» Articles » PMID: 30596648

Transcortical Photothrombotic Pyramidotomy Model with Persistent Motor Deficits

Overview
Journal PLoS One
Date 2019 Jan 1
PMID 30596648
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Traditional pyramidotomy models have a high mortality rate from breathing difficulties and show early recovery from the induced motor deficits. This study establishes a novel pyramidotomy technique in Sprague Dawley rats that generates persistent motor deficits and has a reduced mortality rate. We used viral neural tracing to identify the course and relative distribution of forelimb and hindlimb motor fibers (n = 9). On basis of the neural tracing data, the medullary pyramid was targeted dorsally from the cerebellar cortex for photothrombotic infarct lesioning (n = 18). The photothrombotic technique selectively destroyed the corticospinal fibers in the medullary pyramid with relative preservation of neighboring grey-matter tissue. MicroPET imaging using 2-deoxy-2-[18F]-fluoro-D-glucose (FDG-microPET) showed a decrease in regional cerebral glucose metabolism (rCGM) in the bilateral pyramid and ipsilateral sensory cortex (p < 0.001, FDR q < 0.05). In addition, the trapezoid bodies and superior olivary nuclei showed a decrease in rCGM, compatible with damage caused during the introduction of the optical fiber. Connected structures such as the inferior colliculi and auditory cortices also showed decreases in rCGM in both hemispheres (p < 0.001, FDR q < 0.05). There was a significant and persistent decrease in motor and sensory function in the contralateral limb following pyramidotomy, as demonstrated by performance in the single pellet reaching task and the foot-fault test. There was no operative mortality or loss of respiratory function in this study. These results indicate that photothrombotic pyramidotomy with a dorsal transcortical approach is a safe and reliable technique for generating a pyramidotomy model with persistent motor deficits.

Citing Articles

Saccharomyces boulardii improves the behaviour and emotions of spastic cerebral palsy rats through the gut-brain axis pathway.

Tao D, Zhong T, Pang W, Li X BMC Neurosci. 2021; 22(1):76.

PMID: 34876019 PMC: 8653608. DOI: 10.1186/s12868-021-00679-4.

References
1.
Liu Z, Chopp M, Ding X, Cui Y, Li Y . Axonal remodeling of the corticospinal tract in the spinal cord contributes to voluntary motor recovery after stroke in adult mice. Stroke. 2013; 44(7):1951-6. PMC: 3851018. DOI: 10.1161/STROKEAHA.113.001162. View

2.
Song H, Jung W, Lee E, Park J, Kim M, Lee M . Capsular stroke modeling based on somatotopic mapping of motor fibers. J Cereb Blood Flow Metab. 2016; 37(8):2928-2937. PMC: 5536800. DOI: 10.1177/0271678X16679421. View

3.
Carmel J, Kimura H, Berrol L, Martin J . Motor cortex electrical stimulation promotes axon outgrowth to brain stem and spinal targets that control the forelimb impaired by unilateral corticospinal injury. Eur J Neurosci. 2013; 37(7):1090-102. PMC: 3618589. DOI: 10.1111/ejn.12119. View

4.
Starkey M, Bleul C, Maier I, Schwab M . Rehabilitative training following unilateral pyramidotomy in adult rats improves forelimb function in a non-task-specific way. Exp Neurol. 2011; 232(1):81-9. DOI: 10.1016/j.expneurol.2011.08.006. View

5.
McKenna J, Whishaw I . Complete compensation in skilled reaching success with associated impairments in limb synergies, after dorsal column lesion in the rat. J Neurosci. 1999; 19(5):1885-94. PMC: 6782168. View