米诺环素抑制先天性脑积水H-Tx模型大鼠神经胶质细胞增殖。

James P McAllister, Janet M Miller
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引用次数: 45

摘要

背景:反应性星形细胞增生和小胶质细胞增生是脑积水病理生理的重要特征,持续形成的胶质“疤痕”可加重神经炎症,损害脑灌注,阻碍神经元再生,改变生物力学特性。本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)在H-Tx先天性脑积水大鼠模型中减少胶质瘤的功效。方法:脑积水H-Tx大鼠出生后第15天至第21天,脑室增大至中重度时,给予米诺环素45 mg/kg/d, 5%蔗糖中5 ~ 10 mg/ml滴注。将治疗过的动物与年龄匹配的非脑积水和未治疗的脑积水幼崽进行比较。对大脑皮层(包括灰质层和白质)进行免疫组织化学处理(胶质纤维酸性蛋白,GFAP,用于星形胶质细胞,离子钙结合接头分子,Iba-1,用于小胶质细胞),并通过定性和定量光镜分析。结果:与两种类型的对照组相比,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著增加(p < 0.001)。二甲胺四环素治疗脑积水动物GFAP免疫反应细胞数量显著减少(p < 0.001)。同样,与两种类型的对照组相比,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著高于两种类型的对照组(p < 0.001)。此外,在未接受二甲胺四环素治疗的对照动物和接受二甲胺四环素治疗的对照动物之间,gfap阳性星形胶质细胞或iba -1阳性小胶质细胞的数量没有差异,这表明二甲胺四环素在非损伤条件下不会产生作用。此外,在9个取样区域中的6个,接受二甲胺四环素注射的脑积水动物与未接受治疗的脑积水幼崽相比,皮质明显更厚。结论:总的来说,这些数据表明二甲胺四环素治疗可有效减少脑积水引起的胶质瘤,因此当用作心室分流的补充时可能会提供额外的益处。
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Minocycline inhibits glial proliferation in the H-Tx rat model of congenital hydrocephalus.

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.

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