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碱性成纤维细胞生长因子可保护听觉神经元和毛细胞免受谷氨酸神经毒性和噪声暴露的影响。

Basic fibroblast growth factor protects auditory neurons and hair cells from glutamate neurotoxicity and noise exposure.

作者信息

Zhai Suo-Qiang, Wang Da-Jun, Wang Jia-Ling, Han Dong-Yi, Yang Wei-Yan

机构信息

Institute of Otorhinolaryngology, General Hospital of PLA, Beijing, People's Republic of China.

出版信息

Acta Otolaryngol. 2004 Mar;124(2):124-9. doi: 10.1080/00016480310015939.

Abstract

OBJECTIVE

To determine the protective effects of basic fibroblast growth factor (bFGF) on cochlear neurons and hair cells in vitro and in vivo.

MATERIAL AND METHODS

In Experiment I, cultured spiral ganglion neurons (SGNs) prepared from postnatal Day 3 mice were exposed to 20 mM glutamate for 2 h before the culture medium was replaced with fresh medium containing 0, 25, 50 or 100 ng/ml bFGF. Fourteen days later, all cultures were fixed with 4% paraformaldehyde and stained with 1% toluidine blue. The number of surviving SGNs was counted and the length of the neurites of the SGNs was measured. In Experiment II, in vivo studies were carried out with guinea pigs in which bFGF or normal saline was injected intramuscularly to assess possible protective effects of bFGF on cochlear hair cells and to accelerate the recovery of the auditory brainstem response (ABR). The ABRs were measured before, immediately after and 2 and 4 weeks after exposure to noise.

RESULTS

Exposure to 20 mM glutamate for 2 h resulted in an inhibition of neurite outgrowth of SGNs and an increase in cell death. Treatment of the cultures with bFGF led to promotion of neurite outgrowth and an increase in the number of surviving SGNs. In Experiment II, significant (p < 0.05) differences in ABR thresholds were observed between the groups injected with bFGF and saline (t = 2.689) at 4 weeks after noise exposure. Cochleae were removed and hair cell loss analyzed in surface preparations prepared from all experimental animals. Acoustic trauma caused loss of 240 and 2160 inner hair cells in the groups injected with bFGF and saline, respectively. Similarly, more outer hair cells were lost in the normal saline injection group (99,291) than in the group treated with bFGF (70,377).

CONCLUSIONS

Our results demonstrate that bFGF protects SGNs against glutamate neurotoxicity in vitro. In addition, treatment with bFGF protects hair cells from acoustic trauma.

摘要

目的

确定碱性成纤维细胞生长因子(bFGF)在体外和体内对耳蜗神经元及毛细胞的保护作用。

材料与方法

实验I中,将出生后第3天小鼠制备的培养螺旋神经节神经元(SGNs)暴露于20 mM谷氨酸2小时,之后用含有0、25、50或100 ng/ml bFGF的新鲜培养基替换培养基。14天后,所有培养物用4%多聚甲醛固定,并用1%甲苯胺蓝染色。计数存活的SGNs数量,并测量SGNs的神经突长度。实验II中,对豚鼠进行体内研究,肌肉注射bFGF或生理盐水,以评估bFGF对耳蜗毛细胞的可能保护作用,并加速听觉脑干反应(ABR)的恢复。在暴露于噪声前、暴露后立即以及暴露后2周和4周测量ABR。

结果

暴露于20 mM谷氨酸2小时导致SGNs神经突生长受抑制且细胞死亡增加。用bFGF处理培养物导致神经突生长促进且存活的SGNs数量增加。在实验II中,噪声暴露4周后,注射bFGF和生理盐水的组之间ABR阈值存在显著(p < 0.05)差异(t = 2.689)。取出耳蜗并在所有实验动物制备的表面标本中分析毛细胞损失情况。声损伤分别导致注射bFGF组和生理盐水组的240个和2160个内毛细胞损失。同样,生理盐水注射组(99,291个)比bFGF处理组(70,377个)损失的外毛细胞更多。

结论

我们的结果表明,bFGF在体外可保护SGNs免受谷氨酸神经毒性。此外,bFGF治疗可保护毛细胞免受声损伤。

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