TY - JOUR
T1 - Recent Update on the Protective Potentials of Resveratrol against Cisplatin-induced Ototoxicity
T2 - A Systematic Review
AU - Alsaikhan, Fahad
AU - Jasim, Saade Abdalkareem
AU - Margiana, Ria
AU - Opulencia, Maria Jade Catalan
AU - Yasin, Ghulam
AU - Hammid, Ali Thaeer
AU - Nasretdinova, Makhzuna Tahsinovna
AU - Mahdi, Ahmed B.
AU - Farhood, Bagher
AU - Abedi-Firouzjah, Razzagh
AU - Jamialahmadi, Tannaz
AU - Sahebkar, Amirhosein
N1 - Publisher Copyright:
© 2024 Bentham Science Publishers.
PY - 2024
Y1 - 2024
N2 - Introduction: Although cancer treatment with cisplatin is effective, dose-dependent adverse effects such as ototoxicity occurs often, which limits its clinical use. The use of resveratrol may alleviate the cisplatin-induced ototoxic effects. This study is aimed to review the potential otoprotective effects of resveratrol against cisplatin-induced ototoxicity. Method: According to the PRISMA guideline, a systematic search was accomplished to identify all relevant scientific papers on “the role of resveratrol against cisplatin-induced ototoxicity” in different electronic databases up to May 2021. Fifty-five articles were screened based on a pre-defined set of inclusion and exclusion criteria. Eight eligible studies were finally included in the current systematic review. The in-vitro findings revealed that cisplatin administration significantly decreased the HEI-OC1 cell viability compared to the untreated cells; however, resveratrol co-treatment (in a dose-dependent manner) could protect HEI-OC1 cells against cisplatin-induced decrease in cell viability. Results: Furthermore, the in-vivo finding showed a decreased value of DPOAE, and increased values of ABR threshold, ABR-I, ABR-IV, and ABR I-IV interval in cisplatin-treated animals; in contrast, resveratrol co-administration demonstrated an opposite pattern on these parameters. Conclusion: Thus, it can be mentioned that resveratrol co-treatment alleviates cisplatin-induced ototoxicity. Mechanically, resveratrol exerts its otoprotective effects through various mechanisms such as anti-oxidant, anti-apoptosis, and anti-inflammatory.
AB - Introduction: Although cancer treatment with cisplatin is effective, dose-dependent adverse effects such as ototoxicity occurs often, which limits its clinical use. The use of resveratrol may alleviate the cisplatin-induced ototoxic effects. This study is aimed to review the potential otoprotective effects of resveratrol against cisplatin-induced ototoxicity. Method: According to the PRISMA guideline, a systematic search was accomplished to identify all relevant scientific papers on “the role of resveratrol against cisplatin-induced ototoxicity” in different electronic databases up to May 2021. Fifty-five articles were screened based on a pre-defined set of inclusion and exclusion criteria. Eight eligible studies were finally included in the current systematic review. The in-vitro findings revealed that cisplatin administration significantly decreased the HEI-OC1 cell viability compared to the untreated cells; however, resveratrol co-treatment (in a dose-dependent manner) could protect HEI-OC1 cells against cisplatin-induced decrease in cell viability. Results: Furthermore, the in-vivo finding showed a decreased value of DPOAE, and increased values of ABR threshold, ABR-I, ABR-IV, and ABR I-IV interval in cisplatin-treated animals; in contrast, resveratrol co-administration demonstrated an opposite pattern on these parameters. Conclusion: Thus, it can be mentioned that resveratrol co-treatment alleviates cisplatin-induced ototoxicity. Mechanically, resveratrol exerts its otoprotective effects through various mechanisms such as anti-oxidant, anti-apoptosis, and anti-inflammatory.
KW - Neoplasms
KW - anti-inflammatory
KW - anti-oxidant
KW - cisplatin
KW - ototoxicity
KW - resveratrol
UR - http://www.scopus.com/inward/record.url?scp=85198117514&partnerID=8YFLogxK
U2 - 10.2174/0929867331666230724124013
DO - 10.2174/0929867331666230724124013
M3 - Review article
C2 - 37491852
AN - SCOPUS:85198117514
SN - 0929-8673
VL - 31
SP - 4850
EP - 4866
JO - Current Medicinal Chemistry
JF - Current Medicinal Chemistry
IS - 30
ER -