TABLE 2.
The major effects of natural products in vitro and in vivo models of SLE.
| Nature products | Animal/Cell model/SLE population | Dose | Duration | Therapeutic effects | Ref |
|---|---|---|---|---|---|
| CUR | MRL/lpr mice | 200 mg/kg | 8 weeks | Reduced proteinuria, renal inflammation, serum anti-ds DNA and spleen size | Zhao et al. (2019) |
| PBMCs | 0.1 μg/ml | 48 h | Inhibite the expression and activation of PYK2 in PBMCs from LN patients rather than healthy subjects | Wang et al. (2017) | |
| NZB/W F1 mice | 500 mg/kg | 14 days | Reduced spleen weight and renal injury at 26 weeks of age. Reduced renal injury at 32 weeks of age | Dent et al. (2020) | |
| SLE patients with relapsing or refractory course classified according to ISN/RPS | 3 capsules (contained 500 mg turmeric, of which 22.1 mg was the active ingredient curcumin) daily | 3 months | Significant decrease in proteinuria, systolic blood pressure and hematuria in post-turmeric supplementation | Khajehdehi et al. (2012) | |
| SLE patients with SLEDAI >3 and 25(OH)D level <30 ng/ml | 60 mg daily | 3 months | No significant differences in SLEDAI reduction, decreased serum levels of IL-6, and increased levels of TGF-𝛽1 serum among groups after the treatment | Singgih Wahono et al. (2017) | |
| OL | BALB/c mice | 100 mg/kg | 24 weeks | Reduced renal damage and decreased serum matrix metalloproteinase 3 and prostaglandine E2 kidneys levels | Castejon et al. (2019) |
| PCG | NZB/W F1 mice | 1 and 3 mg/kg | 7 weeks | Alleviate kidney injury and splenomegaly and reduce proteinuria and renal ICAM-1 and VCAM-1 expression | Seo et al. (2020) |
| SFN | MRL/lpr mice | 12.5 mg/kg | 28 weeks | Ameliorate renal function | Jiang et al. (2014) |
| MRL/lpr mice | 82.9 μmol/kg | 27 days | Decrease the percentages of plasma cells, Tfh cells, neutrophils, and dendritic cells | Du et al. (2022) | |
| ICA | MLR/lpr mice | 10 mg/kg | 8 weeks | Decreased serum anti-ds DNA antibody, immune complex and renal disease | Su et al. (2018) |
| API | SNF1 mice | 3,6,20 mg/kg | 8 weeks | Suppressed and promoted apoptosis of the APCs, T and B cells | Kang et al. (2009) |
| RES | PIL mice | 50,75 mg/kg | 7 months | Attenuated glomerulonephritis, proteinuria and immunoglobulin deposition | Wang et al. (2014) |
| MRL/lpr mice | 20 mg/kg | 6 weeks | Reduced serum autoantibodies, relieved lupus nephritis and disease onset, and prolonged survival | Jhou et al. (2017) | |
| ApoE Fas mice | 0.01% in water | 10 weeks | Exerted fewer atherosclerotic plaques | Voloshyna et al. (2016) | |
| BALB/c mice | 25 mg/kg and 50 mg/kg with its bio-enhancer piperine | 4 months | Mitigated renal manifestations | Pannu and Bhatnagar (2020) | |
| MRL/Mp-Faslpr mice | 0.01% in ethanol | 10 weeks | Increased mRNA levels of SIRT1, decreased vascular endothelial growth factor and CX3CL1 mRNA in the hippocampus | Kasselman et al. (2022) |
Abbreviations: SLE: systemic lupus erythematosus; CUR: curcumin; OL: oleuropein; PCG: punicalagin; SFN: sulforaphane; ICA: icariin; API: apigenin; RES: resveratrol; PBMCs: peripheral blood mononuclear cells; PYK2: Proline-rich tyrosine kinase 2; LN: lupus nephritis; ICAM: intercellular adhesion molecule 1; VCAM: vascular cell adhesion molecule 1; Tfh: T follicular helper; APC: antigen-presenting cells; ISN/RPS: The International Society of Nephrology/Renal Pathology Society; SLEDAI: systemic lupus erythematosus disease activity index; SIRT: sirtuin.