miR-23b improves cognitive impairments in traumatic brain injury by targeting ATG12-mediated neuronal autophagy

2018 ◽  
Vol 340 ◽  
pp. 126-136 ◽  
Author(s):  
Liqian Sun ◽  
Aihua Liu ◽  
Jingbo Zhang ◽  
Wenjun Ji ◽  
Youxiang Li ◽  
...  
2018 ◽  
Vol 337 ◽  
pp. 271-279 ◽  
Author(s):  
Liqian Sun ◽  
Manman Zhao ◽  
Man Liu ◽  
Peng Su ◽  
Jingbo Zhang ◽  
...  

2008 ◽  
Vol 23 (3) ◽  
pp. 149-157 ◽  
Author(s):  
Sabrina Breed ◽  
Amanda Sacks ◽  
Teresa A. Ashman ◽  
Wayne A. Gordon ◽  
Karen Dahlman ◽  
...  

2017 ◽  
Vol 88 (Suppl 1) ◽  
pp. A82.2-A82
Author(s):  
Peter Jenkins ◽  
Sara De Simoni ◽  
Niall Bourke ◽  
James Cole ◽  
David Sharp

Brain ◽  
2019 ◽  
Vol 142 (8) ◽  
pp. 2367-2379 ◽  
Author(s):  
Peter O Jenkins ◽  
Sara De Simoni ◽  
Niall J Bourke ◽  
Jessica Fleminger ◽  
Gregory Scott ◽  
...  

Abstract Cognitive impairment is common following traumatic brain injury. Dopaminergic drugs can enhance cognition after traumatic brain injury, but individual responses are highly variable. This may be due to variability in dopaminergic damage between patients. We investigate whether measuring dopamine transporter levels using 123I-ioflupane single-photon emission computed tomography (SPECT) predicts response to methylphenidate, a stimulant with dopaminergic effects. Forty patients with moderate-severe traumatic brain injury and cognitive impairments completed a randomized, double-blind, placebo-controlled, crossover study. 123I-ioflupane SPECT, MRI and neuropsychological testing were performed. Patients received 0.3 mg/kg of methylphenidate or placebo twice a day in 2-week blocks. Subjects received neuropsychological assessment after each block and completed daily home cognitive testing during the trial. The primary outcome measure was change in choice reaction time produced by methylphenidate and its relationship to stratification of patients into groups with normal and low dopamine transporter binding in the caudate. Overall, traumatic brain injury patients showed slow information processing speed. Patients with low caudate dopamine transporter binding showed improvement in response times with methylphenidate compared to placebo [median change = −16 ms; 95% confidence interval (CI): −28 to −3 ms; P = 0.02]. This represents a 27% improvement in the slowing produced by traumatic brain injury. Patients with normal dopamine transporter binding did not improve. Daily home-based choice reaction time results supported this: the low dopamine transporter group improved (median change −19 ms; 95% CI: −23 to −7 ms; P = 0.002) with no change in the normal dopamine transporter group (P = 0.50). The low dopamine transporter group also improved on self-reported and caregiver apathy assessments (P = 0.03 and P = 0.02, respectively). Both groups reported improvements in fatigue (P = 0.03 and P = 0.007). The cognitive effects of methylphenidate after traumatic brain injury were only seen in patients with low caudate dopamine transporter levels. This shows that identifying patients with a hypodopaminergic state after traumatic brain injury can help stratify the choice of cognitive enhancing therapy.


Oncotarget ◽  
2017 ◽  
Vol 8 (35) ◽  
pp. 59181-59203 ◽  
Author(s):  
Liqian Sun ◽  
Manman Zhao ◽  
Jingbo Zhang ◽  
Aihua Liu ◽  
Wenjun Ji ◽  
...  

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