TY - JOUR
T1 - Bliverdin reductase-A improves neurological function in a germinal matrix hemorrhage rat model
AU - Zhang, Yiting
AU - Ding, Yan
AU - Lu, Tai
AU - Zhang, Yixin
AU - Xu, Ningbo
AU - Yu, Lingyan
AU - McBride, Devin W.
AU - Flores, Jerry J.
AU - Tang, Jiping
AU - Zhang, John H.
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2018/2
Y1 - 2018/2
N2 - 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.
AB - 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.
KW - Germinal matrix hemorrhage
KW - Hematoma resolution
KW - Inflammation
KW - Innate immunity
KW - Animals, Newborn
KW - Cerebral Hemorrhage/pathology
KW - Recombinant Proteins/pharmacology
KW - Rats
KW - Lateral Ventricles/drug effects
KW - Rats, Sprague-Dawley
KW - Animals
KW - Oxidoreductases Acting on CH-CH Group Donors/pharmacology
KW - Disease Models, Animal
UR - http://www.scopus.com/inward/record.url?scp=85037640952&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85037640952&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/805cc598-52b1-3301-87b4-fe1ae12fd0e0/
U2 - 10.1016/j.nbd.2017.11.017
DO - 10.1016/j.nbd.2017.11.017
M3 - Article
C2 - 29203281
SN - 0969-9961
VL - 110
SP - 122
EP - 132
JO - Neurobiology of Disease
JF - Neurobiology of Disease
ER -