Paper Details 
Original Abstract of the Article :
Neurons, especially axons, are metabolically demanding and energetically vulnerable during injury. However, the exact energy budget alterations that occur early after axon injury and the effects of these changes on neuronal survival remain unknown. Using a classic mouse model of optic nerve-crush in...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。


引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340706/

データ提供:米国国立医学図書館(NLM)

Altered Energy Metabolism in Optic Nerve Crush Injury

This study investigates the metabolic changes that occur in the retina and optic nerve following optic nerve crush injury. The researchers found that both the injured nerve and retina increase their energy production through both glycolysis and oxidative phosphorylation. However, the study suggests that an increased reliance on oxidative phosphorylation might be detrimental to retinal ganglion cell (RGC) survival.

Energy Metabolism and Optic Nerve Injury

This research sheds light on the complex metabolic changes that occur following optic nerve injury, highlighting the potential for targeting these metabolic pathways to improve RGC survival.

Understanding Optic Nerve Injury

Optic nerve injury can lead to vision loss. Early intervention and management are crucial for minimizing the impact of injury and preserving visual function.

Dr.Camel's Conclusion

Navigating the complexities of optic nerve injury can be like traversing a desert with shifting sands and unpredictable terrain. This study offers valuable insights into the metabolic responses to injury, suggesting that directing energy production towards glycolysis could be a key strategy for protecting RGCs. It's like finding a hidden oasis in the desert, offering a haven for survival and a chance to restore vision.
Date :
  1. Date Completed 2021-07-19
  2. Date Revised 2021-07-19
Further Info :

Pubmed ID

32277382

DOI: Digital Object Identifier

PMC7340706

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Languages

English

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