目的观察宫内生长受限(intrauterine growth restriction,IUGR )幼鼠的神经发育及脑组织氧化应激状况。方法通过对孕鼠进行子宫动脉结扎建立宫内生长受限大鼠模型,以假手术组孕鼠作为对照。通过测量 IUGR幼鼠出生后的体重、身长、尾长、头围和肛殖距评价其体格发育情况;通过平面翻正试验、悬崖回避试验、负性趋地试验及前肢握力试验评价 宫内生长受限幼鼠的神经发育状况;通过检测IUGR幼鼠前额叶皮质、海马以及小脑中的超氧化物歧化酶(SOD)活力、丙二醛(MDA)含量及抑制 羟自由基能力评价其脑组织的氧化应激状况。结果IUGR组幼鼠出生时的体重、身长、尾长、头围及肛殖距均明显小于对照组,差异有统计学意义(P <0.05)。IUGR组幼鼠的翻正反射、悬崖回避、负性趋地时间均显著长于对照组,前肢握杆时间显著短于对照组,差异有统计学意义(P<0.05)。 IUGR组幼鼠前额叶、海马和小脑组织匀浆的SOD活力、抑制羟自由基能力显著低于对照组,MDA水平显著高于对照组,差异有统计学意义(P< 0.05)。结论宫内生长受限幼鼠的神经发育明显延迟,脑组织氧化应激程度显著增高。
ObjectiveTo observe the neurodevelopment and the state of oxidative stress in the brain tissue of immature rats with intrauterine growth restriction (IUGR). MethodsThe IUGR rat model was established by uterine artery ligation on pregnant rats, using pregnant rats in sham operation group as control. By measuring the weight, body length, tail length, head circumference and anogenital distance of IUGR immature rats after birth to evaluate their physical development. The status of neurodevelopment of IUGR immature rats was evaluated by surface righting test, cliff avoidance test, negative geotaxis test and forelimb grip strength test. Through testing superoxide dismutase (SOD) activity and malondialdehyde (MDA) content, and ability to inhibit hydroxyl radical in the prefrontal cortex, hippocampus and cerebellum of IUGR immature rats to evaluate their state of oxidative stress in the brain tissue. ResultsAs compared with the control group, the immature rats in the IUGR group obtained smaller weight, body length, tail length, head circumference and anogenital distance at birth, whereas longer surface righting reflex, cliff avoidance, and negative geotaxis time, while shorter time of forelimb grip strength, with statistically significant differences (P <0.05). The immature rats in the IUGR group obtained lower SOD activity, ability to inhibit hydroxyl radical in the homogenate of the prefrontal cortex, hippocampus and cerebellum, whereas a higher level of MDA in comparison with the control group, with statistically significant differences (P<0.05). ConclusionThe neurodevelopment of IUGR immature rats significantly delays, and the degree of oxidative stress in the brain tissue significantly increases.