Cognitive and Cellular Effects of Combined Organophosphate Toxicity and Mild Traumatic Brain Injury

Author:

Freidin Dor1ORCID,Har-Even Meirav1,Rubovitch Vardit1,Murray Kathleen E.23ORCID,Maggio Nicola456,Shavit-Stein Efrat45ORCID,Keidan Lee1,Citron Bruce A.237ORCID,Pick Chaim G.1689ORCID

Affiliation:

1. Department of Anatomy and Anthropology, Sackler School of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel

2. Laboratory of Molecular Biology, VA New Jersey Health Care System, Research & Development, East Orange, NJ 07018, USA

3. Rutgers School of Graduate Studies, Newark, NJ 07103, USA

4. Department of Neurology, The Chaim Sheba Medical Center, Ramat Gan 52626202, Israel

5. Department of Neurology and Neurosurgery, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel

6. Sagol School of Neuroscience, Tel Aviv University, Tel Aviv 6997801, Israel

7. Department of Pharmacology, Physiology & Neuroscience, Rutgers New Jersey Medical School, Newark, NJ 07103, USA

8. Sylvan Adams Sports Institute, Tel Aviv University, Tel Aviv 6997801, Israel

9. The Dr. Miriam and Sheldon G. Adelson Chair and Center for the Biology of Addictive Diseases, Tel Aviv University, Tel Aviv 6997801, Israel

Abstract

Traumatic brain injury (TBI) is considered the most common neurological disorder among people under the age of 50. In modern combat zones, a combination of TBI and organophosphates (OP) can cause both fatal and long-term effects on the brain. We utilized a mouse closed-head TBI model induced by a weight drop device, along with OP exposure to paraoxon. Spatial and visual memory as well as neuron loss and reactive astrocytosis were measured 30 days after exposure to mild TBI (mTBI) and/or paraoxon. Molecular and cellular changes were assessed in the temporal cortex and hippocampus. Cognitive and behavioral deficits were most pronounced in animals that received a combination of paraoxon exposure and mTBI, suggesting an additive effect of the insults. Neuron survival was reduced in proximity to the injury site after exposure to paraoxon with or without mTBI, whereas in the dentate gyrus hilus, cell survival was only reduced in mice exposed to paraoxon prior to sustaining a mTBI. Neuroinflammation was increased in the dentate gyrus in all groups exposed to mTBI and/or to paraoxon. Astrocyte morphology was significantly changed in mice exposed to paraoxon prior to sustaining an mTBI. These results provide further support for assumptions concerning the effects of OP exposure following the Gulf War. This study reveals additional insights into the potentially additive effects of OP exposure and mTBI, which may result in more severe brain damage on the modern battlefield.

Funder

the Ari and Regine Aprijaskis Fund

Dr. Miriam and Sheldon G. Adelson Center for the Biology of Addictive Diseases

the Sylvan Adams Sports Institute

the Department of Veterans Affairs

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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