Abstract
Germinal matrix hemorrhage is induced by stereotaxic injection of collagenase into the germinal matrix of P7 Sprague-Dawley rats. Hemoglobin assay, western blot, immunofluorescence and neurobehavioral tests were used to test the effects of BLVRA on hematoma resolution and anti-inflammatory response. We showed that BLVRA triggered a signaling cascade that ameliorated post-hemorrhagic neurological deficits in both short-term and long-term neurobehavioral tests in a GMH rat model. Specifically, BLVRA inhibited toll-like receptor 4 (TLR4) expression by translocating to the nucleus in an endothelial nitric oxide (eNOS)/nitric oxide (NO)-dependent manner. BLVRA also induced the upregulation of CD36 scavenger receptor level in microglia/microphages, of which the prominent role is to enhance hematoma resolution. However, the beneficial effects of BLVRA were abolished with the knockdown of eNOS, indicating that the eNOS/NO system is an important downstream factor of BLVRA. Our results demonstrate a mechanism of BLVRA modulating hematoma resolution and suppressing inflammation through eNOS/NO/TLR4 pathway in the GMH rat model.
| Original language | English |
|---|---|
| Pages (from-to) | 122-132 |
| Number of pages | 11 |
| Journal | Neurobiology of Disease |
| Volume | 110 |
| DOIs | |
| State | Published - Feb 2018 |
ASJC Scopus Subject Areas
- Neurology
Keywords
- Germinal matrix hemorrhage
- Hematoma resolution
- Inflammation
- Innate immunity
- Animals, Newborn
- Cerebral Hemorrhage/pathology
- Recombinant Proteins/pharmacology
- Rats
- Lateral Ventricles/drug effects
- Rats, Sprague-Dawley
- Animals
- Oxidoreductases Acting on CH-CH Group Donors/pharmacology
- Disease Models, Animal
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