Related Experiment Video
Updated: Mar 9, 2026

09:52
Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
10.0K
Curcumin: A potentially powerful tool to reverse cisplatin-induced toxicity
Ramin Rezaee1, Amir Abbas Momtazi2, Alireza Monemi3
1Department of Physiology and Pharmacology, School of Medicine, North Khorasan University of Medical Sciences, Bojnurd, Iran.
Pharmacological Research
|January 3, 2017
Summary
Curcumin may protect against cisplatin
Area of Science:
- Natural Products Chemistry
- Pharmacology
- Oncology
Background:
- Curcumin, derived from Curcuma longa, offers health benefits.
- Cisplatin chemotherapy causes adverse effects and resistance.
- Cisplatin toxicity includes ototoxicity, nephrotoxicity, and neurotoxicity.
Purpose of the Study:
- To review curcumin's protective role against cisplatin toxicity.
- To summarize evidence on curcumin combating cisplatin resistance.
Main Methods:
- Literature review of preclinical and clinical studies.
- Analysis of research on curcumin's mechanisms of action.
- Synthesis of data on curcumin's efficacy and safety.
Main Results:
- Curcumin demonstrates protective effects against cisplatin-induced side effects.
- Curcumin shows potential in overcoming cisplatin resistance in cancer cells.
- Studies highlight curcumin's ability to mitigate ototoxicity, nephrotoxicity, and neurotoxicity.
Conclusions:
- Curcumin is a promising agent to reduce cisplatin's adverse effects.
- Curcumin may enhance cisplatin efficacy by overcoming resistance.
- Further research is warranted to explore clinical applications of curcumin in cancer therapy.
Related Concept Videos
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists
701
Neurokinin 1 (NK1) receptors are distributed across the GI tract, vagal afferents, and key CNS regions including the central vomiting center and chemoreceptor trigger zone (CTZ) Chemotherapy agents stimulate enterochromaffin cells in the gastrointestinal (GI) tract to release large amounts of substance P (SP). SP is a neuropeptide released by specific sensory nerves in response to many different stressors, including those in the GI mucosa affected by chemotherapy. SP binds and activates...
701
Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists
755
5-HT3 receptor antagonists, such as dolasetron, granisetron (Kytril), ondansetron (Zofran), and palonosetron (Axoli), are crucial in managing chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea. These drugs selectively block 5-HT3 receptors in the visceral vagal and spinal afferent nerves, chemoreceptor trigger zone, and the vomiting center. They have a rapid onset of action and can be given as a single dose before chemotherapy. Ondansetron and granisetron, in particular,...
755
Chemotherapy-Induced Nausea and Vomiting: Cannabinoids
875
Tetrahydrocannabinol (THC) is a phytocannabinoid that primarily interacts with the CB1 receptor, a type of G protein-coupled receptor (GPCR) predominantly in and around the chemoreceptor trigger zone (CTZ) and emetic center. THC also blocks the serotonin receptor activity in the dorsal vagal complex (DVC) by inhibiting serotonin release. THC exerts its anti-emetic effects through these interactions, which are beneficial for patients undergoing chemotherapy.
Two synthetic agonists of THC,...
Two synthetic agonists of THC,...
875

