BioMed Research International

Volume 2014 (2014), Article ID 872139, 15 pages

http://dx.doi.org/10.1155/2014/872139

Review Article

Glycyrrhizic Acid in the Treatment of Liver Diseases: Literature Review

Jian-yuan Li,1,2 Hong-yan Cao,1,2 Ping Liu,1,2 Gen-hong Cheng,³ and Ming-yu Sun1,2,3

¹Key Laboratory of Liver and Kidney Diseases, Institute of Liver Diseases, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 528 Zhangheng Road, Pudong New District, Shanghai 201203, China

²Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China

³Department of Microbiology, Immunology & Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA

Received 28 February 2014; Revised 11 April 2014; Accepted 11 April 2014; Published 13 May 2014

Academic Editor: Kota V. Ramana

Copyright © 2014 Jian-yuan Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Glycyrrhizic acid (GA) is a triterpene glycoside found in the roots of licorice plants (Glycyrrhiza glabra). GA is the most important active ingredient in the licorice root, and possesses a wide range of pharmacological and biological activities. GA coupled with glycyrrhetinic acid and 18-beta-glycyrrhetic acid was developed in China or Japan as an anti-inflammatory, antiviral, and antiallergic drug for liver disease. This review summarizes the current biological activities of GA and its medical applications in liver diseases. The pharmacological actions of GA include inhibition of hepatic apoptosis and necrosis; anti-inflammatory and immune regulatory actions; antiviral effects; and antitumor effects. This paper will be a useful reference for physicians and biologists researching GA and will open the door to novel agents in drug discovery and development from Chinese herbs. With additional research, GA may be more widely used in the treatment of liver diseases or other conditions.

1. Introduction

The application of natural compounds in the treatment of refractory diseases is a new trend in modern clinical medicine. Because of their satisfactory efficacy in clinic and low toxicity, more natural products are being used as alternative treatments for many diseases. Many hepatoprotective monomers are derived from natural herbs, especially those from China. Glycyrrhizic acid (GA) is an example of one of these hepatoprotective compounds.

The traditional Chinese medicine Gancao (licorice root) is the dried roots of Glycyrrhiza uralensis Fisch (licorice), G. inflata Bat., or G. glabra L. Gancao which was first described in the Chinese book “Shen Nong Ben Cao Jing” in 200 A.D. as an antidote to toxic substances, ache, and other diseases. Gancao can complement other drugs to reduce toxicity and increase efficacy. The traditional use of Gancao involves a decoction of dried plant roots and stems. Some of the possible therapeutic properties of Gancao include antiarthritic [1], antiallergic [2], antiviral [3], antihepatotoxic [4], anticholinergic [5], antiestrogenic [6], anti-inflammatory [6], antileukemogenic [7], and anticarcinogenic effects [8]. It is commonly used for the treatment of acute and chronic liver injury, viral hepatitis, hepatic steatosis, liver fibrosis, hepatoma, viral myocarditis [9], and other diseases like psoriasis [10] or prostate cancer [11].

The known chemical components of Gancao include saponins (mainly glycyrrhizin (GA), 3.63–13.06%), flavonoids (1.5%), coumarin, alkaloids, polysaccharides, sitosterol, and amino acids [12]. GA (Figure 1) and glycyrrhetinic acid (Figure 2) are well-characterized components of Gancao. GA has been developed as a hepatoprotective drug in China and Japan. GA can generate glycyrrhetinic acid through metabolic processes in the human body. Therefore, the pharmacological effects of GA are essentially the same as glycyrrhetinic acid [13]. GA, also called glycyrrhizin, is a triterpene glycoside from licorice root (Glycyrrhiza glabra) and consists of one molecule of 18-glycyrrhetinic acid and two molecules of glucuronic acid (18-glycyrrhetinic acid-3-O--D-glucuronopyranosyl-()-beta-D-glucuronide) [14, 15]. Glycyrrhizin is considered to be the major active component of Gancao as demonstrated by studies with experimental animal models [16] and clinical studies [17]. GA has been used clinically for more than 20 years in patients with chronic hepatitis in China and Japan [18] and shows a satisfactory therapeutic effect in many other diseases. GA is also widely used as a sweetening and flavoring agent in food.

Figure 1: Chemical structure of glycyrrhizin (GA) and its derivatives.

Figure 2: Chemical structure of glycyrrhetinic acid.

GA is a main substance of licorice, which is one of the most important substances utilized as traditional medicine for almost 2000 years. Moreover, GA was reported to have antiallergic, antiviral, and anti-inflammatory activities. GA was also found to suppress the rise in fasting blood glucose and insulin levels and improve glucose tolerance. Additionally, GA may act as an antidiabetic substance without inducing side effects, although the mechanism is unclear [19].

GA can form two epimers: -GA and -GA (Figure 3). -GA is derived from -GA by isomerization, and the - and -forms differ only in their –H–, trans-, and cis-configuration, respectively. Some scholars examined their distribution characteristics in rat tissue and found that the concentrations of -GA in the liver and duodenum were significantly higher than those of -GA after i.v. administration. However, the concentrations of -GA in the other tissues were lower than or similar to those of -GA and declined rapidly. This indicates that the protective and anti-inflammatory effects of -GA on the liver may be better than those of -GA [20].

Figure 3: Chemical structure of 18-glycyrrhetinic acid and 18-glycyrrhetinic acid.

Several clinical studies reported that GA was efficacious in the treatment of various types of inflammation (mainly in liver [21–30] (Table 1), but also in lung, kidney, intestine, and spinal cord [31]). The most common use of GA is in the treatment of liver disease [32]. GA can reduce steatosis and necrosis of liver cells significantly [33] to inhibit the inter-interstitial inflammation and liver fibrosis and promote cell regeneration. GA has few side effects and is therefore considered to be a drug worth attention and promotion for liver disease.

Table 1: Clinical trials using compound glycyrrhizic acid injection.

Experimental drugs
Dose and course of treatment
Combined medication
Case/control
Disease type
Indications and symptoms
Efficacy
Positive control
Side effect
Reference

Glycyrrhizin
200 mg + NaCl

100 mL, i.v., q.d., 4 weeks
Prednisolone

(20–60 mg)
31/14
Acute onset autoimmune hepatitis (AIH)
Fever, general malaise, fatigue, nausea, vomiting, and right upper quadrant discomfort
Recovery rate was higher in the SNMC group than in the SNMC + CS group ()
Glycyrrhizin and corticosteroids (CS)
None
[21]

Glycyrrhizin
200 mg, i.v., q.d., 52 weeks
None
374/129
Chronic hepatitis C
Inflammatory effect
The proportion of patients with ALT reduction ≥50% after 12 weeks was significantly higher with 5×/week glycyrrhizin (28.7%, ) and 3×/week glycyrrhizin (29.0%, ) compared with placebo (7.0%).
Placebo-controlled
None
[22]

Glycyrrhizin
200 mg + NaCl

100 mL, i.v., 6c/week, 4 weeks
None
69/13
Chronic hepatitis C
HCV and HCV-RNA positive;

serum ALT at least 1.5 times;

liver fibrosis or cirrhosis
The mean percentage ALT decrease from baseline at the end of treatment was 26% and 47% for the three times per week and six times per week treatment group, respectively (both versus placebo)
Placebo-controlled
None
[23]

Glycyrrhizin
200 mg + NaCl

100 mL, i.v., q.d. for 8 weeks, then 2–7c/week for 2–16 years
None
453/109
Hepatocellular carcinoma (HCC) occurs in patients with hepatitis C virus-RNA positive chronic liver disease
Inflammatory effect after HCC
Patients treated with SNMC; the 10-year HCC appearance rates in histologic Stages I, II, and III were 3%, and 13%, respectively
Other herbal medicines
None
[24]

Glycyrrhizin
200 mg + NaCl

100 mL, i.v., q.d., 0.1–14.5 years
None
1249/796
Interferon-resistant hepatitis C
Chronic hepatitis effect
Crude carcinogenesis rates in the treated and untreated group were 13.3%, 26.0% at the fifth year and 21.5% and 35.5% at the 10th year, respectively ()
Others without glycyrrhizin therapy
Hypertension skin rash without itching
[25]

Diammonium glycyrrhizinate
150 mg + 5–10% glucose injection liquid 250 mL, i.v., q.d., 1 month, 1-2 cycles
None
629/127
Chronic hepatitis, liver cirrhosis
Fatigue, gastrointestinal symptoms, and discomfort in liver area
After 17-day therapy, there are 93.3% patients with ALT normal level in treating group, but 73.3% in contrast group (). At day 10, the patient’srecovered normal SB were 86.7% in treatment group, but that was 40% in contrast group ()
Compound ammonium glycyrrhetate injection
Headache, facial edema, and blood pressure increased
[26]

-glycyrrhetinic acid
80 mg + 10% glucose injection liquid 250 mL, i.v., q.d., 4 weeks, 100 mg, p.o. tid, 12 weeks
None
80/40
Chronic Hepatitis B
Chronic hepatitis effect
Compared with control group, the TBil, ALT, AST, HA, and IVC are significantly ameliorated in treatment group ()
-glycyrrhizic acid
Edema, blood pressure increased, and serum potassium mildly low
[27]

Magnesium isoglycyrrhizinate
80 mg + 10% glucose injection liquid 250 mL, i.v., q.d., 4 weeks
Hepatoprotective drugs
80/40
Chronic Hepatitis B
Fatigue, gastrointestinal symptoms, and discomfort in liver area
Compared with control group, the TBil, ALT, AST are significantly ameliorated in treatment group ()
Diammonium glycyrrhizinate injection
Headache,and blood pressure increased
[28]

Magnesium isoglycyrrhizinate
150 mg + 5–10% glucose injection liquid 250 mL, i.v., q.d., 4 weeks
None
60/30
Chronic severe hepatitis
Fatigue, gastrointestinal symptoms, discomfort in liver area, and yellow urine
Compared with control group, the TBil, PTA, ALT, and AST are significantly ameliorated in treatment group ()
Hepatocyte generation drugs
None
[29]

Magnesium isoglycyrrhizinate
150 mg + 5–10% glucose injection liquid 250 mL, i.v., q.d., 2 weeks
None
56/28
Liver lesion induced by chemotherapy in cancer
Liver injury effect
Compared with control group, the TBil, PTA, ALT, and AST are significantly ameliorated in treatment group ()
Diammonium glycyrrhizinate injection
None
[30]

GA: glycyrrhizic acid; TBil: total bilirubin; IVC: type IV collagen; ALT: alanine aminotransferase; AST: aspartate transaminase; PTA: prothrombin time activity.

2. Mechanisms of GA Effects

2.1. Inhibition of Hepatic Apoptosis and Necrosis

Tumor necrosis factor-alpha (TNF-) is an important cytokine, which is a key mediator of hepatic apoptosis and necrosis in LPS/D-GaAlN-induced liver failure [34]. Plasma TNF- level is also elevated in patients with chronic hepatitis caused by hepatitis B viral [35] and acute alcoholic hepatitis [36]. Therefore, TNF- plays a key role in the pathogenesis of not only endotoxin-induced experimental liver injury but also many human liver diseases. Caspase-3 activation is an indicator of almost all apoptosis systems [37]. GA has anti-inflammatory and antiapoptotic effects via suppression of TNF- and caspase-3 and these are used to explain the hepatoprotective effect of GA (Table 2) [38]. GA also significantly inhibits the release of cytochrome C from mitochondria into the cytoplasm. The anti-inflammatory activity of GA may rely on the inhibition of release of TNF-, myeloperoxidase activity, and translocation of nuclear factor-B (NF-B) into the nuclei. GA also upregulated the expression of proliferating cell nuclear antigen, implying that it might be able to promote regeneration of liver injury [39]. Activated Kupffer cells are involved in ischemia-reperfusion- (I/R-) induced liver injury and high-mobility group box 1 (HMGB1) production. GA was shown to inhibit HMGB1 production by Kupffer cells and prevented I/R-induced liver injury [40]. GA could also alleviate I/R-induced [41] and spinal cord [42] injury via this mechanism. In addition, GA conjugates free radicals, which might explain the protective action of GA [43]. For example, GA can be an effective chemopreventive agent against lead acetate mediated hepatic oxidative stress in rats because it binds lead [44]. In concanavalin A- (ConA-) induced mouse model, GA alleviated ConA-induced inflammation and fibrosis progression in livers via inhibition of CD4+ T cell proliferation in response to ConA via the Jun N-terminal kinase (JNK), extracellular signal-regulated kinase (ERK), and phosphoinositide 3-kinase (PI3K)/AKT pathways [45].

Table 2: Mechanism of action of glycyrrhizin compound chemotherapy.

Compound
Pharmacological activities
Mechanisms of action
Reference

Glycyrrhizic acid
Anti-inflammatory

antiviral

inhibition of hepatic fibrosis
Regulating the expression of inflammation-related factors;

inhibition replication of viral mRNA
[46–49]

[51, 59]

[45]

Compound glycyrrhizin tablet
Improving the liver dysfunction

augmented the entire cytotoxic function mediated by hepatic lymphocytes

inhibiting the cascade leading to apoptosis
Regulating the expression of inflammation-related factors;

promoting the growth of hepatocyte;

inhibition replication of viral mRNA
[60]

[61]

[62]

Glycyrrhetinic acid
Anti-inflammatory

antiviral

antiallergic

antitumor proliferation
Regulating the expression of inflammation-related factors;

inhibition replication of viral;

inhibition of the expression of sensitizing factors and tumor-associated factor;
[63]

[64]

[65]

[66]

18-glycyrrhetic acid
Antiviral

anti-inflammatory
Regulating the expression of inflammation-related factors;

inhibition replication of viral mRNA
[67]

Diammonium glycyrrhizinate
Anti-inflammatory, resistance to biologic oxidation and membranous protection

neuroprotective effect
Regulating the expression of inflammation-related factors;

regulating the enzymatic reactions’ related oxidation
[68]

Dipotassium glycyrrhizinate
Anti-inflammatory
Regulating the expression of inflammation-related factors
[69]

2.2. Anti-Inflammation and Immunity Regulation

GA suppressed interleukin-6 (IL-6) and TNF- production induced by the lipid A moiety of lipopolysaccharides (LPS) in RAW264.7 cells. It inhibited lipid A-induced NF-B activation in Ba/F3 cells expressing toll-like receptor 4 (TLR4)/myeloid differentiation protein-2 (MD-2), cluster of differentiation 14 (CD14), and bone marrow-derived macrophages (BMMs). GA also inhibited activation of mitogen-activated protein kinase (MAPKs), including JNK, p38 protein, and ERK in BMMs. In addition, GA inhibited NF-B activation and IL-6 production induced by paclitaxel, a nonbacterial TLR4 ligand. It attenuated the formation of the LPS-TLR4/MD-2 complexes, resulting in inhibition of homodimerization of TLR4. Therefore, GA modulated the TLR4/MD-2 complex at the receptor level, leading to suppression of LPS-induced activation of signaling cascades and cytokine production. This indicates that GA can attenuate inflammatory responses and modulate innate immune responses [46]. Moreover, GA can prevent the activation of signal transducers and activators of transcription-3 (STAT-3), reduce the upregulation of intercellular cell adhesion molecule (ICAM-1) and P-selectin expression, reduce formation of poly(adenosine diphosphate-ribose) (PAR) and nitrotyrosine, and reduce polymorphonuclear neutrophil (PMN) infiltration. Some observations suggest that broad anti-inflammatory activity of GA is mediated by interaction with the lipid bilayer, thereby attenuating receptor mediated signaling [47]. GA inhibited the lytic pathway of the complement system and may prevent tissue injury caused by the membrane attack complex. Therefore, GA could be a potent agent for suppressing complement-dependent tissue injury in autoimmune and inflammatory diseases [48]. GA can suppress systemic inflammatory response syndrome (SIRS) associated anti-inflammatory response manifestation via inhibition of CC chemokine ligand 2 (CCL2) production by PMN. It may also have the potential to inhibit anti-inflammatory response-associated opportunistic infections in critically ill patients with severe SIRS [49]. There are also other studies that indicated the same anti-inflammatory mechanisms of GA [50].

2.3. Antiviral Effects

The antiviral mechanisms of GA mainly include the inhibition of viral replication and immunity regulation. GA affects cellular signaling pathways such as protein kinase C and casein kinase II and transcription factors such as activator protein 1 and NF-B. Furthermore, nitrous oxide (NO) inhibits replication of several viruses like Japanese encephalitis virus 4 (a member of the Flaviviridae family), which can also be inhibited by GA. The powerful anti-inflammatory capabilities of GA make it effective in the treatment of various types of hepatitis like viral hepatitis and nonalcoholic hepatitis. GA was found to inhibit the replication of the SARS-associated virus [51]. In the treatment of HCV (hepatitis C virus) infection, GA can inhibit HCV full-length viral particles and HCV core gene expression or function in a dose-dependent manner and have a synergistic effect with interferon [52]. GA is also involved in biliary secretion and excretion. GA can increase hepatic glutathione levels by the inhibition of biliary excretion of glutathione partly through the inhibition of MRP2 [53], an efflux transporter located at the canalicular membrane of a hepatocyte. MRP2 translocates glutathione, LTC4, bilirubin, methotrexate (MTX), glucuronide (e.g., estradiol-17--glucuronide [17G]), or sulfate conjugates and other organic anions from a hepatocyte into the bile canaliculus [54–58].

GA can activate certain immune functions, such as IFN production, augmentation of NK cell activity, and modulation of the growth response of lymphocytes via augmentation of IL-2 production [70]. GA can enhance immune function in mice [71]. GA treatment could significantly reduce blood immunoglobulin E (IgE), interleukin-4 (IL-4), interleukin-5 (IL-5), interleukin-6 (IL-6), NO, TNF- levels, and nitrous oxide synthase (NOS) activity dose-dependently. GA could also enhance blood immunoglobulin A (IgA), immunoglobulin G (IgG), immunoglobulin M (IgM), interleukin-2 (IL-2), and interleukin-12 (IL-12) levels in AR mice. Gr-1⁺CD11⁺b cells are responsible for numerous pathological processes such as T cell dysfunction after severe trauma or major surgery, leading to increased susceptibility to infection [72]. These cells exercise an inhibitory effect on MBD-1 production of EKs mediated via the suppressor molecules CCL-2 and IL-10. GA acts as a potent inhibitor of these cells and therefore restores MBD-1 levels. This restoration affects T cell dysfunction [73]. In thermally injured mice, GA regulates the burn-associated type 2 T cell responses to recover IL-12 and make it unresponsive, thus restoring the impaired cells [74]. GA acts as a promoter of the late signal transduction of T lymphocytes for IL-2 production. The balance between augmenting and suppressing effects might be dependent on the level of stimulation and stage of the cell. Therefore, this determines quality and quantity of the immunomodulatory action of GA [75]. In blood and nasal mucosa, GA consumption decreases antioxidant enzyme activity, lipid peroxidation, Glutathione levels, and IL-4 levels and enhances IFN-γ, thus protecting the nasal mucosa from oxidative injury and improving immunity activity [76].

GA interferes with some viruses, such as H5N1 [77]. The replication and virus-induced proinflammatory gene expression include inhibition of the virus-induced formation of reactive oxygen species and reduced activation of NF-B, JNK, and p38, which are redox-sensitive signaling events known to be relevant for replication.

2.4. Antitumor Effects

CYP enzymes are mainly found in the liver and bowel wall. They are responsible for the bulk of phase I or oxidative metabolism of xenobiotics including dietary toxins, carcinogens, mutagens, and drugs. Administration of GA was able to significantly induce CYP content, which reduces the incidence of cancer [78]. GA can also protect against aflatoxin-induced oxidative stress. The protective effect is likely from its capacity to inhibit the metabolic activation of hepatotoxin, a critical factor in the pathogenesis of chemical-induced carcinogenicity [79]. O-carboxymethyl chitosan nanoparticles (CMCNP) modified by GA with various substitution degrees can efficiently deliver paclitaxel (PTX) to hepatocellular carcinomas (HCC). CMCNP-GA significantly facilitated the increased accumulation of PTX in hepatic tumor tissues and the targeted delivery of PTX to hepatoma carcinoma cells, which resulted in remarkably enhanced in vitro cytotoxicity and in vivo antitumor efficacy [80]. In a diethylnitrosamine-treated experimental animal study, as a chemopreventive agent of HCC, modulation of cell proliferation and apoptosis by GA may be associated with inhibition of HCC. Therefore, GA treatment may inhibit the occurrence of HCC [81].

2.5. Inductive Effect of Liver Enzyme Activity

Some studies showed that GA has an inductive effect on CYP3A activity. Therefore, clinicians should pay attention to other drugs catalyzed by CYP3A, especially those substrates with a narrow therapeutic range such as cyclosporine A, to avoid possible clinically significant interactions with GA [82]. Some studies revealed that the area under concentration-time curve and the mean retention time of methotrexate (MTX) were significantly increased by GA, which increases the adverse reactions of MTX [83]. MTX is an antifolate agent, anticancer agent, and immunosuppressant and is commonly used for anticancer chemotherapy [84], rheumatoid arthritis [85], and severe psoriasis [86]. The adverse reactions of MTX include nausea, vomiting, diarrhea, and hepatotoxicity [87, 88]. A case report showed that combined administration of GA and cilostazol caused pseudoaldosteronism [89]. Therefore, the concurrent use of GA with MTX or cilostazol is not recommended. One report shows a case of hypokalemic rhabdomyolysis secondary to chronic GA intoxication [90]. GA ingestion could therefore potentially aggravate hypokalemia in patients with chronic laxative abuse [91], indicating that the use of GA in hypokalemia should be treated with caution.

3. Other Pharmacological Activities

GA is effective in combating hyperglycemia and associated pathological complications such as hyperlipidemia, abnormal histoarchitectures of different organs, and oxidative stress including hemoglobin-induced iron-mediated free radical reactions. The effects of GA on diabetes-associated changes are almost comparable with those of glibenclamide, a standard antihyperglycemic drug, suggesting a possible use of the herbal agent as a drug to prevent complications of diabetes mellitus [92]. Furthermore, GA regulates renal function through the regulation of water channels [93], and GA administration ameliorates the renal concentrating ability and structural lesions in renal tissues in rats with early-phase of ischemia-acute renal failure [94]. As a reduction inhibitor, GA reduces the therapeutic loss of methylprednisolone produced from methylprednisolone 21-sulfate sodium in the large intestine, thus improving the therapeutic property of the prodrug against inflammatory bowel disease [95]. GA also offers protection from the damage induced by UVB radiation in humans. Therefore, it could be considered as a promising agent for addition to topical formulations for the prevention of skin cancer [96]. GA significantly alleviates asthma symptoms [97], inhibits lung inflammation [98], and relieves acute lung injury [35, 99]. It can directly affect cardiac performance and play a role in myocardial and coronary protection in the presence of cardiovascular diseases [100]. GA may prevent brain tissue damage [101], can be a putative therapeutic drug for neurodegenerative diseases associated with cognitive deficits and neuroinflammation such as Alzheimer’s disease [102], and could suppress ocular hypertension with potential therapeutic effects in eye disease [103]. GA improves resistance to C. albicans infection by inducing CD4+ T cells, which suppress type 2 cytokine production by Th2 cells [104]. GA inhibits activated macrophage (M2M) generation stimulated with neutrophils. The regulation of neutrophil-associated M2M generation by GA may provide a new therapeutic strategy, which could influence the outcome of certain severe infections in hosts with M2M generation [105].

4. Drugs That Include GA

Drugs made with GA have been on the market for many years, and most have important therapeutic uses. Magnesium isoglycyrrhizinate injection (TianQing GanMei, Chia Tai Tainqing, JiangSu, China) is one example of a drug with GA. Magnesium isoglycyrrhizinate is an effective and safe treatment for chronic liver diseases [106] and is capable of slowing down the progress of pulmonary fibrosis [107]. Moreover, diammonium glycyrrhizinate enteric-coated capsules (TianQing GanPing, Chia Tai Tainqing, JiangSu, China) and diammonium glycyrrhizinate injection (GanLiXin, Chia Tai Tainqing, JiangSu, China) are used for acute and chronic hepatitis associated with elevated alanine aminotransferase. Stronger neo-minophagen C (SNMC, Minophagen Pharmaceutical, Tokyo, Japan) is often used in the treatment of chronic liver disease and can improve liver dysfunction [60]. SNMC is a compound GA tablet that includes GA (2 mg) with glycine acid (20 mg) and L-cysteine hydrochloride (1 mg). SNMC has anti-inflammatory, antiallergic, steroid-like, anticomplementary, and immunoregulatory effects.

5. GA Combined with Matrine

GA combined with matrine (Mat) can improve CCL4-induced liver fibrosis effectively. This is evidenced by lower levels of collagen, hyaluronic acid (HA), and laminin (LN), less hepatic stellate cells (HSC) proliferation, collagen I, and HA levels secreted by HSC in vitro with combined therapy compared with GA or Mat alone. GA combination with Mat could protect liver cells and inhibit hepatic fibrosis and may therefore be a safe and effective strategy for improving hepatic fibrosis [108]. In an animal model, GA combined with Mat reduced the mortality of acetaminophen overdosed mice, attenuated acetaminophen-induced hepatotoxicity, and reduced the number and area of y-GT positive foci, thus protecting liver function and preventing HCC from occurring [109]. Additionally, the combination of GA and cyclosporine was an effective treatment for nonsevere aplastic anemia [110].

6. Common Derivatives of Glycyrrhizin

Glycyrrhetinic acid (3β-hydroxy-11-oxo-oleana-12-en-28-oic acid), the aglycone of GA, stimulates glucose-induced insulin secretion in isolated pancreatic islets. Glycyrrhetinic acid treatment enhances plasma insulin levels and reduces the levels of gluconeogenic enzymes in liver. It is a pentacyclic triterpene acid with numerous biological activities, including anti-inflammatory [63], antiviral [64], antiallergic [65], and antitumor proliferative effects [66].

Glycyrrhetinic acid restrains the proliferation of skin tumors in mice and human breast cancer cells (MCF7) and induces apoptosis of cancer cells. The mechanism of apoptosis might be via increased free level in the cells [111]. Mizushina et al. [112] demonstrated that glycyrrhetinic acid potently inhibited the activity of mammalian polymerases, including pol λ. Glycyrrhetinic acid also reduced TNF- production and NF-B activation and suppressed mouse ear inflammation stimulated by tissue plasminogen activator. Therefore, glycyrrhetinic acid could be an anti-inflammatory agent based on pol λ inhibition.

Another licorice acid derivative is 18-glycyrrhetic acid. The triterpene structure of the HMGB1-binding compound is capable of binding to HMGB1 and altering its proinflammatory properties, inhibiting HMGB1-dependent cyclooxygenase (COX) 2 induction [113]. 18-glycyrrhetic acid has significant antiviral activity against rotavirus replication in vitro, and studies to determine whether 18-glycyrrhetic acid attenuates rotavirus replication in vivo are underway, although the exact mechanism is unclear. However, some reports show that 18-glycyrrhetic acid inhibits NF-B activation, which has been interpreted as 18-glycyrrhetic acid-mediated regulation of the inflammatory response [114]. 18-glycyrrhetinic acid can also inhibit the activity of tyrosine and prevent melanin growth and whitening. Some reports show that 18-glycyrrhetinic acid is likely responsible for amelioration of dysfunction of glutamate transport in astrocytes, and the inhibition of protein kinase C activity might be related to its pharmacological efficacy [67].

7. Conclusions and Future Perspectives

This review summarized the efficacy of GA in liver disease from clinical trials and its mechanisms of action in vitro and in vivo. Studies indicate that GA could modulate various molecular pathways in liver disease. There are numerous patents for drugs including GA (Table 3). Studies described here highlight the use of GA as a novel chemopreventive agent for liver injury. It is expected that future studies with GA will help to define various molecular mechanisms and targets for inflammation and steatosis. At present, the number of multicenter, large sample, randomized, double-blind, controlled chemoprevention clinical trials with GA is very limited. Extensive clinical research is warranted to evaluate the safety and chemopreventive efficacy of GA alone or in combination with chemotherapy agents.

Table 3: Patents of glycyrrhizin extracts.

Patent
Patent number

Acetylated 18-alpha glycyrrhizic acid and preparation method thereof
CN102351937 A

Ammoniated glycyrrhizin modified sweetened beverage products
US2008226787(A1)

Application of beta-glycyrrhizic acid and derivatives thereof for radiation protection
CN102206242 A

Application of glycyrrhetinic acid and glycyrrhizic acid in preparing medicaments for preventing or treating pulmonary fibrosis
CN101919870 B

Application of glycyrrhizic acid and glycyrrhetic acid in preparing medicine for inflammatory enteropathy
CN1846705 A

Application of glycyrrhizic acid in preparation of sunitinib malate cardiotoxicity reduction drug
CN103285020 A

Application of glycyrrhizic acid on treating dilated cardiomyopathy cardiac remodeling and cardiac dysfunction
CN102247392 A

Application of glycyrrhizic acid, glycyrrhetinic acid, or salt thereof as well as gel composition and preparation method for gel composition
CN102614213 A

Application of glycyrrhizic acid and its breakdown product glycyrrhetinic acid for the manufacture of a medicament for the treatment of inflammatory bowel disease
US2010087385(A1)

Aqueous pharmaceutical solutions with trisubstituted glycyrrhizic acid salts
EP1226831 A1

Aspergillus niger bacterial strain and glycyrrhizic acid used for production thereof
CN101255401 B

Berberine glycyrrhizic acid enantiomer salt and preparation method and usage thereof
CN101747405 A

Biological extraction process of glycyrrhizic acid
CN101067146 B

Carboxymethyl chitosan nanoparticles modified with glycyrrhizic acid, preparation method, and application thereof
CN102357079 A

Chitosan glycyrrhizic acid nanoparticle and its preparing method
CN1586488 A

Composite glycyrrhizic acid amino acid injection and preparation method as well as applications thereof
CN101669962 A

Compositions containing glycyrrhizin
US4678772(A)

Compound for the control of herpes simplex virus using glycyrrhizic acid, lipoic acid, allantoin, and slippery elm
US2011229584(A1)

Compound glycyrrhizin capsule composition
CN103230407 A

Compound glycyrrhizin soluble powder for livestock and preparation method thereof
CN102526082 B

Dispersed compound tablet of glycyrrhizic acid and glycyrrhizinate and its preparing process
CN100386086 C

Enteric-coated formulation of glycyrrhizic acid and its salt and its preparing method
CN1274309 C

Film-coated tablet of glycyrrhizinic acid monopotassium salt and method for preparing the same
CN100341515 C

Glycyrrhizic acid compounds as foamer in chemically derived surfactant-free dentifrice
US2008274062(A1)

Glycyrrhizic acid and its derivative used as RANTES inducer
CN1498623 A

Glycyrrhizic acid antibody and its preparing method and use
CN1293097 C

Glycyrrhizic acid aureola dimer mediated targeted medication body as well as preparation method and purpose of glycyrrhizic acid aureola dimer mediated targeted medication body
CN102716488 A

Glycyrrhizic acid composition
CN101081227 B

Glycyrrhizic acid derivatives having amino acid, its preparation method, and medicinal composition containing them
CN1911954 A

Glycyrrhizic acid double salt and preparation thereof
CN100537593 C

Glycyrrhizic acid matrine salt and glycyrrhizic acid marine salt, its preparing method and use
CN100564391 C

Glycyrrhizic acid organic salt phospholipid ligand and preparation thereof
CN102716463 A

Glycyrrhizic acid removal glycyrrhiza flavonoid and medicament composition thereof
CN101747307 A

Glycyrrhizic acid sustained-release dropping pills and preparation method thereof
CN101269020 A

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Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work is supported by the National Natural Science Foundation (no. 81273729), Major Project of Shanghai Municipal S&T Commission (no. 11DZ1971702), Shanghai Rising-Star Program (08QA14062), Wang Bao-En Hepatic Fibrosis Research fund (20100048), and E-institute of Shanghai Municipal Education Commission (Project no. E03008). Innovative Research Team in Universities, Shanghai Municipal Education Commission, Shanghai Key Laboratory of Traditional Chinese Clinical Medicine, and Key Disciplines of Liver and Gall Bladder Diseases of State Administration of Traditional Chinese Medicine of the People’s Republic of China.

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