Research, The University Notre Dame Australia, Fremantle, Western Australia, Australia.
Curr Ther Res Clin Exp ; 92: 100584, 2020.
Article en En | MEDLINE | ID: mdl-32322314
BACKGROUND: Despite extensive studies, there are still no clinically available neuroprotective treatments for traumatic brain injury. OBJECTIVES: In previous studies we demonstrated beneficial treatment effects of polyarginine peptides R18 (18-mer of arginine; 300 nmol/kg) and R18D (18-mer of D-arginine; 1000 nmol/kg) in a rat model of impact-acceleration closed-head injury. METHODS: We examined the efficacy of R18D when intravenously administered at a low (100 nmol/kg) and high (1000 nmol/kg) dose, 30 minutes after a closed-head injury in male Sprague-Dawley rats. RESULTS: At postinjury day 3, treatment with R18D at the high dose significantly reduced axonal injury (P = 0.044), whereas the low-dose treatment of R18D showed a trend for reduced axonal injury. Following assessment in the Barnes maze, both doses of R18D treatment appeared to improve learning and memory recovery compared with vehicle treatment at postinjury days 1 and 3, albeit not to a statistically significant level. Rotarod assessment of vestibulomotor recovery did not differ between R18D and the vehicle treatment groups. CONCLUSIONS: R18D modestly decreased axonal injury only at the highest dose used but had no significant effect on functional recovery. These findings warrant further studies with additional doses to better understand peptide pharmacodynamics and provide information to guide optimal dosing.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Curr Ther Res Clin Exp Año: 2020 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Curr Ther Res Clin Exp Año: 2020 Tipo del documento: Article País de afiliación: Australia