» Articles » PMID: 25329574

A Combination Therapy of Neural and Glial Restricted Precursor Cells and Chronic Quipazine Treatment Paired with Passive Cycling Promotes Quipazine-induced Stepping in Adult Spinalized Rats

Overview
Date 2014 Oct 21
PMID 25329574
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: In order to develop optimal treatments to promote recovery from complete spinal cord injury (SCI), we examined the combination of: (1) a cellular graft of neural and glial restricted precursor (NRP/GRP) cells, (2) passive exercise, and (3) chronic quipazine treatment on behavioral outcomes and compared them with the individual treatment elements. NRP/GRP cells were transplanted at the time of spinalization.

Methods: Daily passive exercise began 1 week after injury to give sufficient time for the animals to recover. Chronic quipazine administration began 2 weeks after spinalization to allow for sufficient receptor upregulation permitting the expression of its behavioral effects. Behavioral measures consisted of the Basso, Beattie, and Bresnahan (BBB) locomotor score and percent of weight-supported steps and hops on a treadmill.

Results: Rats displayed an increased response to quipazine (BBB ≥ 9) beginning at 8 weeks post-injury in all the animals that received the combination therapy. This increase in BBB score was persistent through the end of the study (12 weeks post-injury).

Conclusion: Unlike the individual treatment groups which never achieved weight support, the combination therapy animals were able to perform uncoordinated weight-supported stepping without a body weight support system while on a moving treadmill (6.5 m per minute) and were capable of supporting their own weight in stance during open field locomotion testing. No regeneration of descending serotonergic projections into and through the lesion cavity was observed. Furthermore, these results are a testament to the capacity of the lumbar spinal cord, when properly stimulated, to sustain functioning locomotor circuitry following complete SCI.

Citing Articles

Cell transplantation to repair the injured spinal cord.

Hall A, Fortino T, Spruance V, Niceforo A, Harrop J, Phelps P Int Rev Neurobiol. 2022; 166:79-158.

PMID: 36424097 PMC: 10008620. DOI: 10.1016/bs.irn.2022.09.008.


Regenerative Rehabilitation and Stem Cell Therapy Targeting Chronic Spinal Cord Injury: A Review of Preclinical Studies.

Tashiro S, Nakamura M, Okano H Cells. 2022; 11(4).

PMID: 35203335 PMC: 8870591. DOI: 10.3390/cells11040685.


Glial restricted precursor cells in central nervous system disorders: Current applications and future perspectives.

Martins-Macedo J, Lepore A, Domingues H, Salgado A, Gomes E, Pinto L Glia. 2020; 69(3):513-531.

PMID: 33052610 PMC: 7857417. DOI: 10.1002/glia.23922.


Serotonin receptor and dendritic plasticity in the spinal cord mediated by chronic serotonergic pharmacotherapy combined with exercise following complete SCI in the adult rat.

Ganzer P, Beringer C, Shumsky J, Nwaobasi C, Moxon K Exp Neurol. 2018; 304:132-142.

PMID: 29526741 PMC: 5915900. DOI: 10.1016/j.expneurol.2018.03.006.


Passive cycling in neurorehabilitation after spinal cord injury: A review.

Nardone R, Orioli A, Golaszewski S, Brigo F, Sebastianelli L, Holler Y J Spinal Cord Med. 2016; 40(1):8-16.

PMID: 27841091 PMC: 5376131. DOI: 10.1080/10790268.2016.1248524.

References
1.
Winchester P, Smith P, Foreman N, Mosby J, Pacheco F, Querry R . A prediction model for determining over ground walking speed after locomotor training in persons with motor incomplete spinal cord injury. J Spinal Cord Med. 2009; 32(1):63-71. PMC: 2647503. DOI: 10.1080/10790268.2009.11760754. View

2.
Courtine G, Gerasimenko Y, van den Brand R, Yew A, Musienko P, Zhong H . Transformation of nonfunctional spinal circuits into functional states after the loss of brain input. Nat Neurosci. 2009; 12(10):1333-42. PMC: 2828944. DOI: 10.1038/nn.2401. View

3.
Kong X, Wienecke J, Hultborn H, Zhang M . Robust upregulation of serotonin 2A receptors after chronic spinal transection of rats: an immunohistochemical study. Brain Res. 2010; 1320:60-8. DOI: 10.1016/j.brainres.2010.01.030. View

4.
Harkema S . Neural plasticity after human spinal cord injury: application of locomotor training to the rehabilitation of walking. Neuroscientist. 2001; 7(5):455-68. DOI: 10.1177/107385840100700514. View

5.
Chopek J, MacDonell C, Gardiner K, Gardiner P . Daily passive cycling attenuates the hyperexcitability and restores the responsiveness of the extensor monosynaptic reflex to quipazine in the chronic spinally transected rat. J Neurotrauma. 2014; 31(12):1083-7. DOI: 10.1089/neu.2013.3207. View