4.4 Article

Scopolamine disrupts place navigation in rats and humans: a translational validation of the Hidden Goal Task in the Morris water maze and a real maze for humans

期刊

PSYCHOPHARMACOLOGY
卷 234, 期 4, 页码 535-547

出版社

SPRINGER
DOI: 10.1007/s00213-016-4488-2

关键词

Spatial orientation; Scopolamine; Acetylcholinesterase inhibitor; Human; Rat

资金

  1. GACR Center of Excellence [P304/12/G069]
  2. MSMT [LH14053 KONTAKT ll]
  3. Grant Agency of Charles University in Prague [624012, 546113, 1108214, 135215]
  4. Ministry of Health, Czech Republic-conceptual development of research organization, University Hospital Motol, Prague, Czech Republic [00064203]
  5. project National Institute of Mental Health (NIMH-CZ) [ED2.1.00/03.0078]
  6. European Regional Development Fund through the project Sustainability for the National Institute of Mental Health [LO1611]
  7. Ministry of Education, Youth and Sports of the Czech Republic under the NPU I program
  8. European Regional Development Fund-Project FNUSA-ICRC [CZ.1.05/1.1.00/02.0123]
  9. project ICRC-ERA-HumanBridge [316345]
  10. National Program of Sustainability II (MEYS CR) [LQ1605]
  11. Laboratory Research Grant [2/2012 (699002)]
  12. Excellence Grant
  13. [RVO: 67985823]

向作者/读者索取更多资源

Development of new drugs for treatment of Alzheimer's disease (AD) requires valid paradigms for testing their efficacy and sensitive tests validated in translational research. We present validation of a place-navigation task, a Hidden Goal Task (HGT) based on the Morris water maze (MWM), in comparable animal and human protocols. We used scopolamine to model cognitive dysfunction similar to that seen in AD and donepezil, a symptomatic medication for AD, to assess its potential reversible effect on this scopolamine-induced cognitive dysfunction. We tested the effects of scopolamine and the combination of scopolamine and donepezil on place navigation and compared their effects in human and rat versions of the HGT. Place navigation testing consisted of 4 sessions of HGT performed at baseline, 2, 4, and 8 h after dosing in humans or 1, 2.5, and 5 h in rats. Scopolamine worsened performance in both animals and humans. In the animal experiment, co-administration of donepezil alleviated the negative effect of scopolamine. In the human experiment, subjects co-administered with scopolamine and donepezil performed similarly to subjects on placebo and scopolamine, indicating a partial ameliorative effect of donepezil. In the task based on the MWM, scopolamine impaired place navigation, while co-administration of donepezil alleviated this effect in comparable animal and human protocols. Using scopolamine and donepezil to challenge place navigation testing can be studied concurrently in animals and humans and may be a valid and reliable model for translational research, as well as for preclinical and clinical phases of drug trials.

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