A review on the molecular basis underlying the protective effects of Andrographis paniculata and andrographolide against myocardial injury.

Andrographolide is the major compound found in the medicinal plant, Andrographis paniculata (Burm.f.) Nees, which accounts for its medicinal properties. Both the plant extract and compound have been reported to exhibit potential cardiovascular activities. This review summarises related studies describing the biological activities and target mechanisms of A. paniculata and andrographolide in vivo and in vitro. The current evidence unambiguously indicated the protective effects provided by A. paniculata and andrographolide administration against myocardial injury. The intervention ameliorates the symptoms of myocardial injury by interfering with the inductive phase of a) inflammatory response mediated by nuclear factor-kappa B (NF-κB), phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt), mitogen-activated protein kinase (MAPK) and signal transducer and activator of transcription 3 (STAT3) signalling molecules; b) oxidative stress via activation of nuclear factor erythroid 2-related factor (Nrf-2) and reduction of enzymes responsible for generating reactive oxygen and nitrogen species; c) intrinsic and extrinsic mechanisms in apoptosis regulated by upstream insulin-like growth factor-1 receptor (IGF-1R) and peroxisome proliferator-activated receptor-alpha (PPAR-α); d) profibrotic growth factors thus reducing cardiac fibrosis, improving endothelial function and fibrinolytic function. In conclusion, A. paniculata and andrographolide possess therapeutic potential in the management of myocardial injury, which requires further validation in human clinical trials.

Introduction

Myocardial injury is the damage to myocardium affecting the heart function. It can be detected by the elevation of cardiac troponin concentration exceeding the 99th percentile of the reference population or the upper reference limit.1 It can be classified into acute and chronic conditions. Acute myocardial injury refers to dynamic increase and/or decrease of troponin concentration, whereas chronic myocardial injury is characterised by persistent elevated troponin concentration. Both conditions can result from cardiovascular or non-cardiovascular factors in clinical practice.1 Treatment strategies for type I myocardial infarction are well established, but there is no clinical guidance or recommended therapy for patients with other myocardial injury categories.2,3 These shortcomings prompt the search for alternative agents to manage myocardial injury.

Andrographis paniculata (Burm.f.) Nees is a herbaceous plant traditionally used to treat rheumatoid arthritis, diarrhoea, upper respiratory tract infection, laryngitis, fever, and cancer in China, India, and Southeast Asia.4 It is also generally known as “the king of bitters” due to its extremely bitter taste. The local name in Malaysia is “hempedu bumi”, loosely translated as “earthly bile”, reflecting its bitter taste. Andrographolide (Figure 1) is a natural diterpenoid lactone extracted from A. paniculata (Burm.f.) Nees. Scientific research revealed that andrographolide is the phytoconstituent accounts for the medicinal properties of A. paniculata (Burm.f.) Nees. Both plant extract and its bioactive compound are proven through pharmacological research to possess extensive biological effects, such as anti-neoplasm,5–7 anti-bacteria,8,9 anti-malaria,10,11 hepatoprotection,12,13 anti-inflammation,10,13–15 anti-oxidant,15 anti-apoptosis,16,17 anti-fibrosis,14,18 and cardioprotection.19 Among these, the latter three bioactivities are closely associated with the management of myocardial injury.

Figure 1

The chemical structure of andrographolide.

Increasing evidence demonstrated the potential beneficial use of A. paniculata (Burm.f.) Nees in humans against respiratory tract infections,20 diabetes,21 inflammatory bowel diseases,22 fatigue reduction in multiple sclerosis,23 osteoarthritis,24 common cold,25 and hypertriglyceridaemia.26 The doses of A. paniculata (Burm.f.) Nees used in these human trials range from 300 to 1800 mg/day. Clinical trials indicated that andrographolide is a promising therapy for multiple sclerosis,27 rheumatoid arthritis,28 as well as hand, foot, and mouth diseases.29 Much lower doses of andrographolide than A. paniculata (Burm.f.) Nees have been tested, varying from 5 to 140 mg/day. In addition, an array of studies reported that andrographolide and its original plant source, A. paniculata (Burm.f.) Nees are generally non-toxic when taken orally.30,31 For these reasons, studies on the pharmacological functions of andrographolide are still in progress today.

With the presence of diverse pharmacological effects in andrographolide and A. paniculata (Burm.f.) Nees, particularly in reducing cardiac fibrosis and improving cardiac function, it is imperative to review and consolidate current evidence on their beneficial effects against myocardial injury. The molecular mechanism underlying their protective effects are also scrutinised. To date, the investigation on the effects of A. paniculata (Burm.f.) Nees and andrographolide in patients with myocardial injury is limited. This review provides an overview of the pharmacological properties that could promote the development and application of andrographolide and A. paniculata (Burm.f.) Nees as prophylactic or therapeutic agents for myocardial injury.

General Isolation of Andrographolide from A. paniculata (Burm.f.) Nees

Andrographolide has been extracted from A. paniculata (Burm.f.) Nees by researchers using different types of solvents, including dichloromethane, methanol, ethanol, and toluene. A rapid isolation method was developed two decades ago using a mixture of dichloromethane and methanol at 1:1 ratio, methanol, or 95% alcohol as solvents. The extracts were filtered and solvents were removed under vacuum.32 Pundarikakshudu et al employed five simple methods for A. paniculata (Burm.f.) Nees isolation. The three isolation methods used toluene as solvent for cold maceration, followed by refluxing in a mixture of dichloromethane and methanol (1:1), methanol, or ethanol. Another two isolation methods were conducted with maceration in methanol or mixture of dichloromethane and methanol (1:1). The extracts obtained from these approaches were filtered and evaporated to form solid crystalline mass.33 Recently, commercial Andrographis products were used to obtain their methanolic extracts. The product was soaked in methanol, sonicated at room temperature for 60 minutes, filtered through filter paper, and evaporated under vacuum.34 Analysis of thin-layer or high-performance liquid chromatography detected the presence of andrographolide in all these extracts.32–34 In general, the extraction protocol was initiated with maceration of leaf powder in solvent, followed by filtration through filter paper. Next, the solution was evaporated under reduced pressure to yield the green-colour powdered crude extract containing andrographolide.

Literature Search

Literature search was performed using PubMed and Scopus search engines. The keywords used are “(Andrographis paniculata OR andrographolide) AND (myocardial injury OR myocardial infarction OR ischaemia OR endothelial dysfunction OR cardiomyocyte)”. The search identified 17 articles in PubMed and 69 articles in Scopus databases from inception until February 15, 2021. All articles were written in English. We excluded duplicate articles (n=13) retrieved from two search engines. The remaining search results were screened by referring to the title, abstract, and full-text. We included in vitro and in vivo studies demonstrating the effects and mechanism of action of A. paniculata (Burm.f.) Nees and andrographolide on myocardial injuries. The screening of the search results excluded 26 review articles and 32 irrelevant articles not fulfilling the inclusion criteria. A total of 15 original research articles were included in this review (Figure 2).

Figure 2

The framework for the selection of relevant studies.

Nomenclature of the Plant Extract

The accurate nomenclature of plants is crucial in all scientific studies reporting the pharmacological effects of plants to avoid ambiguities and error.35 A total of seven studies in this review examined the effects of A. paniculata (Burm.f.) Nees against myocardial injuries in animals.17,36–41 However, there was only one study performed the verification of plant extract by one of the researchers in their group and the specimen has been deposited in herbarium with a voucher number.17 The correct nomenclature of the plant taxonomically is “A paniculata (Burm.f.) Nees”. This plant is categorised under the family Acanthaceae Juss. and genus Andrographis Wall. ex Nees. Hence, the name of the plant has been written correctly in this review.

Effects of Andrographolide on Myocardial Injury in Animals

A. paniculata (Burm.f.) Nees plant extract or andrographolide increased mean arterial pressure (MAP), heart rate, and improved myocardial function in animals. Left ventricular ejection fraction (LVEF), fractional shortening (LVFS), end-systolic pressure (LVESP), early to late mitral flow (E/A ratio), rate of intra-ventricular pressure rise and decline (±dP/dt), and cardiac output were increased, whereas left ventricular end-diastolic pressure (LVEDP), internal dimension in systole (LVDS), end systolic diameter (LVESd), end diastolic diameter (LVEDd), posterior wall dimension (LVPWd), and infarction size were decreased18,36,40–44 after administration of A. paniculata (Burm.f.) Nees extract or andrographolide. Histological assessment revealed that the pathological changes of heart tissue were repaired after treatment of A. paniculata (Burm.f.) Nees or andrographolide (as seen by reduced interstitial spaces, fibrosis, myocardial degeneration, distortion in the cardiomyocyte arrangement, cell oedema, degree of necrosis, and neutrophil infiltration).17,39–41,45,46 Administration of A. paniculata (Burm.f.) Nees or andrographolide also reversed cardiac fibrosis [indicated by lowered fibrosis marker such as alpha-smooth muscle actin (α-SMA)] and cardiac hypertrophy [cross-sectional area of cardiomyocytes, heart weight normalised with tibia length or body weight, atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and beta-myosin heavy chain were reduced].17,18,43–45 Malignant arrhythmia was absent, ischaemic electrocardiogram and damage to myocardial ultrastructure were milder in mongrel dogs with myocardial ischemia and reperfusion injury receiving A. paniculata (Burm.f.) Nees extract.36,37 The changes in myocyte-specific enzymes, such as creatine phosphokinase-MB (CK-MB) and lactate dehydrogenase, were also noted with A. paniculata (Burm.f.) Nees treatment.40,41 Survival rate was improved in a rat model of autoimmune myocarditis induced by Mycobacterium tuberculosis-supplemented porcine cardiac myosin43 and myocardial infarction induced by left coronary artery ligation18 upon administration of andrographolide.

In summary, A. paniculata (Burm.f.) Nees extract or andrographolide has been consistently reported for its protection against myocardial injury using various types of animal models (Table 1). Based on the accumulated studies, the reported effective doses for A. paniculata (Burm.f.) Nees plant extract against myocardial injury ranged from 100 to 2000 mg/kg with a treatment duration of 7–31 days. For andrographolide, the effective dose ranged from 10 to 100 mg/kg with a treatment duration of 1–12 weeks in animal models. A shorter duration may be sufficient if a higher dose is administered, while a longer treatment duration may be required if lower dose is supplemented. However, their effects in reversing myocardial injury in humans are yet to be investigated. The efficacy of A. paniculata (Burm.f.) Nees or andrographolide need to be further assessed in clinical trial before any conclusion can be drawn.

Table 1

In vivo Studies on the Effects of Andrographolide on Myocardial Injuries

Types of Animal Model	Intervention (Dose, Route, and Duration of Administration)	Findings	Reference
Mongrel dogs with coronary artery thrombosis and acute myocardial infarction by injuring endothelium of coronary artery with a steel wire	A. paniculata (Burm.f.) Nees (4.5 g/kg, i.v., given in bolus followed by infusion)	● ↑ PGI2; ↓ TXA2 synthesis, CK-MB peak, euglobulin lysis time, platelet maximum aggregation rate, size of ischemic area and amplitude of ST-segment elevation● ↓ degree of myocardial degeneration and necrosis	[39]
Mongrel dogs with left anterior descending coronary artery ligation-induced ischaemia and reperfusion injury	A. paniculata (Burm.f.) Nees (9 mg/kg, i.v., given in bolus followed by infusion)	● ↓ LVEDP, infarction size after reperfusion; ↑ cardiac output● Milder ischemic electrocardiogram and damage found in myocardial ultrastructure, absence of malignant arrhythmia	[36]
Mongrel dogs with left anterior descending coronary artery ligation-induced ischaemia and reperfusion injury	A. paniculata (Burm.f.) Nees (5 mL/kg, i.v., given in bolus followed by infusion)	● ↑ SOD; ↓ MDA, and intracellular calcium of ischemic region of myocardial cell● Milder distortion of the ischemic area	[37,38]
Male Wistar rats with myocardial injury induced by isoproterenol (85 mg/kg, s.c.)	A. paniculata (Burm.f.) Nees (100, 200 and 400 mg/kg/day, oral, 31 days)	● ↑ MAP, heart rate, left ventricular peak positive and negative pressure; ↓ LVEDP● ↓ degree of necrosis, oedema and infiltration of inflammatory cells● ↑ CK-MB and lactate dehydrogenase activity● ↓ MDA; ↑ GSH, SOD, CAT, and GPx	[40]
Male Wistar rats with left anterior descending coronary artery ligation-induced ischaemia and reperfusion injury	A. paniculata (Burm.f.) Nees (200 mg/kg/day, oral, 31 days)	● ↑ MAP, heart rate, left ventricular peak positive and negative pressure; ↓ LVEDP● ↓ degree of necrosis, oedema and infiltration of inflammatory cells● ↑ CK-MB and lactate dehydrogenase activity● ↓ MDA; ↑ GSH, SOD, CAT, and GPx	[41]
Obese C57/BL6 mice induced by high-fat diet	A. paniculata (Burm.f.) Nees (2 g/kg/day, oral, a week)	● ↓ heart weight, left ventricle weight, heart weight/tibia and left ventricle weight/tibia↓ ANP and BNP● ↓ COX-2, p-IκBα and NF-κB protein levels● ↓ IL-6, p-MEK5, STAT3, p-MEK1/2 and p-JNK● ↓ abnormal myocardial array and interstitial spaces● ↓ cardiac collagen accumulation and fibrosis● ↓ TUNEL-positive cardiac cells, Fas ligand, Fas receptor, FADD, caspase-8, caspase-3, Bad, Bak, Bid, and cytochrome c● No changes in IGF-1R, p-Akt, Bcl-2, and Bcl-xl	[17]
Obese C57/BL6 mice induced by high-fat diet	Andrographolide (50 mg/kg/day, oral, 1 week)	● ↓ heart weight/tibia length and left ventricle weight/tibia length● ↓ interstitial spaces, fibrosis, and distortion in the cardiomyocyte arrangement● ↓ Fas receptor, FADD, Bak, and cytochrome c; ↑ p-IGF-1R, Bcl-2, and Bcl-xl● ↓ TUNEL-positive cardiomyocytes	[45]
Male C57BL/6 mice fed with high-fat diet and injected (i.p.) with 600,000 U/kg vitamin D3	Andrographolide (10 or 50 mg/kg, 42 days)	● ↓ cell oedema, necrosis, and neutrophil infiltration↓ ET-1 and TXA2; ↑ NO• and PGI2● ↑ t-PA; ↓ PAI-1● ↓ CD86+ cells, TNF-α, MCP-1, hs-CRP, IL-1β, p-IκBα, and p-NF-κB; ↑ CD206+● ↓ caspase-3 and ↑ Bcl-2/Bax● ↓ PPAR-α	[46]
C57/BL6J mice with diabetes-induced myocardial dysfunction induced by streptozotocin (50 mg/kg, i.p.)	Andrographolide (10 or 20 mg/kg/day, oral, 12 weeks)	● ↑ LVEF, LVFS, and E/A ratio● ↓ blood glucose and ↑ insulin● ↓ fibrosis area, collagen I, collagen III, TGF-β1, and fibronectin● ↓ cross-sectional area of cardiomyocytes, heart weight/tibial length, ANP, and BNP● ↓ p-IκBα, p-NF-κB, and COX-2● ↓ ICAM-1, VCAM-1, TNF-α, IL-1β and IL-6● ↑ SOD, Nrf-2, and HO-1; ↓ MDA, 4-hydroxynonenal, 3-nitrotyrosine, O2•−, iNOS, NOX2, NOX4, p47phox● ↓ TUNEL-positive myocardial tissues, cleaved PARP activity, and Bax/Bcl-2 ratio; ↑ p-Akt	[44]
Male BALB/c mice with cardiac malfunctions induced by LPS from E. coli (20 mg/kg, i.p.)	Andrographolide (10 mg/kg/day, oral, 7 days)	● ↑ LVEF, LVFS, and E/A ratio● ↓ TNF-α, IL-1β, NO•, and p-IκBα● No change in thiobarbituric acid reactive substance and SOD● ↓ apoptotic myocytes and caspase-3/7 activity	[42]
Male Lewis rats with autoimmune myocarditis induced by porcine cardiac myosin supplemented by M. tuberculosis (10 mg/mL, s.c.)	Andrographolide (50 or 100 mg/kg/day, oral, 21 days)	● ↓ mortality rate, LVEDP, LVDS, heart weight/body weight; ↑ ±dP/dt and LVEF● ↓ infiltration of inflammatory cells, positive CD3+ cells, positive CD14+ cells, TNF-α, IL-17, and anti-myosin antibody; ↑ IL-10● ↓ p-PI3K and p-Akt	[43]
C57/BL6 mice with myocardial infarction induced by left coronary artery ligation	Andrographolide (25 mg/kg/day, oral, 14 days)	● ↑ survival rate, LVEF, LVFS, cardiac output, LVESP, and dp/dt maximum; ↓ infarction size, LVEDd, LVESd, LVPWd, LVEDP, dp/dt minimum● ↓ cross-sectional area of cardiomyocytes, heart weight/body weight, heart weight/tibial length, lung weight/body weight, ANP, BNP, and β-myosin heavy chain● ↓ myocardial fibrosis, left ventricular collagen volume, TGF-β, p-smad3, collagen I, collagen III, and CTGF● ↓ positive CD45+ cells, positive CD68+ cells, p-IκBα, p-NF-κB, IL-1β, IL-6, TNF-α, and MCP-1● ↓ 4-hydroxynonenal, ROS, p67phox, NOX2, NOX4, and Keap-1; ↑ SOD, GPx, NQO1, HO-1, and Nrf-2	[18]

Abbreviations: ANP, atrial natriuretic peptide; Bad, Bcl-2-associated agonist of cell death; Bak, Bcl-2-antagonist/killer; Bax, Bcl-2-associated X protein; Bcl-2, B-cell lymphoma 2; Bcl-xl, B-cell lymphoma-extra large; Bid, BH3-interacting domain; BNP, brain natriuretic peptide; CD3+, cluster of differentiation 3; CD14+, cluster of differentiation 14; CD45+, cluster of differentiation 45; CD68+, cluster of differentiation 68; CD86+, cluster of differentiation 86; CD206+, cluster of differentiation 206; CK-MB, creatine phosphokinase-MB; COX-2, cyclooxygenase-2; CTGF, connective tissue growth factor; E/A ratio, early to late mitral flow; ET-1, endothelin-1; FADD, Fas-associated death domain protein; GPx, glutathione peroxidase; GSH, reduced glutathione; HO-1, heme oxygenase-1; hs-CRP, high sensitivity C-reactive protein; ICAM-1, intercellular cell adhesion molecules-1; IGF-1R, insulin-like growth factor-1 receptor; IL-1β, interleukin-1 beta; IL-6, interleukin-6; IL-10, interleukin-10; IL-17, interleukin-17; iNOS, inducible nitric oxide synthase; Keap-1, Kelch-like ECH-associated protein 1; LVDS, left ventricular internal dimension in systole; LVEDd, left ventricular end diastolic diameter; LVEDP, left ventricular end-diastolic pressure; LVEF, left ventricular ejection fraction; LVESd, left ventricular end systolic diameter; LVESP, left ventricular end-systolic pressure; LVFS, left ventricular fractional shortening; LVPWd, left ventricular posterior wall dimension; MAP, mean arterial pressure; MCP-1, monocyte chemoattractant protein-1; MDA, malondialdehyde; NO•, nitric oxide; NOX2, NADPH oxidases 2; NOX4, NADPH oxidases 4; NQO1, NADPH dehydrogenase quinone 1; Nrf-2, nuclear factor erythroid 2-related factor; O2•−, superoxide anion; p47phox and p67phox, NADPH oxidase cytosolic proteins; PAI-1, plasminogen activator inhibitor-1; p-Akt, phosphorylated protein kinase B; PARP, poly (ADP-ribose) polymerase; PGI2, prostacyclin or prostaglandin I2; p-IGF-1R, phosphorylated insulin-like growth factor-1 receptor; p-IκBα, phosphorylated inhibitor of NF-κB; p-JNK, phosphorylated c-Jun N-terminal kinase; p-MEK1/2, phosphorylated dual-specificity mitogen/extracellular signal-regulated kinase kinase; p-MEK5, phosphorylated mitogen/extracellular signal-regulated kinase kinase-5; p-NF-κB, phosphorylated nuclear factor-kappa B; PPAR-α, peroxisome proliferator-activated receptor-alpha; p-PI3K, phosphorylated phosphatidylinositol 3-kinase; p-smad3, phosphorylated small mothers against decapentaplegic 3; ROS, reactive oxygen species; SOD, superoxide dismutase; STAT3, signal transducer and activator of transcription 3; TGF-β1, transforming growth factor-beta 1; TNF-α, tumour necrosis factor-alpha; t-PA, tissue plasminogen activator; TUNEL, terminal deoxynucleotidyl transferase dUTP nick end labelling; TXA2, thromboxane A2; VCAM-1, vascular cell adhesion molecule-1; ±dP/dt, rate of intra-ventricular pressure rise and decline.

Mechanism of Action Underlying the Protective Effects of A. paniculata (Burm.f.) Nees and Andrographolide Against Myocardial Injury

Researchers have uncovered the mechanism of action for A. paniculata (Burm.f.) Nees and andrographolide as potential cardioprotective agents through preclinical studies (Tables 1 and 2). The bioactivities of A. paniculata (Burm.f.) Nees and andrographolide include the suppression of inflammatory response, oxidative stress, apoptosis, cardiac fibrosis, and endothelial dysfunction.

Table 2

In vitro Studies on the Effects of Andrographolide on Cardiomyocytes

Types of Cell	Intervention	Findings	Reference
Primary rat myocardial microvascular endothelial cells stimulated by LPS	Andrographolide (10 μg/mL)	● No cytotoxicity● ↓ CAV1, IL-6 and TNF-α	[59]
H9C2 cardiomyocytes stimulated by high concentration of glucose	Andrographolide (1–10 μM)	● ↓ ANP and BNP● ↓ p-IκBα and p-NF-κB● ↓ ROS, NOX2, NOX4, p47phox; ↑ Nrf-2 nuclear translocation● ↓ Bax/Bcl-2 ratio and caspase-3 activity	[44]
H9C2 cardiomyocytes subjected to hypoxia	Andrographolide (12.5–100 μM)	● ↓ α-SMA, TGF-β, p-smad3, collagen I, fibronectin, and CTGF● ↓ ROS, Keap-1, p67phox, and NOX2; ↑ SOD, NQO1, Nrf-2, and HO-1	[18]
Primary neonatal rat cardiomyocytes subjected to hypoxia and reoxygenation injury	Andrographolide (1–10 μM)	● ↓ lactate dehydrogenase● ↑ SOD, CAT, GPx, glutathione reductase, GSH, GCLC, and GCLM	[19]

Abbreviations: ANP, atrial natriuretic peptide; α-SMA, alpha-smooth muscle actin; Bax, Bcl-2-associated X protein; Bcl-2, B-cell lymphoma 2; BNP, brain natriuretic peptide; CAT, catalase; CAV1, caveolin-1; CTGF, connective tissue growth factor; GCLC, glutamate-cysteine ligase catalytic subunit; GCLM, glutamate cysteine ligase modifier; GPx, glutathione peroxidase; GSH, reduced glutathione; HO-1, heme oxygenase-1; IL-6, interleukin-6; Keap-1, Kelch-like ECH-associated protein 1; LPS, lipopolysaccharides; NOX2, NADPH oxidases 2; NOX4, NADPH oxidases 4; NQO1, NADPH dehydrogenase quinone 1; Nrf-2, nuclear factor erythroid 2-related factor; p47phox and p67phox, NADPH oxidase cytosolic proteins; p-IκBα, phosphorylated inhibitor of NF-κB; p-NF-κB, phosphorylated nuclear factor-kappa B; p-smad3, phosphorylated small mothers against decapentaplegic 3; ROS, reactive oxygen species; SOD, superoxide dismutase; TGF-β, transforming growth factor-beta; TNF-α, tumour necrosis factor-alpha.

Regulation of Inflammatory Response

Inflammation is the hallmarks of myocardial injury. Macrophages play an important role in inflammation. They are involved in antigen presentation, phagocytosis, and immunomodulation via the release of cytokines and chemokines.47 Various clusters of differentiation are expressed on the surface of macrophages. Cluster of differentiation 3 (CD3) is a T-cell co-receptor that activates both cytotoxic and helper T cells.48 Cluster of differentiation 14 (CD14) forms a multi-receptor complex with Toll-like receptor for the recognition of lipopolysaccharides (LPS).49,50 Cluster of differentiation 45 (CD45) is a hematopoietic cell marker that indicates the activation of one or more inflammatory cell types.51 Cluster of differentiation 68 (CD68) is a common histochemical/cytochemical marker of inflammation whereby the upregulation is a response of exposure to inflammatory stimuli, such as oxidised low-density lipoprotein (oxLDL).52 Cluster of differentiation 86 (CD86) provides initial co-stimulatory signals for T-cell activation.53,54 The increased expression of these cluster of differentiation activates pro-inflammatory signalling pathways, thereby inducing the secretion of inflammatory cytokines. On the other hand, cluster of differentiation 206 (CD206) involves in the resolution of inflammation. The ligation of CD206 produces anti-inflammatory response by inhibiting pro-inflammatory agents and reactive oxygen species (ROS).55

The initiation and progression of inflammatory response are tightly regulated by a series of signalling molecules, including nuclear factor-kappa B (NF-κB), phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt), and mitogen-activated protein kinase (MAPK). The link between diverse external cell stressors and expression of inflammatory cytokines is mediated through phosphorylation of inhibitor of NF-κB (IκBα) resulting in its ubiquitination and dissociation from NF-κB. The nuclear translocation of activated NF-κB initiates the expression of inflammatory mediators.56 The PI3K/Akt pathway is triggered by the engagement of receptor tyrosine kinase or Toll-like receptor with their respective ligands. PI3K is recruited and activated, facilitating the conversion of phosphatidylinositol (3,4)-bisphosphate (PIP2) to phosphatidylinositol (3,4,5)-trisphosphate (PIP3) and subsequent phosphorylation of Akt. Eventually, the activated Akt promotes inflammatory response.57 Similarly, increased MAPK activity and the crosstalk between MAPK and NF-κB further enhances the transcription and translation of inflammatory mediators.58 Since the activation of NF-κB, PI3K/Akt, and MAPK is involved in modulating an inflammatory response, the targeted therapeutic strategies aiming at inhibition of these signalling molecules could prevent excessive inflammation.

The anti-inflammatory response has been reported in A. paniculata (Burm.f.) Nees extract, conferring protection against pathological cardiac hypertrophy. Apart from causing NF-κB inhibition, oral administration of A. paniculata (Burm.f.) Nees extract suppressed MAPK signalling pathway to mitigate inflammation. The level of IL-6 was decreased and its associated downstream signalling molecules [signal transducer and activator of transcription 3 (STAT3), mitogen/extracellular signal-regulated kinase kinase-5 (MEK5), dual-specificity mitogen/extracellular signal-regulated kinase kinase (MEK1/2) and c-Jun N-terminal kinase (JNK)] were inhibited.17

In autoimmune myocarditis (an inflammation of myocardium induced by autoimmune disease), the untreated rats had higher numbers of positive CD3+ cells, CD14+ cells and inflammatory cells in the myocardial tissue. Plasma inflammatory cytokines and anti-myosin antibody were increased, but interleukin-10 (IL-10) was decreased without treatment of andrographolide. The induction of inflammatory response resulted from the activation of PI3K and its downstream molecule, Akt. All these alterations during autoimmune myocarditis were reversed in the andrographolide-treated group.43 Andrographolide shifted the macrophage phenotype from pro-inflammatory subset (CD86+ cell number was decreased) to anti-inflammatory subset (CD206+ cell number was increased) in mice fed by high-fat diet displaying cardiac injury, subsequently lowered the serum concentration of tumour necrosis factor-alpha (TNF-α), monocyte chemoattractant protein-1 (MCP-1), high sensitivity C-reactive protein (hs-CRP) and interleukin-1 beta (IL-1β). The suppression of inflammatory response was mediated through the inhibition of NF-κB.46 In diabetic cardiomyopathy, andrographolide blocked NF-κB-mediated inflammatory response. As a result, the protein expression of cyclooxygenase-2 (COX-2), TNF-α, IL-1β, interleukin-6 (IL-6), intercellular cell adhesion molecules-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1) were hindered. These findings were supported in vitro using H9C2 cardiomyocytes stimulated by high concentration of glucose. Andrographolide treatment suppressed high glucose-induced IκBα phosphorylation and subsequent active NF-κB nuclear translocation.44 In LPS-induced cardiac malfunctions, Zhang et al proved that the administration of LPS caused phosphorylation of IκBα and overwhelming production of cytokines, which were attenuated by oral administration of andrographolide.42 These findings were in line with in vitro study by Feng et al (2017), describing that the incubation of andrographolide lowered TNF-α and IL-6 in LPS-stimulated primary rat myocardial microvascular endothelial cells.59 In addition, andrographolide protected against adverse cardiac remodelling through the mitigation of inflammation. The dephosphorylation of NF-κB, reduction of cytokines expression, CD45+ cells, and CD68+ cells were noted in the andrographolide-treated mice with myocardial infarction induced by left coronary artery ligation.18 The mechanisms of action of A. paniculata (Burm.f.) Nees and andrographolide in alleviating inflammatory response have been depicted in Figure 3.

Figure 3

The mechanism of action of in the regulation of inflammatory response. During myocardial injuries, the overwhelming inflammatory cytokines activate several essential signalling pathways including TLR, NF-κB, PI3K/Akt, MAPK, JAK-STAT signal transduction pathways. The reductions of inflammation by A. paniculata (Burm.f.) Nees and andrographolide are mainly mediated through the inhibition of these signalling pathways (indicated by green arrows). The arrow pointing upward indicates an increase or activation while the arrow pointing downward indicates a decrease or inhibition.

Regulation of Oxidative Stress

Oxidative and nitrosative stress have been proposed as the molecular events in myocardial injury. It is the consequence of an imbalance between production and elimination of reactive oxygen species (ROS) and reactive nitrogen species (RNS) and/or depletion of antioxidant defence system. Superoxide anion (O2•−), hydroxyl radical (OH•), hydrogen peroxide (H2O2), nitric oxide (NO•), and peroxynitrite (ONOO−) are the most common free radicals produced as metabolic by-products.60 Myocardial injury activates ROS-generating nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, xanthine oxidase, cyclooxygenase, lipoxygenase, myeloperoxidase, and RNS-generating inducible nitric oxide synthase (iNOS) directly or indirectly via increased inflammatory response.61 The production of O2•− coupled with NO• will yield ONOO−. Inadequate antioxidant capacity with low levels of superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), and reduced glutathione (GSH) during myocardial injury further exacerbate oxidative stress and result in lipid peroxidation, protein modification and deoxyribonucleic acid (DNA) damage. Nuclear factor erythroid 2-related factor (Nrf-2) is an important transcription factor for the regulation of oxidative stress. Nrf-2 binds to Kelch-like ECH-associated protein 1 (Keap-1) and sequesters in the cytoplasm under physiological condition, promoting its ubiquitination and degradation. Under oxidative condition, Keap-1 interacts with ROS, thus releasing Nrf-2. Subsequently, Nrf-2 translocates into the nucleus, forms a complex with small musculoaponeurotic fibrosarcoma oncogene homolog (Maf) protein and binds to the antioxidant response element (ARE) to stimulate downstream transcription of heme oxygenase-1 (HO-1), NADPH dehydrogenase quinone 1 (NQO1), glutamate-cysteine ligase catalytic subunit (GCLC), glutathione-S-transferase (GST), SOD, CAT, and GSH.62

The beneficial effects of A. paniculata (Burm.f.) Nees against oxidative stress have been proven in a canine model of left anterior descending coronary artery ligation-induced ischaemia and reperfusion injury. The myocardial tissues of mongrel dogs showed an increase in SOD activity, intracellular calcium, and a decrease in malondialdehyde (MDA) level after treatment with A. paniculata (Burm.f.) Nees.37,38 Ojha and co-researchers reported restoration of antioxidant capacity and inhibition of lipid peroxidation after treatment of A. paniculata (Burm.f.) Nees in two experimental rat models of ischaemia and reperfusion injury induced by left anterior descending coronary artery ligation as well as myocardial injury induced by isoproterenol.40,41

Several reports revealed the beneficial effects of andrographolide against oxidative stress in animals and cardiomyocytes. It has been reported that andrographolide suppressed the level of oxidative stress biomarkers (MDA, 4-hydroxynonenal, 3-nitrotyrosine, and ROS) in myocardial dysfunction induced by diabetes and left coronary artery ligation. The anti-oxidative action of andrographolide was achieved by inhibiting the enzymes responsible for ROS and RNS synthesis as well as targeting the Nrf-2 signalling axis known for the enhancement of antioxidant activities. Andrographolide inhibited the expression of iNOS, NADPH oxidases 2 (NOX2), NADPH oxidase 4 (NOX4), and NADPH oxidase cytosolic proteins (p47phox and p67phox). Additionally, andrographolide enhanced Nrf-2 nuclear translocation and upregulated downstream expression of HO-1, NQO1, SOD, and GPx in the heart.18,44 Cardiac NO• levels enhanced by LPS injection was reversed by andrographolide in male mice.42 Results from in vitro studies demonstrated similar outcomes, in which Nrf-2 nuclear translocation was promoted, whereas NADPH oxidases and their cytosolic proteins were suppressed in cardiomyocytes subjected to high concentration of glucose or hypoxia and treated with andrographolide.18,44 Another cell culture study depicted that andrographolide treatment protected cardiomyocytes against hypoxia and reoxygenation injury by upregulating enzymatic antioxidant activities, non-enzymatic antioxidant content, GCLC and glutamate cysteine ligase modifier (GCLM) expression.19 The anti-oxidative actions of A. paniculata (Burm.f.) Nees and andrographolide have been summarised in Figure 4.

Figure 4

The mechanism of action in the regulation of oxidative stress. During myocardial injuries, the imbalance between ROS/RNS levels and anti-oxidative capacity cause lipid peroxidation and protein modification. The anti-oxidative property A. paniculata (Burm.f.) Nees and andrographolide are accomplished by enhancing the antioxidant system via activation of Nrf-2/Keap-1 pathway as well as decreasing the enzymes responsible for oxidative and nitrosative stress (indicated by green arrows). The arrow pointing upward indicates an increase or activation while the arrow pointing downward indicates a decrease or inhibition.

Regulation of Apoptosis

Apoptosis is a process of programmed cell death, which has a pathological implication in myocardial loss, resulted from the loss of mitochondrial and endoplasmic reticulum mass leading to disruption of cellular integrity.63,64 Apoptosis is tightly regulated by the extrinsic and intrinsic mechanism in response to the exogenous and endogenous triggering stimulus, respectively. The extrinsic mechanism (also known as death receptor pathway) is initiated upon ligation of Fas ligand and tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) with their receptors, Fas and TRAIL receptor. Formation of death-inducing signalling complex (DISC) ensues, comprising Fas-associated death domain protein (FADD) and initiator caspase-8. The intrinsic mitochondrial pathway is promoted in the presence of cellular damage, hypoxia, and survival factor deprivation. These intracellular signals alter the expression of B-cell lymphoma 2 (Bcl-2), B-cell lymphoma-extra large (Bcl-xl), Bcl-2-associated X protein (Bax) and Bcl-2-antagonist/killer (Bak), whereby the former two genes favour apoptosis inhibition, while the latter two genes favour apoptosis activation. Raised pro-apoptotic genes and lowered anti-apoptotic genes enhance the release of cytochrome c, leading to apoptosome formation and initiator caspase-9 activation. The activated initiator caspases from both pathways, in turn, activate executioner caspases (caspase-3, caspase-6, and caspase-7) essential for the cleavage of cellular substrates, such as cytokeratins, cytoskeletal, and poly (ADP-ribose) polymerase (PARP).65,66 The two different apoptosis pathways can be bridged by a pro-apoptotic BH3-interacting domain (Bid), which is cleaved by activated caspase-8 upon death receptor stimulation. The translocation of Bid into mitochondria leads to the release of cytochrome c.67 Insulin-like growth factor-1 (IGF-1) and peroxisome proliferator-activated receptor-alpha (PPAR-α) are pivotal signalling molecules in apoptosis regulation. Interaction between IGF-1 and its receptor (IGF-1R) causes autophosphorylation at β-subunits of the receptor, which provides a docking site for insulin receptor substrate-1 (IRS-1). This eventually drives the phosphorylation and activation of PI3K and its downstream protein kinase, Akt. The activated Akt, in turn, inactivates Bcl-2-associated agonist of cell death (Bad), thus inhibiting apoptosis.68 On the other hand, PPAR-α promotes Bcl-2 ubiquitination and degradation, resulting in cell apoptosis.69

A. paniculata (Burm.f.) Nees and andrographolide potentially provide cardioprotection via mitigation of apoptosis event, indicated by the reduction of terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL)-positive cardiac cells and cleaved PARP activity.17,44,45 A. paniculata (Burm.f.) Nees extract attenuated pathological cardiac hypertrophy governed through its apoptosis-suppressing properties in both extrinsic and intrinsic pathways. Feeding the animals with high-fat diet increased the protein levels of Fas ligand, Fas receptor, FADD, Bid, caspase-8, and caspase 3, in which these apoptotic proteins were decreased after treated with A. paniculata (Burm.f.) Nees extract. Besides, the pro-apoptotic proteins (Bad and Bak) and cytochrome c accumulation were lowered in the A. paniculata (Burm.f.) Nees-treated obese mice.17

Andrographolide exerted anti-apoptotic effects by orchestrating both extrinsic and intrinsic pathways. The expression of Fas receptor and FADD in mice fed with high-fat diet was suppressed by andrographolide.45 For the intrinsic pathway, the protein levels of Bcl-2 and Bcl-xl were upregulated, whereas Bax, Bak, cytochrome c, and caspase-3 were downregulated in high-fat diet-induced obese mice following the administration of andrographolide. Concomitantly, the protein level of phosphorylated IGF-1R was increased, while the expression of PPAR-α was downregulated after being treated with andrographolide.45,46 A comprehensive study consisting of in vivo and in vitro experiments found reductions of Bax/Bcl-2 ratio and caspase-3 activity in the andrographolide-treated diabetic mice with myocardial dysfunction and in H9C2 cardiomyocytes stimulated by high concentration of glucose. The authors suggested that the anti-apoptotic activity of andrographolide was mediated through activation of Akt activity.44 Another study showed that andrographolide suppressed LPS-induced myocardial apoptosis as well as inhibited the executioner caspase-3 and caspase-7 activities for in mouse heart.42 The molecular mechanisms underlying the anti-apoptotic effects of A. paniculata (Burm.f.) Nees and andrographolide have been summarised in Figure 5.

Figure 5

The mechanism of action in the regulation of apoptosis during myocardial injuries. In the extrinsic pathway, the interaction between Fas ligand and its receptor causes the recruitment of FADD and procaspase-8 to form DISC. In the intrinsic pathway, the increases in pro-apoptotic genes and the decrease in anti-apoptotic genes resulted from oxidative stress and cellular damage lead to the release of cytochrome c from mitochondria. Apoptosome formation ensues, consisting of cytochrome c, deoxyadenosine triphosphate (dATP), apoptotic protease-activating factor 1 (Apaf-1), and procaspase-9. The activated initiator caspases (caspase-8 and caspase-9) further activates executioner caspases (caspase-3, caspase-6, and caspase-7), promoting the cleavage of cellular substrate. A. paniculata (Burm.f.) Nees and andrographolide prevent apoptosis by suppressing the mitochondrial and death receptor pathways. The upstream signalling events involved are the activation of IGF-1R and inhibition of PPAR-α. The anti-apoptotic effects of A. paniculata (Burm.f.) Nees and andrographolide are indicated (green arrows). The arrow pointing upward indicates an increase or activation while the arrow pointing downward indicates a decrease or inhibition.

Prevention of Cardiac Fibrosis and Endothelial Dysfunction

Cardiac fibrosis is defined as an imbalance between the production and degradation of extracellular matrix (ECM), leading to scar tissue accumulation, heart architecture distortion, and cardiac dysfunction.70 During myocardial injury, the pathogenesis of cardiac fibrosis is initiated with the increases in numerous profibrotic growth factors, such as transforming growth factor-beta (TGF-β), connective tissue growth factor (CTGF), and endothelin-1 (ET-1). TGF-β is a pleiotropic regulator in cardiac fibrosis. It stimulates the conversion of cardiac fibroblasts into myofibroblasts, promotes collagen deposition by decreasing the activity of plasminogen activators [such as urokinase plasminogen activator (u-PA) and tissue plasminogen activator (t-PA)] as well as inhibiting ECM degradation by decreasing matrix metalloproteinases (MMPs) activation via stimulation of plasminogen activator inhibitor-1 (PAI-1).71 In addition to the role as mediators for collagen synthesis and ECM degradation, plasminogen activators are proteins that facilitate the conversion of plasminogen to plasmin (an enzyme involved in the physiological breakdown of blood clot), whereas PAI-1 is a principal inhibitor of plasminogen activators, thus suggesting their functions in fibrinolytic activity. The expression of CTGF in myocardium is highly induced by cytokines and it creates a fibrotic environment and modulates the activity of other growth factors in ECM. Endothelin-1 promotes cardiac fibroblast proliferation, collagen production, and microfibroblast differentiation. Apart from the role of ET-1 in regulating cardiac fibrosis, it is also a powerful endogenous vasoconstrictor produced predominantly by endothelial cells. Its action is opposed to the function of NO•, whereby ET-1 exerted an inhibitory effect on NO•-mediated vasodilatation. Hence, the changes in NO• and ET-1 cause vascular endothelial dysfunction.72 Endothelial dysfunction is characterised by the reduction in bioavailability of NO• (a vasodilator) and/or an imbalance between endothelium-derived contracting and relaxing factors. Endothelial dysfunction precedes the development of myocardial injury. Mechanistically, these profibrotic growth factors trigger small mothers against decapentaplegic (Smad)-dependent and Smad-independent pathways to regulate ECM homeostasis. All the profibrotic growth factors are positively correlated with each other, further providing a positive feedback loop on fibrotic response.70 Thromboxane A2 (TXA2) is a potent vasoconstrictor and has a prothrombotic property. It is produced by activated platelet to promote platelet aggregation. Nonetheless, prostacyclin or prostaglandin I2 (PGI2) is an effective vasodilator produced by vascular endothelium and has an inhibitory effect on platelet activation. Therefore, changes in TXA2 and PGI2 affect endothelial function and they work as physiological antagonists for the regulation of blood coagulation in the vascular system. In the endothelial cells, caveolin-1 (CAV1) binds to endothelial nitric oxide synthase (eNOS) and inhibits NO• production.73

The promising effects of A. paniculata (Burm.f.) Nees against ischemic myocardium in experimental dogs were also mediated through its fibrinolytic action. The levels of PGI2 in platelets and euglobulin lysis time (a measure of fibrinolysis) were elevated, whereas the level of TXA2 was lowered in the A. paniculata (Burm.f.) Nees-treated group.39 Andrographolide has been proven to alleviate cardiac fibrosis through the TGF-β/Smad pathway. The collagen deposition and expression of fibrosis markers, including collagen I, collagen III, TGF-β, and fibronectin, were markedly reduced by andrographolide in streptozotocin-induced diabetic mice as compared to non-treated negative controls.44 In recent year, Xie et al performed preclinical studies utilising a mouse model of myocardial infarction induced by left coronary artery ligation and hypoxia-induced cardiomyocytes. The results showed the increases in TGF-β, collagen I, collagen III, CTGF, and phosphorylated Smad caused by myocardial infarction or hypoxia were attenuated by andrographolide treatment.18 Andrographolide also mitigated vascular endothelial dysfunction caused by chronic heart disease by decreasing ET-1 and TXA2 while increasing the levels of NO• and PGI2. Besides, andrographolide elevated t-PA and reduced PAI-1 content, indicating the improvement of fibrinolytic function and reduction of blood coagulation in mice with chronic heart disease.46 Microarray analysis also showed a reduction in CAV1 by andrographolide, which might help in maintaining NO• level and improved endothelial function in LPS-stimulated primary rat myocardial microvascular endothelial cells.59 The postulated mechanisms of A. paniculata (Burm.f.) Nees and andrographolide in the prevention of cardiac fibrosis and endothelial dysfunction have been summarised in Figure 6.

Figure 6

The mechanism of action in the prevention of cardiac fibrosis and endothelial dysfunction. In myocardial injuries, the increased expressions of collagen I, collagen III, fibronectin, PAI-1, and CTGF are mediated through TGF-β/SMAD signalling pathway, leading to the increase in blood coagulation and cardiac fibrosis. High levels of ET-1, TXA2 and low level of PGI2 cause the inhibition of vasodilatation, resulting in endothelial dysfunction. Treatment with A. paniculata (Burm.f.) Nees and andrographolide reverse all these changes, leading to the reduction of cardiac fibrosis, improvement of endothelial function and fibrinolytic function (indicated by green arrows). The arrow pointing upward indicates an increase or activation while the arrow pointing downward indicates a decrease or inhibition.

Taken together, the evidence showed that A. paniculata (Burm.f.) Nees and andrographolide potentially mitigate myocardial injury in animal and cellular models via its anti-inflammatory, anti-oxidative, and anti-apoptotic properties. The inhibition of important signalling molecules (such as NF-κB, PI3K/Akt, and MAPK) is responsible for regulating the crosstalk between myocardial injury and inflammation. The reduction of oxidative stress by A. paniculata (Burm.f.) Nees and andrographolide is in part modulated through the activation of Nrf-2 signalling axis. Both extrinsic and intrinsic pathways are involved in anti-apoptotic effects of A. paniculata (Burm.f.) Nees and andrographolide in heart tissues. Moreover, A. paniculata (Burm.f.) Nees and andrographolide prevents cardiac fibrosis, endothelial dysfunction, and enhances fibrinolytic activity, conferring cardioprotective effects for the prevention of myocardial injury.

Safety and Toxicity of Andrographolide

A wide array of cellular, animal, and human studies revealed that A. paniculata (Burm.f.) Nees and andrographolide are safe and non-toxic. There was no observable adverse effect reported in rats even at a relatively high dose of andrographolide or A. paniculata (Burm.f.) Nees (up to 5 g/kg).30,74,75 The cytotoxic effect of andrographolide was not seen in primary rat myocardial microvascular endothelial cells at the dose of 10 μg/mL.59 Batran et al evaluated the acute toxicity of andrographolide (100 or 500 mg/kg) in healthy male and female rats by observing the behavioural changes, abnormal manifestation, and mortality rate up to 24-hour post-treatment. There were no death or hazardous signs in biochemical parameters and histological evaluation in renal, liver, and kidney after andrographolide administration.76 In humans, the subjects were well tolerated with the doses of A. paniculata (Burm.f.) Nees (3 or 6 g/kg) provided and it is effective in relieving fever and sore throat in a randomised double-blind study recruiting patients with pharyngotonsillitis.77 A Phase I trial of andrographolide from A. paniculata (Burm.f.) Nees was conducted on human immunodeficiency virus-positive patients and healthy individuals. The regimen used was the dose escalation of andrographolide at the doses of 5, 10, and 20 mg/kg over a 9-week period (3 weeks for each dose). No adverse medical outcomes were observed, whereby the levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were in the normal range throughout the study period.78 In brief, the scientific data obtained from preclinical and clinical settings assure the safety and medicinal use of A. paniculata (Burm.f.) Nees and andrographolide, which requires further validation in patients with myocardial injury.

Perspectives

The pharmacokinetics of A. paniculata (Burm.f.) Nees or andrographolide serve as the essential information for determining their optimum treatment dose, route, frequency, and duration for potential clinical utility. The absorption of A. paniculata (Burm.f.) Nees is almost complete following its oral administration. Plasma concentration of andrographolide reaches the peak at two hours after oral administration of A. paniculata (Burm.f.) Nees at the dose of 20 and 200 mg/kg.79 In terms of distribution, andrographolide can be detected in the kidney, liver, heart, spleen, lung, and brain of rats after orally treated with A. paniculata (Burm.f.) Nees extract (133.33 mg/kg) and andrographolide (100 mg/kg), with the maximum concentration of andrographolide in these organs was observed at one-hour post-administration.80 The half-life of andrographolide was approximately 2.5 hours and excreted within 8 hours.79,80

As mentioned earlier, the effective doses of andrographolide against myocardial injury ranged from 10 to 100 mg/kg in animals. The calculated human equivalent dose is estimated to be 48–1000 mg for a 60 kg adult, which can be used as dose reference for future human trials. However, it is worthy to note that treatment with the lowest dose of andrographolide for a week might exert lesser beneficial effects. For instance, significant changes were not observed in the levels of thiobarbituric acid reactive substance and SOD in male mice with LPS-induced cardiac malfunction.42 In addition, higher dosage of A. paniculata (Burm.f.) Nees (100–2000 mg/kg) than andrographolide might be required, possibly attributed to a lower amount of andrographolide or the presence of other phytoconstituents in the plant extract as compared to the pure compound. Likewise, a shorter period of treatment (one week) for A. paniculata (Burm.f.) Nees was also insufficient to induce changes in some apoptosis parameters in obese mice fed with high-fat diet.17 In this context, the use of andrographolide at lower dose can be considered over the use of A. paniculata (Burm.f.) Nees extract at higher dose if comparable protective action against myocardial injury can be achieved. Another possible factor influencing the effective dose of A. paniculata (Burm.f.) Nees is the quality of plant extract, whereby andrographolide content may vary geographically, environmentally, and seasonally.81,82 The evaluation of plant extracts and andrographolide content present in different extracts should be mentioned along with the geographical distribution. Thus, pure compound is preferable compared to its original plant extract for better estimation of effective dose.

To our knowledge, there is a lack of clinical trial assessing the effect of A. paniculata (Burm.f.) Nees and andrographolide in patients with myocardial injury. The absence of data on the comparison between the efficacy of A. paniculata (Burm.f.) Nees or andrographolide with standard therapy is the shortcoming of current preclinical evidence. It will be rather challenging to translate the findings clinically. However, the combination of A. paniculata (Burm.f.) Nees or andrographolide with standard therapy may be possible in future human trials.

Conclusion

The abilities of A. paniculata (Burm.f.) Nees and andrographolide in resolving overwhelming inflammatory response, oxidative stress, apoptosis event, cardiac fibrosis, and endothelial dysfunction contribute to their protective effects against myocardial injury. From the evidence gathered, it would appear that both A. paniculata (Burm.f.) Nees and andrographolide may have the potential to be developed as prophylactic agents against future myocardial injury. They appear to be less effective for short-term relief of myocardial events. There are also no obvious differences in the myocardial protective effects between A. paniculata (Burm.f.) Nees and andrographolide. However, the effective dose of A. paniculata (Burm.f.) Nees is generally higher than andrographolide. Thus, andrographolide may be a better choice to consider whereby a lower dose may be sufficient. To confirm whether andrographolide is the specific bioactive compound responsible for beneficial properties of A. paniculata (Burm.f.) Nees, both plant extract and andrographolide isolated from the plant should be tested in vitro or in vivo under the same experimental setting to compare their myocardial protective effects. Researchers should further evaluate the effects of A. paniculata (Burm.f.) Nees and andrographolide in clinical trials to verify the positive outcomes reported in vivo and in vitro, thus promoting their potential clinical application as the management for myocardial injury.