Research Progress in the Pharmacological Activities, Toxicities, and Pharmacokinetics of Sophoridine and Its Derivatives.

Sophoridine is a natural quinolizidine alkaloid and a bioactive ingredient that can be isolated and identified from certain herbs, including Sophora flavescens Alt, Sophora alopecuroides L, and Sophora viciifolia Hance. In recent years, this quinolizidine alkaloid has gained widespread attention because of its unique structure and minimal side effects. Modern pharmacological investigations have uncovered sophoridine's multiple wide range biological activities, such as anti-cancer, anti-inflammatory, anti-viral, anti-arrhythmia, and analgesic functions, among others. These pharmacological activities and beneficial effects point to sophoridine as a strong potential therapeutic candidate for the treatment of various diseases, including several cancer types, hepatitis B virus, enterovirus 71, coxsackievirus B3, cerebral edema, cancer pain, heart failure, acute myocardial ischemia, arrhythmia, inflammation, acute lung injury, and osteoporosis. The data showed that sophoridine had adverse reactions, including hepatotoxicity and neurotoxicity. Additionally, analyses of sophoridine's safety, bioavailability, and pharmacokinetic parameters in animal models of research have been limited, especially in the clinic, as have been investigations on its structure-activity relationship. In this article, we comprehensively summarize the biological activities, toxicity, and pharmacokinetic characteristics of sophoridine and its derivatives, as currently reported in publications, as we attempt to provide an overall perspective on sophoridine analogs and the prospects of its application clinically.

Introduction

Currently, various plant-derived metabolites are increasingly being used in drug synthesis or semi-synthesis, with a variety of plant extracts seeing extensive use in the treatment of specific diseases. Nitrogen compounds play specific roles in different plant secondary metabolites, including sophoridine, a widely distributed natural quinolizidine alkaloid (Figure 1A) that can be isolated and identified in the Leguminosae of the leguminous family, like Sophora flavescens Alt,1 Sophora alopecuroides L2 and Sophora viciifolia Hance.3 The pharmacological activities of sophoridine, including anti-cancer, anti-inflammatory, anti-viral, anti-arrhythmia, and analgesic properties, have been reported broadly in recent years. The main biological activities and some underlying molecular mechanisms are summarized in Table 1 and suggest that sophoridine is a potential drug candidate for the treatment of a variety of diseases, such as cancers, viruses, and cardiovascular diseases.

Figure 1

The chemical structural formula of sophoridine (A), matrine (B), sophocarpine (C), sophoramine (D), oxymatrine (E) and oxysophoridine (F).

Table 1

Pharmacological Activities of Sophoridine Both in vitro and in vivo Studies

Biological Activity	Types	Cell Lines/Model	Dosage/Route of Administration	Effects/Mechanisms	Ref.
Anti-cancer
	In vitro	HepG2 cells	20, 40, and 80 μM	Regulating PTEN/PI3K/Akt signaling pathway and caspase-3/-9 and MMP-2/-9 signaling pathway.	[10]
	In vivo	Nude mice	20, 40, and 80 μM	Decreasing the PTEN protein expression, tumor volume and weight	[10]
	In vitro	HepG2 and Huh7 human HCC cell lines	20, 40, and 80 μM	Reducing VEGFR2 expression and RAS/MEK/ERK axis	[17]
	In vivo	BALB/c nude mice	50 mg/kg, ip	Inhibiting the tumour cell proliferation and angiogenesis.	[17]
	In vitro	BRL-3A cells	1, 2, and 3 mM	Up-regulating intracellular ROS accumulation	[16]
	In vitro	MKN45 cells	8, 14 mM	Down-regulation of HMGB3 protein expression	[20]
	In vitro	Gastric cancer cell lines (SGC7901 and AGS)	1, 3, and 5 μM	Up-regulating ESRRG /β-catenin pathway	[21]
	In vitro	MFC cancer cells	2, 4, and 8 mM	Up-regulating TLR4/IRF3 signal pathway and CD8+ T cytotoxic function against gastric cancer	[12]
	In vitro	SW480 cells	1.6, 3.2 mM	Activating apoptosis-related proteins caspases (caspase −3, caspase-9 and caspase-7) and PARP regulation	[13]
	In vivo	Nude mice	15, 25 mg/kg, ip	Inhibiting tumor growth	[13]
	In vitro	Miapaca-2 and PANC-1	20 μM	Activation of the phosphorylation of ERK and JNK, induced cell cycle arrest at S phase and mitochondrial related apoptosis.	[11]
	In vivo	Balb/c nude mice	20, 40 mg/kg, ip	Inhibiting tumor growth	[11]
	In vitro	A549 cells	20, 40 μM	Down-regulating AKT /NF-κB signaling pathway	[9]
	In vitro and in vivo	NCL-H460, A549 cells BALB/c mice	20, 40 μM; 16.9 mg/kg, ip	Activating the Hippo and p53 signaling pathways	[24]
	In vitro	D283-Med cells	2, 4, and 8 mM	Inhibition of the FoxM1, NF-κB and AP-1 signaling pathway	[30]
	In vitro	U87MG cells	2, 4, and 8 mM	Inducing ROS accumulation and activating mitochondrial signal pathways	[31]
Anti-virus activity
	In vitro	HepG2.2.15 cells	0.4, 0.8 and 1.6 mM	Down-regulation of p38 MAPK, TRAF6, ERK1, NLRP10 and caspase-1 expression	[42]
	In vitro	HepG2.2.15 cells	0.4, 0.8 and 1.6 mM	Elevating methylation of HBV DNA	[42]
	In vivo and in vitro	BALB/c mice, Primarily cultured myocardial cells	20 and 40 mg/kg, ig; 4, 20 μM	Increasing cytokines IL-10, IFN-γ levels and reducing the expression of TNF-α	[52
Neuroprotection and analgesic activities
	In vivo	SD rats	2.5, 5, and 10 mg/kg, ip	Down-regulation of TRAF6 expression and up-regulation of erk1/2 phosphorylation	[56]
	In vivo	CD-1 mice	2.5, 10 mg/kg, ip	Inhibiting the TLR4/NF -κB signal pathway	[57]
	In vivo	SD rats	25 mg/kg, ip	Increasing the mechanical withdrawal threshold and the thermal withdrawal latency and down-regulation of COX-2 and VEGF expression	[59]
	In vivo	SD rats	25 mg/kg, ip	Down-regulating NMDAR-nNOS/NO-cGMP pathway	[62]
Effect on cardiovascular system
	In vivo	Male SD rats	2.5, 5, and 10 mg/kg, ip	Ameliorating cardiac Ca2+ induced Ca2+ transients through upregulating DHPR	[68]
	In vivo	Male SD rats	5, 10, and 20 mg/kg, ip	Recovering of sarcoplasmic reticulum calcium Capacity, and up-regulation of SERCA2a expression	[69]
	In vivo	Male SD rats	2.5, 5, and 10 mg/kg, iv	Decreasing LVSP and ± dp/dtmax changes, and LVEDP in AMI	[72]
	In vivo	Male SD rats	2.5, 5, and 10 mg/kg, iv	Decreasing myocardial ischemic infarct size	[73]
	In vitro	hERG-expressing HEK293 cell lines	30, 100, and 300 μM	Down-regulating the channel kinetics: block hERG K+ channels	[77]
Anti-inflammation activity
	In vitro and in vivo	HL-60 cells and the mouse peritoneal macrophages; Kunming mice	0.01, 0.1, and 1 μM; 12.15, 48.60 mg/kg, ig	Inhibiting the production of inflammatory cytokine (TNF-a and IL-8) and inflammatory media PGE2	[80]
	In vivo	Female C57BL/6 mice	25, 50 mg/kg, ig	Inhibiting the expression of ICAM-1 gene	[83]
	In vivo	BALB/c mice	3, 6 and 12mg/kg, ip	Inhibiting the expression of p-ERK and TNF-a	[84]
	In vitro	RAW264.7 cells	62.9 μM	Decreasing expression of CD14, P38 and i NOS	[85]
	In vitro	RAW264.7 cells	125.8 μM	Inhibiting TLR4/JNK signal transduction pathway	[86]
	In vivo	Kunming mice	2.5, 5, and 9 mg/kg, ip	Inhibiting the NF-κB signaling pathway	[89]
	In vivo	BALB/c mice	3, 6, and 12 mg/kg, ip	Inhibiting MAPK/AP-1 signaling pathway	[88]
	In vivo	Kunming mice	2.5, 5, and 9 mg/kg, ip	Inhibition of IL-6, IL-10, NO and MDA, and elevation of SOD.	[90]
Others
	In vivo and in vitro	Mice bone marrow macrophage, Female FVB mice	20, 40, and 60 μM; 15 mg/kg, ip	Inhibition of OCs formation through the RANKL-ERK-NFAT pathway	[93]
	In vitro	Sperm	4, 20.1, 36.2, 42.3, 44.3, 120.8 μM	Inhibition sperm motility, change the morphology and structure, and even crack sperm	[94]

Over the past decades, the pharmacological properties of sophoridine have seen increased testing, as have its pharmacokinetics and toxicity in recent years. However, most previous reports on the alkaloid are scattered and lack systematic summaries and generalizations. Therefore, we have systematically reviewed and critically discussed the pharmacological activity, pharmacokinetics, and toxicity of sophoridine in this paper, as currently available in publications, in the hope of providing some perspective to the development of sophoridine and the prospects of its application clinically (Figure 2).

Figure 2

The schematic representation of biological activities, toxicity, and pharmacokinetic characteristics of sophoridine and its derivatives.

Chemical Properties and Plant Sources of Sophoridine

Sophoridine, also known as allomatrine or (5-β)-matridin-15-one, is a common quateracyclic quinolizidine alkaloid. Its basic structure consists of two dipiperidine rings with two trivalent nitrogen atoms, its molecular formula is C15H24N2O (Figure 1A), and its relative molecular weight is 248.36 g/mol, CAS No. 6882-68-4. Sophoridine has several structurally similar derivatives, including sophocarpine, sophoramine, matrine, and oxymatrine (Figure 1B–E), can be chemically converted to oxysophoridine (Figure 1F) by oxidizing its 1-nitrogen with oxygen in the presence of hydrogen peroxide, and is a white or light-yellow crystalline alkaloid monomer soluble in solvents, like water, methanol, ethanol, or carbon tetrachloride.

Sophoridine is a metabolite in plant metabolism and is reportedly one of the major alkaloids in several representative plants, such as Sophora flavescens Alt,1 Sophora alopecuroides L,2 Sophora viciifolia Hance3 and Oxytropis ochrocephala Bunge.4 It is found primarily in the roots, flowers, and seeds of the aforementioned plants. The general steps for its extraction from plants are shown in Figure 3, with the plants yielding varying contents of isolated sophoridine: higher amounts of Sophora alopecuroides L and Sophora flavescens Alt than the others. Differences in the growth period and propagation mode also affect the content of sophoridine in Sophora flavescens Alt roots. According to Hu and his colleagues (2004), sophoridine contents increase with longer growing seasons and are highest during asexual reproduction.5 These contents differ in Sophora alopecuroides L seeds and cotyledon pseudoactinine; cotyledon contains the most significant amount (5.16 mg/g) and the seed coat (2.25 mg/g)6 the least significant amount. However, the alkaloid contents in Sophora flavescens Alt and Sophora alopecuroides L seeds are highly similar.2

Figure 3

Extraction process for sophoridine from Sophora alopecuroides L.

Pharmacological Activities of Sophoridine

Anti-Cancer Activity

Sophoridine, a natural agent extracted from medicinal plants, exhibits a wide spectrum of pharmacological properties, including anti-cancer effects, and selectively induces apoptotic cell death in a variety of human cancer cells in vitro and in vivo; however, its mechanism of action remains to be elaborated further. The main active ingredient of Kushen extract, the traditional Chinese medicine commonly known as Compound Kushen Injection (CKI) and approved as an anti-cancer agent in 1995, is sophoridine, which exhibits an excellent anti-cancer effect.7 In 2005, the State Food and Drug Administration of China (SFDA) approved the clinical application of sophoridine hydrochloride injection as a treatment for cancer patients;8 it is used to treat patients with malignant trophoblastic tumors who cannot tolerate standard chemotherapy but is contraindicated in patients with a history of hypersensitivity to quinolizidine alkaloids. The recommended dose of this injection is 125 mg/m2 diluted to 500 mL of 5% glucose solution and continuously administered intravenously for no less than 6 hours. A multicenter clinical study on sophoridine conducted in ten hospitals across the country showed that sophoridine had an acceptable therapeutic effect on malignant trophoblastic tumors.8

Broad-spectrum anti-cancer activities of sophoridine have also been reported in cancer cells from different tissues, including lung,9 hepatoma,10 pancreatic,11 gastric,12 and colon13 tissues. Several investigations have demonstrated that sophoridine and most of its derivatives inhibit cancer cell proliferation, as well as induce apoptosis, cell cycle arrest, and reverse multidrug resistance in cancer cells.

Anti-Liver Cancer Cells

Many studies have demonstrated sophoridine’s potency against cancer, with multiple underlying mechanisms. Wang et al (2017) revealed that sophoridine (20, 40 μM) suppresses liver cancer cell survival in vitro by regulating the PTEN/PI3K/Akt, caspase-3/-9, and MMP-2/-9 signaling pathways.10 Bcl-2 and Bax are two significant regulators of mitochondria-dependent apoptosis, with a decrease in Bcl-2 and an increase in Bax resulting in apoptosis.14,15 Additionally, sophoridine has been shown to induce apoptosis in rat liver BRL-3A cells through the excessive ROS accumulation-induced redox imbalance pathway.16 Its effect is also markedly associated with enhancing the expressions of cleaved PARP and Bax in BRL-3A cells and lessening Bcl-2 protein expression. In in vivo experiments, sophoridine considerably reduces tumor volume and tumor weight in nude mice by down-regulating PTEN protein expression.10

Furthermore, one recent study demonstrated sophoridine’s ability to enhance lenvatinib-resistant hepatocellular carcinoma (LR HCC) sensitivity to lenvatinib through a molecular mechanism in which sophoridine drastically suppresses ETS-1 expression to reduce VEGFR2 levels and the downstream RAS/MEK/ERK axis in LR HCC cells. The same investigation established and analyzed an in vivo HepG2-LR cell subcutaneous tumor model in BALB/c nude mice, finding that sophoridine also sensitized LR HCC to lenvatinib via a mechanism of action possibly closely associated with the inhibition of tumor cell proliferation and angiogenesis. Per these reports, combining sophoridine with lenvatinib could be a novel therapeutic strategy for HCC treatment.17

Anti-Stomach Cancer Cells

Stomach cancer is the third leading cause of cancer deaths and the most diagnosed cancer, with an incidence twice as high in men as in women.18 While surgical resection is currently the most effective treatment, most patients tend to be diagnosed with advanced-stage gastric cancer because early-stage gastric cancer is asymptomatic.19 Therefore, the development of new gastric cancer treatments is of great significance to patients with advanced-stage disease. Sophoridine has an anti-gastric cancer effect. In vitro, it has been shown to inhibit the proliferation of MKN45 cells and promote their apoptosis, possibly via a mechanism associated with the down-regulation of HMGB3 protein expression.20 Sophoridine concentration- and time-dependently inhibited the growth of gastric cancer cell lines (SGC7901 and AGS), including suppressing proliferation, migration, invasion, and colony formulation, as well as inducing apoptosis, with IC values of 3.52 and 3.91 μM, respectively.

According to Peng and his colleagues (2020), sophoridine induces G2/M cell cycle arrest by inhibiting double-stranded DNA break repairs in gastric cancer cells, which is inseparable from the targeted ESRRG/β-catenin pathway. Furthermore, combining sophoridine and cisplatin enhances the efficacy of cisplatin in gastric cancer cells.21 In their study assessing how CD8+ T cells modulate the tumor microenvironment, Zhuang et al (2020) found sophoridine to exert its anti-gastric cancer effect by inhibiting macrophage-mediated immunosuppression through the TLR4/IRF3 signaling pathway, subsequently up-regulating CD8+ T cytotoxic function against gastric cancer.12

Anti-Colorectal Cancer Cells

Sophoridine has been reported to have an anti-colorectal cancer effect that is possibly linked to the regulation of MAPKAPK2 targeting and could serve as a prognosis marker in colorectal cancer patients.22 Liang et al (2012) showed that sophoridine inhibited SW480 cell (IC50 = 3.14 mM) growth time- and dose-dependently by activating the mitochondrial apoptosis pathway. The studies have reported sophoridine’s exertion of its anti-colorectal carcinoma effect through the activation of apoptosis-related protein caspases (caspase-3, caspase-7, and caspase-9) and PARP regulation, thereby inducing apoptosis. In in vivo xenograft tumor model established via the subcutaneous injection of SW480 cells into the armpits of nude mice, sophoridine (15 and 25 mg/kg) inhibited tumor growth (weight and volume of tumors). Moreover, the pathological and ultrastructure of xenograft tumor cells in the drug treatment group showed apoptotic changes, suggesting that sophoridine-induced apoptosis of tumor cells.13

This demonstrably potent quateracyclic quinolizidine alkaloid has also demonstrated potential apoptosis effects on two pancreatic cancer cell lines, Miapaca-2 and PANC-1. Specifically, it effectively inhibited the proliferation of pancreatic cancer cells by blocking cells in the S phase and decreasing mitochondria-related apoptosis, as well as provoking the initiation of ERK and JNK phosphorylation and inducing ROS generation in pancreatic cancer cells. In vivo, 20 and 40 mg/kg of sophoridine drastically suppressed tumor growth in mouse xenograft models.11 Ren et al (2016) reported that sophoridine can effectively inhibit human pancreatic cancer capan-1 cell proliferation and reduce cell invasion ability by down-regulating the expression levels of MMP-2 and MMP-9.23

Anti-Lung Cancer Cells

Li et al (2015) showed that the intracellular ROS level and apoptosis rate of A549 cells were up-regulated after sophalidine (20 and 40 μM) treatment, and the cell cycle was arrested in G2/M phase. In addition, the expression of pro-apoptotic protein caspase-3/8 was up-regulated, the expression of apoptotic protein Survivin and bcl-2 was down-regulated, and the expression of cycle-related protein CDK-2, adhesion molecule CD44 and matrix metalloproteinase MMP-2/9 were down-regulated. These results suggest that sophoridine inhibits the proliferation and invasion of lung cancer by increasing ROS levels, promoting apoptosis and blocking cell cycle.9 Zhu et al (2020) revealed that sophoridine inhibits the proliferation and colony formation of lung cancer and enhances the effects of cisplatin against lung cancer cells, possibly via the activation of the Hippo and p53 signaling pathways.24 In Lewis mouse model, Zhao et al (2014) found that sophoridine (15 and 25 mg/kg) effectively inhibits tumor growth of non-small lung cancer by activating MAPKs signaling pathway and increasing expression of pro-inflammatory cytokines and M1 surface marker CD86.25

Dong et al (2014) assessment of these properties revealed that mesoporous silica nanospheres effectively regulated the uptake and release of sophoridine; however, how these nanospheres perform in vivo remains unknown.26 Inspired by the above ideas, Wang et al (2016) prepared sophoridine-loaded PLGA microspheres using the O/O emulsion-solvent evaporation method, which exhibited combined lung-targeting and sustained drug release properties.27 Thus, the sustained release of loaded sophoridine by PLGA microspheres suggests that sophoridine has a remarkable potential value for lung cancer treatment.

Others

Forkhead box M1 (FOXM1) is a key regulator of the cell cycle and is expressed during the G1, S, and mitotic phases,28 and the activator protein 1 (AP-1) compound is vital in the event of cancer metastasis.29 Yue et al (2017) demonstrated that sophoridine markedly attenuated cancer cell growth, induced apoptosis by suppressing the FOXM1, NF-κB, and AP-1 signaling pathways, and significantly up-regulated cytotoxicity and caspase-3/8 activity in the human medulloblastoma cell line D283-Med.30 In addition, sophoridine significantly up-regulated cytotoxicity and caspase-3/8 activity in human medulloblastoma. In human glioma U87MG cell, Wang and his colleagues (2015) found that sophoridine shows obvious anti-cancer activity on glioma cells by inducing cell apoptosis, inducing ROS accumulation, and activating mitochondrial signal pathways.31

Anti-Cancer of Sophoridine Derivatives

While sophoridine has been approved as an anti-cancer agent, its anti-cancer property has only been observed in malignant trophoblastic tumors.8 To improve this property, a series of structural modifications have been conducted on sophoridine, and the resulting derivatives have been examined for anti-cancer effects. This endeavor has yielded a well-developed structure–activity relationship (SAR) for sophoridine. Chemically, sophoridine belongs to one kind of matrine-type alkaloid formed from two piperidine rings by the thickening of trivalent nitrogen atoms. Structural modifications on the lactam ring of matrine-type alkaloids are currently a popular subject of research among investigators. Sophoridine derivatives can be classified based on structural modifications: i) at the N-16 position; ii) at the C-14 position of the lactam ring; and iii) on sophoridine by opening the lactam ring (Figure 4).

Figure 4

Synthetic routes of sophoridine derivatives 1, 2 and 3 that have anti-cancer effects.

The SAR indicates that the introduction of an aliphatic acyl on the 16-nitrogen atom of sophoridine could considerably enhance its anti-cancer effect. For instance, the compound 1-bearing bromoacetyl side-chain is active against four human tumor cell line types: liver, colon, breast, and lung cell lines, with an IC50 value of 0.062 mM and a mechanism of action aimed at inhibiting the activity of DNA topoisomerase I (Figure 4).32 According to findings from SAR analyses, two suitable substitutions on the 16-nitrogen atom and carboxyl region can help maintain a satisfactory anti-tumor activity: two moieties could be introduced as decorators of various substitutions to regulate the drug-like physical-chemical properties of the compounds.33

Among the newly synthesized derivatives, compound 2 displays a potential anti-proliferative activity in both wild MCF-7 and adriamycin (AMD)-resistant MCF-7 (MCF-7/AMD) breast carcinoma cell lines, with an IC50 value of 3.1 μM. Its mechanism of action is associated with the arrest of the cell cycle at the G0/G1 phase, consistent with that of sophoridine. Compound 2 also has a reasonable clogp value and a favorable pharmacokinetic property with rapid absorption at a Tmax of 4.6 h, a favorable half-life of 12 h, and a mean residence time (MRT) of 5.4 h if administered orally at a dose of 25 mg/kg (Figure 4).34 Therefore, the SAR results suggest that a sophoridinic acid with a 3-ring structure scaffold is more promising than sophoridine with a 4-ring scaffold.

Per further SAR analyses, the R-configuration at the 5-position is crucial and the introduction of a chlorobenzyl to the 12-nitrogen atom of sophoridinol significantly enhances sophoridine’s activity.35 Compound 3 is synthesized by introducing a benzyl chloride group to nitrogen atoms, which can result in a more potent anti-proliferative property against various cancer cell line types (HepG2, HCT116, H1299, U87, MCF-7, and KB), with IC values ranging from 0.011 to 0.041 mM and much better than that of the parent sophoridine (>0.08 mM) and a mode of action that constitutes inhibiting the activity of DNA topo I, followed by the G0/G1 phase arrest. Compound 3 also has high solubility and decent safety profiles (Figure 4).36

A previous SAR analysis revealed that the 16-N-p-cholobenzyl substituent boosts sophoridine’s anti-tumor activity. Taking 16-N-p-chlorobenzyl Compound 3 as a lead compound, numerous novel sophoridinic derivatives with various 3′-substituents at the 11-attachment have been synthesized and evaluated for their anti-cancer properties. Among them, sophoridinic ketones 4a-b, alkenes 4c-d, and sophoridinic amines 4e-f have displayed adequate anti-proliferative activity, with IC50 values ranging from 3.8 to 5.4 μM. Particularly, compounds 4a and 4d were shown to exhibit an equipotency in both AMD-susceptible and AMD-resistant MCF-7 breast carcinoma cells, indicating that they possess a different mechanism from AMD (Figure 5).37

Figure 5

Synthetic routes of sophoridine derivatives 4a-f and 5 that have anti-cancer effects.

Recently, Zhao et al (2020) found that compound 5 (Figure 5) induced DNA breakage and cell apoptosis by blocking STAT5a nuclear translocation and inhibiting STAT5a phosphorylation at 694 and 780.38 Compared to other derivatives, compound 5 also displayed outstanding water solubility and lower toxicity properties, and its synthesis is straightforward, suggesting that it could be applied as an anti-cancer compound and, therefore, should be explored further.

The synthesis of novel sophoridine derivatives using acyclic aryloxy phosphoramidate mustard can greatly improve sophoridine’s anti-cancer activity. For instance, compound 6a-6e, containing a phosphoramidate mustard motif substituted at the lactam ring-opened sophoridine skeleton was shown to markedly suppress the viability of S180 and H22 cells (IC50 = 1.01–3.56 μM). In addition, compounds 6a, 6c, and 6e (Figure 6) hindered cancer growth with apparent organ toxicity in mice bearing liver tumors, and molecular docking showed compounds 6a-6e binding well with DNA topoisomerase.39

Figure 6

Synthetic routes of sophoridine derivatives 6a-e and 7 that have anti-cancer effects.

SAR analyses in a series of sophoridine derivatives show that the introduction of the N-benzyl indole group to the 14-carbon atom of sophoridine can significantly enhance sophoridine’s anti-proliferative activity. Of 58 compounds, 33 displayed improved anti-proliferative properties, with IC50 values less than 10 µM; compound 7 exhibited the most potent anti-proliferative activity in all tested cell lines (HepG2, SMMC-7721, Hela, CNE1, CNE2, and MCF7), with IC50 values ranging from 0.93 to 1.89 μM and much lower than that of the parent sophoridine. Anti-cancer mechanisms are strongly associated with the suppression of DNA topo I and the activation of caspase-3 via molecular docking and enzyme assays. In vivo, anti-tumor assays demonstrated that compound 7 suppresses the growth of HepG2 xenografts in nude mice without obvious side effects.40

Per SAR analyses (Figure 7), i) methoxy and N-(4-(phenylmethoxy) benzyl) groups at the indole ring boost anti-cancer activity; ii) the connecting site of indole (attached to sophoridine) at position 3 is preferable to positions 4 or 5; iii) sophoridine derivatives bearing an α, β-unsaturated ketone scaffold are essential to their anti-cancer inhibitory activity; iv) the (R)-configuration of the 6-chiral center is considerably more adequate for anti-cancer activity enhancement than the (S)-configuration. Therefore, the structural modification of sophoridine is a key strategy to enhance its anti-cancer properties.

Figure 7

Structure activity relationship analysis of sophoridine derivatives.

Anti-Virus Activity

Hepatitis B virus (HBV) infection is a severe global health problem caused by the hepatotropic double-stranded DNA virus, with long-term infection capable of causing a series of pathological changes in the liver, such as fatty liver, chronic hepatitis, and advanced liver diseases, including cirrhosis and liver cancer.41 Chen et al (2016) reported that sophoridine inhibits HBV in HepG 2.2.15 cells by reducing HBsAg and intracellular HBV DNA levels. Additionally, sophoridine (at doses of 0.4, 0.8, and 1.6 mM) showed a more potent anti-HBV activity than other matrine-type alkaloids (matrine, oxymatrine, and sophocarpine) by effectively down-regulating the mRNA expressions of p38 MAPK, TRAF6, ERK1, NLRP10, and caspase-1; its anti-HBV effect might be partly attributable to the rise in the methylation of HBV DNA.42 Matrine-type alkaloids from Sophora flavescens Alt have also been shown to exhibit potent antiviral activity against HBV.43 Sophoridine was revealed to significantly inhibit HBsAg in the HepG2.2.15 cell line by 40.2% at non-cytotoxic concentrations of 0.4 mM, with a potency degree comparable to matrine’s (34.7% at a concentration of 0.4 mM) but superior to the positive control, lamivudine’s (31.5% at a concentration of 1.0 mM).44 These findings provide a new perspective for the application of sophoridine as an anti-HBV agent.

Enterovirus 71 (EV71) is the main pathogen that causes hand, foot, and mouth disease (HFMD) epidemics.45 It is characterized by single-stranded and positive polarity RNA viruses and belongs to group A of enteroviruses in the family of small RNA viruses.46 Ou et al (2016) found that sophoridine inhibited the EV71 virus adsorption and its RNA replication in vitro (SI = 3.99).47 Using the attachment and penetration assays, Ren et al (2019) established that sophoridine (IC50 = 0.25 mM) displayed significant antiviral activity against EV71 when Vero cells were pretreated with the alkaloid.48

Coxsackievirus B3 (CVB3) also belongs to the enterovirus family of small RNA viruses, which can cause viral myocarditis, hepatitis, and meningoencephalitis in adults.49 Although the pathogenesis of CVB3 has been studied extensively in mouse models and a lot of work has been done on the development of vaccines and therapeutic agents against CVB3, no effective clinical therapeutic methods have been established so far.50,51 Per Zhang et al (2006) sophoridine exhibited antiviral properties against CVB3 both in vitro (primary myocardial cells) and in vivo (BALB/c mice) by speeding up IL-10 and IFN-γ production and shrinking TNF-α levels, possibly through locatine itself rather than via a metabolite.52

Neuroprotection and Analgesic Activities

Sophoridine is a quinolizine alkaloid and a structural isomer of matrine whose biological activities have been scrutinized extensively and shown to be similar to its pharmacological activities. Studies have revealed that matrine is an effective neuroprotective substance against cerebral ischemia.53–55 Researchers examining the effect of sophoridine (10, 20, and 40 mM) on nerves in a model of permanent middle cerebral artery occlusion (PMCO) found that it had a potential neuroprotective activity, including diminishing cerebral edema and infarct volume, possibly via the down-regulation of TRAF6 expression and the up-regulation of erk1/2 phosphorylation.56 In Miao et al’s research (2013), sophoridine significantly improved neural dysfunction in ischemia-reperfusion injury by inhibiting the TLR4/NF-κB signal pathway.57 These findings indicate that sophoridine possesses a decent neuroprotective activity.

Compound matrine injection is clinically used primarily against cancer pain and bleeding, with sophoridine one of its main components.58 Yan et al (2013) found that sophoridine significantly alleviated pain and inhibited tumor progression in rats with W256 tumor cell transfection-induced bone cancer pain by enhancing the mechanical withdrawal threshold and thermal withdrawal latency via a mechanism associated considerably with the inactivation of the expression of cyclooxygenase-2 (COX-2) and vascular endothelial growth factor (VEGF) or linked to nitric oxide (NO),59 a neurotransmitter with a key role in the intermediation stage of pain signaling.60,61 Further research has shown that the mechanism of sophoridine’s analgesic property against bone cancer pain may be associated with its down-regulation of the “NMDAR-nNOS/NO-cGMP” signal transduction pathway that is closely linked to hyperalgesia.62 Zhang et al (2012) also demonstrated sophoridine’s outstanding analgesic activity in traditional pain model-induced hot-plate, writhing, and tenderness tests, which was more potent than those of other matrine-type alkaloids (oxymatrine, sophocarpine, and oxysophocarpine) in acetic acid writhing pain.63 These reports provide experimental bases for the further development of alkaloids; however, their specific mechanisms must be investigated further.

Effect on Cardiovascular System

Heart failure (HF) is characterized by contractile dysfunction and the activation of neurohumoral factors and is escalating major health problems worldwide.64 Studies have demonstrated matrine-type alkaloids’ positive inotropic activity on the myocardium, which could be associated with the activation of the calcium channel. For example, matrine, oxymatrine, sophoridine, and sophocarpine, with common molecular structures of O = C = N-CC-CC-N, possess positive ion effects and hERG blocking activities.65,66 Some investigations have suggested that this structure may be responsible for the positive inotropic effect of matrine-type alkaloids, possibly in association with the activation of calcium channels. The abnormal regulation of Ca2+ by the L-type Ca2+ channel (LTCC)/dihydropyridine receptor (DHPR) and Ca2+-ATPase (SERCA2a) is the underlying mechanism for muscle dysfunctions in HF.67 Our assessment of the effect of sophoridine on heart failure in a rat model of chronic HF revealed that sophoridine (5 and 10mg/kg) improved HF by ameliorating cardiac Ca2+-induced Ca2+ transients through the up-regulation of the dihydropyridine receptor (DHPR).68 The administration of 5 mg/kg of sophoridine provided sufficient significant cardioprotection against myocardial infarction-induced heart injury. Similarly, Hu et al (2014) found that sophoridine protects myocardial in rats with chronic HF by recovering the sarcoplasmic reticulum calcium capacity via a mechanism that is possibly associated with the up-regulation of SERCA2a expression in cardiomyocytes.69 Therefore, sophoridine can become a novel, effective therapeutic drug for the treatment of HF.

Acute myocardial ischemia (AMI) is a pathological condition marked by failure of the heart to function properly in which blood perfusion in the heart rapidly decreases, leading to an abnormal heart function.70,71 Ding et al (2010) established an AMI model in vivo by ligating the left anterior descending coronary artery (LAD) to evaluate the effects of sophoridine on cardiac function in rats with AMI. By recording the cardiac function indexes of pre-LAD occlusion using the BL-420 biological function experimental system, the authors noted that sophoridine improved the cardiac function of rats with LAD acduion-induced acute myocardial ischemia injury, boosting the left ventricular systolic pressure (LVSP) and ± dp/dtmax changes and decreasing the left ventricular end-diastolic pressure (LVEDP) of AMI.72 They also observed that acute myocardial infarction caused irreversible myocardial necrosis due to sudden and persistent AMI, with the changes and recovery of various cardiac function indexes associated with the scope of myocardial infarction. Ding et al (2009) noted that sophoridine ameliorated cardiac damage in a rat model of AMI by shrinking the myocardial ischemic infarct size dose-dependently.73

Sophoridine is protective against arrhythmia too. The human ether-à-go-go-related gene (hERG), which encodes the rapid component of the cardiac delayed rectifier K+ current (IKr), has a significant role in the repolarization of the cardiac action potential.74–76 One study assessed the effects of sophoridine on hERG-encoded K+ channels in HEK293 cells stably transfected with hERG cDNA using the whole-cell patch-clamp technique and found that sophoridine acted as a low potency blocker of hERG K+ channels by altering the channels’ kinetics. Additionally, sophoridine had a higher binding affinity for the open state; however, it had no impact on the generation and transport of the hERG protein.77 According to Hu and his colleagues (2016), the anti-arrhythmia effect of sophoridine is closely associated with the inhibition of cardiomyocytes’ scavenging of hydroxy radicals and effect on the ion channels.68 In other studies, sophoridine significantly inhibited aconitine, BaCl2, and coronary ligation-induced ventricular arrhythmias in rats.78 Therefore, sophoridine harbors significant anti-arrhythmia properties whose specific mechanism must be researched further.

Anti-Inflammatory Activity

Inflammation is associated with the development and progression of many diseases, including pneumonia and colitis. Therefore, the search for effective and low-toxicity anti-inflammatory drugs remains a research hotspot. Endotoxin or lipopolysaccharide (LPS) is crucial to the infection-triggered systemic inflammatory response syndrome.79 In recent years, many investigations have focused on the antagonistic effect of sophoridine on LPS. Huang et al (2014) demonstrated sophoridine’s excellent anti-inflammatory activity in which the alkaloid protected mouse macrophages from LPS-induced apoptosis and inhibited the production of inflammatory cytokines (TNF-α and IL-8) and inflammatory media prostaglandin E2 (PGE2) in vitro and in vivo.80 The intercellular adhesion molecule-1 (ICAM-1) gene is a member of the immunoglobulin superfamily (IGSF) of adhesion molecules and plays a pivotal role in the body’s immune response.81,82 In a dextran sulfate sodium (DSS)-induced colitis C57BL/6 mouse model, Zhao et al (2010) revealed for the first time that sophoridine markedly attenuated colonic inflammatory response by negatively mediating the expression of the ICAM-1 gene.83 Another in vivo experiment detailed sophoridine’s significant protective effect against acute LPS-induced liver injury via a mechanism possibly associated with the inhibition of p-ERK expression in liver tissues and TNF-α expression in serum.84 Similarly, Zhang et al (2015) reported that sophoridine suppressed RAW264.7 cell inflammatory response by mitigating the expressions of CD14, P38, and iNOS.85 The TLR4/JNK axis also allegedly participates in the execution of sophoridine’s (125.8 μM) protective effect on LPS-induced RAW264.7 cells.86

Acute lung injury (ALI) is a primary cause of morbidity and mortality worldwide and is characterized by extensive inflammation of the lungs.87 In an LPS-induced lung injury mouse model, researchers found that sophoridine alleviated inflammatory response by suppressing the NF-κB (phosphorylation of p65 and IκB) and MAPK (phosphorylation of p38 and JNK) pathways.88,89 On their part, Yang et al (2012) demonstrated that the anti-inflammatory activity of sophoridine on lungs relies on its inhibition of IL-6, IL-10, NO, and malondialdehyde (MDA) and elevation of superoxide dismutase (SOD).90 These results indicate that sophoridine could treat inflammation-related diseases.

Others

The pharmacological properties of sophoridine against other conditions have also been examined. The formation of osteoclasts (OCs) is one of the decisive pathological processes in the occurrence and development of osteoporosis.91,92 In Zhao et al (2011), ovariectomized mice (OVX) treated with sophoridine (15mg/kg) dose-dependently and time-dependently blocked RANKL-induced OC formation and activation of ERK and c-fos, as well as NFATc1 induction and nuclear translocation. Therefore, sophoridine protected against ovariectomy-induced osteoporosis, possibly by inhibiting OC formation through the RANKL-ERK-NFAT pathway.93

Sophoridine, it is alleged, also inhibits sperm motility in vitro dose-dependently. One study noted that a low dose of sophoridine (44.3 μM) inhibited sperm motor function, while a considerably higher dose (120.8 μM) concentration altered the morphological structure of sperm, including sperm crack. Per a drug sensitivity test, sophoridine did not interfere with the growth and reproduction of normal vaginal flora, especially lactobacillus. Therefore, sophoridine as a vaginal spermatostatic agent cannot destroy the normal physiological environment of the vagina.94

Sophoridine also inhibits a variety of bacteria. Zhou et al (2001) observed that sophoridine significantly inhibited five environmental bacterial strains (Escherichia coli, Enterobacter aerogenes, Proteus vulgaris, Bacillus subtilis, and Staphylococcus epidermidis) at a minimum inhibitory concentration (MIC) of 20–40 mM.95 Another study elaborated on sophoridine’s bacteriostatic effect on bacteria that cause common urogenital tract infection, like Escherichia coli (MIC = 32.2 mM), Pseudomonas aeruginosa (MIC = 32.2 mM), and Staphylococcus epidermidis (MIC = 16.1 mM): sophoridine’s bacteriostatic effect was stronger than that of oxysophoridine.96 Sophoridine undoubtedly possesses a broad spectrum of pharmacological activities and can be used to treat specific diseases (Table 1), which points to its far-reaching application prospects.

Pharmacokinetics of Sophoridine

The development of pharmacochemistry has seen the pharmacokinetic characteristics of drugs become more and more complex and establishing them become progressively more challenging. Presently, the acceptability of a drug requires assessing its characteristics and application prospects based not only on high efficiency and low toxicity but also on excellent pharmacokinetic properties.97 A study found that intravenously administering 20 mg/kg of sophoridine to rats resulted in the following body tissue distribution order: kidney > spleen > uterus > gastrointestinal tract > liver > lung > heart > muscle > brain > blood.98

Liu et al (2014) reported a low absolute bioavailability (Fabs) of sophoridine via gavage (Fabs = 41.8%), as well as an increased area under the plasma concentration–time curve and improved sophoridine bioavailability post-intravenous administration (AUC0-18h = 3005.3 ng.h.mL−1) compared to intragastric administration (AUC0-18h = 1256.2 ng.h.mL−1). The low absolute bioavailability via gavage was probably due to the first-pass effect of oral administration during which part of sophoridine is destroyed in the liver so that the effect of what is left of the drug absorbed into blood circulation is reduced.99 In Wu and colleagues’ (2005) high-performance liquid chromatography-mass spectrometry (HPLC-MS) investigation to examine the pharmacokinetic features of sophoridine in rabbit plasma, they established a decent linear relationship between the peak area and concentration at sophoridine doses ranging from 0.05 to 4 μM.100 In another trial, 16 tumor patients were given sophoridine (75, 125, and 144 mg.m−2) by intravenous infusion at a constant rate for 3 h, and subsequent analyses revealed that the drug was rapidly distributed and eliminated (t1/2β = 5.22, 7.42, and 7.41 h) in the body, eventually excreting mainly in its original form through the kidney.8

A liposome is a type of microcapsule with a bilayer structure similar to a biofilm; it has low toxicity, low irritation, and excellent biocompatibility.101 Nano-liposomes were prepared from sophoridine and used to alter the distribution of drugs in the body, prolong the action time of drugs in target tissues, improve drug efficacy, and reduce the side effects of drugs.102 In an HPLC analysis of the pharmacokinetics and distribution of sophoridine nano-liposome injections in rats after administration through the tail vein using sophoridine injection as control, results showed that the AUC curve of sophoridine nano-liposomes was 2.42 times as much as that of sophoridine injection, with prolonged retention time in vivo.103

Bovine serum albumin (BSA) is the most abundant carrier protein in serum, which can combine with many compounds and is an important carrier and target of drugs. To explore the interaction between drugs and BSA is of great significance for understanding the distribution, transport, efficacy and metabolism of drugs in vivo, revealing pharmacokinetics, guiding clinical rational drug use and new drug design and development.104,105 There is a strong binding effect between sophoridine and BSA, and the main driving force behind this binding effect is electrostatic attraction. In a study on the binding sites of sophoridine on BSA using sites I and II probes, sophoridine liaised with the site I loci on BSA hydrophobic cavities. The results provided important information for studying the storage, transportation and pharmacodynamics of sophoridine in vivo.106

Traditional Chinese medicine often contains multiple ingredients, with other ingredients also capable of impacting the elimination of the drug. Wu et al (2005) found that the elimination half-life of sophoridine in Kuhuang injection (T1/2β = 67.2 min) was shorter than that of standard sophoridine (T1/2β = 84.5 min), suggesting that other components in Kuhuang injection promote the elimination of sophoridine.107 In their investigation, Hu and his colleagues (1995) demonstrated that sophoridine was eliminated primarily through excretion via the kidney and urine after it was injected into the tail vein of rats.98 In Li et al’s research (2006), sophoridine was excreted as a prototype through the kidney in the human body.8 Further relevant pharmacokinetic parameters of sophoridine in vivo are summarized in Table 2; these also provide meaningful references for the pharmacokinetic study of sophoridine.

Table 2

Pharmacokinetic Parameters of Sophoridine in vivo

Inclusion of Drug Components	Administration Route	Dosage	In vivo/Model	Pharmacokinetic Parameters of Sophoridine	Ref.
Sophoridine	iv drip	75, 125, 144 mg/m2	Cancer patients	T1/2β=5.22, 7.42,7.41hMRT=7.64, 7.73, 7.16hAUC=17.35, 41.50, 45.97 mg.h/L	[8]
Sophoridine	iv	10 mg/kg	SD rats	T1/2=1.75 h,Cmax=5.56 mg/L,AUC=12.80 mg.h./LMRT=1.56 hCL=0.81L/(mg.h)	[126]
Sophoridine injection and sophoridine nano-liposome	iv	6.25 mg/kg	SD rats	T1/2α=0.496,1.113 hT1/2β=2.494,2.323 hAUC=215.542, 522.215 mg.h/LMRT=37.50,95.72hCL=0.029, 0.011 L/(mg.h)	[103]
Sophora alopecuroides L.	ig	40 mg/kg (equivalent to sophoridine)	SD rats	T1/2α=0.28 hT1/2β=3.66 hCmax=1.62 mg/LAUC=4.84 mg.h/ulTmax=0.75 hCL=0.1 L/(mg.h)	[127]
Sophoridine	iv	2 mg/kg	KM mouse	T1/2β=2.7±0.2 hAUC=3.038±0.023 mg.h/LCL=5.8±1.8 mL/h	[99]
Sophoridine	ig	2 mg/kg	KM mouse	T1/2β=3.6±0.5 hAUC=1.265±0.042 mg.h/LCL=7.5 ±1.2mL/hTmax=1±0.33 h,Cmax=0.756±0.057 mg/L	[99]
Sophoridine	ig	200 mg/kg	Rabbit	T1/2α=78.68 minT1/2β=187.07 minCmax=10.91 mg/LAUC=2303.16 (mg.min) /LTmax=45.52 minCL=0.2171 L/(min)	[128]
Kuhuang injection	iv	1.5 mL/kg (equivalently sophoridine with 0.122 mg/kg)	Rabbit	T1/2α=4.90 minT1/2β=67.2 minAUC=2957 ug.min/LCL=130.8 mL/(min.kg)	[107]

Abbreviations: Cmax, maximum plasma concentration; Tmax, the time of maximum plasma concentration; AUC, the area under the plasma concentration time curve; T1/2α, the distributed half-life; T1/2β, the elimination half-life; MRT, mean residence time; CL, clearance.

Toxicology of Sophoridine

In addition to the numerous pharmacological studies, experiments to understand the toxicology of sophoridine against normal cells and mice have been conducted. One reported sophoridine’s cytotoxicity against Vero cells (African green monkey kidney cell), with an IC50 value of 5.69 mM via an MTT assay.48 However, in Wang et al’s investigation (2019), sophoridine displayed no cytotoxicity against two non-tumorigenic cell lines (HKC and LX-2), even at a high concentration of 160 μM.22 Another report found sophoridine to concentration- and time-dependently inhibit the activity of BRL-3A cells (rat normal liver cells) at IC50 values of 2.94 mM (12 h), 1.9 mM (24 h), and 1.29 mM (48 h), respectively. Perhaps, sophoridine reduces ATP levels and the mitochondrial membrane potential, thereby inducing apoptosis through the mitochondria-dependent apoptosis pathway.16 Lower degrees of cytotoxicity to human pancreatic ductal epithelial (HPDE) cells and human bronchial epithelial (BEAS-2B) cells have also been demonstrated, with corresponding IC50 values of 0.402 and 0.458 mM.11

Sophoridine toxicity assessments have also been carried out in vivo in recent years. In Shi et al’s (2020) acute evaluations of sophoridine (ip), the alkaloid had an acute toxic LD50 of 62.6 mg/kg in mice. Its continuous administration for 30 days caused substantial organ damage, including the liver and kidney; however, these recovered after 30 days of discontinuing the treatment.108 Yu et al (2006) derived an LD50 of 47.6 mg/kg for sophoridine injection into the tail vein of mice,109 while Zhang et al (2011) showed that a one-time intraperitoneal injection of sophoridine (32–78.1 mg/kg) reduced the autonomous activity of mice, with an LD50 (65.19 mg/kg) of the drug close to LD1 (39.74 mg/kg).110 According to Zhu et al (1995), intraperitoneally injecting 27 mg/kg (about 27 times the clinical therapeutic dose) of sophoridine resulted in embryotoxicity in Wistar pregnant mice, including decreased weight gain and increased stillbirth rates; however, no teratogenic effect was noted.111 In contrast, Zhang et al (2006) reported no sophoridine-related toxicity in mice, not even at an oral dose of 40 mg/kg, suggesting it can be used in a clinical setting.52

After intraperitoneally injecting rats with sophoridine (32 mg/kg) for 60 days, Li et al (2004) found that the rats developed various neurotoxic reactions, including fluffiness, tail erection, muscle tremor, and convulsion. However, the investigators established no histopathological changes or delayed alterations in the nervous system. Therefore, sophoridine-caused neurological symptoms are functional, stressful, and reversible without late-onset and sequelae.112

Cheng et al’s analyses (2010) yielded sophoridine (47.83 mg/kg)-induced increases in the expressions of ERK1, ERK2, and p-ERK1/2 proteins in hippocampal CA1 neurons and epileptic damage to rat hippocampal tissues through the activation of the ERK signaling pathway.113 Another investigation examined the effects of sophoridine on the morphology and ultrastructure of hippocampal neurons in the CA3 region and revealed that sophoridine induced hippocampal neuronal damage, including the destruction of the nuclear membrane bilayer structure, severe nuclear pyknosis, and mitochondrial swelling, which resulted in epilepsy.114 The authors subsequently demonstrated that sophoridine shortens the incubation period of epilepsy, prolongs the onset of time, and its effect is stronger than that of penicillin,115 with the mechanisms possibly associated with sophoridine’s elevation of TNF-α, IL-2, and IL-6 in serum.116 The contradictory nature of reports on sophoridine toxicity suggests that the toxicology of this alkaloid requires further research and exploration to ascertain its safety and efficacy. The toxicity of sophoridine is summarized in Table 3 for additional reference.

Table 3

Toxicity of Sophoridine Both in vitro and in vivo Studies

Activity/Mechanism (s) of Action	Cells Lines/Model	Dosage/Route of Administration	Application	Ref.
Inhibiting of cell viability	Vero cells	IC50 = 5.69 mM	In vitro	[48]
Down-regulating the ATP levels and mitochondrial membrane potential; Mitochondria - dependent apoptosis pathway induces apoptosis	BRL-3A cells	IC50 = 1.9 mM	In vitro	[16]
Inhibiting of cell viability	HPDE cells	IC50 = 0.402 mM	In vitro	[11]
Inhibiting of cell viability	BEAS-2B cells	IC50 = 0.458 mM	In vitro	[11]
Liver and kidney damage, recovery after 30 days of drug withdrawal	KM mice	LD50 = 62.6 mg/kg, ip	In vivo	[108]
Mice showed irritability, vertical tail, clonus and even death	ICR mice	LD50 = 47.6 mg/kg, iocv	In vivo	[109]
Reduced autonomic activity and crouching	KM mice	LD50 = 65.19mg/kg, LD1 = 39.74mg/kg, ip	In vivo	[110]
Weight gain decreased and stillbirth rates increased	Wistar pregnant mice	27 mg/kg, ip	In vivo	[111]
Neurotoxic reaction	SD rats	32 mg/kg, ip	In vivo	[112]
Up-regulating ERK1, ERK2 and p-ERK1/2 proteins in hippocampal neurons; Epileptic damage to hippocampus is caused by activation of ERK signaling pathway	SD rats	47.83 mg/kg, ip	In vivo	[113]
Nuclear membrane bilayer structure destruction, severe nuclear pyknosis, mitochondrial swelling, resulting in epilepsy	SD rats	47.83 mg/kg, ip	In vivo	[114]
Shorten the incubation period of epilepsy, prolong the attack time	SD rats	47.83 mg/kg, ip	In vivo	[115]
Up-regulating TNF-α, IL-2 and IL-6	SD rats	55 mg/kg, ip	In vivo	[116]

Conclusion and Future Perspectives

Natural products are key sources for the development of new drugs.117–119 In recent years, artemisinin, camptothecin, and others have been examined and have seen increased use thanks to their acceptable efficacy and low toxicity. Sophoridine is another natural compound with a unique chemical structure and pharmacological action. It can be extracted from some commonly used traditional herbal medicines. In this review, we have systematically summarized the chemical properties, plant origin, pharmacological activities, toxicity, and pharmacokinetic characteristics of sophoridine and hope that the material we have put together provides a reference point for future research and the further development of sophoridine.

At present, sophoridine is used mostly to treat malignant trophoblastic tumors that cannot be attended to with standard chemotherapy. However, many investigations have demonstrated excellent inhibitory effects of this substance on other forms of tumors. As mentioned previously, sophoridine has shown good anti-cancer effects by blocking cells in the S phase and decreasing mitochondrial-related apoptosis, up-regulating cytotoxicity in human medulloblastoma, and regulating the TLR4/IRF3, RAS/MEK/ERK, NF-κB, and PTEN/PI3K/Akt signaling pathways. In addition, sophoridine also regulated apoptosis proteins and cell cycle-related genes (cleaved caspase-3, caspase-7, caspase-9, Bcl-2, MMP-2, and MMP-9) in tumor cells. Research can, therefore, utilize nanotechnology and structural modifications (new sophoridine derivatives) to promote its anti-tumor activity for clinical use.

Because the risk of cancer is further amplified by chronic inflammation considered one of the hallmarks of cancer,120,121 we have also presented findings on sophoridine’s significant anti-inflammatory activity mediated mainly by modulating immune cells and related cytokines, including TNF-α, IL-6, IL-8, IL-10, NO and iNOS, etc. Furthermore, we have digested results on sophoridine’s therapeutic potential against viruses and cardiovascular diseases. As mentioned above, experiments with some animal models have demonstrated that sophoridine not only inhibits cardiomyocytes’ scavenging of hydroxyl radicals and effect on cardiac ion channels but also has positive inotropic effects. Sophoridine, as presented above, also inhibits HBV, EV71, and CBV3 viruses. According to literature reports, sophoridine through structural modification (benzyl indole group or chlorobenzyl), can improve its anti-tumor pharmacological activity, but in other pharmacological activities (inflammatory and viruses) are relatively lack, later can increase this aspect of research, screen more activity and lower side effects of sophoridine derivatives. Its therapeutic mechanism must also be established with the help of metabolomics and pharmacology.

In addition to the therapeutic effects of drugs, their pharmacokinetic properties and safety are key factors in determining their potential for clinical application. It has been reported that sophoridine is widely distributed in various tissues, including kidney, liver, gastrointestinal, uterus, lung and other organs. Sophoridine showed hepatotoxicity, reproductive toxicity and neurotoxicity. Therefore, it is necessary to further study the methods to reduce the toxicity of sophoridine in order to improve its medicinal value. The structure can be modified to produce sophoridine derivatives that are specific to specific organs and reduce their widespread distribution and resulting toxicity.

Added to that, a recent study reported that the support vector machine (SVM) classifier and physiologically based pharmacokinetic (PBPK) modeling can be optimized to predict the oral hepatotoxicity dose of natural products derived from traditional Chinese medicines (NP-TCMs).122,123 Therefore, if these methods can be used to predict the hepatotoxicity of sophoridine in future experiments, evaluating its safety and clinical applicability will take one step forward. To better assess its side effects or toxicity and render it safe to use, rigorous in vivo testing must be performed.

Sophoridine and berberine are both bioactive alkaloids derived from many herbs, but they have some differences in pharmacological activity and pharmacokinetics. Berberine is widely used to treat diabetes mellitus, and its mechanism probably consists of inhibiting hepatic gluconeogenesis and inducing hyperglycolysis and insulin sensitivity.124 On the other hand, sophoridine is the focus of anti-tumor research, particularly malignant trophoblastic tumors. Many experimental studies have confirmed that berberine is metabolized rapidly in vivo, primarily by the liver and intestinal flora, and its content and structure change after metabolism.124 In contrast, research shows that sophoridine is metabolized primarily through urine excretion as a prototype of the human kidney.8,98 Still, the difference in LD50 between sophoridine and berberine (65.19 vs 57.6 mg/kg) by intraperitoneal injection is miniscule.110,125

Collectively, sophoridine has multiple biological activities. To promote its development for acceptable clinical application, future research should consider focusing primarily on the following aspects: (i) elucidating its anti-cancer molecular mechanism using scientific techniques and methods; (ii) conducting more in-depth investigations to demonstrate the potential of sophoridine in the treatment of viruses and arrhythmias; (iii) performing more in vivo experiments to clarify its safety; (iv) improving oral availability and drug treatment potential through nanotechnology and chemical structure modification.