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The impact of phosphodiesterase inhibition on neurobehavioral outcomes in preclinical models of traumatic and non-traumatic spinal cord injury: a systematic review.

Title: The impact of phosphodiesterase inhibition on neurobehavioral outcomes in preclinical models of traumatic and non-traumatic spinal cord injury: a systematic review.
Authors: Butler, Max B; Vellaiyappan, Sundar K; Bhatti, Faheem; Syed, Fazal-E-Momin; Rafati Fard, Amir; Teh, Jye Quan; Grodzinski, Ben; Akhbari, Melika; Adeeko, Sylva; Dilworth, Rory; Bhatti, Aniqah; Waheed, Unaiza; Robinson, Sophie; Osunronbi, Temidayo; Walker, Benn; Ottewell, Luke; Suresh, Gayathri; Kuhn, Isla; Davies, Benjamin M; Kotter, Mark RN; Mowforth, Oliver D
Publisher Information: Frontiers; //doi.org/10.3389/fmed.2023.1237219
Publication Year: 2023
Collection: Apollo - University of Cambridge Repository
Subject Terms: neurobehavioral outcomes; phosphodiesterase inhibitor; preclinical model; spinal cord; spinal cord injury
Description: Peer reviewed: True ; Acknowledgements: We gratefully acknowledge support from the Cambridge NIHR Brain Injury MedTech Cooperative. ; STUDY DESIGN: Systematic review. OBJECTIVE: The objective of this study was to evaluate the impact of phosphodiesterase (PDE) inhibitors on neurobehavioral outcomes in preclinical models of traumatic and non-traumatic spinal cord injury (SCI). METHODS: A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines and was registered with PROSPERO (CRD42019150639). Searches were performed in MEDLINE and Embase. Studies were included if they evaluated the impact of PDE inhibitors on neurobehavioral outcomes in preclinical models of traumatic or non-traumatic SCI. Data were extracted from relevant studies, including sample characteristics, injury model, and neurobehavioral assessment and outcomes. Risk of bias was assessed using the SYRCLE checklist. RESULTS: The search yielded a total of 1,679 studies, of which 22 met inclusion criteria. Sample sizes ranged from 11 to 144 animals. PDE inhibitors used include rolipram (n = 16), cilostazol (n = 4), roflumilast (n = 1), and PDE4-I (n = 1). The injury models used were traumatic SCI (n = 18), spinal cord ischemia (n = 3), and degenerative cervical myelopathy (n = 1). The most commonly assessed outcome measures were Basso, Beattie, Bresnahan (BBB) locomotor score (n = 13), and grid walking (n = 7). Of the 22 papers that met the final inclusion criteria, 12 showed a significant improvement in neurobehavioral outcomes following the use of PDE inhibitors, four papers had mixed findings and six found PDE inhibitors to be ineffective in improving neurobehavioral recovery following an SCI. Notably, these findings were broadly consistent across different PDE inhibitors and spinal cord injury models. CONCLUSION: In preclinical models of traumatic and non-traumatic SCI, the administration of PDE inhibitors appeared to be associated with statistically significant improvements ...
Document Type: article in journal/newspaper
File Description: application/pdf; application/zip; application/octet-stream; text/xml
Language: English
Relation: https://www.repository.cam.ac.uk/handle/1810/356900
Availability: https://www.repository.cam.ac.uk/handle/1810/356900
Accession Number: edsbas.3963524A
Database: BASE