Mechanisms by which seizures affect cerebral circulation in newborns are of physiological and potentially clinical importance. Carbon monoxide (CO) and biliverdin/bilirubin formed in the brain from intracellular heme I via the heme oxygenase (HO) pathway are a vasodilator and antioxidants, respectively. My published and preliminary data suggest: 1) seizures dilate cerebral arterioles and increase cerebral blood flow, 2) seizures cause activation of HO in the brain, 3) HO inhibition attenuates cerebral dilation to seizures and results in sustained postictal cerebral vascular dysfunction, 4) HO upregulation may prevent postictal cerebral vascular dysfunction, 5) the seizure-associated excitotoxic neuromediator, glutamate, dilates cerebral arterioles and increases cerebral vascular HO activity, 6) glutamate receptors are detected in cerebral microvascular endothelial cells (CMVEC). The research proposed will pursue the hypothesis that heme oxygenase provides endogenous vascular protection against seizure-induced postictal vascular dysfunction in the neonatal cerebral circulation.
Three specific aims will be addressed using in vivo and in vitro techniques in newborn pigs.
SPECIFIC AIM 1. Evaluate, in vivo, the relationship between activation of HO and cerebrovascular dysfunction secondary to glutamatergic seizures.
SPECIFIC AIM 2. Examine the mechanism(s) by which HO diminishes postictal cerebrovascular dysfunction.
SPECIFIC AIM 3. To explore a potential mechanism by which glutamate increases the protective HO activity, test, in vitro, the hypothesis that cerebral microvessels express glutamate receptors (GluRs) that are functionally linked to HO. I will use in vivo and in vitro techniques to investigate intact cerebral microcirculation, isolated cerebral arterioles, and CMVEC. Cranial window techniques allow investigation of cerebral circulation in vivo. Intact and endothelium-denuded isolated pressurized cerebral arterioles will be used to examine vascular responses to glutamate in situ. CMVEC in primary cultures in vitro will be studied to uncover the cellular and molecular mechanisms by which glutamate stimulates HO activity. Seizures in newborn children are frequently associated with long-lasting neurological disabilities and increase chances of subsequent development of chronic epilepsy. Better understanding of the mechanisms of postictal cerebral vascular dysfunction is needed to improve the long-term neurological outcome in human newborns.
| Parfenova, Helena; Tcheranova, Dilyara; Basuroy, Shyamali et al. (2012) Functional role of astrocyte glutamate receptors and carbon monoxide in cerebral vasodilation response to glutamate. Am J Physiol Heart Circ Physiol 302:H2257-66 |
| Parfenova, Helena; Leffler, Charles W; Basuroy, Shyamali et al. (2012) Antioxidant roles of heme oxygenase, carbon monoxide, and bilirubin in cerebral circulation during seizures. J Cereb Blood Flow Metab 32:1024-34 |
| Xi, Qi; Tcheranova, Dilyara; Basuroy, Shyamali et al. (2011) Glutamate-induced calcium signals stimulate CO production in piglet astrocytes. Am J Physiol Heart Circ Physiol 301:H428-33 |
| Basuroy, Shyamali; Tcheranova, Dilyara; Bhattacharya, Sujoy et al. (2011) Nox4 NADPH oxidase-derived reactive oxygen species, via endogenous carbon monoxide, promote survival of brain endothelial cells during TNF-?-induced apoptosis. Am J Physiol Cell Physiol 300:C256-65 |
| Leffler, Charles W; Parfenova, Helena; Jaggar, Jonathan H (2011) Carbon monoxide as an endogenous vascular modulator. Am J Physiol Heart Circ Physiol 301:H1-H11 |
| Leffler, Charles W; Parfenova, Helena; Basuroy, Shyamali et al. (2011) Hydrogen sulfide and cerebral microvascular tone in newborn pigs. Am J Physiol Heart Circ Physiol 300:H440-7 |
| Parfenova, Helena; Leffler, Charles W; Tcheranova, Dilyara et al. (2010) Epileptic seizures increase circulating endothelial cells in peripheral blood as early indicators of cerebral vascular damage. Am J Physiol Heart Circ Physiol 298:H1687-98 |
| Basuroy, Shyamali; Bhattacharya, Sujoy; Leffler, Charles W et al. (2009) Nox4 NADPH oxidase mediates oxidative stress and apoptosis caused by TNF-alpha in cerebral vascular endothelial cells. Am J Physiol Cell Physiol 296:C422-32 |
| Leffler, Charles W; Parfenova, Helena; Jaggar, Jonathan H et al. (2006) Carbon monoxide and hydrogen sulfide: gaseous messengers in cerebrovascular circulation. J Appl Physiol 100:1065-76 |
