| Literature DB >> 21682914 |
Thomas Freret1, Pascale Schumann-Bard, Michel Boulouard, Valentine Bouet.
Abstract
Despite extensive research efforts in the field of cerebral ischemia, numerous disappointments came from the translational step. Even if experimental studies showed a large number of promising drugs, most of them failed to be efficient in clinical trials. Based on these reports, factors that play a significant role in causing outcome differences between animal experiments and clinical trials have been identified; and latest works in the field have tried to discard them in order to improve the scope of the results. Nevertheless, efforts must be maintained, especially for long-term functional evaluations. As observed in clinical practice, animals display a large degree of spontaneous recovery after stroke. The neurological impairment, assessed by basic items, typically disappears during the firsts week following stroke in rodents. On the contrary, more demanding sensorimotor and cognitive tasks underline other deficits, which are usually long-lasting. Unfortunately, studies addressing such behavioral impairments are less abundant. Because the characterization of long-term functional recovery is critical for evaluating the efficacy of potential therapeutic agents in experimental strokes, behavioral tests that proved sensitive enough to detect long-term deficits are reported here. And since the ultimate goal of any stroke therapy is the restoration of normal function, an objective appraisal of the behavioral deficits should be done.Entities:
Year: 2011 PMID: 21682914 PMCID: PMC3141537 DOI: 10.1186/2040-7378-3-6
Source DB: PubMed Journal: Exp Transl Stroke Med ISSN: 2040-7378
Available and helpful sensorimotor tests assessing longitudinal and long-term functional recovery.
| Behavioral test | Brief description | Time points | Advantages | Concerns | |
|---|---|---|---|---|---|
| SENSORI-MOTOR FUNCTIONS | Neurological scales | Few days to a week[ | * Inter-species comparisons: non-human primate and rodents (mouse, rat, gerbil) | * Requires animal contention | |
| Limb placing test | Till 2 - 3 weeks[ | ||||
| Cylinder test | Few weeks[ | * Easy to perform | * Cannot be done in the acute phase, since it needs a certain level of recovery | ||
| Grip strength test | Few weeks to a month[ | * Quantitatively measured by a Newton meter | * Specific apparatus required | ||
| Beam walking test | Few weeks[ | * Easy to perform | * Cannot be done until postural bias and circling behaviors have not disappeared | ||
| Rotarod test | weeks[ | * Easy to perform | * Cost of apparatus | ||
| Adhesive removal test | From weeks[ | * Inter-species comparisons: non-human primate and rodents (mouse, rat, gerbil) | * May require a training session | ||
| Reach to grasp test/Skilled reaching test/staircase test | From weeks[ | * Inter-species comparisons: non-human primate and rodents (mice, rat) | * Requires a food restriction | ||
| MNESIC FUNCTIONS | Morris water maze | weeks[ | * Highly develop since 80's, numerous protocols existing that can fit all request | * Require a training session for the learning phase and a retention phase | |
| Passive avoidance | From days[ | * One-trial task with no need to learn a rule | * Require electrical foot shock that may interfere with other behavioral test | ||
| Object recognition test | weeks[ | * One-trial task with no need to learn a rule | |||
| EMOTIONAL-TRAIT | Elevated plus maze | Few months[ | * Easy to perform | * Cannot be done until postural bias and circling behaviors have not disappeared | |
| Black & white box | |||||
Time points when behavioral tests can discern sham-operated from stroked animals are given as an indication for a typical 30-50% lesion size.