Center for Hearing and Deafness, University at Buffalo, 137 Cary Hall, Buffalo, NY, 14214, USA.
Department of Otolaryngology Head and Neck Surgery, The Third People's Hospital of Chengdu, Chengdu, China.
Neurotox Res. 2020 Mar;37(3):743-752. doi: 10.1007/s12640-020-00170-8. Epub 2020 Jan 29.
A wide variety of ototoxic drugs are capable of damaging the sensory hair cells in the mammalian cochlea resulting in permanent hearing loss. However, the toxic properties of these drugs suggest that some could potentially damage cochlear support cells as well. To test the hypothesis, we treated postnatal day three rat cochlear cultures with toxic doses of gentamicin, cisplatin, mefloquine, and cadmium. Gentamicin primarily destroyed the hair cells and disrupted the intercellular connection with the surrounding support cells. Gentamicin-induced hair cell death was initiated through the caspase-9 intrinsic apoptotic pathway followed by activation of downstream executioner caspase-3. In contrast, cisplatin, mefloquine, and cadmium initially damaged the support cells and only later damaged the hair cells. Support cell death was initiated through the caspase-8 extrinsic apoptotic pathway followed later by downstream activation of caspase-3. Cisplatin, mefloquine, and cadmium significantly reduced the expression of actin and laminin, in the extracellular matrix, leading to significant disarray of the sensory epithelium.
多种耳毒性药物能够损伤哺乳动物耳蜗中的感觉毛细胞,导致永久性听力损失。然而,这些药物的毒性特征表明,它们可能会潜在地损伤耳蜗支持细胞。为了验证这一假说,我们用庆大霉素、顺铂、甲氟喹和镉的毒性剂量处理了出生后 3 天的大鼠耳蜗培养物。庆大霉素主要破坏毛细胞,并破坏与周围支持细胞的细胞间连接。庆大霉素诱导的毛细胞死亡是通过 caspase-9 内在凋亡途径启动的,随后激活下游效应 caspase-3。相比之下,顺铂、甲氟喹和镉最初损伤支持细胞,随后才损伤毛细胞。支持细胞死亡是通过 caspase-8 外在凋亡途径启动的,随后下游激活 caspase-3。顺铂、甲氟喹和镉显著降低了细胞外基质中肌动蛋白和层粘连蛋白的表达,导致感觉上皮显著紊乱。