Omeprazole Suppresses Oxaliplatin-Induced Peripheral Neuropathy in a Rodent Model and Clinical Database.
Keisuke MineTakehiro KawashiriMizuki InoueDaisuke KobayashiKohei MoriShiori HiromotoHibiki KudamatsuMayako UchidaNobuaki EgashiraSatoru KoyanagiShigehiro OhdoTakao ShimazoePublished in: International journal of molecular sciences (2022)
(1) Background: Oxaliplatin is used as first-line chemotherapy not only for colorectal cancer but also for gastric and pancreatic cancers. However, it induces peripheral neuropathy with high frequency as an adverse event, and there is no effective preventive or therapeutic method. (2) Methods: The effects of omeprazole, a proton pump inhibitor (PPI), on oxaliplatin-induced peripheral neuropathy (OIPN) was investigated using an in vivo model and a real-world database. (3) Results: In a rat model, oxaliplatin (4 mg/kg, i.p., twice a week for 4 weeks) caused mechanical hypersensitivity accompanied by sciatic nerve axonal degeneration and myelin sheath disorder. Repeated injection of omeprazole (5-20 mg/kg, i.p., five times per week for 4 weeks) ameliorated these behavioral and pathological abnormalities. Moreover, omeprazole did not affect the tumor growth inhibition of oxaliplatin in tumor bearing mice. Furthermore, clinical database analysis of the Food and Drug Administration Adverse Event Reporting System (FAERS) suggests that the group using omeprazole has a lower reporting rate of peripheral neuropathy of oxaliplatin-treated patients than the group not using (3.06% vs. 6.48%, p < 0.001, reporting odds ratio 0.44, 95% confidence interval 0.32-0.61). (4) Conclusions: These results show the preventing effect of omeprazole on OIPN.
Keyphrases
- adverse drug
- high frequency
- drug induced
- end stage renal disease
- newly diagnosed
- transcranial magnetic stimulation
- chronic kidney disease
- high glucose
- drug administration
- emergency department
- ejection fraction
- diabetic rats
- spinal cord injury
- electronic health record
- prognostic factors
- signaling pathway
- risk assessment
- multiple sclerosis
- small molecule
- metabolic syndrome
- endothelial cells
- mass spectrometry
- gestational age
- ultrasound guided
- skeletal muscle
- study protocol
- young adults
- patient reported outcomes