CORM‑2 reduces cisplatin accumulation in the mouse inner ear and protects against cisplatin-induced ototoxicity

顺铂 耳毒性 球茎 医学 药理学 化学 癌症研究 内科学 化疗 生物 农学
作者
Ah‐Ra Lyu,Soo Jeong Kim,Min Jung Park,Yong‐Ho Park
出处
期刊:Journal of Advanced Research [Elsevier]
被引量:2
标识
DOI:10.1016/j.jare.2023.11.020
摘要

Cisplatin is a life-saving anticancer compound used to treat multiple solid malignant tumors, while it causes permanent hearing loss. There is no known cure, and the FDA has not approved any preventative treatment for cisplatin-based ototoxicity.This study investigated whether the carbon monoxide (CO)-releasing tricarbonyldichlororuthenium (II) dimer, CORM-2, reverses cisplatin-induced hearing impairment and reduces cisplatin accumulation in the mouse inner ear.Male 6-week-old BALB/c mice were randomly assigned to one of the following groups: control (saline-treated, i.p.), CORM-2 only (30 mg/kg, i.p., four doses), cisplatin only (20 mg/kg, i.p., one dose), and CORM-2 + cisplatin, to determine whether cisplatin-based hearing impairment was alleviated by CORM-2 treatment.Our results revealed CORM-2 significantly attenuated cisplatin-induced hearing loss in young adult mice. CORM-2 co-treatment significantly decreased platinum accumulation in the inner ear and activated the plasma membrane repair system of the stria vascularis. Moreover, CORM-2 co-treatment significantly decreased cisplatin-induced inflammation, apoptosis, and cochlear necroptosis. Because the stria vascularis is the likely cochlear entry point of cisplatin, we next focused on the microvasculature. Cisplatin induced increased extravasation of a chromatic tracer (fluorescein isothiocyanate [FITC]-dextran, MW 75 kDa) around the cochlear microvessels at 4 days post-treatment; this extravasation was completely inhibited by CORM-2 co-therapy. CORM-2 co-treatment effectively maintained the integrity of stria vascularis components including endothelial cells, pericytes, and perivascular-resident macrophage-type melanocytes.CORM-2 co-therapy substantially protects against cisplatin-induced ototoxicity by reducing platinum accumulation and toxic cellular stress responses. These data indicate that CORM-2 co-treatment may be translated into clinical strategy to reduce cisplatin-induced hearing loss.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
yx发布了新的文献求助10
1秒前
奋斗靖仇发布了新的文献求助10
1秒前
天天发布了新的文献求助10
1秒前
灿灿陈发布了新的文献求助30
1秒前
香蕉觅云应助山野桃饼采纳,获得10
2秒前
2秒前
从容芮应助谜墨采纳,获得30
3秒前
3秒前
3秒前
kaisihs完成签到,获得积分10
4秒前
zcg发布了新的文献求助10
5秒前
5秒前
5秒前
萧布完成签到,获得积分10
6秒前
三柒完成签到,获得积分10
6秒前
耳东完成签到,获得积分10
6秒前
wwhdream完成签到,获得积分10
6秒前
Efei完成签到,获得积分10
6秒前
淇淇发布了新的文献求助10
7秒前
7秒前
memo发布了新的文献求助30
7秒前
Lucas完成签到,获得积分10
8秒前
8秒前
9秒前
失似发布了新的文献求助10
9秒前
李健应助危机的依柔采纳,获得10
10秒前
任性的卿发布了新的文献求助10
10秒前
11秒前
奋斗靖仇完成签到 ,获得积分10
11秒前
慕青应助青山采纳,获得10
11秒前
11秒前
6666666666完成签到,获得积分10
12秒前
zcg完成签到,获得积分20
12秒前
葛辉辉发布了新的文献求助10
12秒前
zhugepengju完成签到,获得积分10
13秒前
怡然雨雪完成签到,获得积分10
14秒前
眯眯眼的篮球完成签到,获得积分10
14秒前
我爱学习完成签到,获得积分10
15秒前
波波啵啵发布了新的文献求助10
15秒前
高分求助中
Exploring Mitochondrial Autophagy Dysregulation in Osteosarcoma: Its Implications for Prognosis and Targeted Therapy 2000
Impact of Mitophagy-Related Genes on the Diagnosis and Development of Esophageal Squamous Cell Carcinoma via Single-Cell RNA-seq Analysis and Machine Learning Algorithms 2000
LNG地下式貯槽指針(JGA指-107) 1000
什么是会话分析 888
QMS18Ed2 | process management. 2nd ed 600
LNG as a marine fuel—Safety and Operational Guidelines - Bunkering 560
Clinical Interviewing, 7th ed 400
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 电极
热门帖子
关注 科研通微信公众号,转发送积分 2942717
求助须知:如何正确求助?哪些是违规求助? 2601799
关于积分的说明 7006084
捐赠科研通 2242961
什么是DOI,文献DOI怎么找? 1190285
版权声明 590292
科研通“疑难数据库(出版商)”最低求助积分说明 582718