Developmental Neuroscience · 2015 · 24 citations · 33 references
MedicineNeurobiologyNeuroscienceDevelopmental NeuroscienceDevelopmental PhysiologyNeurophysiologyCerebral Blood FlowCerebral PhysiologyHypoxic-ischemic Brain InjuryHypoxic-ischemic EncephalopathyCerebral Blood Flow AlterationsCerebral HemodynamicsCerebral Hypoxic-ischemic InjuryHypothermiaHypoxiaHypoxic-ischemic Encephalopathy MonitoringNeonatal Cerebral Blood FlowNeonatal Hypoxic-ischemic Encephalopathy
<b><i>Background:</i></b> Neonatal hypoxic-ischemic (HI) encephalopathy occurs in 1-4 per 1,000 live term births and can cause devastating neurodevelopmental disabilities. Currently, therapeutic hypothermia (TH) is the only treatment with proven efficacy. Since TH is associated with decreased cerebral metabolism and cerebral blood flow (CBF), it is important to assess CBF at the bedside. Diffuse correlation spectroscopy (DCS) has emerged as a promising optical modality to noninvasively assess an index of CBF (CBF<sub>i</sub>) in both humans and animals. In this initial descriptive study, we employ DCS to monitor the evolution of CBF<sub>i</sub> following HI with or without TH in immature rats. We investigate potential relationships between CBF and subsequent cerebral damage. <b><i>Methods:</i></b> HI was induced on postnatal day 10 or 11 rat pups by right common carotid artery ligation followed by 60-70 min hypoxia (8% oxygen). After HI, the pups recovered for 4 h under hypothermia (HI-TH group, n = 23) or normothermia (HI-N group, n = 23). Bilateral measurements of hemispheric CBF<sub>i</sub> were made with DCS in unanesthetized animals at baseline, before HI, and 0, 1, 2, 3, 4, 5, and 24 h after HI. The animals were sacrificed at either 1 or 4 weeks, and brain injury was scored on an ordinal scale of 0-5 (0 = no injury). <b><i>Results:</i></b> Carotid ligation caused moderate bilateral decreases in CBF<sub>i</sub>. Following HI, an initial hyperemia was observed that was more prominent in the contralateral hemisphere. After initiation of TH, CBF<sub>i</sub> dropped significantly below baseline levels and remained reduced for the duration of TH. In contrast, CBF<sub>i</sub> in the HI-N group was not significantly decreased from baseline levels. Reductions in CBF<sub>i</sub> after 4 h of TH were not associated with reduced damage at 1 or 4 weeks. However, elevated ipsilateral CBF<sub>i</sub> and ipsilateral-to-contralateral CBF<sub>i</sub> ratios at 24 h were associated with worse outcome at 1 week after HI. <b><i>Conclusions:</i></b> Both HI and TH alter CBF<sub>i</sub>, with significant differences in CBF<sub>i</sub> between hypothermic and normothermic groups after HI. CBF<sub>i</sub> may be a useful biomarker of subsequent cerebral damage.
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