Abstract

BackgroundOur past researches suggested that L. barbarum exhibits direct neuroprotective and immune regulatory effects on the central nervous system, which are highly related to the events involved in the spinal cord injury, but not yet been investigated. Immune responses play an important role in the development of the pathology after secondary injury, particularly the M1 and M2 types of macrophage, on which special emphasis was laid in this study.MethodsIn our previous studies L. barbarum was administrated orally from 7 days before the injury to ensure a stabilized concentration in the blood. For clinical application, L. barbarum can only be administered after the injury. Therefore, both pre-injury and post-injury administration protocols were compared. In vivo and in vitro studies were conducted and analyzed immunohistochemically, including Western blotting.ResultsThe lesion size in the pre-treated group was much larger than that in the post-treated group. To explain this difference, we first studied the effect of L. barbarum on astrocytes, which forms the glial scar encircling the lesion. L. barbarum did not significantly affect the astrocytes. Then we studied the effect of L. barbarum on microglia/macrophages, particularly the M1 and M2 polarization. After spinal cord injury, the deleterious M1 cells dominant the early period, whereas the beneficial M2 cells dominate later. We found that in the pre-treated group L. barbarum significantly enhanced the expression of M1 cells and suppressed that of M2 cells, while in the post-treated group LBP markedly promoted the activity of M2 cells. This explained the difference between the pre- and post-treated groups.ConclusionsLycium barbarum has been wildly accepted to have beneficial effects in various central nervous system diseases. Our finding of deleterious effect of LBP administered at early period of spinal cord injury, indicates that its application should be avoided. The substantial beneficial effect of LBP when administered at later stage has an important impact for clinical application.

Highlights

  • Our past researches suggested that L. barbarum exhibits direct neuroprotective and immune regulatory effects on the central nervous system, which are highly related to the events involved in the spinal cord injury, but not yet been investigated

  • In Ocular hypertension model, we found a correlation between microglial activation and protection of RGC by Lycium barbarum polysaccharide (LBP) [16,17]

  • Our finding of deleterious effect of LBP administered at early period of spinal cord injury, so that its application should be avoided, and the substantial beneficial effect of LBP when administered at later stage has an important impact for clinical application

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Summary

Introduction

Our past researches suggested that L. barbarum exhibits direct neuroprotective and immune regulatory effects on the central nervous system, which are highly related to the events involved in the spinal cord injury, but not yet been investigated. Our past researches suggested a direct neuroprotective effect on CNS of LBP, in models of Alzheimer's disease (Amyloid-β toxicity) [9,10,11,12,13,14], glutamate excitotoxicity [15], and Ocular hypertension [16,17,18], by down-regulation of c-Jun N-terminal signaling, RNA-dependent protein kinase phosphorylation, caspase-3 and caspase-2 activities, endoplasmic reticulum stress and up-regulation of Akt signaling or crystalline [11,12,13,15,17,18]. It has been reported that LBP can be anti-oxidative [22,23,24,25,26]

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