Prospective, randomized, blinded, and placebo-controlled study of Cerebrolysin dose-response effects on long-term functional outcomes in a rat model of mild traumatic brain injury
Recommended Citation
Zhang Y, Chopp M, Gang Zhang Z, Zhang Y, Zhang L, Lu M, Zhang T, Winter S, Brandstätter H, Mahmood A, Xiong Y. Prospective, randomized, blinded, and placebo-controlled study of Cerebrolysin dose-response effects on long-term functional outcomes in a rat model of mild traumatic brain injury. J Neurosurg. 2018 Nov 1;129(5):1295-1304.
Document Type
Article
Publication Date
11-1-2018
Publication Title
Journal of neurosurgery
Abstract
Using a prospective, randomized, blinded, placebo-controlled protocol, the authors demonstrated that Cerebrolysin at doses of 0.8-7.5 ml/kg, administered 4 hours after injury and then once daily for a total of 10 consecutive days, improves long-term functional outcomes in a rat model of mild closed head injury; a 2.5-ml/kg dose was identified as optimal. These findings suggest that Cerebrolysin has the potential to treat mild traumatic brain injury, the incidence of which is high without effective treatments.
Medical Subject Headings
Amino Acids/pharmacology/therapeutic use; Animals; Brain Concussion/drug therapy; Cognition/drug effects; Disease Models; Animal; Dose-Response Relationship; Drug; Double-Blind Method; Male; Maze Learning/drug effects; Neuroprotective Agents/pharmacology/therapeutic use; Rats; Rats; Wistar; Recovery of Function/drug effects; Treatment Outcome; Cerebrolysin; MWM = Morris water maze; NOR = novel object recognition; RCT = randomized controlled trial; TBI = traumatic brain injury; cognitive recovery; dose-response; mNSS = modified neurological severity score; mTBI = mild TBI; mild traumatic brain injury; neurological outcome
PubMed ID
29303438
Volume
129
Issue
5
First Page
1295
Last Page
1304
