Chronic inflammatory systemic diseases like rheumatoid arthritis are considered whole lifetime debilitating disorders, increasing the mortality rate bringing about high costs in healthcare for the patients and public health organizations (
50). Accordingly, pharmacotherapy in these inflammatory disorders is one of the vital healthcare issues. Herbal products hold a unique place among the public and researchers, revealing appealing natural sources for detection and proceeding with novel drug candidates. Regarding the natural products, different constitutes and preparations from
S. officinale L. have been extensively used to treat inflammatory disorders such as painful muscle and joint illnesses bone and wound healing (
18). In a study by Thibane et al., leaves of
S. officinale L. were used to stimulate healing, reduce inflammation, resulting in the alleviation of joint and muscle disorders and more facilitated functional improvements (
51). In a randomized, placebo-controlled, double-blind study by Koll et al., this genus was also renowned for its effectiveness in treating gonarthrosis, acute lower and upper back pain, and blunt injuries (
52).
S. officinale L. has oral and topical preparations (
53), used for its analgesic and anti-inflammatory activities, validated by modern clinical studies; however, the molecular base of action is still elusive (
18,
54). Some scientific shred of evidence is explaining the pathogenesis of inflammation and inflammatory diseases, underlining the role of the
Symphytum L. genus in this process (
5,
24). A reputable source, European Scientific Cooperative on Phytotherapy Monograph (ESCOP), introduced a monograph for
S. officinale L. discussing some properties of this plant. Specifically, it has been indicated that the roots have beneficial diverse therapeutic indications such as discolorations and wound healing, strains recovery, osteoarthritis, tend vaginitis, epicondylitis, arthritis, knee joint injuries, skin inflammation, tendinitis syndrome, non-active gonarthrosis, mastitis, insect bites, and fractures, proved by numerous clinical trials (
55,
56). Although
S. officinale L. is the most acknowledged species in this genus, other species represent significant bioactivities like
S. x uplandicum L. (Russian comfrey) with wound healing effect, and another plant is
S. caucasicum L. with burn healing effects (
57,
58). Diverse biological effects have been reported from the selected species of the Boraginaceae family, which especially have a reputation in the treatment process of inflammation (
Table 1).
| Genus | Active Components | Biological Activity | Geographical Distribution | References |
|---|
| Symphytum | Allantoin, pyrrolizidine alkaloids, choline, tannins, rosmarinic acid, and triterpenoid saponins. | Wound healing effects, strains recovery, osteoarthritis, tend vaginitis, epicondylitis, arthritis, knee joint injuries, skin inflammation. | Europe, Asia, and America | (59) |
| Pulmonaria | Allantoin, Rosmarinic acid, flavenoides, and phenolic compounds. | Treating respiratory disorders and urinary disorders anti-lithiasis activities. Wound healing effects. | Europe and western Asia | (47) |
| Nonea | Phenolic compounds, pyrrolizidine alkaloids, fatty acids, flavonoid, and saponines. | Treating diabetes, respiratory disorders, and wound healing agent. | the Mediterranean districts | (44) |
| Anchusa | Allantoin, pyrrolizidine alkaloids, tannins, triterpenes, and phenolic compounds. | Antiulcer, wound healing, Diaphoretic, antipyretic, narcotic, antipyretic, antirheumatic, and antiarthritis. | tropical and Mediterranean districts | (38, 60) |
| Echium | Allantoin, naphthoquinones,flavonoids, terpenoids, and phenolic compounds. | sedative, and anxiolytic, treating disorders including fissures of the hands, general scratches, and snakebites. | Mediterranean, North Africa and Europe | (49) |
| Borage | Allantoin and gamma-linolenic acid | Treating multiple sclerosis, diabetes, arthritis, eczema, and autoimmune disorders. | Europe, North Africa and Asia | (39) |
| Lithospermum | Allantoin, pyrrolizidine alkaloids, shikonin, shikalkin, flavonoids, and phenolic compounds. | Wounds and burns healing, antimicrobial, and antiparasitic agent. | Native to Europe, Asia, Africa. | (61) |
Diverse mechanisms of the anti-inflammatory preparations from the
Symphytum and selected members of the Boraginaceae family L. spp. have been revealed to the constituents playing roles in these procedures (
62). It has been confirmed that allantoin, choline, tannins, rosmarinic acid and its derivatives, poly[3-(3,4-dihydroxyphenyl) glyceric acid], shikonin, triterpenoid saponins, and essential oil were of the leadings phytopharmaceuticals present in these plants (
63,
64). Considerably, these constituents vary depending on the plant species and special part of the herb. The chemical structures of phytochemicals, structure activity relationship (SAR), and the source of the phytochemicals have important effects on the anti-inflammatory activities of a plant (
Table 2 and
Figure 2) (
65,
66).
| Group Compound | Compound Name | Source | Anti-inflammatory Effects | References |
|---|
| Imidazolidine-type alkaloid | Allantoin | Aerial parts and roots of Symphytum, Aerial parts of Borage, Aerial parts and roots of Lithospermum, Aerial parts and roots of Anchusa, Aerial parts and roots of Echium, Aerial parts and roots of Nonea, Aerial parts and roots of Pulmonaria | stimulating cell proliferation, improving regeneration of damaged tissues | (67, 68) |
| Phenolic acid | Rosmarinic acid | Aerial parts and roots of Symphytum, Aerial parts and roots of Borage, Aerial parts and roots of Lithospermum, Aerial parts and roots of Anchusa, Aerial parts and roots of Echium, Aerial parts and roots of Nonea, Aerial parts and roots of Pulmonaria | inhibits the formation of pro-inflammatory mediators, inhibits the formation of lipoxygenase, inhibits the formation of 5-HETE, inhibits cytokine release | (67, 69) |
| Naphthoquinone | Shikonin | Roots of Symphytum, Roots of Lithospermum, Roots of Echium | suppresses the transcriptional activation of the TNF-α promoter | (67, 70, 71) |
| Phenolic acid | Hydrocaffeic acid | Aerial parts and roots of Symphytum, Aerial parts and roots of Lithospermum, Aerial parts and roots of Echium, Aerial parts and roots of Nonea | inhibited the release of IL-1β | (67, 72) |
| Phenolic acid | Chlorogenic acid | Aerial parts of Symphytum, Aerial parts of Lithospermum, Aerial parts of Nonea, Aerial parts and roots of Pulmonaria | inhibits NO, inhibits pro-inflammatory cytokines | (67, 73-75) |
| Flavonoid | Rutin | Aerial parts of Symphytum, Aerial parts of Lithospermum, Aerial parts of Anchusa, Aerial parts of Echium | suppresses the production of TNF-α, suppresses interleukin 6, suppresses the activation of NF-κB | (68, 73, 76) |
The chemical structures of the important phytochemicals used in the treatment of inflammation
Allantoin, 5-ureide-hydantoin, is a metabolic compound of uric acid oxidation stimulating cell proliferation and improving regeneration of damaged tissues, while the compound choline decreases capillary permeability and, as a result, acts as an anti-oedemateous (
77,
78). It has been reported that the quantity of allantoin in the selected species was in the range of 0.6 - 11.8 mg.g
-1 air-dried matter in the aerial parts and 0.1 - 34.9 mg.g
-1 air-dry matter in the roots. The maximum amount of this compound was detected in
Echium italicum L. aerial parts (9.59 ± 1.96 mg.g
-1) and roots (34.89 ± 10.4 mg.g
-1), whereas in
S. officinale aerial parts, it was reported as 9.38 ± 2.72 and in roots, it was 25.77 ± 17.02 mg.g
-1 (
67). However, allantoin's molecular mechanism of action and its pharmacodynamic have remained unknown (
79). Choline increases tissue perfusion through vasodilatation and supports the clearance of inflammations mediators from the involved tissue (
78). Choline shows its anti-inflammatory effect by triggering alpha-7 nicotinic receptors and reducing cytokine production in macrophages (
80). Rosmarinic acid, a phenolic compound in
Symphytum L. spp., inhibits the formation of pro-inflammatory mediators, lipoxygenase, and 5-HETE also expresses antiphlogistic activity with no relative activity upon prostaglandin synthesis (
81,
82). Moreover, rosmarinic acid binds to T-cells and blocks signaling pathways to the nucleus resulting in cytokine release inhibition like IL-1 that would be used in treating autoimmune diseases (
83). The rosmarinic acid quantity in the selected plant species was in the range of 1.2 - 36.6 mg.g
-1 air-dry matter in the aerial parts and 1.3 - 27.0 mg.g
-1 air-dried matter in the roots. The maximum amount of this compound was detected in
Pulmonaria mollis aerial parts (36.6 ± 1.2 mg.g
-1) and roots of
Anchusa undulata (27.0 ± 5.65 mg.g
-1). In aerial parts of
S. officinale, rosmarinic acid quantity was detected as 4.5 ± 1.5, and in roots, it was 7.1 ± 2.63 mg.g
-1. Compared to
S. officinale, the amount of rosmarinic acid was much more in the other species,
S. cordatum, in aerial parts (12.4 ± 1.3) and less in the amount in the roots (7.19 ± 0.75) (
67). Allantoin, rosmarinic acid, and choline were believed to be the most responsible components for the anti-inflammatory and wound-healing properties in the mentioned plants (
84). Phenolic compounds of
S. officinale L. have been ascertained to be used as an anti-inflammatory agent in experimentations both in-vitro and in-vivo (
85). A polysaccharide; Poly[3-(3,4-dihydroxyphenyl)glyceric acid], showed antioxidant and anti-complement effects putting a stop to tissue damage that would be beneficial in several pathological disorders (
86).
S. officinale L. has anti-inflammatory properties that could be attributed to inhibition of IL-1β release, significantly (
87). Shikonin suppresses the transcriptional activation of the TNF-α promoter concluded inhibiting the binding of Transcription factor II D (a complex of proteins that binds to a TATA series on the DNA) complex to TATA box (a sequence of DNA) within the basal transcription machinery and so the consequent expression of the TNF-α protein. It is well accepted that shikonin possesses valuable therapeutic profits for skin-related inflammatory diseases and conceivably in inflammatory disorders attendant with increased TNF-α mediators (
88). There are various molecular mechanisms accredited in the treatment of inflammations commended to describe their functioning mechanism, containing the targeting of various intracellular signaling pathways provoking through Nrf2, MAPK, NF-κB, PPAR, and AP1 (
Figure 3) (
20).
Anti-inflammatory components pharmacodynamics figure
NF-κB signaling regulated several innate and adjustable immune functions. It is believed that NF-κB is a transcription factor that adjusts pro-inflammatory cytokine gene transcription. In the study, the roots of
S. officinale L. were extracted by hydroalcoholic; solution. The mucilage depleted fraction impaired the interleukin-1 (IL-1) through induction of pro-inflammatory markers, an expression containing E-selectin, VCAM1, ICAM1, and COX-2. Data afforded evidence that
S. officinale L. obstructed NF-κB signaling at two different stages: at first, it reduced the activation of IKK1/2, and later degradation of IκBα, and secondly, it inhibited the NFκB p65 nucleo-cytoplasmatic transporting and transactivation (
18,
26). There is another established mechanism for diverse anti-inflammatory effects of
Symphytum L. spp. through the two cyclooxygenase isoforms in charge of several signs of inflammation such as vascular disorders and pain. Logically, COX-1 and COX-2 are the main enzymes in the arachidonic acid metabolism pathway resulting in the synthesis of prostaglandins. The inhibitory action of the
Symphytum L. spp. was determined to be specifically on COX-2, with no effect on COX-1 enzymatic activity. Of note, no direct inhibitory activity on the enzymatic activity was detected, but the expression of COX-2 itself was powerfully blocked (
18,
89). Various genera of the Boraginacea family inhibits numerous inflammatory factors (
Table 3).
| Genus | Inhibited Inflammation Factors | References |
|---|
| Symphytum | COX-2, iNOS, NF-κB, NO, LOX | (24) |
| Pulmonaria | TNF-α, COX-2 | (90) |
| Nonea | COX-2, Complement | (91) |
| Anchusa | COX-2, LOX, Complement | (92, 93) |
| Echium | COX-2, iNOS, PGE2, NO, | (94, 95) |
| Borage | TNF-α, PGE2 | (96, 97) |
| Lithospermum | TNF-α, COX-2, NF-κB | (88, 98) |
The aqueous extract of
S. officinale L. aerial parts stimulated peroxisome proliferator-activated receptor (PPARs) and down-regulated E-selectin (expressed on endothelial cells after activation by IL-1 or TNFα and played an essential role in inflammation) mRNA and IL-8 (
15,
99). The wound healing activity of
S. officinale L. leaves was evaluated using three preparations via carbomer gel, glycero-alcoholic solution, and emulsion/soft lotion upon open wound rat model, using allantoin as the positive control. The results showed that the emulsion induced healing of the tissue injury and proliferation in collagen deposition from 40% to 240% and reduced cellular inflammatory infiltration by 3 - 46% (
15,
99,
100). Polysaccharides like poly[3-3,4-dihydroxyphenyl) glyceric acid] from
S. officinale showed the ability to deactivate the formation of active oxygen species (AOS) that are molded by activated polymorphonuclear neutrophils (PMN), performing a significant role in the protection of the body from invasive microorganisms (
101). The tissue was threatened when PMN initiated extra AOS production (
102). When AOS rises, the enzyme xanthine oxidase (XO) catalyzes the oxygen transformation into a superoxide anion, causing tissue damage. It was concluded that the binding of superoxide anion formed by activation of PMN and by XO was essential for healing wounds and treating inflammations (
103). Another study assessed the effects of hydroalcoholic extract on healing osteoarthritis pain on 200 patients divided into two groups. One group used
S. officinale L. extract cream, and the other applied placebo cream. The results showed that the patients who applied
S. officinale L. cream rated their pain 16 points lower than the other group in a short time (
104,
105). Elsewhere, the effectiveness of the ointment of
S. officinale L. extracts compared to diclofenac gel was evaluated in an observer-blinded study reporting the curve (AUC), the tenderness, and pain assessment at rest, movement by the patient, swelling, and ankle movement. According to the statistical data, the difference between the two groups was significant, and the benefit of the herbal ointment in excess of the diclofenac gel in the treatment process of distortions was observed. The
S. officinale L. products were suggested as a safe and effective alternative to the standard topical treatments (
Table 4) (
5,
106).
| Species | Anti-inflammatory Activity | Active Components | References |
|---|
| Symphytum officinale L. | Wound healing effects, Treating swelling of muscles, Treating arthritis, Treating sprains, contusions and strains after accidents | Allantoin, Rosmarinic acid, Hydro caffeic acid, Chlorogenic acid | (107-109) |
| Symphytum asperum Lepech. | Treating fractures and strains, Treating thrombophlebitis, Treating rheumatism , Treating gout, Wound healing effects | Poly [3-(3, 4-dihydroxyphenyl) glyceric acid], Caffeic acid, Rosmarinic acid, Chlorogenic acid, Salvianolic acid | (110) |
| Symphytum caucasicum | Burning healing effects, Wound healing effects | Poly [3-(3, 4-dihydroxyphenyl) glyceric acid], Allantoin | (63, 111) |
| Symphytum cordatum | Wound healing effects | Allantoin, Rosmarinic acid, Hydrocaffeic acid, P-hydroxybenzoic acid | (14, 67) |
| Symphytum × uplandicum Nyman | Wound healing effects, Treating swelling of muscles and myalgia, Treating arthritis, Treating sprains, contusions and strains after accidents, Treating joint distortion | Allantoin | (58, 112) |
| Symphytum anatolicum | Wound healing effects, Treating sprains and bruises | Caffeic acid, Allantoin, Chlorogenic acid, Rosmarinic acid, Isoquercitrin, Rutin, Hyperoside, Salvianolic acid C | (72, 113) |