Ginger Polyphenols Reverse Molecular Signature of Amygdala Neuroimmune Signaling and Modulate Microbiome in Male Rats with Neuropathic Pain: Evidence for Microbiota-Gut-Brain Axis.
Chwan-Li ShenJulianna Maria SantosMoamen M ElmassryViren BhaktaZarek DriverGuangchen JiVadim YakhnitsaTakaki KiritoshiJacob LovettAbdul Naji HamoodShengmin SangVolker NeugebauerPublished in: Antioxidants (Basel, Switzerland) (2024)
Emerging evidence shows that the gut microbiota plays an important role in neuropathic pain (NP) via the gut-brain axis. Male rats were divided into sham, spinal nerve ligation (SNL), SNL + 200 mg GEG/kg BW (GEG200), and SNL + 600 mg GEG/kg BW (GEG600) for 5 weeks. The dosages of 200 and 600 mg GEG/kg BW for rats correspond to 45 g and 135 g raw ginger for human daily consumption, respectively. Both GEG groups mitigated SNL-induced NP behavior. GEG-supplemented animals had a decreased abundance of Rikenella , Muribaculaceae , Clostridia UCG-014 , Mucispirillum schaedleri , RF39 , Acetatifactor , and Clostridia UCG-009 , while they had an increased abundance of Flavonifactor , Hungatella , Anaerofustis stercorihominis , and Clostridium innocuum group. Relative to sham rats, Fos and Gadd45g genes were upregulated, while Igf1 , Ccl2 , Hadc2 , Rtn4rl1 , Nfkb2 , Gpr84 , Pik3cg , and Abcc8 genes were downregulated in SNL rats. Compared to the SNL group, the GEG200 group and GEG600 group had increases/decreases in 16 (10/6) genes and 11 (1/10) genes, respectively. GEG downregulated Fos and Gadd45g genes and upregulated Hdac2 genes in the amygdala. In summary, GEG alleviates NP by modulating the gut microbiome and reversing a molecular neuroimmune signature.
Keyphrases
- neuropathic pain
- genome wide
- spinal cord
- spinal cord injury
- bioinformatics analysis
- genome wide identification
- endothelial cells
- resting state
- genome wide analysis
- physical activity
- blood brain barrier
- multiple sclerosis
- high glucose
- stress induced
- drug induced
- preterm birth
- subarachnoid hemorrhage
- mouse model
- liver injury
- prefrontal cortex
- induced pluripotent stem cells