Inhibiting Inducible Nitric Oxide Synthase with 1400W Reduces Soman (GD)-Induced Ferroptosis in Long-Term Epilepsy-Associated Neuropathology: Structural and Functional Magnetic Resonance Imaging Correlations with Neurobehavior and Brain Pathology

• Published in: The Journal of pharmacology and experimental therapeutics 2024-02, Vol.388 (2), p.724-738
• Main Authors: Putra, Marson, Vasanthi, Suraj S., Rao, Nikhil S., Meyer, Christina, Van Otterloo, Madison, Thangi, Lal, Thedens, Daniel R., Kannurpatti, Sridhar S., Thippeswamy, Thimmasettappa
• Format: Article
• Language: English
• Subjects: Amidines - pharmacology; Amidines - therapeutic use; Animals; Benzylamines - pharmacology; Brain; Enzyme Inhibitors - pharmacology; Enzyme Inhibitors - therapeutic use; Epilepsy - drug therapy; Ferritins - pharmacology; Ferroptosis; Iron; Magnetic Resonance Imaging; Nitric Oxide - metabolism; Nitric Oxide Synthase Type II - metabolism; Rats; Soman - toxicity; Toxicology
• ISSN: 0022-3565; 1521-0103; 1521-0103
• DOI: 10.1124/jpet.123.001929

Organophosphate (OP) nerve agent (OPNA) intoxication leads to long-term brain dysfunctions. The ineffectiveness of current treatments for OPNA intoxication prompts a quest for the investigation of the mechanism and an alternative effective therapeutic approach. Our previous studies on 1400W, a highly selective inducible nitric oxide synthase (iNOS) inhibitor, showed improvement in epilepsy and seizure-induced brain pathology in rat models of kainate and OP intoxication. In this study, magnetic resonance imaging (MRI) modalities, behavioral outcomes, and biomarkers were comprehensively investigated for brain abnormalities following soman (GD) intoxication in a rat model. T1 and T2 MRI robustly identified pathologic microchanges in brain structures associated with GD toxicity, and 1400W suppressed those aberrant alterations. Moreover, functional network reduction was evident in the cortex, hippocampus, and thalamus after GD exposure, and 1400W rescued the losses except in the thalamus. Behavioral tests showed protection by 1400W against GD-induced memory dysfunction, which also correlated with the extent of brain pathology observed in structural and functional MRIs. GD exposure upregulated iron-laden glial cells and ferritin levels in the brain and serum, 1400W decreased ferritin levels in the epileptic foci in the brain but not in the serum. The levels of brain ferritin also correlated with MRI parameters. Further, 1400W mitigated the overproduction of nitroxidative markers after GD exposure. Overall, this study provides direct evidence for the relationships of structural and functional MRI modalities with behavioral and molecular abnormalities following GD exposure and the neuroprotective effect of an iNOS inhibitor, 1400W. Our studies demonstrate the MRI microchanges in the brain following GD toxicity, which strongly correlate with neurobehavioral performances and iron homeostasis. The inhibition of iNOS with 1400W mitigates GD-induced cognitive decline, iron dysregulation, and aberrant brain MRI findings.: ▪