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Minocycline inhibits glial proliferation in the H-Tx rat model of congenital hydrocephalus

机译:米诺环素抑制先天性脑积水H-Tx大鼠模型中的神经胶质增生

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Background Reactive astrocytosis and microgliosis are important features of the pathophysiology of hydrocephalus, and persistent glial "scars" that form could exacerbate neuroinflammation, impair cerebral perfusion, impede neuronal regeneration, and alter biomechanical properties. The purpose of this study was to determine the efficacy of minocycline, an antibiotic known for its anti-inflammatory properties, to reduce gliosis in the H-Tx rat model of congenital hydrocephalus. Methods Minocycline (45 mg/kg/day i.p. in 5% sucrose at a concentration of 5-10 mg/ml) was administered to hydrocephalic H-Tx rats from postnatal day 15 to day 21, when ventriculomegaly had reached moderate to severe stages. Treated animals were compared to age-matched non-hydrocephalic and untreated hydrocephalic littermates. The cerebral cortex (both gray matter laminae and white matter) was processed for immunohistochemistry (glial fibrillary acidic protein, GFAP, for astrocytes and ionized calcium binding adaptor molecule, Iba-1, for microglia) and analyzed by qualitative and quantitative light microscopy. Results The mean number of GFAP-immunoreactive astrocytes was significantly higher in untreated hydrocephalic animals compared to both types of controls (p < 0.001). Minocycline treatment of hydrocephalic animals reduced the number of GFAP immunoreactive cells significantly (p < 0.001). Likewise, the mean number of Iba-1 immunoreactive microglia was significantly higher in untreated hydrocephalic animals compared to both types of controls (p < 0.001). Furthermore, no differences in the numbers of GFAP-positive astrocytes or Iba-1-positive microglia were noted between control animals receiving no minocycline and control animals receiving minocycline, suggesting that minocycline does not produce an effect under non-injury conditions. Additionally, in six out of nine regions sampled, hydrocephalic animals that received minocycline injections had significantly thicker cortices when compared to their untreated hydrocephalic littermates. Conclusions Overall, these data suggest that minocycline treatment is effective in reducing the gliosis that accompanies hydrocephalus, and thus may provide an added benefit when used as a supplement to ventricular shunting.
机译:背景反应性星形细胞增多症和小胶质细胞增生是脑积水病理生理学的重要特征,形成的持续的神经胶质“瘢痕”会加剧神经炎症,损害脑灌注,阻碍神经元再生并改变生物力学特性。这项研究的目的是确定米诺环素(一种以其抗炎特性而闻名的抗生素)减轻先天性脑积水的H-Tx大鼠模型中神经胶质增生的功效。方法从出生后第15天到第21天,当脑室肥大达到中度至重度阶段时,对脑积水H-Tx大鼠给予米诺环素(45 mg / kg /天,腹腔注射5%蔗糖,浓度为5-10 mg / ml)。将治疗的动物与年龄匹配的非脑积水和未治疗的脑积水同窝仔进行比较。对大脑皮层(灰质薄片和白质)进行免疫组织化学处理(神经胶质纤维酸性蛋白GFAP用于星形胶质细胞,离子钙结合衔接分子Iba-1用于小胶质细胞),并通过定性和定量光学显微镜进行分析。结果与两种类型的对照相比,未经治疗的脑积水动物中GFAP免疫反应性星形胶质细胞的平均数量显着更高(p <0.001)。米诺环素治疗脑积水动物可显着减少GFAP免疫反应性细胞的数量(p <0.001)。同样,与两种类型的对照相比,未经治疗的脑积水动物中Iba-1免疫反应性小胶质细胞的平均数量显着更高(p <0.001)。此外,在未接受美满霉素的对照动物与接受美满霉素的对照动物之间,未观察到GFAP阳性星形胶质细胞或Iba-1阳性小胶质细胞数量的差异,这表明美满环素在非损伤条件下不会产生作用。此外,在九个采样区域中的六个区域中,接受米诺环素注射的脑积水动物与未经处理的脑积水同窝仔相比,皮质明显增厚。结论总体而言,这些数据表明,米诺环素治疗可有效减少伴随脑积水的神经胶质细胞增生,因此当用作心室分流的补充剂时可能会提供额外的益处。

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