Amantadine ameliorates dopamine-releasing deficits and behavioral deficits in rats after fluid percussion injury

Eagle Yi Kung Huang, Pi Fen Tsui, Tung Tai Kuo, Jing Tsai, Yu Ching Chou, Hsin I. Ma, Yung Hsiao Chiang, Yuan Hao Chen

研究成果: 雜誌貢獻文章

16 引文 (Scopus)

摘要

Aims: To investigate the role of dopamine in cognitive and motor learning skill deficits after a traumatic brain injury (TBI), we investigated dopamine release and behavioral changes at a series of time points after fluid percussion injury, and explored the potential of amantadine hydrochloride as a chronic treatment to provide behavioral recovery. Materials and Methods: In this study, we sequentially investigated dopamine release at the striatum and behavioral changes at 1, 2, 4, 6, and 8 weeks after fluid percussion injury. Rats subjected to 6-Pa cerebral cortical fluid percussion injury were treated by using subcutaneous infusion pumps filled with either saline (sham group) or amantadine hydrochloride, with a releasing rate of 3.6mg/kg/hour for 8 weeks. The dopamine-releasing conditions and metabolism were analyzed sequentially by fast scan cyclic voltammetry (FSCV) and high-pressure liquid chromatography (HPLC). Novel object recognition (NOR) and fixed-speed rotarod (FSRR) behavioral tests were used to determine treatment effects on cognitive and motor deficits after injury. Results: Sequential dopamine-release deficits were revealed in 6-Pa-fluid-percussion cerebral cortical injured animals. The reuptake rate (tau value) of dopamine in injured animals was prolonged, but the tau value became close to the value for the control group after amantadine therapy. Cognitive and motor learning impairments were shown evidenced by the NOR and FSRR behavioral tests after injury. Chronic amantadine therapy reversed dopamine-release deficits, and behavioral impairment after fluid percussion injuries were ameliorated in the rats treated by using amantadine-pumping infusion. Conclusion: Chronic treatment with amantadine hydrochloride can ameliorate dopamine-release deficits as well as cognitive and motor deficits caused by cerebral fluid-percussion injury.

原文英語
文章編號e86354
期刊PLoS One
9
發行號1
DOIs
出版狀態已發佈 - 一月 30 2014

指紋

Percussion
Amantadine
dopamine
Rats
Dopamine
Fluids
rats
Wounds and Injuries
Rotarod Performance Test
Object recognition
Animals
learning
Learning
High pressure liquid chromatography
Therapeutics
Subcutaneous Infusions
Infusion Pumps
therapeutics
Motor Skills
fluids

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

引用此文

Huang, E. Y. K., Tsui, P. F., Kuo, T. T., Tsai, J., Chou, Y. C., Ma, H. I., ... Chen, Y. H. (2014). Amantadine ameliorates dopamine-releasing deficits and behavioral deficits in rats after fluid percussion injury. PLoS One, 9(1), [e86354]. https://doi.org/10.1371/journal.pone.0086354

Amantadine ameliorates dopamine-releasing deficits and behavioral deficits in rats after fluid percussion injury. / Huang, Eagle Yi Kung; Tsui, Pi Fen; Kuo, Tung Tai; Tsai, Jing; Chou, Yu Ching; Ma, Hsin I.; Chiang, Yung Hsiao; Chen, Yuan Hao.

於: PLoS One, 卷 9, 編號 1, e86354, 30.01.2014.

研究成果: 雜誌貢獻文章

Huang, Eagle Yi Kung ; Tsui, Pi Fen ; Kuo, Tung Tai ; Tsai, Jing ; Chou, Yu Ching ; Ma, Hsin I. ; Chiang, Yung Hsiao ; Chen, Yuan Hao. / Amantadine ameliorates dopamine-releasing deficits and behavioral deficits in rats after fluid percussion injury. 於: PLoS One. 2014 ; 卷 9, 編號 1.
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abstract = "Aims: To investigate the role of dopamine in cognitive and motor learning skill deficits after a traumatic brain injury (TBI), we investigated dopamine release and behavioral changes at a series of time points after fluid percussion injury, and explored the potential of amantadine hydrochloride as a chronic treatment to provide behavioral recovery. Materials and Methods: In this study, we sequentially investigated dopamine release at the striatum and behavioral changes at 1, 2, 4, 6, and 8 weeks after fluid percussion injury. Rats subjected to 6-Pa cerebral cortical fluid percussion injury were treated by using subcutaneous infusion pumps filled with either saline (sham group) or amantadine hydrochloride, with a releasing rate of 3.6mg/kg/hour for 8 weeks. The dopamine-releasing conditions and metabolism were analyzed sequentially by fast scan cyclic voltammetry (FSCV) and high-pressure liquid chromatography (HPLC). Novel object recognition (NOR) and fixed-speed rotarod (FSRR) behavioral tests were used to determine treatment effects on cognitive and motor deficits after injury. Results: Sequential dopamine-release deficits were revealed in 6-Pa-fluid-percussion cerebral cortical injured animals. The reuptake rate (tau value) of dopamine in injured animals was prolonged, but the tau value became close to the value for the control group after amantadine therapy. Cognitive and motor learning impairments were shown evidenced by the NOR and FSRR behavioral tests after injury. Chronic amantadine therapy reversed dopamine-release deficits, and behavioral impairment after fluid percussion injuries were ameliorated in the rats treated by using amantadine-pumping infusion. Conclusion: Chronic treatment with amantadine hydrochloride can ameliorate dopamine-release deficits as well as cognitive and motor deficits caused by cerebral fluid-percussion injury.",
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