Kim Shin Hye, Jung Gaon, Kim Sangjae, Koo Ja-Won
Department of Otorhinolaryngology-Head and Neck Surgery, Korea University Medical Center, Korea University College of Medicine, Seoul, South Korea.
Department of Otorhinolaryngology-Head and Neck Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, South Korea.
Front Cell Neurosci. 2018 Jan 19;12:3. doi: 10.3389/fncel.2018.00003. eCollection 2018.
The cell-penetrating peptide GV1001 has been investigated as an anticancer agent and recently demonstrated anti-oxidant and anti-inflammatory effects. It has shown a protective effect on a kanamycin (KM)-induced ototoxicity mouse model. In the present study, we administered GV1001 at different time points after inducing hair cell damage, and examined if it rescues hair cell loss and restores hearing. A deaf mouse model was created by intraperitoneal injection of KM and furosemide. First, to test the early temporal change of hearing and extent of hair cell damage after KM and furosemide injection, hearing and outer hair cells (OHCs) morphology were evaluated on day 1, day 2 and day 3 after injection. In the second experiment, following KM and furosemide injection, GV1001, dexamethasone, or saline were given for three consecutive days at different time points: D0 group (days 0, 1, and 2), D1 group (days 1, 2, and 3), D3 group (days 3, 4, and 5) and D7 group (days 7, 8, and 9). The hearing thresholds were measured at 8, 16, and 32 kHz before ototoxic insult, and 7 days and 14 days after KM and furosemide injection. After 14 days, each turn of the cochlea was imaged to evaluate OHCs damage. GV1001-treated mice showed significantly less hearing loss and OHCs damage than the saline control group in the D0, D1 and D3 groups ( < 0.0167). However, there was no hearing restoration or intact hair cell in the D7 group. GV1001 protected against cochlear hair cell damage, and furthermore, delayed administration of GV1001 up to 3 days rescued hair cell damage and hearing loss in KM/furosemide-induced deaf mouse model.
细胞穿透肽GV1001已作为一种抗癌药物进行研究,最近还显示出抗氧化和抗炎作用。它对卡那霉素(KM)诱导的耳毒性小鼠模型具有保护作用。在本研究中,我们在诱导毛细胞损伤后的不同时间点给予GV1001,并检查它是否能挽救毛细胞损失并恢复听力。通过腹腔注射KM和速尿建立耳聋小鼠模型。首先,为了测试注射KM和速尿后听力的早期时间变化以及毛细胞损伤程度,在注射后的第1天、第2天和第3天评估听力和外毛细胞(OHC)形态。在第二个实验中,注射KM和速尿后,在不同时间点连续三天给予GV1001、地塞米松或生理盐水:D0组(第0、1和2天)、D1组(第1、2和3天)、D3组(第3、4和5天)和D7组(第7、8和9天)。在耳毒性损伤前以及注射KM和速尿后7天和14天测量8、16和32kHz的听力阈值。14天后,对耳蜗的每一旋进行成像以评估OHC损伤。在D0、D1和D3组中,GV1001治疗的小鼠听力损失和OHC损伤明显少于生理盐水对照组(<0.0167)。然而,D7组没有听力恢复或完整的毛细胞。GV1001可防止耳蜗毛细胞损伤,此外,在KM/速尿诱导的耳聋小鼠模型中,将GV1001的给药延迟至3天可挽救毛细胞损伤和听力损失。