Evidence-Based Complementary and Alternative Medicine

Volume 2013 (2013), Article ID 925625, 14 pages

http://dx.doi.org/10.1155/2013/925625

Review Article

Effects and Mechanisms of Chinese Herbal Medicine in Ameliorating Myocardial Ischemia-Reperfusion Injury

Qing Liu,1,2 Jiqiang Li,² Jing Wang,² Jianping Li,¹ Joseph S. Janicki,¹ and Daping Fan¹

¹Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, SC 29208, USA

²The Second Clinical School of Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510405, China

Received 24 July 2013; Revised 26 August 2013; Accepted 4 September 2013

Academic Editor: Joen-Rong Sheu

Copyright © 2013 Qing Liu 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.

Myocardial ischemia-reperfusion (MIR) injury is a major contributor to the morbidity and mortality associated with coronary artery disease, which accounts for approximately 450,000 deaths a year in the United States alone. Chinese herbal medicine, especially combined herbal formulations, has been widely used in traditional Chinese medicine for the treatment of myocardial infarction for hundreds of years. While the efficacy of Chinese herbal medicine is well documented, the underlying molecular mechanisms remain elusive. In this review, we highlight recent studies which are focused on elucidating the cellular and molecular mechanisms using extracted compounds, single herbs, or herbal formulations in experimental settings. These studies represent recent efforts to bridge the gap between the enigma of ancient Chinese herbal medicine and the concepts of modern cell and molecular biology in the treatment of myocardial infarction.

1. Introduction

Myocardial infarction (MI) and the accompanying acute loss of viable myocardium is the leading cause of death in industrialized countries. Even if the patient survives the acute phase of MI, the subsequent adverse myocardial remodeling and impairment of cardiac function severely impact their quality of life and 5-year survival. Early restoration of blood flow to the ischemic myocardium is a common treatment strategy aimed at limiting myocardial infarct size. However, reperfusion can cause additional cell death and, in many cases, paradoxically increase infarct size, a situation referred to as myocardial ischemia-reperfusion (MIR) injury. MIR is characterized by a rapid increase in cytokines and chemokines and an influx of leukocytes into the vulnerable region bordering the infarcted site. This inflammatory response not only results in cardiomyocyte apoptosis during the acute phase, but also results in an adverse myocardial remodeling that further compromises cardiac function. Therefore, limiting ischemia-reperfusion (I/R) induced myocardial inflammation may not only lower the acute death rate, but also improve long term survival and quality of life [1]. Chinese herbal medicine, especially combined herbal formulations, has been widely used in traditional Chinese medicine for the treatment of MI for hundreds of years. The purpose of this review is to highlight recent studies that experimentally address the mechanistic effects of extracted compounds, single herbs, or herbal formulations on several factors and pathways known to be involved in MIR injury.

2. Myocardial Ischemia-Reperfusion Injury

2.1. Oxidative Stress

Reactive oxygen species (ROS) have both a physiological and pathological role in cellular and tissue adaptation to environmental factors. Normally, low levels of oxygen radicals and oxidants are present in cells and are important in maintaining cellular homeostasis, mitosis, differentiation, and signaling [2]. However, during MIR, ROS formation is markedly increased and cellular injury occurs (Figure 1). Although mammalian cells express endogenous free radical scavenging enzymes, such as superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), these antioxidative defenses are insufficient during MIR [3, 4]. Oxidative stress during MIR injury contributes to a vicious cycle as it promotes mitochondrial dysfunction, excitotoxicity, lipid peroxidation, and inflammation [5–7].

Figure 1: Effects and mechanisms of Chinese herbal medicine in myocardial ischemia-reperfusion (MIR) injury. During ischemia, oxygen is not available to accept the electrons in the metabolic degradation of substrates, and consequently anaerobic metabolites become important in the preservation of myocardial viability. However, free radicals and reactive oxygen species (ROS) formation is markedly increased in this procedure. Reperfusion also generates high ROS levels which have an adverse impact on specific signal transduction systems, thereby predisposing the heart to further oxidative cell damage. Damaged cell debris, fibrinogen, cytokines, and chemokines will activate the receptors, including TLRs, TNFR, and ILR, in the host inflammatory cells as well as the cardiomyocytes. This sterile inflammatory process leads to the formation of a vicious circle, whereby the cardiomyocyte TLRs, TNFR, and ILR are activated by inflammatory cell-generated ligands. Typically, this has an adverse impact on specific signal transduction systems (e.g., AMPK, JNK, and NF-κB pathways), thereby activating the caspase cascade. Elevated ROS levels also result in intracellular Ca²⁺ overload which adversely affects mitochondrial function by opening the mitochondrial permeability transition pore (MPTP). As a result, the balance between Bax and Bcl is interrupted and the caspase cascade is further activated, leading to apoptotic cell death and myocardial tissue damage. Injured tissue expresses SDF-1, which interacts with its specific receptors (e.g., CXCR4) to facilitate the trafficking, adhesion, and infiltration of bone marrow derived stem cells (BMSCs). BMSCs produce high levels of the endothelial cell-specific angiogenic factor, VEGF, which is a critical regulator of angiogenesis that includes the stimulation of proliferation, migration, and proteolytic activity of endothelial cells and eventually leads to an increase in vessel density and the facilitating of myocardial regeneration and remodeling. During the MIR injury process, there are seven target areas where Chinese herbal medicine can exert protective effects on cardiomyocyte. Examples are as follows: (1) anti-oxidation actions of Palmatine, Forsythoside B, and SiNi Decoction; (2) anti-inflammatory properties of Tanshinone IIA, Schisandrin B, and ShuMai Decoction; (3) anti-apoptosis ability of Salidroside, Tyrosol, and Cardiotonic Pill; (4) protection of mitochondrial function by Herba Cistanches, Cistanche, and Guanxin II; (5) increasing BMSCs migration by Tanshinone IIA and Salvianolic acid B (6) promoting angiogenesis by Radix et Rhizoma Rhodiolae Kirilowii, ShuMai Decoction and TongXinLuo Superfine; and (7) inhibiting Ca²⁺ overload by Astragaloside IV, Lycium barbarum, and Acanthopanax senticosus injection.

2.2. Sterile Inflammation

Ischemia and reperfusion cause sterile inflammation. Nevertheless, the consequences of MIR share many phenotypic parallels with activation of a host immune response directed toward invading microorganisms [8]. This sterile inflammation is mainly triggered by the interactions between toll-like receptors (TLRs) and their endogenous ligands generated in ischemic and reperfused myocardium, such as apoptotic cell debris, fibrinogen, high mobility group box (HMGB) 1, and heat shock proteins (HSPs) [9]. The activation of immune cell and cardiomyocyte TLR and other signaling pathways results in a vicious cycle of inflammatory response in the I/R region and causes significant cardiomyocyte apoptosis (Figure 1). Following the acute I/R period, the cardiac function is further compromised by adverse myocardial remodeling [10]. The magnitude of the inflammation during the acute phase determines the extent to which cardiac function is compromised during the following myocardial remodeling phase.

During the sterile inflammation phase of MIR, TLRs play detrimental roles as demonstrated by extensive experimental evidence [11]. To date, 11 TLRs (TLR1–TLR11) have been identified in mammals. It should be noted that, during MIR, the expression of TLR4 is significantly increased in both the failing myocardium, and infiltrated macrophages and thus TLR4 is thought to be a central mediator of inflammation and cardiac injury. TLR4 has been identified as a mediator of inflammation and organ injury in several models of sterile tissue injury including MIR, and a soluble inhibitor of TLR4 was able to prevent contractile dysfunction in wild-type cells [12]. Using a temporary left anterior descending (LAD) artery occlusion model, Oyama et al. first observed myocardial infarct size reductions in 2 distinct strains of mice that lack functional TLR4 signaling, accompanied with reduced neutrophil infiltration in the affected myocardium [13]. TLR2, which is expressed in cardiomyocytes and many other cell types, also contributes to the pathogenesis of cardiac dysfunction during MIR [14, 15]. Activation of TLR2, TLR4, and TLR5 increases the myocardial level of the inflammatory cytokines, chemokines, and cell surface adhesion molecules [16]. Given the known role of TLR4 and TLR2 in MIR, inhibition of TLR4 and TLR2 signaling is a promising approach to reduce morbidity and mortality in MI patients.

There are a variety of TLR ligands generated during MIR. For example, heat shock proteins (HSPs) are a class of molecular chaperones that promote intracellular protein folding. They may be released into the extracellular space after cell trauma and interact with adjacent cells or distant cells via bloodstream delivery [17]. Extracellular HSP60 induced apoptotosis via the activation of TLRs [18]. Another example is HMGB1 which is a damage-associated molecular pattern (DAMP) protein secreted by injured cells [19]. It plays a major role in early MIR by binding to TLRs and the receptor for advanced glycation end products (RAGE), resulting in the activation of proinflammatory pathways and enhanced myocardial injury [20]. In fact, a prerequisite for neutrophil-mediated tissue damage is the “priming” effect of various pro-inflammatory stimuli generated by damaged tissue during MIR, such as HSP60 and HMGB1 [21]. Cytokines released by TLR-activated cells such as tumor necrosis factor-alpha (TNF-α) and IL-1 can elicit neutrophil polarization and upregulation of cell-surface glycoproteins such as macrophage adhesion molecule-1 (Mac-1) [22]; Mac-1 upregulation in peripheral neutrophils is a very early event in MIR [23].

2.3. Apoptosis and Mitochondrial Function

MIR leads to the activation of cell death programs, including apoptosis, autophagy-associated cell death, and necrosis [24]. Apoptosis involves an orchestrated caspase signaling cascade, including caspase-3 and caspase-9, which induces a self-contained program of cell death, characterized by the shrinkage of the cell and its nucleus, with plasma membrane integrity persisting until late in the process [25]. The balance between apoptotic factors Bcl-2 and Bax has been found altered in cardiomyocytes during ischemia [26]. Autophagy is stimulated by nutrient starvation and growth factor deprivation when cells are unable to take up external nutrients. Autophagy is also activated by decreases in ATP in order for the cell to maintain energy homeostasis and survival. Autophagy may serve primarily to maintain energy production during acute ischemia but switch to clear up damaged organelles during chronic ischemia or reperfusion [27].

Multiple cell signaling pathways, such as the AMPK, JNK, and NF-κB pathways, have been shown to be involved in MIR-induced cardiomyocyte apoptosis (Figure 1). AMPK orchestrates the regulation of energy-generating and energy-consuming pathways; its activation has been shown to protect the heart against ischemic injury [28, 29]. Activated JNK signaling, especially in mitochondria, is associated with oxidative stress, mitochondrial dysfunction, and cell death [30]; it is a key modulation event in cell death mediated by reactive oxygen and nitrogen species [31]. JNK is also required for TNF-α-stimulated ROS production and cytochrome c-mediated cell death; Bcl-2 family members are essential components of this mitochondrial apoptotic machinery. Studies have suggested that blockage of JNK mitochondrial translocation or JNK inhibition prevents ROS production and mitochondrial dysfunction and may be an effective treatment for I/R-induced cardiomyocyte death [32–35]. The nuclear factor kappa B (NF-κB) also modulates apoptosis during ischemia and reperfusion [36]. TLR signaling pathway leads to translocation of NF-κB to the nucleus and thus up-regulation of expression of proinflammatory cytokines. However, there is the possibility that a crosstalk between the TLR/NF-κB and PI3K/Akt signaling pathways and modulation of the crosstalk could protect the myocardium from I/R injury [37].

Within the mitochondria dependent intrinsic apoptosis pathway, which has an important function in cardiac cell injury under various pathological conditions [38], mitochondrial permeability transition pore (MPTP) opening plays a pivotal role [39]. The event of MPTP opening is affected by various factors including intracellular Ca²⁺, oxidative radicals, ATP levels and the levels of Bcl-2 family proteins [40].

2.4. Bone Marrow Stem Cell Migration

Bone marrow mesenchymal stem cells (BMSCs) are multipotent cells that secrete angiogenic factors. Injured tissues express specific receptors, such as CXCR4, and/or their ligands including stromal cell-derived factor-1 (SDF-1), to facilitate trafficking, adhesion, and infiltration of BMSCs. During MIR, BMSCs are preferentially attracted to and retained in the ischemic tissue [41, 42]. As a result of the hypoxic microenvironment, these BMSCs produce high levels of vascular endothelial growth factor (VEGF), leading to an increase in vessel density and facilitating myocardial regeneration and remodeling [43, 44] (Figure 1).

2.5. Angiogenesis

Angiogenesis refers to the sprouting, bridging, intussusception, and/or enlargement of capillaries. In the late stage of MI repair, enhancement of blood flow to ischemic myocardium can result from either true angiogenesis or the recruitment of preexisting coronary collaterals [45]. VEGF is an endothelial cell-specific angiogenic factor and also a critical regulator of angiogenesis that stimulates proliferation, migration, and proteolytic activity of endothelial cells [46]. Ischemia or coronary artery occlusion induces myocardial VEGF expression, which leads to an angiogenesis-induced restoration of tissue blood flow and the prevention of further tissue damage (Figure 1). In addition, VEGF is a potent survival factor during physiological and tumor angiogenesis, and has been shown to induce expression of anti-apoptotic proteins in endothelial cells [47, 48].

2.6. Other Factors

The activation of ATP-sensitive potassium (KATP) channel subunits and ATPase, and calcium (Ca²⁺) overload are also involved in MIR (Figure 1). Ischemia-reperfusion may activate some ion channels that do not open under normal physiological conditions. One such channel is the KATP channel, whose activation facilitates potassium ion efflux, hyperpolarization, and action potential repolarization. The resulting shortening of the action potential duration decreases the total influx of sodium and calcium, which alleviates overloading of intracellular calcium (Ca²⁺) which in turn weakens myocardial contraction force and reduces myocardial oxygen consumption. Therefore, the opening of KATP channels plays an active role in protecting the heart against MIR injury.

3. Effects and Mechanisms of Chinese Herbal Medicine in MIR

The typical symptoms of cardiovascular diseases induced by MIR have been recorded in several ancient books of Traditional Chinese Medicine (TCM), such as Inner Canon of Huangdi and Treatise on Febrile Diseases. In TCM, Qi (energy) and Blood (material) are the main components compromised in MIR, whereby the principal mechanism is considered to be a disorder or deficiency of Qi and a disorder of the circulation (blood stasis) that results in severe pain and even death. Therefore, the main aims of Chinese herbs and herbal formulations in MIR treatment are to regulate or replenish Qi, and to unblock circulation or resolve blood stasis. In Tables 1–4, we list four categories of Chinese herbal medicine that have been used in the practice of TCM and/or recent research, including compounds extracted from herbs (Table 1), single herbs (Table 2), decoctions (Table 3), and patent drugs made up of Chinese herbs (Table 4). All of the abbreviations used in these tables are listed at the end of the paper, and the main mechanisms and the representatives of Chinese herbal medicine in MIR treatment are schematized in Figure 1. In the following sections, these herbal medicines are grouped according to their efficacy in TCM terminology, and the underlying cellular and molecular mechanisms demonstrated by experimental investigations are discussed.

Table 1: Efficacy and mechanisms of Chinese herb-derived compounds in the treatment of MIR.

Mechanism of action in TCM terminology
Plant
Compound
Mechanism
Biomarker/Targets
In vivo/In vitro
References

Tonifying Qi (energy) to activate circulation and enrich Blood
Salvia miltiorrhiza
Tanshinone IIA
Anti-inflammation
MCP-1, TGF-β1, TNF-α, NF-κB
In vivo
[56]

Antioxidant
VEGF, HIF-1; MDA, SOD, GPx
Both
[68, 72]

Antiapoptosis
Bcl-2/Bax, caspase-3
Both
[72]

Promote angiogenesis
VEGF, HIF-1
In vivo
[68]

Promote BMSCs migration
SCF-1, CXCR-4
In vivo
[67]

Sodium tanshinone IIA sulfonate
Anti-apoptosis
LDH, JNK, p38
In vivo
[73]

Magnesium tanshinoate B
Anti-apoptosis
p-JNK, cytochrome c, caspase-3
In vitro
[74]

Salvianolic acid A
Activate calcium channels
I-CaL
In vivo
[75]

Salvianolic acid B
Promote angiogenesis
VEGF
In vivo
[76]

Salvianolic acids
Antioxidant
15-F2t-IsoP, ET-1, CK-MB
In vivo
[77]

Reduce ME
CK
In vitro
[78]

Tanshinone combined with salvianolic acids
Inhibit of intracellular calcium, and anti-apoptosis, antioxidants
ICAM-1, Ca²⁺
In vivo
[79]

Tanshinone IIA combined with salvianolic acid B
Antioxidant
CAT, L-arginine, eNOS, AMPK, Akt
In vivo
[80]

Danshensu
Antioxidant, reduce ME
SOD, MDA; CKMB, LDH
In vivo
[81]

Salvia miltiorrhiza extract
Antioxidant, reduce ME
MDA, SOD, and GPx; LDH, CK, GOT
In vivo
[82, 83]

Aqueous extracts of Salvia miltiorrhizae
Reduce ME, promote angiogenesis
CK-MB and cTnT, 6-keto-PGF-1/TXB-2
In vivo
[84]

Salvia miltiorrhizae
Antioxidant
COX-2; TXB2, 6-keto-PGF1-
In vivo
[85]

Radix Ginseng
Saponin of red ginseng
Inhibit Ca²⁺ overload, up-regulate KATP
Ca²⁺; KATP; cTnI; PI3K
Both
[86, 87]

Total ginsenosides
Antioxidant, anti-apoptosis
Ca²⁺; eNOS, iNOS, GR; PI3K, Akt
In vivo
[87, 88]

Radix Ginseng extracts
Antioxidant, reduce ME
NO, eNOS; CK, LDH
In vivo
[88]

Astragalus membranaceus
Astragaloside IV
Up-regulate KATP channel subunits, facilitate KATP currents
KATP channel subunits Kir6.1, Kir6.2, SUR2A, SUR2B
In vivo
[70]

Rhodiola
Salidroside, tyrosol
Anti-apoptosis
caspase-3, p-JNK, cytochrome c
In vitro
[60]

Millettia pulchra
17-Methoxyl-7-hydroxy-benzene-furanchalcone
Antioxidant, anti-inflammation, and anti-apoptosis
MDA; TNF-α; NF-κB p65, Bcl-2-associated X protein
Both
[89]

Schisandra chinensis
Schisandrin B
Anti-inflammation and
Hsp25, Hsp70
In vivo
[57]

Antioxidant
cytochrome P-450
In vivo
[90]

Lycium barbarum
Lycium barbarum polysaccharides
Increase Na⁺-K⁺-ATPase and Ca²⁺-ATPase, anti-apoptosis
Na⁺-K⁺-ATPase, Ca²⁺-ATPase; Bax, Bcl-2
In vivo
[71]

Moving Qi and activating circulation to resolve stasis
Ligusticum wallichii
Tetramethylpyrazine
Antioxidant, inhibit neutrophil
HO-1; Migrated neutrophil
In vivo
[91]

Aqueous extracts of Rhizoma Chuanxiong
Reduce ME, promote angiogenesis
CK-MB, cTnT; 6-keto-PGF-1/TXB-2
In vivo
[84]

Carthamus tinctorius L.
Extracts of Carthamus tinctorius
Antioxidant, anti-inflammation
ROS, MDA, SOD; CRP, TNF-, IL-1; PI3K
Both
[92, 93]

Panax notoginseng
Extracts of Panax notoginseng
Antioxidant, anti-inflammation
MDA, SOD; CRP, TNF-, IL-1
In vivo
[92]

Notoginsengnosides
Reduce ME
CK
In vitro
[78]

Dipsacus asper
Asperosaponin VI
Antioxidant, reduce ME, and protect mitochondrial function
SOD, GOT, GPx, MDA; CK-MB, LDH, cTnT; ICDH, MDH, -KGDH, ATP, Ca²⁺
In vivo
[94]

Anti-apoptosis, reduce ME
Bcl2/Bax, caspase-3; LDH, CREB, PI3K
In vitro
[95]

Pyrolae
Flavonoid of Herba Pyrolae
Antioxidant, reduce ME
SOD, MDA; CK, LDH
In vivo
[96]

Lamiophlomis rotata
Forsythoside B
Antioxidant, anti-inflammation
MDA, MPO, SOD, GPx;Tn-T, TNF-, IL-6, HMGB1; IkBa, NF-κB
In vivo
[50]

Sida cordifolia L.
Hydroalcoholic extract of Sida cordifolia L.
Antioxidant, reduce ME
SOD, CAT; LDH, CK-MB
In vivo
[24]

Desmodium
Desmodium gangeticum
Stimulate muscarinic receptors
Muscarinic receptor
In vivo
[97]

Inducing Diuresis to resolve stasis
Leonurus
3,5-Dimethoxy-4-(3-(2-carbonyl-ethyldisulfanyl)-propionyl)-benzoic acid

4-Guanidino-butyl ester
Anti-apoptosis
Caspase-3, Bcl-2/Bax, Akt
In vitro
[61]

4-Guanidino-n-butyl syringate
Inhibit Ca²⁺ overload, antiapoptosis
Ca²⁺; Bcl-2, Bax, LDH
In vivo
[98]

Acorus gramineus
Acori graminei Rhizoma
Inhibit calcium overload
Ca²⁺
In vivo
[99]

Phytolacca
Oleanolic Acid
Anti-apoptosis
AMPK, p38, FOXO3
In vitro
[100]

Tetrandra
Tetrandrine
Inhibit neutrophil, antioxidant
neutrophil adhesion, Mac-1; ROS
In vivo
[23]

Cooling Blood to stop bleeding
Baicalensis
Botanical Flavonoids
Antioxidant
ROS, NO, SOD, CAT, GPx
Both
[101, 102]

Coptidis rhizoma
Palmatine
Antioxidant, reduce ME
SOD, MDA, COX-2; LDH, CK
In vivo
[49]

Buxus microphylla
Cyclovirobuxine D
Antioxidant, reduce ME
KATP channel opening; NO, ROS, SOD, MDA; CPK, LDH, FFA
In vivo
[52, 103]

Tonifying Qi to invigorate Yang
Cinnamon
2-Methoxycinnamaldehyde
Antioxidant, anti-inflammation
VCAM-1,TNF-, HO-1
In vivo
[51]

Herba Cistanches
A semipurified fraction of Herba Cistanches
Protect mitochondrial function, antioxidant, and anti-apoptosis
ATP-generation, mitochondrial uncoupling; GSH; caspase-3
Both
[65]

Regulating Qi and moving Qi
Corydalis
Corydalis yanhusuo extract
Anti-apoptosis
Bax, Bcl-2
In vivo
[104]

Magnolia officinalis
Magnolol
Antioxidant; inhibit neutrophil
MPO, superoxide anion; migrated neutrophil
In vivo
[105]

Table 2: Efficacy and mechanism of single Chinese herbs in the treatment of MIR.

Mechanism of action in TCM terminology
Herb
Mechanism
Biomarker/Targets
In vivo/In vitro
References

Replenishing and moving Qi
Rhodiola
Promote angiogenesis
VEGFR (Flt-1, KDR, and Tie-2)
In vivo
[106]

Euryale ferox (Makhana)
Antioxidant
TRP32, ROS, and Trx-1
Both
[53]

Aurantii Fructus
Recovery of contractile dysfunction
Perfusion pressure, aortic flow, and coronary flow
In vivo
[107]

Table 3: Efficacy and mechanisms of Chinese herb decoctions in the treatment of MIR.

Mechanism of action in TCM terminology
Decoction
Constituent herbs
Mechanism
Biomarker/Targets
In vivo/In vitro
References

Tonifying Qi to enrich Blood
DangGui BuXue Decoction
Astragali and Angelica roots
Antioxidant, protect mitochondrial function
GSH, GSSG, GRD
In vivo
[108]

BuYang HuanWu Decoction
Astragalus, angelica, red peony, earthworm, and so forth
Reduce ME
LDH, CK, AST; CD40-CD40L
In vivo
[109]

Replenishing Qi to activate Blood and recover circulation
ShuMai Decoction
Astragalus mongholicus, Salvia miltiorrhiza, Eupolyphaga,

Wallich and Hirudo nipponica Whitman, Moschus berezovskii
Anti-inflammation
TNF-α, p38, MAPK, TIMP-1
In vivo
[58]

Promote angiogenesis
VEGF, PDGF-BB, PI3K, Akt
In vivo
[110]

Invigorating Yang to recover circulation
Sini Decoction
Aconite, ginger, and licorice
Antimitochondrial oxidation
SOD, MDA, MnSOD mRNA
In vivo
[54]

Moving Qi to activate circulation
Dan-Chuan-Hong Decoction
Salvia, Rhizoma Chuanxiong, and safflower
Anti-apoptosis
TUNEL
In vivo
[111]

Enriching Blood to engender fluid
DanShen GeGen Decoction
Radix Salvia miltiorrhiza, and Radix Puerariae lobatae
Antioxidant
Redox-sensitive PKCε/mKATP pathway
In vivo
[112]

Enrich Qi and cool Blood
Radix et Rhizoma Rhodiolae Kirilowii
Radix, Rhizoma Rhodiolae kirilowii
Promote angiogenesis
vWF, VEGF, HIF-1α, HIF-1β
In vivo
[69]

Table 4: Efficacy and mechanism of patent drugs made up of Chinese herbs in the treatment of MIR.

Mechanism of action in TCM terminology
Patent drug name
Main ingredient
Mechanism
Biomarker/Targets
In vivo/In vitro
References

Activating Blood to resolve stasis, and moving Qi to relieve pain
XinKeShu Tablet
Salvia, arrowroot, woody, hawthorn, panax
Antioxidant, promote angiogenesis
eNOS; VCAM-1
In vivo
[113]

TongXinLuo Superfine
Ginseng, leeches, scorpion, Eupolyphaga, centipede, et al
Antioxidant, proangiogenesis
NO, eNOS; vWF, Hhcy
In vivo
[114]

ShuMai Capsule
Peanut shells
Promote angiogenesis
vWF, VEGF
In vivo
[115]

Moving Qi to activate circulation and relieve pain
GuanXin ErHao (Guanxin II)
Safflower, red peony, salvia, Chuanxiong, and so forth
Anti-apoptosis, protect mitochondrial function
Caspase-3, Caspase-9, Bcl-2/Bax, cytochrome c, Akt
In vivo
[63, 64]

XiongShao Capsule
Rhizoma Chuanxiong, Radix Paeoniae Rubra
Anti-inflammation
TNF-, MCP-1, ICI
In vivo
[59]

Replenishing Qi to activate circulation, and moving Qi to relieve pain
Vigconic 28 (VI-28)
Radix Ginseng, Cornu Cervi, Cordyceps, Radix Salviae, Semen Allii, and so forth
Antioxidant, protect mitochondrial function
GSH, -TOC, CuZn-SOD, Ca²⁺-induced permeability, mitochondrial MDA, Ca²⁺, cytochrome c
In vivo
[116]

Acanthopanax Senticosus Injection
Acanthopanax
Antioxidant, inhibit Ca²⁺ overload
SOD, MDA, GPx; Ca²⁺
In vivo
[55]

ShuangShen NingXin Capsule
Ginseng total saponins, total salvianolic, corydalis
Antioxdiant
SOD, MDA
In vivo
[117]

ShuangShen TongGuan Recipe
Ginseng, astragalus, Atractylodes, and so forth
Anti-inflammation
NF-κB, p65, TNF-, ICAM-1, MJIC-Cx43
In vivo
[118]

Replenishing Qi and invigorating Yang
ShenFu Injections
Red ginseng, Monkshood
Antioxdiant, reduce ME, up-regulate-ATPase
SOD, GPx; LDH, CK; Na⁺-K⁺-ATP and Ca²⁺-ATP
In vivo
[119]

Replenishing Blood and activating circulation
DanHong Injection
Salvia, safflower
Antioxidant
SOD, MDA
In vivo
[120]

Cardiotonic Pill
Salvia miltiorrhiza
Anti-apoptosis
Caspase-3, Akt
In vivo
[62]

3.1. Anti-Oxidation

Many Chinese herbal medicines, including extracted compounds, single herbs, decoctions, and patent drugs, exert their beneficial effects on MIR via their anti-oxidative activity. A number of biomarkers have been used to evaluate the antioxidative effects of these Chinese herbal medicines, such as ROS, SOD, GPx, CAT, nitric oxide synthase (NOS), malondialdehyde (MDA), myeloperoxidase (MPO), heme oxygenase (HO)-1, superoxide anion, GOT, 15-F2t-isoprostane (15-F2t-IsoP), ET-1, cycloxygenase-2 (COX-2), thioredoxin-1 (Trx-1), thioredoxin-related protein-32 (TRP32), redox-sensitive PKCε/mKATP pathway, glutathione (GSH), oxidized glutathione (GSSG), glutathione reductase (GRD), CuZn-superoxide dismutase (CuZn-SOD), and Mn-SOD.

Through in vivo and in vitro experiments, Kim et al. revealed that palmatine, a compound extracted from the Chinese herb, Coptidis rhizome, markedly reduced serum MDA level, and the activity of SOD and CAT in the cardiac tissues, as well as the COX-2 and iNOS expressions in MIR myocardium of rats [49]. Jiang et al. reported that the MDA content and MPO activity in ischemic myocardial tissue of rats treated with Forsythoside B, a compound derived from the Chinese herb, Lamiophlomis rotate (Benth.) Kudo, were both significantly reduced. These reductions were accompanied by a significantly improved recovery in myocardial function [50]. Hwa et al. reported that 2-Methoxycinnamaldehyde (2-MCA), a compound derived from the Chinese herb, Cinnamomum cassia, significantly increased HO-1 induction by promoting the translocation of Nrf-2 from cytosol to nucleus in endothelial cells in an MIR model [51]. In addition, Hu et al. demonstrated that cyclovirobuxine D, a compound derived from the Chinese herb, Buxus microphylla, significantly protected rat aorta endothelial cells against hypoxia-induced injury and enhanced nitric oxide (NO) release from endothelial cells; these effects were inhibited by nitric oxide synthase (NOS) inhibitor N-nitro-L’argininemethyl ester (L-NAME) [52]. Das et al. studied the effects of a single herb, Makhana, and demonstrated that the cardioprotective properties of Makhana were linked to its ability to scavenge ROS [53]. Some decoctions and patent drugs made up of Chinese herbs have also been shown to exert the anti-oxidative effects on MIR. Zhao et al. found that SiNi Decoction (SND), composed of Chinese herbs, Aconite, Ginger and Licorice, could enhance the activity of myocardial and myocyte mitochondrial SOD and reduce MDA by increasing the expression of Mn-SOD mRNA [54]. Wang et al. reported that in rats treated with Acanthopanax Senticosus Injection (ASI) at doses of 25, 50, and 100 mg/kg via femoral vein infusion 30 min after coronary occlusion, the content of myocardial MDA was decreased significantly and dose-dependently and the activities of myocardial SOD and GSH-Px were increased dramatically [55].

3.2. Anti-Inflammation

The manifestation of MIR shares many phenotypic similarities with the activation of a host immune response directed toward invading microorganisms. HSPs and HMGB1 are both involved in the initiation of host defense and tissue repair. Molecules derived from immune cells and cardiomyocytes have been utilized as biomarkers to evaluate the anti-inflammatory effects of Chinese herbal medicine on MIR, including IL-6, MCP-1, TGF-β1, TNF-α, CRP, IL-1β, VCAM-1, ICAM-1, HMGB1, HSP25 and Hsp70, macrophage adhesion molecule-1 (Mac-1), troponinT (Tn-T), phosphorylated p38, activated MAPK, and tissue inhibitor of matrix metalloproteinase (TIMP)-1.

Ren et al. indicated that Tanshinone IIA (Tan IIA), a compound extracted from the Chinese herb, Salvia miltiorrhiza Bunge, attenuated expression of MCP-1, TGF-β1, and TNF-α as well as macrophage infiltration in rats when administered intragastrically at a dose of 60 mg/kg/day [56]. Jiang et al. reported that treatment with Forsythoside B significantly decreased the levels of TNF-β, IL-6, and HMGB1 in a rat MIR model [24, 50]. Results of a study by Chiu and Ko indicated that the reduction of Hsp25 and Hsp70 expression by Schisandrin B (Sch B), a compound extracted from Chinese herb, Schisandra chinensis, in MIR rats resulted in cardioprotection [57]. Shen et al. reported that neutrophils from MIR animals displayed a significant morphological change and Mac-1 up-regulation, both of which could be prevented by Tetrandrine (TTD), a compound extracted from the Chinese herb, Stephania tetrandra [23].

Decoctions and patent drugs made up of Chinese herbs have also been demonstrated to exert anti-inflammatory effects in MIR. Yin et al. showed that a significant reduction in TIMP-1 and TNF levels and improved cardiac function in MIR rats were achieved by treatment with ShuMai Decoction consisting of Astragalus mongholicus Bunge, Salvia miltiorrhiza Bge, and Eupolyphaga sinensis, in a dose-dependent manner [58]. Zhang et al. studied the patent drug Xiongshao Capsule (XSC), comprised of Chinese herbs, Rhizoma Chuanxiong and Radix Paeoniae Rubra, and found that it reduced levels of MCP-1 and TNF-α as well as inflammatory cell infiltration (ICI) in the ischemic myocardium [59].

3.3. Anti-Apoptosis

Alterations of pro and antiapoptotic signaling pathways, including changes in the levels of apoptosis-modulating molecules and induction of caspases, have been used to examine the anti-apoptotic effects of Chinese herbal medicine in MIR. Levels and/or activities of caspase-3, caspase-9, Bcl-2/Bax, p-JNK, p-AMPK, p-p38, phosphatidylinositol 3-kinase (PI3 K), Akt, p-IκB-α, NF-κB, p65, Bcl-2-associated X protein, cytochrome c, and forkhead transcription factor 3 (FOXO3) are among the commonly used biomarkers.

Sun et al. revealed that Salidroside and Tyrosol, two compounds extracted from the Chinese herb, Rhodiola, separately or in combination, significantly reduced caspase-3 activity, cytochrome c release, and JNK activation in an in vitro study [60]. Liu et al. reported that 3,5-Dimethoxy-4-(3-(2-carbonyl-ethyldisulfanyl)-propionyl)-benzoic acid 4-guanidino-butyl ester, derived from the Chinese herb, Leonurus, inhibited apoptosis by increasing the ratio of Bcl-2/Bax, decreasing the level of cleaved-caspase-3, and enhancing the phosphorylation of Akt [61]. An in vivo study by Jiang et al. demonstrated that rats treated with Forsythoside B showed a significant recovery in myocardial function due to down-regulated phosphorylation of IkB-α and NF-κB [50].

Ling et al. studied the effects of the patent drug, Cardiotonic Pill (CP) combined with the Chinese herb, Salvia miltiorrhiza, and found that CP treatment (50 mg/mL) significantly inhibited TNF-α-induced apoptosis in cardiomyocytes through activating Akt signaling [62]. Others have showed that Guan xin er hao (Guanxin II), which consists of the Chinese herbs, Safflower, red peony, salvia, Chuanxiong, and Dalbergiae Odoriferae, tilted the balance between Bax and Bcl-2 toward an anti-apoptotic state, decreased mitochondrial cytochrome c release, reduced caspase-9 activation, and attenuated subsequent caspase-3 activation and postischemic myocardial apoptosis in rats [63, 64].

3.4. Protecting Mitochondrial Function

MPTP has been used as a target for protecting mitochondrial function by Chinese herbal medicine in the treatment of MIR. ATP-generation capacity, mitochondrial uncoupling, cAMP response element-binding protein (CREB), cytochrome c, cytochrome P-450, mitochondrial glutathione (GSH), mitochondrial Ca²⁺, and mitochondrial MDA have been used as biomarkers to evaluate the effects of Chinese herbal medicine.

Wong and Ko reported that a semipurified fraction of Herba Cistanches (HCF1) increased mitochondrial ATP-generation capacity and ADP-stimulated state respiration in H9c2 cardiomyocytes during MIR. HCF1 pretreatment could protect against MIR injury in rats presumably mediated by the induction of glutathione antioxidant [65]. Siu and Ko studied the single Chinese herb, Cistanche, and found it enhanced mitochondrial glutathione status, decreased mitochondrial Ca²⁺ level, and increased the mitochondrial membrane potential and respiration rate in rat hearts [66]. Others reported that the patent drug, Guanxin II, decreased mitochondrial cytochrome c release and attenuated caspase-3 activation in rat MIR myocardium [63, 64].

3.5. Increasing BMSCs Migration

Bone marrow mesenchymal stem cells (BMSCs) are preferentially attracted to and retained in ischemic tissue. SDF-1 and CXCR4 have been used as targets for increasing BMSC migration to protect cardiomyocytes against MIR.

Tong et al. studied the effect of Tan IIA on MIR both in vitro and in vivo. Their data showed that combination treatment with Tan IIA and BMSCs significantly reduced the infarct size and improved cardiac function after MI, which primarily resulted from Tan IIA induced increase of the migration of BMSCs to ischemic region [67].

3.6. Promoting Angiogenesis

Angiogenesis limits MIR damage by restoring tissue blood flow. Related molecules such as VEGF, von Willebrand factor (vWF), hypoxia-inducible factor 1α (HIF-1α), VEGFR (Flt-1, KDR, and angiopoietin receptor (Tie-2)), platelet-derived growth factor (PDGF-BB), and phosphatidylinositol 3-kinase (PI3K) have been used as the targets for angiogenesis promotion to protect cardiomyocytes against MIR.

Xu et al. found that the compound, Tanshinone IIA, elicited a significant cardioprotective effect by up-regulating VEGF expression in MI rats and enhancing HIF-1α expression [68]. Experiments of Gao et al. showed that the expressions of vWF, HIF-1α, HIF-1β, and VEGF were significantly increased in myocardium treated with Radix et Rhizoma Rhodiolae Kirilowii Decoction [69].

3.7. Up-Regulating KATP Channel Subunits and ATPase, and Inhibiting Calcium Overload

KATP channel subunits Kir6.1, Kir6.2, SUR2A and SUR2B, Na⁺-K⁺-ATPase, Ca²⁺-ATPase and intracellular calcium (Ca²⁺), and L-type calcium current (I-CaL) have been used to assess the effects of Chinese herbal medicine in protecting cardiomyocytes against MIR.

Han et al. examined the effects of Astragaloside IV (As IV), a compound extracted from the Chinese herb, Astragalus membranaceus. They found that As IV significantly up-regulated mRNA and protein levels of KATP channel subunits Kir6.1, Kir6.2, and SUR2A and SUR2B [70]. Lu and Zhao reported that Lycium barbarum polysaccharides, extracted from the Chinese herb, Lycium barbarum, significantly increased Na⁺-K⁺-ATPase and Ca²⁺-ATPase activities in myocardium of ischemia-reperfusion rats [71].

4. Summary and Perspective

In summary, significant progress has been made regarding the mechanistic research into the efficacy of Chinese herbal medicine for the treatment of MIR. However, much work remains. Most clinical studies were of limited extrapolatable value because of the small sample sizes and/or incomplete data. Experimental studies have focused mainly on single compounds extracted from Chinese herbs. Studies of Chinese decoctions or formulations are relatively scarce, although decoction and formulations are the main forms of therapy in TCM practice. Capitalization of the interactions between the different components and herbs is the essence of TCM. Many herbs are paired together to attenuate toxicity as well as to enhance efficacy. Encouragingly, the number of studies on patent Chinese herbs has been gradually increasing. These studies help us to understand the mechanisms underlying the use of Chinese herbs and formulations for the treatment of MIR. Accordingly, there is a strong likelihood that such ongoing research will lead to novel therapies for the treatment of myocardial ischemia and reperfusion injury using Chinese herbs and herbal formulations.

Abbreviations

ROS: | Reactive oxygen species
NOS: | Nitric oxide synthase
MDA: | Malondialdehyde
SOD: | Superoxide dismutase
GSH: | Glutathione
GPx: | Glutathine peroxidease
MPO: | Myeloperoxidase
CAT: | Catalase
COX-2: | Cycloxygenase-2
GOT: | Glutamic oxalacetic transaminase
ME: | Myocardial enzymes
TRP32: | Thioredoxin-related protein-32
GSH: | Glutathione
GSSG: | Oxidized glutathione
GRD: | Glutathione reductase
CuZn-SOD: | CuZn-superoxide dismutase
PI3K: | Phosphatidylinositol 3-kinase
HMGB1: | High-mobility group box1
HSP: | Heat shock protein
TIMP: | Tissue inhibitor of matrix metalloproteinase
ICI: | Inflammatory cell infiltration
LDH: | Lactate dehydrogenase
CK: | Creatine kinase
CK-MB: | Creatine kinase isoenzyme-MB
TXB2: | Thromboxane B2
VEGF: | Vascular endothelial growth factor
HIF-1a: | Hypoxia-inducible factor 1a
Vwf: | Von Willebrand factor
SDF-1: | Stromal cell-derived factor-1
SCF-1: | Stem cell factor-1
CXCR4: | CXC chemokine receptor 4
I-CaL: | L-type calcium current
15-F2t-IsoP: | 15-F2t-isoprostane
6-keto-PGF1-a: | 6-keto-prostaglandin F1alpha
GR: | Glucocorticoid receptor
CREB: | cAMP response element-binding protein
Tn-T: | TroponinT
FOXO3: | Forkhead transcription factor 3
Mac-1: | Macrophage adhesion molecule-1
HO-1: | Heme oxygenase-1
Tie-2: | Angiopoietin receptor
TRP32: | Thioredoxin-related protein-32
Trx-1: | Thioredoxin-1
GSSG: | Oxidized glutathione
GRD: | Glutathione reductase
PDGF-BB: | Platelet-derived growth factor
Hhcy: | Hyperhomocysteinemia
MJIC-Cx43: | Myocardial junction intercellular communication connexin 43.

Conflict of Interests

The authors declare that they have no conflict of interests regarding the publication of this paper.

Acknowledgment

This work was supported by Grants from the National Institute of Health nos. R21AT006767 and R01HL116626 (to D. Fan).

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