2016
DOI: 10.1016/j.neuroscience.2016.07.040
|View full text |Cite
|
Sign up to set email alerts
|

Electrical muscle stimulation elevates intramuscular BDNF and GDNF mRNA following peripheral nerve injury and repair in rats

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
48
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 61 publications
(48 citation statements)
references
References 75 publications
0
48
0
Order By: Relevance
“…Electrical stimulation elevates intramuscular trophic factor mRNA levels which may explain how electrical stimulation enhances neural regeneration following nerve injury. 57 In addition, the impact of stimulation on terminal sprouting, a mentioned negative aspect of electrical muscle stimulation, was a minor contributor to long term functional reinnervation of stimulated muscles in that study. 56 …”
Section: Co-expression Of Fast and Slow Mchs Is Detected In Muscle Bimentioning
confidence: 62%
“…Electrical stimulation elevates intramuscular trophic factor mRNA levels which may explain how electrical stimulation enhances neural regeneration following nerve injury. 57 In addition, the impact of stimulation on terminal sprouting, a mentioned negative aspect of electrical muscle stimulation, was a minor contributor to long term functional reinnervation of stimulated muscles in that study. 56 …”
Section: Co-expression Of Fast and Slow Mchs Is Detected In Muscle Bimentioning
confidence: 62%
“…The release of neurotrophic factors is thus considered as an important index for evaluating the normal biological function of Schwann cells. Therefore, two key growth factors, BDNF and GDNF, were mainly measured in the present study, as these growth factors could be released by Schwann cells and were found to have positive effect on peripheral nerve regeneration in the previous study . The released amount of BDNF and GDNF by Schwann cells in various PCL scaffolds after culture for 24 h is shown in Figure (a).…”
Section: Resultsmentioning
confidence: 84%
“…The expression of stress and senescence markers was evaluated by staining sections for senescence‐associated ÎČ‐galactosidase (SA‐ÎČ‐gal) activity and p16 INK4A expression . The gene expression of select neurotrophic factors ( Gdnf and Bdnf ) was analyzed using qRT‐PCR, where Gdnf and Bdnf expression are known to have a major role in promoting nerve regeneration …”
Section: Methodsmentioning
confidence: 99%