4.7 Article

The Anti-Inflammatory Agent Bindarit Attenuates the Impairment of Neural Development through Suppression of Microglial Activation in a Neonatal Hydrocephalus Mouse Model

Journal

JOURNAL OF NEUROSCIENCE
Volume 42, Issue 9, Pages 1820-1844

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1160-21.2021

Keywords

bindarit; microglia; neonatal hydrocephalus; white matter injury

Categories

Funding

  1. Hydrocephalus Association Innovator Award
  2. Center for Clinical and Translational Science and Training at the University of Cincinnati - National Institutes of Health (NIH) Clinical and Translational Service Award (CTSA) Program Award [2UL1TR001425-05A1]
  3. Rudi Schulte Research Institute
  4. NIH [NS121946]
  5. Japan Society for the Promotion of Science

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This study demonstrates that the use of the anti-inflammatory drug bindarit can effectively improve the neurological development of patients with hydrocephalus and alleviate the damage caused by neuroinflammation.
Neonatal hydrocephalus presents with various degrees of neuroinflammation and long-term neurologic deficits in surgically treated patients, provoking a need for additional medical treatment. We previously reported elevated neuroinflammation and severe periventricular white matter damage in the progressive hydrocephalus (prh) mutant which contains a point mutation in the Ccdc39 gene, causing loss of cilia-mediated unidirectional CSF flow. In this study, we identified cortical neuropil maturation defects such as impaired excitatory synapse maturation and loss of homeostatic microglia, and swimming locomotor defects in early postnatal prh mutant mice. Strikingly, systemic application of the anti-inflammatory small molecule bindarit significantly supports healthy postnatal cerebral cortical development in the prh mutant. While bindarit only mildly reduced the ventricular volume, it significantly improved the edematous appearance and myelination of the corpus callosum. Moreover, the treatment attenuated thinning in cortical Layers II-IV, excitatory synapse formation, and interneuron morphogenesis, by supporting the ramified-shaped homeostatic microglia from excessive cell death. Also, the therapeutic effect led to the alleviation of a spastic locomotor phenotype of the mutant. We found that microglia, but not peripheral monocytes, contribute to amoeboid-shaped activated myeloid cells in prh mutants' corpus callosum and the proinflammatory cytokines expression. Bindarit blocks nuclear factor (NF)-kB activation and its downstream proinflammatory cytokines, including monocyte chemoattractant protein-1, in the prh mutant. Collectively, we revealed that amelioration of neuroinflammation is crucial for white matter and neuronal maturation in neonatal hydrocephalus. Future studies of bindarit treatment combined with CSF diversion surgery may provide long-term benefits supporting neuronal development in neonatal hydrocephalus.

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