Details

Autor(en) / Beteiligte

• Chan, Hugh H.
• Hogue, Olivia
• Mathews, Nicole D.
• Hunter, Joshua G.
• Kundalia, Ronak
• Hermann, John K.
• Floden, Darlene P.
• Machado, Andre G.
• Baker, Kenneth B.

Titel

Deep cerebellar stimulation enhances cognitive recovery after prefrontal traumatic brain injury in rodent

Ist Teil von

• Experimental neurology, 2022-09, Vol.355, p.114136-114136, Article 114136

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2022

Quelle

MEDLINE

Beschreibungen/Notizen

• Functional outcome following traumatic brain injury (TBI) varies greatly, with approximately half of those who survive suffering long-term motor and cognitive deficits despite contemporary rehabilitation efforts. We have previously shown that deep brain stimulation (DBS) of the lateral cerebellar nucleus (LCN) enhances rehabilitation of motor deficits that result from brain injury. The objective of the present study was to evaluate the efficacy of LCN DBS on recovery from rodent TBI that uniquely models the injury location, chronicity and resultant cognitive symptoms observed in most human TBI patients. We used controlled cortical impact (CCI) to produce an injury that targeted the medial prefrontal cortex (mPFC-CCI) bilaterally, resulting in cognitive deficits. Unilateral LCN DBS electrode implantation was performed 6 weeks post-injury. Electrical stimulation started at week eight post-injury and continued for an additional 4 weeks. Cognition was evaluated using baited Y-maze, novel object recognition task and Barnes maze. Post-mortem analyses, including Western Blot and immunohistochemistry, were conducted to elucidate the cellular and molecular mechanisms of recovery. We found that mPFC-CCI produced significant cognitive deficits compared to pre-injury and naïve animals. Moreover, LCN DBS treatment significantly enhanced the long-term memory process and executive functions of applying strategy. Analyses of post-mortem tissues showed significantly greater expression of CaMKIIα, BDNF and p75NTR across perilesional cortex and higher expression of postsynaptic formations in LCN DBS-treated animals compared to untreated. Overall, these data suggest that LCN DBS is an effective treatment of cognitive deficits that result from TBI, possibly by activation of ascending, glutamatergic projections to thalamus and subsequent upregulation of thalamocortical activity that engages neuroplastic mechanisms for facilitation of functional re-organization. These results support a role for cerebellar output neuromodulation as a novel therapeutic approach to enhance rehabilitation for patients with chronic, post-TBI cognitive deficits that are unresponsive to traditional rehabilitative efforts. •LCN DBS promoted prefrontal-dependent cognitive recovery of rodent post-mPFC TBI.•LCN DBS enhanced prefrontal-dependent strategy application in Barnes maze searching.•The cognitive recovery are possibly mediated with the BDNF-mediated synaptogenesis.•LCN DBS possibly restored the hippocampal-prefrontal connection.•This neuromodulation is with a strong translational value of in the clinical use.