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[Primary study on proteomics about Ganoderma lucidium spores promoting survival and axon regeneration of injured spinal motor neurons in rats]. | LitMetric

[Primary study on proteomics about Ganoderma lucidium spores promoting survival and axon regeneration of injured spinal motor neurons in rats].

Zhong Xi Yi Jie He Xue Bao

Division of Neuroscience, Department of Histology and Embryology, Zhongshan Medical College, Sun Yat-sen University, Guangzhou, Guangdong Province 510080, China.

Published: May 2006

AI Article Synopsis

  • The study aimed to investigate how ganoderma lucidium spores (GASP) affect protein expression related to the survival and regeneration of spinal motor neurons after injury in rats.
  • Rats were divided into three groups: a control group, an untreated group, and a group treated with GASP for 14 days after spinal nerve injury, with protein analysis conducted post-treatment.
  • The results showed six proteins that were differently expressed, with some protein levels being higher in the GASP-treated group, suggesting that GASP could enhance neuron survival and regeneration by modulating these protein expressions.

Article Abstract

Objective: To detect some proteins associated with the effect of ganoderma lucidium spores (GASP) on promoting the survival and axon regeneration of injured spinal motor neurons in rats.

Methods: The rats were divided into normal control group, untreated group and GASP-treated group, and the rats in the last two groups received ventral root avulsion. GASP preparation was fed to the rats in the GASP-treated group for 14 days. The gray matter tissues of the lumbar spinal were sampled from rats in each group after 14 days following ventral root avulsion, and the extracted proteins from these tissues were detected by using 2-dimensional electrophoresis. Matrix assisted laser desorption/ionization time-of-flight mass spectroscopy (MALDI-TOF MS) was utilized to identify the differentially expressed proteins among these three groups.

Results: There were six kinds of proteins differentially expressed among the three groups, which were collapsin response mediator protein 2 (CRMP-2), F-actin capping protein beta subunit (FCP-beta), isocitrate dehydrogenase [NAD] subunit beta (IDH-beta), ATPase, glutamate oxaloacetate transaminase-1 (GOT1) and M2 pyruvate kinase (M2-PK). The expression levels of CRMP-2, IDH-beta, ATPase and GOT1 were higher in the GASP-treated group than those in the untreated group, while the expression levels of FCP-beta and M2-PK were lower than those in the untreated group.

Conclusion: GASP maybe promotes the survival and axon regeneration of injured spinal motor neurons in rats by virtue of up- or down-regulating the expression levels of the proteins mentioned above.

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Source
http://dx.doi.org/10.3736/jcim20060316DOI Listing

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