TY - JOUR
T1 - Hypoxia-ischemia causes persistent movement deficits in a perinatal rabbit model of cerebral palsy
T2 - assessed by a new swim test
AU - Derrick, Matthew
AU - Drobyshevsky, Alexander
AU - Ji, Xinhai
AU - Chen, Lina
AU - Yang, Yirong
AU - Ji, Haitao
AU - Silverman, Richard B.
AU - Tan, Sidhartha
PY - 2009/10
Y1 - 2009/10
N2 - The relationship of movement between different muscle groups has not been quantified before in the newborn period. Cerebral palsy (CP), which often occurs as a result of perinatal hypoxia-ischemia (H-I), is categorized depending on clinical presentation, brain region involvement and extent of involvement. In order to test different brain region involvement, this study investigates individual and multi-joint involvement in a rabbit model of CP. Pregnant rabbits at 70% gestation were subjected to 40-min uterine ischemia. Newborn rabbit kits were subjected to a swim test at 5 time points over the first 11 days of life. H-I kits were divided into hypertonic and non-hypertonic groups based on muscle tone at birth. The ranges and velocity of angular movement of the forelimb and hind limb joints (wrist, elbow, shoulder, ankle, knee and hip) during supported swimming were determined. Severely impaired (hypertonic) animals have significantly reduced range and angular velocity of joint motion, which do not improve over time. The non-hypertonic group showed deficits in wrist and hind limb movements that were not evident on prolonged observation. Preventive treatment with an inhibitor of neuronal nitric oxide synthase decreased the incidence of severely impaired kits; the non-hypertonic kits showed a different pattern of swimming. Supported swimming allows quantification of limb and joint motion in the principal plane of movement in the absence of weight bearing and decreases the need for balance control. Identification and quantification of milder deficits allows mechanistic studies in the causation of H-I injury as well as estimation of recovery with therapeutic agents.
AB - The relationship of movement between different muscle groups has not been quantified before in the newborn period. Cerebral palsy (CP), which often occurs as a result of perinatal hypoxia-ischemia (H-I), is categorized depending on clinical presentation, brain region involvement and extent of involvement. In order to test different brain region involvement, this study investigates individual and multi-joint involvement in a rabbit model of CP. Pregnant rabbits at 70% gestation were subjected to 40-min uterine ischemia. Newborn rabbit kits were subjected to a swim test at 5 time points over the first 11 days of life. H-I kits were divided into hypertonic and non-hypertonic groups based on muscle tone at birth. The ranges and velocity of angular movement of the forelimb and hind limb joints (wrist, elbow, shoulder, ankle, knee and hip) during supported swimming were determined. Severely impaired (hypertonic) animals have significantly reduced range and angular velocity of joint motion, which do not improve over time. The non-hypertonic group showed deficits in wrist and hind limb movements that were not evident on prolonged observation. Preventive treatment with an inhibitor of neuronal nitric oxide synthase decreased the incidence of severely impaired kits; the non-hypertonic kits showed a different pattern of swimming. Supported swimming allows quantification of limb and joint motion in the principal plane of movement in the absence of weight bearing and decreases the need for balance control. Identification and quantification of milder deficits allows mechanistic studies in the causation of H-I injury as well as estimation of recovery with therapeutic agents.
KW - Cerebral palsy
KW - Hypoxia-ischemia
KW - Perinatal
KW - Rabbit
UR - http://www.scopus.com/inward/record.url?scp=68549095940&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=68549095940&partnerID=8YFLogxK
U2 - 10.1016/j.ijdevneu.2009.06.008
DO - 10.1016/j.ijdevneu.2009.06.008
M3 - Article
C2 - 19573586
AN - SCOPUS:68549095940
SN - 0736-5748
VL - 27
SP - 549
EP - 557
JO - International Journal of Developmental Neuroscience
JF - International Journal of Developmental Neuroscience
IS - 6
ER -