Figure 6From: Complex pattern of interaction between in uterohypoxia-ischemia and intra-amniotic inflammation disrupts brain development and motor function Prenatal injury significantly impacts motor function in juvenile rats. Digigait analyses at postnatal day 28 demonstrate significant motor impairment and gait abnormalities in both forelimbs and hindlimbs of lipopolysaccharide (LPS; n = 13), transient systemic hypoxia-ischemia (TSHI; n = 14) and TSHI + LPS (n = 21) rats, compared to shams (n = 18). Impairment includes (A) decreased stride length, (B) increased stride variation, (C) decreased time in the propel phase, (D) decreased paw area at peak stride, consistent with toe-walking, and (E) increased stride frequency, which all culminate in (F) increased ataxia coefficients. *P < 0.05, ** P < 0.01, *** P < 0.001, versus shams. CV, Coefficient of variation.Back to article page