Table 5.
In vivo effects of ginger phenolics in animal models of autoinflammatory and autoimmune diseases.
| Compounds | Models | Administration routes | Observed effects | Potential mechanisms | Ref. |
|---|---|---|---|---|---|
| 6-, 8-, and 10-gingerols | DSS-induced rat colitis model | intraperitoneal | • attenuated DSS-induced symptoms of colitis • accelerated mucosal damage healing • decreased neutrophil infiltration in the colon • reduced TNF and IL-1β serum levels |
• increased SOD activity • decreased MPO activity |
(67) |
| 6-gingerol | DSS-induced mouse colitis model | oral | • decreased DSS-induced weight loss • decreased IL-17 levels and increased IL-10 levels both in serum and bowel tissue |
• inhibited IκB phosphorylation • suppressed NF-κB nuclear translocation in the bowel tissue |
(68) |
| 6-shogaol | DSS-induced mouse colitis model | oral | • alleviated colitis symptoms • accelerated wound repair • decreased the levels of TNF, IL-6, IL-1β and iNOS |
• increased HO-1 and NRF2 expression in the colon tissues | (69) |
| 6-, 8-, 10-gingerols and 6-, 8-, 10-shogaols | DSS-induced mouse colitis model | oral | • prevent DSS-induced weight loss, colon length reduction • reduced IL-1β, IL-6 and IFN-γ serum levels • downregulated iNOS and COX-2 levels |
• reduced NF-κB phosphorylation | (70) |
| 6-gingerol | EAE mice | intraperitoneal | • decreased inflammatory cell infiltration and demyelination in spinal cord and CNS • lowered number of inflammatory cells in the spleen • inhibited Th17 polarization |
– | (53) |
| 6-shogaol, 6-paradol | EAE mice | oral | • decreased demyelination, cell accumulation and TNF expression in spinal cord • reduced astrogliosis and microglial activation |
– | (72) |
| 6-gingerol | lupus and APS mouse model | intraperitoneal | • reduced serum level of anti-dsDNA, cell-free DNA, MPO-DNA complexes, TNF, IFN-γ • suppressed netosis • inhibited thrombosis in APS |
– | (47) |
| 8-shogaol | AIA rats | intraperitoneal | • reduced paw thickness and weight loss • improved walking • decreased bone erosion and cellular infiltration to the joints • reduced TNF, IL-6 and IL-8 levels in serum and synovial tissues |
– | (76) |