Electroacupuncture combined with botulinum toxin type A promotes common peroneal nerve repair and activation of GDNF-BDNF/TrkB signaling pathway in post-stroke limb spasticity rats.
Abstract
[BACKGROUND] Post-stroke limb spasticity (PSLS) is a rehabilitation problem that needs to be solved urgently, electroacupuncture (EA), a safe and effective adjunctive rehabilitation therapy with relatively few side effects, and botulinum toxin type A (BTX-A) can improve motor function; however, it is not clear whether EA combined with BTX-A is more effective in improving PSLS. This study will investigate the effects and mechanisms of EA combined with BTX-A to improve PSLS in rats.
[METHODS] PSLS rat model was prepared and treated with EA, BTX-A, or EA+BTX-A, Zea longa, modified Ashworth, and modified neurological severity score to assess the changes of neurological function and dystonia, and to observe the cerebral infarction condition, fibers changes of gastrocnemius muscle, common peroneal nerve pathology morphology, changes of neural repair factors and GDNF/BDNF/TrkB signaling pathway in the rats, respectively.
[RESULTS] The results showed that EA combined with BTX-A effectively promotes the recovery of neurological function in rats with post-stroke limb spasticity, improves axonal and myelin regeneration of the gastrocnemius nerve on the operated side, promotes the repair of the common peroneal nerve, and activates the GDNF-BDNF/TrkB signaling pathway.
[CONCLUSIONS] Collectively, EA combined with BTX-A for the treatment of PSLS may be associated with the promotion of common peroneal nerve repair and modulation of the GDNF-BDNF/TrkB signaling pathway.
[METHODS] PSLS rat model was prepared and treated with EA, BTX-A, or EA+BTX-A, Zea longa, modified Ashworth, and modified neurological severity score to assess the changes of neurological function and dystonia, and to observe the cerebral infarction condition, fibers changes of gastrocnemius muscle, common peroneal nerve pathology morphology, changes of neural repair factors and GDNF/BDNF/TrkB signaling pathway in the rats, respectively.
[RESULTS] The results showed that EA combined with BTX-A effectively promotes the recovery of neurological function in rats with post-stroke limb spasticity, improves axonal and myelin regeneration of the gastrocnemius nerve on the operated side, promotes the repair of the common peroneal nerve, and activates the GDNF-BDNF/TrkB signaling pathway.
[CONCLUSIONS] Collectively, EA combined with BTX-A for the treatment of PSLS may be associated with the promotion of common peroneal nerve repair and modulation of the GDNF-BDNF/TrkB signaling pathway.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | botulinum toxin
|
보툴리눔독소 주사 | dict | 2 | |
| 해부 | limb
|
scispacy | 1 | ||
| 해부 | PSLS
→ Post-stroke limb spasticity
|
scispacy | 1 | ||
| 해부 | cerebral
|
scispacy | 1 | ||
| 해부 | gastrocnemius muscle
|
scispacy | 1 | ||
| 해부 | neural
|
scispacy | 1 | ||
| 해부 | myelin
|
scispacy | 1 | ||
| 약물 | [BACKGROUND] Post-stroke limb spasticity
|
scispacy | 1 | ||
| 약물 | BTX-A
→ botulinum toxin type A
|
scispacy | 1 | ||
| 약물 | [CONCLUSIONS]
|
scispacy | 1 | ||
| 질환 | Electroacupuncture
|
C0013794
Electroacupuncture
|
scispacy | 1 | |
| 질환 | post-stroke limb spasticity
|
scispacy | 1 | ||
| 질환 | dystonia
|
C0013421
Dystonia
|
scispacy | 1 | |
| 질환 | cerebral infarction
|
C0007785
Cerebral Infarction
|
scispacy | 1 | |
| 질환 | axonal and myelin regeneration
|
scispacy | 1 | ||
| 질환 | PSLS
→ Post-stroke limb spasticity
|
scispacy | 1 | ||
| 기타 | peroneal nerve
|
scispacy | 1 | ||
| 기타 | rats
|
scispacy | 1 | ||
| 기타 | botulinum toxin type A
|
scispacy | 1 | ||
| 기타 | BTX-A
→ botulinum toxin type A
|
scispacy | 1 | ||
| 기타 | Zea longa
|
scispacy | 1 | ||
| 기타 | post-stroke limb spasticity
|
scispacy | 1 | ||
| 기타 | gastrocnemius nerve
|
scispacy | 1 | ||
| 기타 | PSLS
→ Post-stroke limb spasticity
|
scispacy | 1 |
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