Herbal Treatment for Management of Psoriasis: An Overview
Ravindra G. Gaikwad, Anilkumar J. Shinde*, Ashok A. Hajare
Department of Pharmaceutics, Bharati Vidyapeeth College of Pharmacy, Kolhapur, Maharashtra India – 416013.
*Corresponding Author E-mail: anilkumar.shinde@bharatividyapeeth.edu
ABSTRACT:
Psoriasis is an inflammatory skin condition characterised by scaling with inflammation (pain, edema, warmth, and redness) that results in regions of thick, red skin covered in silvery scales. These spots can be itchy or painful. Systemic treatment, topical therapy, and phototherapy are all now used to treat psoriasis. These treatments have a variety of negative and perhaps fatal side effects. Patients with psoriasis are more likely to acquire other conditions such as psoriatic arthritis, anxiety and depression, cancer, metabolic syndrome, cardiovascular disease, and Crohn's disease. The majority of people use herbal medicine because it is readily available, inexpensive, and effective. Many plants have promising features, including significant results in the treatment of psoriasis. The present study plans to emphasize such plants, herbal formulations, and associated therapy, which could add value to the development of a better, safe, and efficacious formulation to treat psoriasis that may help new researchers in this field.
KEYWORDS: Psoriasis, autoimmune disease, medicinal plants, herbal formulation, topical therapy.
INTRODUCTION:
Psoriasis is a well-known chronic, non-infectious, inflammatory dermatitis characterised by an acute exanthematous plaque bearing more adherent, silvery scales. Psoriasis is an organ-specific autoimmune syndrome activated by the cellular immune system1,2. Word Psoriasis is derived from the Greek word "psora", meaning "itch", and "sis" means "action," that is, "roughly itching condition." Psoriasis is divided into five types: guttate psoriasis, inverse psoriasis, plaque psoriasis, pustular psoriasis, and erythrodermic psoriasis. Along with it is also observed in case nail and psoriasis arthritis. The major characteristics are redness, irritation, and blistering patches on the skin3.
Pathophysiology of Psoriasis:
T-cell mediated cutaneous inflammation develops in psoriasis when activation is dependent on two signals. Surface proteins and antigen-presenting cells like dendritic cells and macrophages mediate this signal throughout cell-cell interaction.
T-cells that have been activated go from lymph nodes and into the circulation onto the skin region, where they release cytokines that cause pathological change. Other cytokines, such as TNF- and IL-8, are produced locally by keratinocytes and neutrophils. The growth of keratinocytes at that site is stimulated which leads to T-cell production and activation4.
ETIOLOGY OF PSORIASIS:
Immunological Factors:
In an autoimmunity situation, the body attacks itself. Psoriasis is an autoimmune disease. Invading WBCs assault and obliterate invading bacteria and scrap infection. In psoriasis, T cells attack the skin cells. This assault may cause the skin cell construction procedure to go into overdrive. The speed-up of skin cell construction causes fresh skin cells to expand excessively. The hyper proliferated skin cells are come towards the exterior skin, wherever they piled up5.
Genetic Factors:
One of the causes of psoriasis is the genetic component supported by family aggregation. The 1st and 2nd generations of sick people have an amplified frequency of emergent psoriasis. Whereas dizygotic twins have a two-to-three-fold amplified possibility, monozygotic twins have a two-to-three-fold amplified possibility6. Wide linkage report of families affected by psoriasis has so far detected at least 60 chromosomal loci linked to psoriatic susceptibility. PSORS1 is situated on chromosome 6P21, contained by the main histocompatibility complex7,8. PSORS1 is a risk factor exposed to more than 50 single- nucleotide polymorphisms (SNPs) that are connected to psoriasis9-11.
Environmental Factors:
Environmental factors such as ultraviolet rays, mechanical injury, different infections chemical injury, prescribed drug, and smoking may trigger psoriasis. Psychological stress is also one of the reasons for psoriasis12,13.
Figure 1. Etiolgy of Psoriasis
Figure 2. Types of psoriasis: (a) Single plaque of psoriasis; (b) Chronic plaque psoriasis; (c) Inverse psoriasis; (d) Guttate psoriasis; (e)
Pustular psoriasis; (f) Palmoplantar pustulosis; (g) Erythroderma and (h) Psoriatic arthritis
Types of Psoriasis:
(a) Single plaques psoriasis:
In case of this type of psoriasis reddish or salmon pink shading, covered with whitish or gleaming scales also, might be thick, flimsy, huge or little shown in Figure 2(a). They are generally active at the edge: quickly advancing sores might be annular, with normal skin in the middle.
(b) Chronic plaques psoriasis:
This type of psoriasis arises generally lying on the skeletal muscle of elbows, scalp, knees, lumbosacral area, and umbilicus, Figure 2(b). It is characterized by the koebner occurrence, in this development of new lesions at sites of pressure. It appears as small to big, well-defined regions of skin that are red, scaly, and thickened.
(c) Inverse psoriasis:
This type of psoriasis is a characterised by site-responsive form of vulgaris. In this inter triginous site are glossy, reddish, and characteristically without of scales, Figure 2(c). Psoriasis vulgaris will almost certainly show several intimately connected except phenotypically and genotypically different situation. It may describe the inconsistency of reaction to treatment, mainly through the T-cell embattled pharmacological agents.
(d) Guttate psoriasis:
It is developed in children and adolescents. In this psoriasis papules may be less than one centimeter in span blows upon the trunk, Figure 2(d). This psoriasis develops oneself in and sort-out within 120-130 days of arrival, even though its long-term prognosis is unidentified.
(e) Pustular psoriasis:
It is a severe sort of condition in which microscopic monomorphic sterile pustules proliferate within painful reddish skin, Figure 2(e). Fever, intercurrent infection, and the unexpected removal of general and, in some cases, ultra-potent topical corticosteroids may be experienced by the patient.
(f) Palmoplantar pustulosis:
This type of psoriasis characterized as recurring inflammatory condition that affects the palms and soles of the feet, Figure 2(f). On the palms of the hands and/or the soles of the feet, affected persons develop small to large sterile blisters filled with a yellow turbid liquid (pustules). Yellowish-brown pustules on soles and palm occurred. Generally, more than 25% of the community among palmoplantar pustulosis too has chronic plaque psoriasis. Palmoplantar pustulosis have diverse demographics to psoriasis vulgaris. Most of women who are current or previous smokers are affected by it. Usually onset occurrence age is 40-50. The hereditary examination has oblique to palmoplantar pustulosis and psoriasis vulgaris has diverse reasons.
(g) Erythroderma:
The erythroderma psoriasis, the entire skin is pretentious due to psoriasis. It leads to hypothermia, hypoalbuminemia, and elevated cardiac output. Erythroderma, Figure 2(g), is a condition due to other diseases; include drug eruptions, atopic dermatitis, and cutaneous T-cell lymphoma.
(h) Psoriatic arthritis:
Psoriatic arthritis is type of psoriasis characterized by inflammation at joints which may flare and subside, Figure 2(h). Peoples of psoriatic arthritis are affected with the condition of morning stiffness. Even in case of mild skin psoriasis patient can have a significant degree of arthritis. Nail psoriasis seen in nearly in patients with psoriatic arthritis. More than 10% of people by psoriatic arthritis faced skin embodiment of psoriasis.
The current available for the treatment of psoriasis includes topical agents, phototherapies and systemic medications. Systemic medication includes methotrexate, cyclosporine, retinoid and corticosteroids. The main difficulty related to using these drugs is they may show to augmented some side effects. Usually, herbal medicines are significant over allopathic drugs to treat skin disorders due to increased activity and lesser side effects14.
The allopathic system of medicine mainly concentrates on disease symptoms, but not on the main reason of the diseased condition. Ayurvedic treatment based on five elements theory, by this, these elements should survive in concord by the ‘fault’, ‘tissue’ and the ‘impurity’. Ayurvedic treatment makes the equilibrium between Dosha, Vatt and Pitta. Allopathy therapy has several side effects; may be every prescribe drug has connected with different side effect. Ayurvedic medicines, on the other hand, are made up of herbal and natural ingredients. As a result, there are no or very few chances of side effects. The use of herbal formulation increased in skin diseases15, 16. The current review was created with the goal of gathering comprehensive information on plants used for the management of psoriasis. There are also some recently marketed formulations and herbal formulations listed.
1. Silybum marianum:
The plant Silybum marianum is generally known as milk thistle plant. It belongs to the family Asteraceae. Silymarin is the main active constituent of Silybum marianum seeds. Silymarin is a flavolignan mixture of silybinin, silychristin, silydianin, and isosilybinin. Silybum marianum is used as an anti-inflammatory, hepatoprotective, antioxidant, immunomodulatory, and anti-fibrotic17. In the market, silymarin is available in different form of formulations for treatment of variety of diseases. The topical gel of silymarin was prepared by using methanol as a co-solvent, carbopol/HPMC used as a gelling agent & methyl/propyl paraben act as a preservative18, 19. In pathogenesis of psoriasis, abnormal level of cAMP and leukotriene has been observed. Silymarin can remove endotoxin from the liver and inhibit the synthesis of phosphodiesterase. Silymarin also inhibits leukotriene20. Silybin used in various cosmetics and dermatological preparations. Silymarin did not show phototoxicity21.
2. Coleus forskohlii Linn:
The family of Coleus forskohlii is Lamiaceae. It has fasciculate roots and is one of the sources of diterpenoid forskolin. It is an imperative medicinal plant in the ayurvedic system. It is used to management of cardiovascular disorders, asthma, eczema, hypertension and psoriasis. This plant promotes cell division. It increases isoform selectivity by acting on adenylyl cyclase to improve the intracellular level of cAMP. Coleus oil is effective against Propioni bacterium acnes. It is effective against skin infection, yeast culture and eruptions22. The herbal root extract of Coleus forskohlii incorporated into the gel. Propylene glycol acts as a penetration improver and sodium CMC act as a gel forming agent. The physical appearance, rheological properties, drug content, and rapid stability testing were all used to characterize the formulation. Drug concentration leftovers are unaffected by storage space for 90 days at 40°C23.
3. Pongamia pinnata Linn:
The family of Pongamia pinnata is Fabaceae and generally known as ‘Karanj’. It contains flavonoid and fixed oil. It is a versatile plant due to its chemical constituents, Pongamia pinnata sprouts and fruits used in folk remedies for abdominal cancer; the seeds for keloid tumors and powder of plant for tumors. The oil used in the preparation of liniments and skin preparations. The juice of leaves used in dyspepsia, cold, diarrhea, cough, flatulence, leprosy and gonorrhea. Karanj root meant for clean-up gums, teeth, and ulcers. It is used in anti-plasmodial, anti-inflammatory, anti-nociceptive, anti-lipid oxidative, anti-hyperammonic, anti-diarrheal, and antioxidant24. Oil of karanj is a source of biodiesel25. Karanj oil shows antipsoriatic activity. QRT-PCR is used to confirm cytokines attentiveness in the blood serum26. Gel has been prepared by means of methylsulphonylmethane crush and seed oil of Pongamia pinnata Linn. The prepared gel shows good antipsoriatic activity. The activity of the gel was evaluated by using the HaCaT cell line and mouse tail model27. Aqueous bark extract of plant Pongamia pinnata was incorporated in commercial preparation SUEX gel, used for psoriasis treatment. This new formulation successfully reduces retention of stratum granulosum and epidermal thickness. This gel shows that the attendance of the water extract of the bark shows an enhancement in the effectiveness of the ointment (SUEX GEL) used in the management of psoriasis28. Karanjin and pongapin furanoflavone was isolated from the air-dried root bark, both isolated compounds show antipsoriatic activity29.
4. Thespesia populnea Linn:
Thespesia populnea Linn belonging to the family Malvaceae; traditionally used to treat scabies, psoriasis, ringworm, eczema and herpetic diseases30. The ground bark is boiled in coconut oil; it is useful superficially in management of scabies and psoriasis. Different parts of the plant possess antibacterial, anti-inflammatory, antioxidant, antifertility, and purgative activity. The bark contains carbohydrates, tannins, glycosides, triterpenoids, flavonoids, fixed oil and phytosterols. The cream made by different extract and isolated compound shows antipsoriatic activity. The petroleum ether extract of bark shows the highest activity than other extracts. Every extract of plant (100 mg) & separated compounds (50 mg) were used for the formulation of a cream, by adding liquid paraffin (10 ml) and beeswax (3 g) and used topically31.
5. Memecylon malabaricum Cogn:
The plant Memecylon malabaricum family of Melastomaceae is used to treat a variety of ailments such as inflammatory, bacterial infections, diabetes conditions, herpes simplex, skin disorders, chickenpox, and psoriasis. It contains steroids, saponins, flavonoids, tannins, and alkaloids. Memecylaene isolated from leaves possesses potent anti-inflammatory activity. Extract of leaves shows in vitro antipsoriatic activity. This extract shows good inhibition of lipoxygenase. Memecylon malabaricum decoction shows thymidine phosphorylase inhibition32.
6. Cassia tora Linn:
Cassia tora leaf is rich by anthraquinone glycosides. Traditionally it is profess that used in the cure of skin diseases and psoriasis. Luteolin-7-O-β-glucopyranoside, formononetin-7-O-β-D-glucoside and quercetin-3-O-β-D- glucuronide was isolated from the tora leaf. The ethanolic extract of Cassia tora leaf was evaluated for antipsoriatic activity. Ethanol extract and isolated compound exhibit a momentous fraction decrease of epidermal thickness. Luteolin, quercetin and formononetin was isolated and used as marker33. Oil in water cream was prepared with methanolic extract and tested using ultraviolet-B-induced psoriasis in the rat. Acute dermal toxicity, sensitivity, and grittiness were tested. According to the study, acute dermal toxicity was observed, and the creams were appropriate and safe at a dose of 2000 mg/kg 34.
7. Givotia rottleriformis Griff. Ex Wight:
Plant Givotia rottleriformis Griff. Ex Wight belongs to the family Euphorbiaceae. An ethanolic extract of bark contains carbohydrates, alkaloids, glycosides, proteins, saponins, and flavonoids35.Luteolin-7-O-β-D-glucuronide, rutin, and kaempferol 3-O-[2-O-(6-O-feruloyl)-β-Dglucopyranosyl]-β-D-galactopyranoside flavonoids are extracted and evaluated. Isolated flavonoid shows antipsoriatic activity by HaCaT human keratinocytes cell line36. Ethanolic extract of Givotia rottleriformis bark shows effective antipsoriatic activity. The extract shows major decrease in the epidermal thickness representing to delay the hyperproliferation37.
8. Wrightia tinctoria:
Plant Wrightia tinctoria belongs to family Apocynaceae. This herb contains various secondary metabolites like alkaloids, triterpenoids, steroids, flavonoids, lipids and carbohydrates. Hydroalcoholic extract of leaves of Wrightia tinctoria shows antipsoriatic activity which is evaluated by means of mouse tail test. The extract shows the important quantity of orthokeratosis38. The oil extracted from herb Wrightia tinctoria incorporated in beads formulations, which shows excellent activity. The beads formulation was prepared from extracted oil, acacia powder, and pectin and sodium alginate polymer39. The most significant bioactive principles in seeds are quercitin, lupeol, α-amyrin, β-amyrin, wrightial and β-sitosterol. The nanosponge of Wrightia tinctoria was prepared from methanolic seed extract and these were incorporated into a gel base and used as a topical gel40.
9. Wannachawee Recipe:
Wannachawee Recipe (WCR) efficiently used as Thai folk medicine for treatment of psoriasis. Wannachawee Recipe contains 8 Thai herbs as Alpinia galanga Linn Willd, Smilax glabra Wall, Smilax corbularia Kunth, Smilax species, Stemonacollinsae Craib, Rhinacanthus nasutus Linn Kurz., Acanthus ilicifolius Linn. The water extract of this all plant dissolved in DMSO and screened for its antipsoriatic activity. Wannachawee Recipe considerably decreased the mRNA expression 41.
10. Strobilianthes ciliates:
Plant Strobilianthes ciliatus belongs to family Acanthaceae. Strobilianthes ciliatus is extremely prospective remedial plant in ayurveda for the dealing of inflammation and skin problems. Petroleum ether and ethanolic extract of leaf of Strobilianthes ciliatus and ethanolic extract of stem of Strobilianthes ciliatus were evaluated for anti-psoriatic by in-vitro models. Psoriatic activity was screened with MTT assay on HACAT cell lines. Petroleum ether extract of leaf showed high anti-psoriatic activity42.
11. Solanum xanthocarpum:
Plant Solanum xanthocarpum belongs to the Solanaceae. It is members of the dashamula in Ayurvedic medicine. Ethanolic steam extract of Solanum xanthocarpum was incorporated in gel. The gel of ethanolic extract of 2.5,5 and 10 % was prepared and orally 100, 200 and 400 mg/kg screened for antipsoriatic activity by imiquimod-induced psoriatic mouse model. Gel of 10 % and orally 200 and 400 mg/kg shows excellent antipsoriatic activity43.
12. Citrus aurantium:
Citrus aurantium is plant from family Rutaceae it contains significant pharmacologically active compounds such as phenethylamine alkaloids, synephrine, tyramine, octopamine, hordenine and n-methyltyramine44. It is affluent in flavonoids, vitamin C, and volatile oil. Hexane, ethyl acetate and methanolic extract of Citrus aurantium tested for anti-psoriatic activity by MTT assay. All the extract of plant Citrus aurantium shows major inhibits activity on the proliferative of THP1 cell lines45.
13. Citrus sinensis:
Citrus sinensis belongs to the family Rutaceae. Cream prepared from ethanol and aqueous extract of Citrus sinensis shows antipsoriatic activity46. Citrus sinensis oil was used in preparation of lotion. Psoralea corilyfolia oil, Aloe barbadensis leaves, Ocimum sanctum leaves, Azadirachta indica leaves, Curcuma longa rhizomes), Ammi visnaga fruits, Citrus limonum Peel, and Citrus sinensis oil were used to prepare lotion47.
14. Curcuma longa:
Curcuma longa belonging to family Zingiberaceae is originating from south‑eastern Asia. Curcuma longa has long olden times to use as medicine in ayurveda. Curcuma longa is well-known as turmeric. Curcuma longa contains three main curcuminoids such as curcumin, demethoxycurcumin and bisdemethoxycurcumin.
Curcuma longa contain volatile oil like tumerone, atlantone and zingiberone48. It is a potential plant for treating anti-inflammatory, anti-allergic, antioxidant, antihyperglycemic, and anticancer properties. Molecular study of turmeric includes fingerprinting by RAPD, SCAR, ISSR, and AFLP plays a principal role in developing a molecular marker for the authenticity and diversity of plants49. Various products containing Curcuma longa frequently used to treat ringworm, obstinate itching, eczema, and other parasitic skin diseases50, 51.
The antipsoriatic activity of Curcuma longa is due to the existence of antioxidants components in the plant. Curcuminoids of Curcuma (curcumin) has poor water solubility and permeability that limits transdermal absorption. Saponin acts as a surfactant that promotes transdermal absorption. Isolated saponins and curcumin used in different concentration for the formulation of gel. Curcumin and curcumin-saponin incorporated gel show potent antipsoriatic activity52. Caffeine synergizes the action of curcumin. Methylxanthine moiety caffeine is proficient to inhibit the phosphodiesterase enzyme. Phosphodiesterase enzyme helps to hydrolysis of cyclic nucleotide elevates the concentration of intracellular cAMP. In psoriasis intracellular, cAMP levels reduced from cutaneous leukocytes. Phosphodiesterase inhibitor caffeine increases intracellular cAMP levels53. Nanosponge based gel of curcumin and caffeine so act as a potential treatment of psoriasis. A crosslinker dimethyl carbonate and polymer beta-cyclodextrin used to prepare nanosponge; this incorporated in topical gel54. O/W cream prepare by ethyl alcohol extract of Curcuma shows significant antipsoriatic activity55. Curcumin microemulison gel is used in dermatocosmetics56. SmartPearls tools, which loads medicine into spongy material to get steady amorphous contemporary relief. Penetration and efficacy enhanced by smartPearl tools with the addition of glycyrrhizic acid57.
15 Azadirachta indica:
Azadirachta indica is plant from Meliaeae family. The active constituent of Azadirachta indica is nimbidin, nimbolides, salanin, azadirachtin, meliacin, gedunin, nimbin, valassin, meliacin. The seed contains tignic acid, limnoids. Azadirachta indica kernels were used in making soap, pesticide and pharmaceutical industries. Neem shows analgesic, abortifacient, antibacterial, anti-yeast, anthelminthic, anti-inflammatory and antiviral. Azadirachta indica also shows diuretic, antinematodal, antipyretic, antispasmodic, immunomodulators and antinematodal activity58. Topical cream consists of the nanostructured lipid carriers of Azadirachta leaves extract; Lawsonia inermis leaves extract, and fruit extract of Mallotus philippensis, which show anti-psoriatic activity59. O/W cream of extract of Azadirachta indica leaf extract, Bereris aristata root extract, Psoralia corylifolia seed extract and Hemidesmus indicus root show excellent antipsoriatic activity60.
Recent drugs available in market:
Psoriasis is a chronic reoccurring disease that required long term therapy. Therapy depends on severity and comorbidity. Nature of the medical sternness of lesions, the fraction of exaggerated body surface region is divided into mild or moderate psoriasis. Gentle to modest psoriasis treated topically, whereas sensible to severe psoriasis often requires systemic treatment61.
Table 1: List of some recent drugs available in market
|
Drugs |
Mechanism of action |
Marketed preparation |
|
Methotrexate |
Inhibition DNA production by blocking thymidine and purine synthesis |
Methocip® Tablet (Cipla) Methorex® Tablet (Zydus) Folitrax® Tablet (Ipca Lab) |
|
Cyclosporine |
T cell-inhibitor |
Imusporin® Capsule (Cipla) Cyclophil® ME 25 Tablet (Biocon) Psorid® Capsule (Biocon) |
|
Acitretin (Retinoids) |
Transcriptional process by acting throughout nuclear receptors and normalizes keratinocyte proliferation and separation |
A Treat Capsule (Kaizen Pharma.) Acipsor Capsules (Kivi Labs) Acetroin (Nidus Pharma) |
|
Apremilast |
Inhibition the hydrolyzation of the second messenger cAMP. |
Aprezo tablet (Glenmark Pharma. Ltd.) Apxenta tablet (Ajanta Pharma.) Apraize (Ipca Lab.) |
|
Etanercept |
Dimeric human fusion protein mimicking TNF-αR |
Intacept 25 solution for Injection (Intas Pharma.) Etacept 25 mg Injection (Cipla) Enbrel 25 mg Injection (Pfizer) |
|
Infliximab |
Chimeric IgG1κ monoclonal antibody that binds to soluble and transmembrane forms of TNF-α |
Infimab Injection (Sun Pharma.) Remicade Injection (Janssen Pharma.) |
|
Adalimumab |
Human monoclonal antibody against TNF-α |
Plamumab Injection (Cipla) Adalirel 40 mg Injection (Reliance Life Sci) Adalimac 40 mg injection (Macleods Pharma) |
|
Tofacitinib |
Janus kinase (JAK) inhibitor |
Jaknat Tablet (Natco Pharma) Tofe Tablet (Alkem Lab.) Tfct-Nib Tablet (Ipca Lab.) |
|
Halobetasol |
Blocks chemical messenger responsible for inflammation |
Hobs 0.05% cream (Aamorb Pharma.) Haloderm Ointment (Micro Labs) Haloderm Lotion (Micro Labs) |
Some herbal formulations available on market include Psoraze Cream (contains Cestrum Diurnum; Ayushavedam), Psoraksha oil (contains Cestrum Diurnum, by Ayushavedam), 4G green powder (contains Cestrum Diurnum; Ayushavedam), Regsor Psoriasis Oil (contains Wrightia Tinctori;, Apptec Inc.), Vasu Cutisora Lotion and Oil (contains Neem, Karanj, Haridra, Kali mirch, Shwet Kutaj, Vasa, Kantakari, Guduchi; Vasu Healthcare), Sornip Cream (contains herbal oil containing 3-O-Acetyl-11-Keto β-Boswellic acid; Cipla), Soricure Cream (contains Wrightia Tinctoria; Indian Herbs Specialities).
Many medicines are available in the market and the effectiveness of treatment depends on many factors, including severity of the condition or the time of diagnosis. Though they can cause side effects these herbal remedies are usually safe to use. It is advisable for people to always consult a doctor before using any of the new herbs, herbal remedies, or natural treatments.
ACKNOWLEDGEMENTS:
Authors kindly acknowledge Dr. H. N. More the Principal of Bharati Vidyapeeth College of Pharmacy Kolhapur Maharashtra for proving facility to conduct literature work. The authors are also thankful to Chhatrapati Shahu Maharaj Research, Training and Human Development Institute (SARTHI), Pune for providing financial assistance in the work.
CONFLICT OF INTREST:
The authors have no conflicts of interest regarding views expressed in this review.
REFERENCES:
1. Krueger JG, The immunologic basis for the treatment of psoriasis with new biologic agents, Journal of American Academy of Dermatology. 2002; 46: 1–23. doi:10.1067/mjd.2002.120568
2. Sumithra M, Mohamed A, Chitra. V. Cell lines and animal models of psoriasis. Research Journal of Pharmacy and Technology. 2020; 13(3):1601-1608. doi: 10.5958/0974-360X.2020.00290.5
3. Jobling R, A patient’s journey, Psoriasis. British Medical Journal. 2007; 334:953-954. doi: 10.1136/bmj.39184.615150.802
4. DiPiro JT. Pharmacotherapy Handbook. Wells BG, Schwinghammer TL, DiPiro CV, Education MH, editors. Appleton & Lange; 2000.
5. Bissonnette R, Fuentes DJ, Mashiko S, Li X, Bonifacio KM, Cueto I, Suárez FM, Maari C, Bolduc C, Nigen S, Sarfati M. Palmoplantar pustular psoriasis (PPPP) is characterized by activation of the IL-17A pathway. Journal of Dermatological Science. 2017; 85(1):20-6. doi:10.1016/j.jdermsci.2016.09.019
6. Farber EM, Nall ML, Watson W. Natural history of psoriasis in 61 twin Pairs. Archives of Dermatol. 1974; 109:207–211. doi:10.1001/archderm.1974.01630020023005.
7. Mallon E, Bunce M, Savoie H, Rowe A, Newson R, Gotch F, Bunker CB. HLA‐C and guttate psoriasis. British Journal of Dermatology. 2000; 143(6):1177-82. doi: 10.1046/j.1365-2133.2000.03885.x
8. Gudjonsson JE, Karason A, Antonsdottir A, Runarsdottir E, Hauksson VB, Upmanyu R, Gulcher J, Stefansson K. and Valdimarsson H. Psoriasis patients who are homozygous for the HLA‐Cw 0602 allele have a 2· 5‐fold increased risk of developing psoriasis compared with Cw6 heterozygotes. British Journal of Dermatology. 2003; 148(2):233-235. doi:10.1046/j.1365-2133.2003.05115.x
9. Elder JT. Genome-wide association scan yields new insights into the immunopathogenesis of psoriasis. Genes & Immunity. 2009; 10(3):201-9. doi:10.1038/gene.2009.11
10. Sakthi PS, Vani PB, Kumar PR. A comparative review on conventional and traditional medicine in the treatment of psoriasis. Research Journal of Pharmacy and Technology. 2020; 13(11):5642-5646. doi:10.5958/0974-360X.2020.00983.X
11. Yin X, Low HQ, Wang L, Li Y, Ellinghaus E, Han J, Estivill X, Sun L, Zuo X, Shen C, Zhu C. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Nature communications. 2015; 23; 6(1):1-1. doi: 10.1038/ncomms7916
12. Deka D, Borah T, Swarnakar A, Baruah D, Bharali BK. Psoriasis: A comparative study as per ayurvedic and modern classics. Journal of Ayurvedic and Herbal Medicine. 2016; 2: 186-191.
13. Haslett C, Haslett C, Davidson SS. Davidson's principles and practice of medicine. Churchill Livingstone; 2002.
14. Padmini IR, Gupta VN. Formulation and evaluation of herbal cream for treating psoriasis. Research Journal of Pharmacy and Technology. 2021; 14(1):167-170. doi: 10.5958/0974-360X.2021.00029.9
15. Kulkarni UM, Shetty YC, Dongre AM, Dave JS, Khopkar US. The perception of dermatologists towards the outcome of ayurvedic therapy for psoriasis. Journal of Clinical & Experimental Dermatology Research. 2018; 9(465):2. doi: 10.4172/2155-9554.1000465
16. Menter A, Griffiths CE, Current and future management of psoriasis, Lancet. 2007; 370:272–284. doi:10.1016/S0140-6736(07)61129-5
17. Qavami N, Naghdi BH, Labbafi MR, Mehrafarin A. A review on pharmacological, cultivation and biotechnology aspects of milk thistle Silybum marianum L. Gaertn. Journal of Medicinal Plants. 2013; 12(47):19-37.
18. Khedekar YB, Mojad AA, Malsane PN. Formulation, development, and evaluation of silymarin loaded topical gel for fungal infection. International Journal of Advances in Pharmaceutics. 2019; 08(01): e5041. doi: https://doi.org/10.7439/ijap.v8i1.5041
19. Khan PA, Thube R, Rab RA, Formulation development and evaluation of silymarin gel for psoriasis treatment, Journal of Innovations in Pharmaceuticals and Biological Sciences. 2013; 1(1):021-026.
20. Singh KK, Tripathy S. Natural treatment alternative for psoriasis: a review on herbal resources. Journal of Applied Pharmaceutical Science. 2014; 4(11):114-21. doi: 10.7324/JAPS.2014.41120
21. Svobodová AR, Zálešák B, Biedermann D, Ulrichová J, Vostálová J. Phototoxic potential of silymarin and its bioactive components. Journal of Photochemistry and Photobiology B: Biology. 2016; 1; 156:61-8. doi:10.1007/s00403-018-1828-6
22. Lokesh B, Deepa R, Divya K. Medicinal Coleus (Coleus forskohlii Briq): A phytochemical crop of commercial significance. Journal of Pharmacognosy and Phytochemistry. 2018; 7:2856-64. doi:10.1016/j.phytochem.2018.08.003
23. Damle MC, Bhalekar MR, Lonkar SA, Formulation and evaluation of herbal gel for the treatment of psoriasis, World Journal of Pharmacy and Pharmaceutical Sciences. 2017; 6(7):1199-1210. doi: 10.20959/wjpps20177-9521.
24. Manikannan M, Arumugam S, Rangasamy B, Selvaraj J. Immune Stimulation effects of Pongamia pinnata extracts an in vitro analysis. Research Journal of Pharmacy and Technology. 2020; 13(1): 308-312. doi: 10.5958/0974-360X.2020.00062.1
25. Chopade VV, Tankar AN, Pande VV, Tekade AR, Gowekar NM, Bhandari SR, Khandake SN. Pongamia pinnata: phytochemical constituents, traditional uses and pharmacological properties: a review. International Journal of Green Pharmacy. 2008; 2(2):72-75.
26. Alex T, Mansuri S, Chaudhary S, Malviya N, Evaluation of anti psoriatic activity of karanjin oil, Journal of Drug Delivery and Therapeutics. 2017; 7(7):206-207. doi: https://doi.org/10.22270/jddt.v7i7.1638
27. Salunke PB, Kadam SS, Patil SB, Kolap MB, Antipsoriatic activity of gel containing methylsulphonylmethane powder and seed oil of pongamia pinnata Linn, Der Pharma Chemica. 2017; 9(18):12-20.
28. Divakara P, Nagaraju B, Buden RP, Sekhar HS, Ravi CM. Antipsoriatic activity of ayurvedic ointment containing aqueous extract of the bark of Pongamia pinnata using the rat ultraviolet ray photodermatitis model. Advancement in Medicinal Plant Research. 2013; 1:8-16.
29. Ghosh A, Tiwari GJ. Role of nitric oxide-scavenging activity of karanjin and pongapin in the treatment of psoriasis. Biotech. 2018; 8(8):1-4. doi:org/10.1007/s13205-018-1337-5
30. Hiteksha SP, Mamta BS. Thespesia populnea linn. A review. International Journal of Pharmacognosy. 2017; 4(1):1-05. doi:10.13040/IJPSR.0975-8232.IJP.4(1).1-05
31. Shrivastav S, Sindhu RK, Kumar S, Kumar P, Anti-Psoriatic and phytochemical evaluation of thespesia populnea bark extracts, International Journal of Pharmacy and Pharmaceutical Sciences. 2009; 1(1):176-185.
32. Abi PK, Madhusudhanan K. Memecylon malabaricum Cogn, plant profile, pharmacology and phytochemistry-a review. International Journal of Biosciences, Alternative and Holistic Medicine. 2017; 5(1):1.
33. Dhanabal SP, Muruganantham N, Basavaraj KH, Wadhwani A, Shamasundar NM. Antipsoriatic activity of extracts and fractions obtained from Memecylon Malabaricum leaves. Journal of Pharmacy and Pharmacology. 2012; 64(10):1501-9.
34. Vijayalakshmi A, Madhira G. Anti-psoriatic activity of flavonoids from Cassia tora leaves using the rat ultraviolet B ray photodermatitis model. Revista Brasileira de Farmacognosia. 2014; 1; 24(3):322-9. doi: http://dx.doi.org/ 10.1016/j.bjp.2014.07.010
35. Singhal M, Kansara N. Cassia tora Linn cream inhibits ultraviolet-B-induced psoriasis in rats. International Scholarly Research Notices. 2012; 1-6. doi:10.5402/2012/346510
36. Geetha M, Vijayalakshmi A. Pharmacognostic and phytochemical investigation of Givotia rottleriformis Griff. Ex Wight bark. Journal of Pharmacognosy and Phytochemistry. 2013; 2(3):188-94.
37. Niper J. Anti-Psoriatic activity of flavonoids from the bark of Givotia rottleriformis Griff. Ex Wight. Iranian Journal of Pharmaceutical Sciences. 2014; 10(3):81-94.
38. Vijayalakshmi A, Geetha M. Anti-psoriatic activity of Givotia rottleriformis in rats. Indian journal of pharmacology. 2014; 46(4):386. doi:10.4103/0253-7613.135949
39. Dhanabal SP, Raj BA, Muruganantham N, Praveen TK, Raghu PS. Screening of Wrightia tinctoria leaves for anti psoriatic activity. Hygeia-Journal for Drugs and Medicine. 2012; 4(1):73-8.
40. Singh D, Rawat S, Riyal N, Aman S, Khulbe P. Determining anti-psoriatic activity of salicylic acid and wrightia tinctoria herb using extemporaneous formulation. 2018; 7 (4): 562-585.
41. Iriventi P, Gupta NV. Development and evaluation of nanosponge loaded topical herbal gel of wrightia tinctoria. International Journal of Applied Pharmaceutics. 2020; 15:89-95.
42. Takuathung MN, Wongnoppavich A, Pitchakarn P, Panthong A, Khonsung P, Chiranthanut N, Soonthornchareonnon N, Sireeratawongs S, Effects of wannachawee recipe with antipsoriatic activity on suppressing inflammatory cytokine production in HaCaT human keratinocytes, Hindawi Evidence-Based Complementary and Alternative Medicine. 2017; 1-12. doi: doi.org/10.1155/2017/5906539
43. Shalini K, Aleykutty NA, Harindran J. In vitro antipsoriatic effect of extract of Strobilianthes ciliatus using Hacat cell lines and its cyclooxygenase inhibition using RAW 264.7 cell lines. The Pharma Innovation Journal. 2018; 7(3): 253-256.
44. Parmar KM, Itankar PR, Joshi A, Prasad SK. Anti-psoriatic potential of Solanum xanthocarpum stem in imiquimod-induced psoriatic mice model. Journal of Ethnopharmacology. 2017; 23; 198:158-66.
45. Suryawanshi JS. An overview of Citrus aurantium used in treatment of various diseases. African Journal of Plant Science. 2011; 5(7):390-5.
46. Vardhan TV, Kumar M, Arumugam P. Anti-psoriatic activity of orange peel extract using monocytic cell line. 2015; 8(3):119-129.
47. Kumar BV, Sekhar GC, Venkatesh C, Manikanta Y, Nagalakshmi J, Rao NR. Phytochemical screening and anti-psoriatic evaluation of citrus sinensis peel extracts on mouse tail model. World Journal of Pharmaceutical Research. 2019; 8(2):1210-1219. doi:10.20959/wjpr20192-14147
48. Yadav D, Yadav SK, Khar RK, Mujeeb M, Akhtar M. Turmeric (Curcuma longa L.): A promising spice for phytochemical and pharmacological activities. International Journal of Green Pharmacy. 2013; 7(2):85-89. doi:10.4103/0973-8258.116375
49. Ashraf K, Sulatan S, A comprehensive review on Curcuma longa Linn. Phytochemical, pharmacological, and molecular study. International Journal of Green Pharmacy. 2018; 11; 11(04).S671-S685. doi: http://dx. doi.org/10.22377/ijgp.v11i04.1343
50. Miquel J, Bernd A, Sempere JM, Dıaz-Alperi J, Ramırez A. The curcuma antioxidants: pharmacological effects and prospects for future clinical use. A review. Archives of Gerontology and Geriatrics. 2002; 1; 34(1):37-46. doi:10.1016/s0167-4943(01)00194-7.
51. Badmanaban R, Saha D, Sen DJ Biswas A, Mandal S, Basak S. Turmeric: A holistic solution for biochemical malfunction. Research Journal of Pharmacy and Technology. 2021; 14(10):5540-0. doi:10.52711/0974-360X.2021.00966
52. Morankar PG, Kumbhare MR, Shelke SJ, Diwane CM. Enhancement of skin permeability and anti-inflammatory, antipsoriatic efficacy of curcumin through a gel formulation. Innoriginal: International Journal of Sciences. 2021; 28:22-9.
53. Duvoix A, Blasius R, Delhalle S, Schnekenburger M, Morceau F, Henry E, Dicato M, Diederich M. Chemopreventive and therapeutic effects of curcumin. Cancer letters. 2005; 8; 223(2):181-90. doi: 10.1016/j.canlet.2004.09.041.
54. Iriventi P, Gupta NV, Osmani RA, Balamuralidhara V. Design & development of nanosponge loaded topical gel of curcumin and caffeine mixture for augmented treatment of psoriasis. DARU Journal of Pharmaceutical Sciences. 2020; 29:1-8. doi:10.1007/s40199-020-00352-x
55. Hassan BA. Evaluation of Antipsoriatic activity of topical curcumin by using mouse tail model. University of Thi-Qar Journal of Medicine. 2018; 16(2):172-84.
56. Scomoroscenco C, Teodorescu M, Raducan A, Stan M, Voicu SN, Trica B, Ninciuleanu CM, Nistor CL, Mihaescu CI, Petcu C, Cinteza LO. Novel gel microemulison as topical drug delivery system for curcumin in dermatocosmetics. Pharmaceutics. 2021; 13(4):505.
57. Jin N, Lin J, Yang C, Wu C, He J, Chen Z, Yang Q, Chen J, Zheng G, Lv L, Liang H. Enhanced penetration and anti-psoriatic efficacy of curcumin by improved smartPearls technology with the addition of glycyrrhizic acid. International journal of pharmaceutics. 2020; 30; 578:119101. doi: 10.1016/j.ijpharm.2020.119101.
58. Hashmat I, Azad H, Ahmed A. Neem Azadirachta indica (A. Juss) a nature’s drugstore: an overview. International Research Journal of Biological Sciences. 2012; 1(6):76-9.
59. Khan S, Mulla G, Bhise K. Development and characterization of topical nanoparticulate antipsoriatic polyherbal cream. International Journal of Applied Pharmaceutics. 2020:7:67-73.
60. Mundada AS, Mahajan MS, Gangurde HH, Borkar VS, Gulecha VS, Khandare RA. Formulation and evaluation of polyherbal antipsoriatic cream. Pharmacology online. 2009; 2:1185-91.
61. Mrowietz U, Kragballe K, Reich K, Spuls P, Griffiths CE, Nast A, Franke J, Antoniou C, Arenberger P, Balieva F, Bylaite M. Definition of treatment goals for moderate to severe psoriasis: a European consensus. Archives of Dermatological Research. 2011; 303(1):1-10.
Received on 08.01.2022 Modified on 14.02.2022
Accepted on 10.03.2022 © RJPT All right reserved
Research J. Pharm.and Tech 2022; 15(3):1385-1392.
DOI: 10.52711/0974-360X.2022.00231