Red Ginger Extract Prevents the Development of Oxaliplatin-Induced Neuropathic Pain by Inhibiting the Spinal Noradrenergic System in Mice.
Keun-Tae ParkHeejoon JoBonlgee KimWoojin KimPublished in: Biomedicines (2023)
Oxaliplatin is a well-known chemotherapeutic drug that is widely used to treat colorectal cancer. However, it can induce acute side effects in up to 90% of patients. Serotonin and norepinephrine reuptake inhibitors (SNRIs) are used as first-choice drugs; however, even SNRIs are known to be effective only in treatment and not for prevention. Therefore, finding a drug that can prevent the development of cold and mechanical forms of allodynia induced by oxaliplatin is needed. This study demonstrated that multiple oral administrations of 100 mg/kg and 300 mg/kg of red ginger extract could significantly prevent pain development in mice. The role of the noradrenergic system was investigated as an underlying mechanism of action. Both the spinal α1- and α2-adrenergic receptors were significantly downregulated after treatment. Furthermore, the noradrenaline levels in the serum and spinal cord were upregulated and downregulated after treatment with paclitaxel and red ginger, respectively. As the active sub-component of red ginger, ginsenoside Rg3 (Rg3) was identified and quantified using HPLC. Moreover, multiple intraperitoneal injections of Rg3 prevented the development of pain in paclitaxel-treated mice, suggesting that RG3 may induce the effect of red ginger extract.
Keyphrases
- neuropathic pain
- spinal cord
- spinal cord injury
- drug induced
- end stage renal disease
- oxidative stress
- high fat diet induced
- pain management
- chronic kidney disease
- newly diagnosed
- emergency department
- ejection fraction
- metabolic syndrome
- liver failure
- intensive care unit
- combination therapy
- acute respiratory distress syndrome
- peritoneal dialysis
- mouse model
- adipose tissue
- smoking cessation
- mass spectrometry
- high performance liquid chromatography
- decision making
- patient reported outcomes
- platelet rich plasma
- patient reported