Near-Term Fetal Hypoxia–Ischemia in Rabbits

Author:

Drobyshevsky Alexander1,Derrick Matthew1,Luo Kehuan1,Zhang Li-Qun1,Wu Yi-Ning1,Takada Silvia Honda1,Yu Lei1,Tan Sidhartha1

Affiliation:

1. From the Department of Pediatrics, NorthShore University Health Systems, Evanston, IL (A.D., M.D., K.L., L.Y., S.T.); Rehabilitation Institute of Chicago and Northwestern University, Chicago, IL (L.-Q.Z., Y.-N.W.); and the Laboratory of Neurosciences, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil (S.H.T.).

Abstract

Background and Purpose— The pattern of antenatal brain injury varies with gestational age at the time of insult. Deep brain nuclei are often injured at older gestational ages. Having previously shown postnatal hypertonia after preterm fetal rabbit hypoxia–ischemia, the objective of this study was to investigate the causal relationship between the dynamic regional pattern of brain injury on MRI and the evolution of muscle tone in the near-term rabbit fetus. Methods— Serial MRI was performed on New Zealand white rabbit fetuses to determine equipotency of fetal hypoxia–ischemia during uterine ischemia comparing 29 days gestation (E29, 92% gestation) with E22 and E25. E29 postnatal kits at 4, 24, and 72 hours after hypoxia–ischemia underwent T2- and diffusion-weighted imaging. Quantitative assessments of tone were made serially using a torque apparatus in addition to clinical assessments. Results— Based on the brain apparent diffusion coefficient, 32 minutes of uterine ischemia was selected for E29 fetuses. At E30, 58% of the survivors manifested hind limb hypotonia. By E32, 71% of the hypotonic kits developed dystonic hypertonia. Marked and persistent apparent diffusion coefficient reduction in the basal ganglia, thalamus, and brain stem was predictive of these motor deficits. Conclusions— MRI observation of deep brain injury 6 to 24 hours after near-term hypoxia–ischemia predicts dystonic hypertonia postnatally. Torque-displacement measurements indicate that motor deficits in rabbits progressed from initial hypotonia to hypertonia, similar to human cerebral palsy, but in a compressed timeframe. The presence of deep brain injury and quantitative shift from hypo- to hypertonia may identify patients at risk for developing cerebral palsy.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialised Nursing,Cardiology and Cardiovascular Medicine,Clinical Neurology

Reference26 articles.

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