Department of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, North Carolina, 27710, USA.
Department of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, North Carolina, 27710, USA.
Toxicology. 2018 Sep 1;408:11-21. doi: 10.1016/j.tox.2018.06.008. Epub 2018 Jun 20.
Glucocorticoids are given in preterm labor to prevent respiratory distress but these agents evoke neurobehavioral deficits in association with reduced brain region volumes. To determine whether the neurodevelopmental effects are distinct from growth impairment, we gave developing rats dexamethasone at doses below or within the therapeutic range (0.05, 0.2 or 0.8 mg/kg) at different stages: gestational days (GD) 17-19, postnatal days (PN) 1-3 or PN7-9. In adolescence and adulthood, we assessed the impact on noradrenergic systems in multiple brain regions, comparing the effects to those on somatic growth or on brain region growth. Somatic growth was reduced with exposure in all three stages, with greater sensitivity for the postnatal regimens; brain region growth was impaired to a lesser extent. Norepinephrine content and concentration were reduced depending on the treatment regimen, with a rank order of deficits of PN7-9 > PN1-3 > GD17-19. However, brain growth impairment did not parallel reduced norepinephrine content in magnitude, dose threshold, sex or regional selectivity, or temporal pattern, and even when corrected for reduced brain region weights (norepinephrine per g tissue), the dexamethasone-exposed animals showed subnormal values. Regression analysis showed that somatic growth impairment accounted for an insubstantial amount of the reduction in norepinephrine content, and brain growth impairment accounted for only 12%, whereas specific effects on norepinephrine accounted for most of the effect. The adverse effects of dexamethasone on noradrenergic system development are not simply related to impaired somatic or brain region growth, but rather include specific targeting of neurodifferentiation.
糖皮质激素在早产中被用于预防呼吸窘迫,但这些药物会引起神经行为缺陷,同时伴随着脑区体积减少。为了确定神经发育的影响是否与生长受损不同,我们在不同阶段给发育中的大鼠给予地塞米松,剂量低于或处于治疗范围内(0.05、0.2 或 0.8mg/kg):妊娠第 17-19 天、出生后第 1-3 天或第 7-9 天。在青春期和成年期,我们评估了其对多个脑区去甲肾上腺素系统的影响,将其与对躯体生长或脑区生长的影响进行比较。所有三个阶段的暴露都导致了躯体生长的减少,而对出生后方案的敏感性更高;脑区生长的受损程度较轻。去甲肾上腺素含量和浓度取决于治疗方案而降低,其缺陷程度的顺序为 PN7-9 > PN1-3 > GD17-19。然而,脑生长受损的程度与去甲肾上腺素含量的减少并不平行,无论是在幅度、剂量阈值、性别还是区域选择性上,或在时间模式上,即使校正了脑区重量减少(去甲肾上腺素每克组织),地塞米松暴露的动物仍表现出低于正常的数值。回归分析表明,躯体生长受损仅占去甲肾上腺素含量减少的一小部分,而脑生长受损仅占 12%,而对去甲肾上腺素的特定影响则占大部分影响。地塞米松对去甲肾上腺素系统发育的不良影响与其说是与躯体或脑区生长受损有关,不如说是包括对神经分化的特定靶向。