Table 1.
Liver Injury | |||
---|---|---|---|
Model | Prebiotic or Probiotic Species/Treatments | Effect | Reference |
C57BL/6 mice. Obesity and NAFLD induced by HFD |
|
↓TNF-α ↓SREBP-1c ↑PPAR-α ↑A. muciniphila |
[34] |
Wistar rats. Fibrosis induced by TAA |
|
↓TNF-α ↓TGF-β ↓α-SMA ↓ALT, AST, AP |
[55] |
Sprague Dawley rats. Acute liver injury induced by D-galactosamine |
|
↓GGTP ↓TBA ↓G-CSF ↓RANTES ↓IL-5 ↑IL-10 |
[56] |
Patients with NAFLD |
|
↓ALT, AST, GGTP, AP ↓TG, TC, LDL |
[57] |
Patients with NAFLD |
|
↓ALT, GGTP ↓TNF-α ↓NF-κB |
[58] |
Patients with NASH |
|
↓AST ↓TNF-α ↓LDL-C ↓CRP ↓Serum endotoxin Insulin resistance, steatosis, and NASH activity index were improved |
[59] |
Wistar rats. Acute liver injury induced by acetaminophen |
|
↓AST, ALT ↓TNF-α, ↓IL-1β ↓Necrosis Antioxidant capacity |
[60] |
Zucker-Lepr fa/fa rats (NAFLD). |
|
↓MDA, MPO ↓Hepatic lipids ↓TNF-α, IL-6, LPS ↑IgA |
[61] |
Colitis | |||
C57BL/6 mice. Colitis-associated cancer induced by azoxymethane and DSS |
|
Fewer and smaller tumors than the control Attenuation of intestinal inflammation ↑INF-γ ↓TNF-α ↓IL-1β, IL-23, IL-17, IL-6 |
[62] |
BALB/c mice. Colitis induced by DSS |
|
↑ Abundance and diversity of gut microbiota ↑Hemoglobin content ↓MPO ↓TNF-α ↓IL-1β, IL-6 ↑IL-10 |
[63] |
C57BL/6 mice. Colitis induced by DSS |
|
↑Abundance and diversity of gut microbiota ↓Abundance of potentially harmful bacteria ↓TNF-α ↓IL-1β, IL-6 ↑IL-10 Regulated expression of T-bet |
[64] |
C57BL/6 mice. Colitis induced by DSS |
|
Attenuation of intestinal inflammation Balance of intestinal microbiota |
[65] |
C57BL/6J mice. Colitis induced by DSS |
|
↓TNF-α ↓IL-1β, IL-6 ↑IL-10 ↑Firmicutes ↓STAT3 |
[66] |
C57BL/6 mice. Colitis induced by DSS |
|
↓TNF-α ↓IL-1β, IL-6 ↓IL-17 ↑IL-10 ↑Foxp3 ↓α-SMA ↓MCP-1 in HT-29 cells |
[67] |
Diabetes/Obesity/Hyperlipidemia | |||
Wistar rats. Diabetes (type 2) induced by HFD and STZ |
|
Glucose levels restored Prevention against hyperlipidemia Improved glucose tolerance |
[68] |
Sprague-Dawley rats. Diabetes (type 2) induced by HFD and STZ |
|
↓HbA1C, fasting blood glucose Glucose tolerance and insulin resistance improved ↓TC, LDL-C ↓LPS ↓TNF-α ↑IL-10 ↓ALT and AST IRS-2/PI3K/Akt-2 signal Pathway improved ↓PEPCK, G6Pase |
[69] |
Diabetic (type 2) female patients. |
|
↓Fasting serum glucose ↓HbA1C ↓ALT, AST, AP Reductions in systolic and diastolic blood pressure |
[70] |
Diabetic (type 2) patients. |
|
Insulin resistance improved ↓IL-1β, IL-6, IL-8 ↓TNF-α |
[71] |
C57BL/6 JRj mice. Obesity-induced by HFD |
|
↑PPAR-γ ↑Lipoprotein lipase ↑GLP-1 ↑IL-10 ↓Lipids accumulation in adipocytes Restored gut barrier Limited body weight gain |
[72] |
Wistar rats. Obesity and insulin resistance induced by HFD |
|
↓Plasma insulin ↓TC ↓LDL-C Insulin resistance improved Bodyweight and visceral fat weight reduced ↓BP and MAP ↓Oxidative stress |
[73] |
Sprague Dawley rats. Hyperlipidemia induced by HFD |
|
↓TC, VLDL-C, LDL-C ↓TG ↓TBA ↓SREBP-1c ↓ChREBP ↑PPAR-α ↓CYP7A1 |
[74] |
Please see the glossary for abbreviations; ↓ (decrease), ↑ (increase).