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Review Article

Hepatoprotective properties of extensively studied medicinal plant active constituents: Possible common mechanisms

, &
Pages 781-791 | Received 04 Apr 2014, Accepted 25 Jul 2014, Published online: 09 Dec 2014

Figures & data

Table 1. Most frequently studied hepatoprotective phytochemicals.

Figure 1. Common in vivo models of liver damage.

Figure 1. Common in vivo models of liver damage.

Figure 2. The most important multiple pathways in the liver pathobiology that can be interrupted at one or more levels by hepatoprotective plant constituents (not shown) to interfere with oxidative stress. ACC, acetyl-CoA carboxylase; AMPK, adenosine-5′-monophosphate-activated protein kinase; ATP, adenosine triphosphate; Bax, proapoptotic protein of Bcl-2 family; BSEP, bile salt export pump; CAT, catalase; CO, carbon monoxide; COX-2, inducible cyclooxygenase; CYP, cytochrome P450; eCa2+, extracellular calcium; ECM, extracellular matrix; eNOS (NOS-1), endothelial nitric oxide synthase; ER, endoplasmic reticulum; GPx, glutathione peroxidase; GSH, reduced glutathione; GST, glutathione-S-transferase; HO-1, inducible heme oxygenase; IL, interleukin; iCa2+, intracellular calcium; iNOS (NOS-2), inducible nitric oxide synthase; MDR3, multidrug resistance protein 3; MRP2, multidrug resistance-related protein 2; NO, nitric oxide; NF-κB, nuclear factor kappa-B; NRS, nitrogen reactive species; ONOO−, peroxynitrite anion; p53, protein p53; PPAR-α/γ, peroxisome proliferator-activated receptor-α/γ; ROS, reactive oxygen species; SIRT1, silent information regulator T1; SOD, superoxide dismutase; TGF-β, transforming growth factor-β; TNF-α, tumor necrosis factor-α, VCAM-1, vascular cell adhesion molecule-1.

Figure 2. The most important multiple pathways in the liver pathobiology that can be interrupted at one or more levels by hepatoprotective plant constituents (not shown) to interfere with oxidative stress. ACC, acetyl-CoA carboxylase; AMPK, adenosine-5′-monophosphate-activated protein kinase; ATP, adenosine triphosphate; Bax, proapoptotic protein of Bcl-2 family; BSEP, bile salt export pump; CAT, catalase; CO, carbon monoxide; COX-2, inducible cyclooxygenase; CYP, cytochrome P450; eCa2+, extracellular calcium; ECM, extracellular matrix; eNOS (NOS-1), endothelial nitric oxide synthase; ER, endoplasmic reticulum; GPx, glutathione peroxidase; GSH, reduced glutathione; GST, glutathione-S-transferase; HO-1, inducible heme oxygenase; IL, interleukin; iCa2+, intracellular calcium; iNOS (NOS-2), inducible nitric oxide synthase; MDR3, multidrug resistance protein 3; MRP2, multidrug resistance-related protein 2; NO, nitric oxide; NF-κB, nuclear factor kappa-B; NRS, nitrogen reactive species; ONOO−, peroxynitrite anion; p53, protein p53; PPAR-α/γ, peroxisome proliferator-activated receptor-α/γ; ROS, reactive oxygen species; SIRT1, silent information regulator T1; SOD, superoxide dismutase; TGF-β, transforming growth factor-β; TNF-α, tumor necrosis factor-α, VCAM-1, vascular cell adhesion molecule-1.

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