Summary: Researchers say a novel enzyme treatment may reduce inflammation and scarring that prevents neural regeneration in spinal cord injury.
Spinal cord injury or damage causes permanent changes in strength, sensation and other body functions. Hope of recuperation is slim to none. Now a new Tel Aviv University study finds the intravenous injection of a potent enzyme, just hours after an accident, has the potential to diminish a cascade of pathological events responsible for neuronal death, such as inflammation and scarring.
The study was conducted by Dr. Angela Ruban of TAU’s Sackler Faculty of Medicine and Dr. Yona Goldshmit of TAU’s Sackler Faculty of Medicine and the Australian Regenerative Medicine Institute, Monash University. It was published in May in the Journal of Neurotrauma.
“Primary mechanical damage to spinal cord tissue kills a certain amount of neuronal cells. But there’s secondary damage due to the release of excess glutamates, which are responsible for additional functional disability,” Dr. Goldshmit says. “The main idea is to reduce the secondary damage as soon as possible — to block the body’s natural reaction to spinal cord trauma. This is the role of the enzyme injection we devised.”
“When this new treatment will be available to paramedics, the consequences of injuries could be dramatically reduced,” Dr. Ruban says.
“Don’t wait to diagnose”
Dr. Ruban worked with the late Prof. Vivian I. Teichberg of the Weizmann Institute of Science to develop the “blood glutamate scavenging approach,” a treatment based on controlling the levels of glutamate, the most abundant free amino acid in the central nervous system. Glutamate accounts for approximately 60 percent of total neurotransmitter activity in the brain. Dr. Ruban’s research has shown the positive effect of the blood glutamate treatment in models of glioblastoma, ALS and others.
“Our takeaway is, ‘Don’t wait to diagnose it, treat it,'” Dr. Ruban says. “It’s similar to aspirin, which can rescue a cardiac patient from irreversible damage if taken within the first few hours of a heart attack. We suggest administering the injection even in cases of uncertain diagnosis. There’s no side effect to the injection, but it might just mitigate secondary damage and dramatically improve the quality of a person’s life.”
According to the research, neurotrauma produces the immediate elevation of extracellular glutamate levels, which leads to inflammation, scar formation and, consequentially, neuronal death.
“Our new treatment aims to lower levels of glutamate, which is released in toxic quantities after trauma, by intravenous administration of blood glutamate scavengers (BGS), such as recombinant enzyme glutamate-oxaloacetate transaminase (rGOT1) and its cosubstrate,” Dr. Ruban says.
“If we manage to reduce the amount of glutamate that is released initially, we can moderate the inflammation and scarring, thereby moderating the damage to the tissue and enabling neuronal cells to survive,” Dr. Goldshmit adds.
Initial success in mouse models
The research team studied the neuroprotective effect of the blood glutamate scavengers in mouse models of spinal cord injury. After receiving the treatment for five consecutive days, the mice significantly recovered from the injury.
“The treatment increased the survival of neurons at the lesion site and enabled axonal regeneration into the injury site, which resulted in significant functional recovery compared with the untreated mice,” Dr. Ruban concludes. “This indicates that drug intervention with blood glutamate scavengers following spinal cord injury may be neuroprotective and may create a regenerative environment.”
About this neuroscience research article
Source: George Hunka – AFTAU Publisher: Organized by NeuroscienceNews.com. Image Source: NeuroscienceNews.com image is credited to AFTAU. Original Research:Abstract for “Blood Glutamate Scavenger as a Novel Neuroprotective Treatment in Spinal Cord Injury” by Yona Goldshmit, Ghil Jona, Eran Schmukler, Shira Solomon, Ronit Pinkas-Kramarski, and Angela Ruban in Journal of Neurotrauma. Published May 15 2018. doi:10.1089/neu.2017.5524
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[cbtabs][cbtab title=”MLA”]AFTAU”New Study Offers Hope of Recovery From Spinal Cord Injury.” NeuroscienceNews. NeuroscienceNews, 27 July 2018. <https://neurosciencenews.com/sci-recovery-9624/>.[/cbtab][cbtab title=”APA”]AFTAU(2018, July 27). New Study Offers Hope of Recovery From Spinal Cord Injury. NeuroscienceNews. Retrieved July 27, 2018 from https://neurosciencenews.com/sci-recovery-9624/[/cbtab][cbtab title=”Chicago”]AFTAU”New Study Offers Hope of Recovery From Spinal Cord Injury.” https://neurosciencenews.com/sci-recovery-9624/ (accessed July 27, 2018).[/cbtab][/cbtabs]
Blood Glutamate Scavenger as a Novel Neuroprotective Treatment in Spinal Cord Injury
Neurotrauma causes immediate elevation of extracellular glutamate (Glu) levels, which creates excitotoxicity and facilitates inflammation, glial scar formation, and consequently neuronal death. Finding factors that reduce the inflammatory response and glial scar formation, and increase neuronal survival and neurite outgrowth, are of major importance for improving the outcome after spinal cord injury (SCI). In the present study, we evaluated a new treatment aiming to remove central nervous system (CNS) Glu into the systemic blood circulation by intravenous (IV) administration of blood Glu scavengers (BGS) such as the enzyme recombinant glutamate-oxaloacetate transaminase 1 (rGOT1) and its co-substrate. In this study we induced in mice an SCI (hemisection), and 1 h post-injury started administering BGS treatment for 5 consecutive days. The treatment reduced the expression levels of p-p38, which regulates apoptosis and increased the expression of p-Akt, which mediates cell survival. Moreover, this treatment decreased pro-inflammatory cytokine expression and microglia activation, reduced astrocytes’ reactivity, and facilitated expression of radial glia markers such as Pax6 and nestin. BGS treatment increased the survival of neurons at lesion site and enabled axonal regeneration into the injury site. These effects were correlated with improved functional recovery of the left paretic hindlimb. Thus, early pharmacological intervention with BGS following SCI may be neuroprotective and create a pro-regenerative environment by modulating glia cell response. In light of our results, the availability of the method to remove excess Glu from CNS without the need to deliver drugs across the blood–brain barrier (BBB) and with minimal or no adverse effects may provide a major therapeutic asset.